Contribution of DOCK11 to the Expansion of Antigen-Specific Populations among Germinal Center B Cells

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Contribution of DOCK11 to the Expansion of Antigen-Specific
Populations among Germinal Center B Cells
Akihiko Sakamoto and Mitsuo Maruyama

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ImmunoHorizons 2020, 4 (9) 520-529
doi: https://doi.org/10.4049/immunohorizons.2000048
http://www.immunohorizons.org/content/4/9/520
This information is current as of January 30, 2022.

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ISSN 2573-7732.
RESEARCH ARTICLE

                                                                                                                                     Adaptive Immunity

Contribution of DOCK11 to the Expansion of Antigen-Specific
Populations among Germinal Center B Cells
Akihiko Sakamoto* and Mitsuo Maruyama*†
*Department of Mechanism of Aging, National Center for Geriatrics and Gerontology, Obu, Aichi 474-8511, Japan; and †Department of Aging
Research, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan

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ABSTRACT
Germinal centers (GCs) are a structure in which B cell populations are clonally expanded, depending on their affinities to Ag. Although
we previously isolated a characteristic protein called dedicator of cytokinesis 11 (DOCK11) from GC B cells, limited information is
available on the roles of DOCK11 in GC B cells. In this study, we demonstrate that DOCK11 may contribute to the expansion of Ag-
specific populations among GC B cells upon immunization of mice. The lack of DOCK11 in B cells resulted in the lower frequency of
Ag-specific GC B cells along with enhanced apoptosis upon immunization. Under competitive conditions, DOCK11-deficient B cells
were dramatically prevented from participating in GCs, in contrast to DOCK11-sufficient B cells. However, minor impacts of the
DOCK11 deficiency were identified on somatic hypermutations. Mechanistically, the DOCK11 deficiency resulted in the suppression
of B cell–intrinsic signaling in vitro and in vivo. Although DOCK11 expression by B cells was required for the induction of T follicular
helper cells at the early stages of immune responses, minor impacts were identified on the expansion of Ag-specific populations
among GC B cells. Thus, DOCK11 appears to contribute to the expansion of Ag-specific populations among GC B cells through the
stimulation of B cell–intrinsic signaling. ImmunoHorizons, 2020, 4: 520–529.

INTRODUCTION                                                                           rho family GTPase cell division cycle 42 (CDC42), resulting in
                                                                                       cytoskeletal reorganization (13, 14). Because the cytoskeleton plays
Germinal centers (GCs) are a structure in which B cell populations                     an important role in humoral immune responses (15–18), DOCK11,
are clonally expanded, depending on their affinities to Ag (1–4).                        similar to CDC42 (19–22), may play some roles in B cells.
Upon Ag binding, B cells are activated and proliferate to form GCs.                        Among DOCK-D family proteins (23–25), DOCK10 and
Ig genes are somatically hypermutated, resulting in the generation                     DOCK11 are expressed by B cells (12, 26). We and other groups
of BCR with high affinities to Ag. High-affinity B cell clones are                         previously reported that the lack of DOCK10 caused mild to no
selectively expanded with help from T follicular helper (Tfh) cells                    defects in the development of B cells or humoral immune
(5–11). Thus, GCs are an important structure for the selection of                      responses (26–29). Similarly, the lack of DOCK11 caused only
high-affinity B cell clones.                                                             mild, if any, defects in the development of B cells (28). Limited
    We previously isolated a characteristic protein called dedicator                   information is currently available on the roles of DOCK11 in
of cytokinesis 11 (DOCK11, also known as Zizimin2) from GC B cells                     humoral immune responses, including the clonal expansion of GC
(12). As a guanine nucleotide exchange factor, DOCK11 activated the                    B cell populations.

Received for publication June 7, 2020. Accepted for publication August 13, 2020.
Address correspondence and reprint requests to: Dr. Mitsuo Maruyama, Department of Mechanism of Aging, National Center for Geriatrics and Gerontology, 7-430
Morioka-cho, Obu, Aichi 474-8511, Japan. E-mail address: michan@ncgg.go.jp
ORCID: 0000-0003-0788-3646 (A.S.).
This work was partially supported by research funding for longevity sciences from the National Center for Geriatrics and Gerontology (30-41 to A.S. and 29-26 and 19-1
to M.M.).
Abbreviations used in this article: AF, Alexa Fluor; Cg1, Cg1, IgG1 C region; CDC42, cell division cycle 42; CGG, chicken g globulin; DOCK11, dedicator of cytokinesis 11;
GC, germinal center; Igk, Ig L chain k; KO, knockout; NP, 4-hydroxy-3-nitrophenylacetyl; Tfh, T follicular helper; VH186.2, IgH V region 186.2.
The online version of this article contains supplemental material.
This article is distributed under the terms of the CC BY-NC 4.0 Unported license.
Copyright © 2020 The Authors

520                                                                                                                  https://doi.org/10.4049/immunohorizons.2000048

ImmunoHorizons is published by The American Association of Immunologists, Inc.
ImmunoHorizons                                                         CONTRIBUTION OF DOCK11 TO Ag-SPECIFIC GC B CELLS             521

   In the current study, we examined the impact of the DOCK11           CD21/CD35 allophycocyanin (clone no. 7E9, 0.25 mg/ml; Bio-
deficiency on the formation of GC B cells upon immunization.             Legend), anti-CD23 PE (clone no. B3B4, 0.25 mg/ml; BioLegend),
Because DOCK11 was found to contribute to the expansion of              anti-CD38 PE-Dazzle594 (clone no. 90, 0.5 mg/ml; BioLegend),
Ag-specific populations among GC B cells, the underlying                 anti-CD44 FITC (clone no. IM7, 0.63 mg/ml; BioLegend), anti-
mechanisms were examined in more detail.                                CD45R (B220) PE-Cy7 (clone no. RA3-6B2, 0.25 mg/ml; Bio-
                                                                        Legend), anti-CD45.1 (Ly5.1) FITC or allophycocyanin-Cy7
                                                                        (clone no. A20, 1.25 mg/ml; BioLegend), anti-CD45.2 (Ly5.2)
MATERIALS AND METHODS                                                   Brilliant Violet 605 (clone no. 104, 0.25 mg/ml; BioLegend),
                                                                        anti-CD62L Alexa Fluor (AF) 700 (clone no. MEL-14, 0.63 mg/ml;
Mice                                                                    BioLegend), anti-CD95 allophycocyanin (clone no. REA453,
All mice were maintained on a C57BL/6 background under specific          0.15 mg/ml; Miltenyi Biotec), anti-CD185 (CXCR5) biotin
pathogen-free conditions. Dock11 knockout (KO) (28), Cd19-Cre           (clone no. L138D7, 1.25 mg/ml; BioLegend), anti-CD279 (PD1)
(30), IgG1 C region (Cg1)-Cre (31), Dock11 flox (28), Cdc42 flox (32),    PE (clone no. 29F.1A12, 0.5 mg/ml; BioLegend), anti-Foxp3 AF 647
and B1-8f mice (33) were described previously. Ly5.1 mice were          (clone no. MF23, 0.5 mg/ml; BD Biosciences), anti-IgG1 FITC or BV605
obtained from Sankyo Labo Service (Tsukuba, Japan). Dock10 flox          (clone no. A85-1, 0.5 mg/ml; BD Biosciences), anti-IgG1 PE-

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mice were recovered from frozen embryos by the German                   Dazzle594 (clone no. RMG1-1, 0.5 mg/ml; BioLegend), anti-Igk AF
Research Center for Environmental Health (Neuherberg,                   700 (clone no. RMK-45, 1.25 mg/ml; BioLegend), antiphosphorylated
Germany) and backcrossed to C57BL/6 mice for more than                  Bruton tyrosine kinase (BTK) (Y223) BV421 (clone no. N35-86,
10 generations. Each genotype was elucidated by PCR. All                1:400; BD Biosciences), antiphosphorylated spleen tyrosine kinase
animal experiments were performed using 2- to 4-mo-old male             (SYK) (Y352) PE (clone no. 17A/P-ZAP70, 1:400; BD Biosciences),
and female mice with the approval of the Institutional Review           Ghost Dye Red 780 (1:1000; Tonbo Biosciences), NP23 PE (0.5 mg/ml;
Board at the National Center for Geriatrics and Gerontology.            LGC Biosearch Technologies), propidium iodide (1 mg/ml; Sigma-
                                                                        Aldrich), streptavidin Brilliant Violet 605 (0.25 mg/ml; Bio-
Immunization                                                            Legend), and Zombie NIR (1:1000; BioLegend). Apoptotic cells
Primary immunization was performed by an i.p. injection of 50 mg        were identified using a CaspGLOW fluorescein active caspase
of 4-hydroxy-3-nitrophenylacetyl (NP) coupled to Ficoll (NP53-Ficoll;   staining kit (BioVision, Milpitas, CA). Intracellular staining
LGC Biosearch Technologies, Teddington, Middlesex, U.K.),               was performed using a Foxp3/transcription factor staining
100 mg of alum-precipitated chicken g globulin (CGG) (Calbiochem,       buffer set (Thermo Fisher Scientific, Waltham, MA), according
currently Sigma-Aldrich, St. Louis, MO), or 100 mg of alum-             to the manufacturer’s instructions. A flow cytometric analysis was
precipitated NP33-CGG (LGC Biosearch Technologies). Secondary           performed on a Gallios cytometer (Beckman Coulter, Indianapolis,
immunization was performed by an i.p. injection of 50 mg of             IN) equipped with a bandpass filter (605BP30; Omega Optical,
NP33-CGG.                                                               Brattleboro, VT). Cell sorting was performed on a FACSAria II
                                                                        cytometer (BD Biosciences).
MACS
A single-cell suspension was prepared by passing tissues through
                                                                        Quantitative RT-PCR
a 100-mm nylon cell strainer. RBC lysis was performed in lysis
                                                                        RNA was extracted with a TRI reagent (Molecular Research
buffer (150 mM NH4Cl, 14 mM NaHCO3, and 2 mM EDTA). To
                                                                        Center, Cincinnati, OH), followed by reverse transcription to
isolate B cells, cells were incubated with anti-CD43 microbeads
                                                                        cDNA with ReverTra Ace transcriptase (Toyobo, Osaka, Japan).
(Miltenyi Biotec, Bergisch Gladbach, Germany). More than 90%
                                                                        Quantitative PCR was performed using a THUNDERBIRD SYBR
purity was achieved, as measured by flow cytometry. To enrich GC
                                                                        mix (Toyobo). The primers used were as follows: 59-GCTTGACAG
B cells, cells were incubated with anti-CD4 biotin (clone no. GK1.5,
                                                                        CATGGCCAAAA-39 and 59-AACGCTGAACACCCACTAGG-39 for
0.63 mg/ml; BioLegend, San Diego, CA), anti-CD8a biotin (clone
                                                                        Dock11 (34); 59-TAGTGCCACCTCCTGCTCACT-39 and 59-
no. 53-6.7, 1:800; Tonbo Biosciences, San Diego, CA), anti–TER-119
                                                                        CAACAATTCCACGTGGCAGCC-39 for Aicda (35); and 59-AGT
biotin (clone no. TER-119, 0.63 mg/ml; BioLegend), anti-CD38 biotin
                                                                        CCCTGCCCTTTGTACACA-39 and 59-GATCCGAGGGCCTCACTA
(clone no. 90, 1.25 mg/ml; BD Biosciences, San Jose, CA), and, in
                                                                        AAC-39 for 18S ribosomal RNA (34). All samples were run in
some cases, anti–Ig L chain k (Igk) biotin (clone no. RMK-12,
                                                                        duplicate on a PikoReal real-time PCR system (Thermo Fisher
1.25 mg/ml; BioLegend) and anti-CD45.1 (Ly5.1) biotin (clone
                                                                        Scientific). The DD cycle threshold method was applied for the
no. A20, 1.25 mg/ml; BioLegend), followed by an incubation
                                                                        relative quantification of RNA expression levels.
with antibiotin microbeads (Miltenyi Biotec).

Flow cytometry                                                          Preparation of NP-BSA
The following Abs and reagents were used for flow cytometry:             For ELISA of anti-NP Abs, varied concentrations of 4-hydroxy-3-
anti-BCL6 BV421 (clone no. K112-91, 1:400; BD Biosciences), anti-       nitrophenylacetic acid succinimide ester (LGC Biosearch Tech-
CD4 PE-Cy7 (clone no. GK1.5, 0.25 mg/ml; BioLegend), anti-CD19          nologies) were conjugated to BSA, according to the manufacturer’s
allophycocyanin-Cy7 (clone no. 6D5, 0.25 mg/ml; BioLegend), anti-       instructions. The resultant NP-BSA conjugates were purified

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522    CONTRIBUTION OF DOCK11 TO Ag-SPECIFIC GC B CELLS                                                                     ImmunoHorizons

through a PD-10 desalting column (Cytiva, Marlborough, MA). The        follicular B cells. Naive follicular B cells were isolated from spleens
conjugation ratio was determined by the absorbance value at 430 nm.    of naive mice (Supplemental Fig. 1A). B1-8 IgH forms an NP-
                                                                       specific BCR when combined with an Ig L chain l (39). To obtain
ELISA                                                                  Ag-specific GC B cells, B1-8 IgH-carrying mice (33) were i.p.
Serum was collected from mice under anesthesia with isoflurane.         immunized with alum-precipitated NP-CGG. NP-specific IgG1+
For sandwich ELISA, 96-well plates were coated with 2 mg/ml            GC B cells were then isolated from spleens (Supplemental Fig. 1B).
NP20-BSA or NP4-BSA. Serially diluted samples were loaded,             The isolation of GC B cells was confirmed by the upregulation
followed by incubations with 1 mg/ml anti-IgG1 biotin (clone no.       of activation-induced cytidine deaminase (40) (Fig. 1A). In
A85-1; BD Biosciences) and streptavidin HRP (1:3000; Cytiva).          contrast, the expression levels of DOCK11 in NP-specific IgG1+ GC
Color development was performed with tetramethylbenzidine              B cells were decreased to 27% of those in naive follicular B cells
and stopped by acidification. Absorbance at 450 nm was measured         (Fig. 1B).
on a 680 microplate reader (Bio-Rad Laboratories, Hercules, CA).
Dose-response curves were analyzed, using R software (R Founda-        Impact of the DOCK11 deficiency on the frequency of
tion for Statistical Computing, Vienna, Austria) (36). Ab concentra-   Ag-specific GC B cells
tions were determined, based on the EC50 values of dilution factors.   Although DOCK11 was originally isolated from GC B cells (12), the

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N1G9 anti-NP IgG1 (37) was used as a standard.                         expression levels of DOCK11 were rather downregulated in GC
                                                                       B cells as compared with those in naive follicular B cells. Thus,
Adoptive transfer                                                      DOCK11 seemed to be dispensable in GC B cells. To examine
B1-8 IgH-bearing B cells were isolated by MACS using spleens           whether the remaining expression of DOCK11 is still required in
pooled from three or more mice. The numbers of NP-binding cells        GC B cells, we generated mice lacking DOCK11 in B cells. Dock11
were enumerated by flow cytometry. Adoptive transfer was                flox mice (28) were crossed with Cd19-Cre mice (30). After
performed by an i.v. injection of B cells, including 1 3 105 of NP-
specific cells per recipient.

BCR sequencing
BCR sequencing was performed, as previously described (38), with
some modifications. Briefly, NP-specific IgG1+ GC B cells were
single-cell sorted into 10 ml of RNase-free water containing 50 ng
of carrier RNA (Thermo Fisher Scientific). Gene segments of IgH
V region 186.2 (VH186.2) linked to Cg1 were amplified, using a
SuperScript IV one-step RT-PCR system (Thermo Fisher Scientific).
Primers for nested PCR were as follows: 59-TTCTTGGCAGCAA
CAGCTACA-39 (VH186.2 sense), 59-GGATCCAGAGTTCCAGGT
CACT-39 (Cg1 external antisense), and 59-GGAGTTAGTTTGGG
CAGCAG-39 (Cg1 internal antisense).

Cell stimulation
To stimulate B cells, DMEM was supplemented with 10% heat-
inactivated FBS, 1 mM sodium pyruvate, 10 mM HEPES, 1%
nonessential amino acids, 100 U/ml penicillin, 100 mg/ml
streptomycin, and 52 mM 2-ME. B1-8 IgH-bearing B cells were
incubated at 37°C with or without 0.2 mg/ml NP53-Ficoll. The
stimulation was stopped by directly adding twice the volume of
ice-cold fixation/permeabilization working solution in a Foxp3/         FIGURE 1. Downregulation of DOCK11 in GC B cells.
transcription factor staining buffer set.                               The expression levels of activation-induced cytidine deaminase (A) and
Statistical analysis                                                   DOCK11 (B) by the indicated splenic B cells were measured by quan-
Statistical analyses were performed using R software. A p value        titative RT-PCR and normalized to those of 18S ribosomal RNA. GC B
,0.05 was considered to be significant.                                 cells were isolated from the spleens of B1-8 IgH-carrying mice 14 d
                                                                       postimmunization with alum-precipitated NP-CGG. Gating strategies
                                                                       for naive follicular B cells (B220+CD19+CD23+CD21–) and NP-specific
RESULTS                                                                IgG1+ GC B cells (B220+CD19+CD95+CD38–NP+IgG1+Igk–) are shown
                                                                       in Supplemental Fig. 1A, 1B, respectively. Each symbol represents an
Downregulation of DOCK11 in GC B cells                                 individual mouse. Horizontal lines represent geometric means. Data are
To identify the roles of DOCK11 in GC B cells, we compared the         pooled from two independent experiments, using six or more mice per
expression levels of DOCK11 in GC B cells with those in naive          experimental group. ***p , 0.001, **p , 0.01 (Welch t test).

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ImmunoHorizons                                                              CONTRIBUTION OF DOCK11 TO Ag-SPECIFIC GC B CELLS                523

immunization with NP-CGG, the numbers of NP-specific
IgG1+ GC B cells were enumerated by flow cytometry (Fig.
2A). NP-specific IgG1 + GC B cells were similarly formed to

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                                                                             FIGURE 3. Impact of the DOCK11 deficiency after the B cell
                                                                             activation stage.
                                                                             (A) Numbers of NP-specific and whole IgG1 + GC B cells
                                                                             (B220+CD19+CD95+CD38–IgG1+) in the spleens of the indicated strains
                                                                             14 d postimmunization with NP-CGG. Each symbol represents an in-
                                                                             dividual mouse. Horizontal lines represent geometric means. Data are
                                                                             pooled from four independent experiments, using eight or more mice
                                                                             per experimental group. (B) Frequencies of NP-specific cells among
                                                                             IgG1+ GC B cells in (A). (C) Levels of NP-specific IgG1 in serum of the
                                                                             indicated strains 14 d postimmunization with NP-CGG, as measured by
                                                                             ELISA. Each symbol represents an individual mouse. Horizontal lines
                                                                             represent means. Data are pooled from two independent experiments,
                                                                             using nine or more mice per experimental group. **p , 0.01, *p , 0.05
                                                                             (Welch t test). cKO, conditional KO.
FIGURE 2. Impact of the DOCK11 deficiency on the specificity of
GC B cells.
(A) Gating strategies for NP-specific IgG1+ GC B cells. The left contour
plots are gated on B220+ cells. Numbers show the percentages of cells        the levels of those in Cd19-Cre mice (Fig. 2B). In contrast, the
in each gate. (B) Numbers of NP-specific and whole IgG1+ GC B cells          frequencies of NP-specific cells among IgG1 + GC B cells were
(B220+CD19+CD95+CD38–IgG1+) in the spleens of the indicated strains          decreased in DOCK11-deficient mice (Fig. 2C). Thus, the
14 d postimmunization with NP-CGG. Each symbol represents an individual      DOCK11 deficiency appeared to affect the frequency of Ag-
mouse. Horizontal lines represent geometric means. Data are pooled from      specific populations among GC B cells.
three independent experiments, using eight or more mice per experimental         The frequencies of Ag-specific GC B cells were further
group. (C) Frequencies of NP-specific cells among IgG1+ GC B cells in (B).   examined using mice lacking other DOCK11-related proteins,
(D) Gating strategies for apoptotic cells among NP-specific IgG1+ GC B       including another DOCK-D family protein DOCK10 and the
cells. The contour plots are gated on B220+CD19+CD95+CD38–NP+IgG1+           DOCK11 substrate CDC42 (12, 14). Dock10 and Cdc42 flox mice
cells. Numbers show the percentages of cells in each gate. (E) Frequencies   (32) were crossed with Cd19-Cre mice. After immunization with
of apoptotic cells among NP-specific IgG1+ GC B cells in (D). Each symbol    NP-CGG, NP-specific IgG1+ GC B cells were similarly formed in
represents an individual mouse. Horizontal lines represent means. Data are   these mice (Supplemental Fig. 2A). The frequencies of NP-specific
pooled from two independent experiments, using four or more mice per         cells among IgG1+ GC B cells were decreased in CDC42-deficient
experimental group. *p , 0.05 (Welch t test). cKO, conditional KO.           mice but not in DOCK10-deficient mice (Supplemental Fig. 2B).

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524    CONTRIBUTION OF DOCK11 TO Ag-SPECIFIC GC B CELLS                                                                          ImmunoHorizons

 A                                                                       Collectively, the DOCK11-CDC42 axis may contribute to the
                                                                         frequency of Ag-specific GC B cells.
                                                                             We then examined the impact of the DOCK11 deficiency on
                                                                         the apoptosis of Ag-specific GC B cells. Apoptotic cells were
                                                                         identified by binding of a fluorophore-conjugated VAD-FMK
                                                                         inhibitor to activated caspases (Fig. 2D). After immunization of
                                                                         DOCK11-deficient mice with NP-CGG, NP-specific IgG1+ GC
                                                                         B cells contained larger numbers of apoptotic cells than those
 B                                                C                      from Cd19-Cre mice (Fig. 2E). Thus, DOCK11 may be required
                                                                         for the survival of Ag-specific GC B cells.

                                                                         Impact of the DOCK11 deficiency after the B cell
                                                                         activation stage
                                                                         We then investigated the stage at which the DOCK11 deficiency
                                                                         may affect the frequency of Ag-specific GC B cells. Cg1-Cre mice

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                                                                         are a strain in which the expression of Cre recombinase is induced
                                                                         by transcription of the Cg1 (31). Reflecting the finding that Ig class-
 D                                                E                      switching starts as early as the B cell activation stage (41), Cre-mediated
                                                                         recombination occurs within a few days after immunization
                                                                         (31). Therefore, by crossing Dock11 flox mice with Cg1-Cre mice
                                                                         instead of Cd19-Cre mice, one would be able to examine the
                                                                         impact of the DOCK11 deficiency in GC B cells while DOCK11
                                                                         expression is maintained in naive B cells. After immunization of
                                                                         the resultant mice with NP-CGG, NP-specific IgG1+ GC B cells
                                                                         were similarly formed to the levels of those in Cg1-Cre mice
                                                                         (Fig. 3A). In contrast, the frequencies of NP-specific cells among
 F                        G                                              IgG1+ GC B cells were decreased in mice lacking DOCK11 by Cg1-
                                                                         Cre recombinase (Fig. 3B). These results indicate that the lack
                                                                         of DOCK11 after the B cell activation stage still affects the
                                                                         frequency of Ag-specific populations among GC B cells.
                                                                             We next examined whether the serum Abs were reflected by
                                                                         the frequency of Ag-specific GC B cells. After immunization with
FIGURE 4. Impact of the DOCK11 deficiency on the expansion of            NP-CGG, serum levels of both high- and low-affinity Abs were
Ag-specific populations among GC B cells.                                decreased in mice lacking DOCK11 by Cg1-Cre recombinase (Fig.
(A) Experimental outline to examine the impact of the DOCK11 de-         3C). Additionally, the ratios between the levels of high- and low-
ficiency on the selection of GC B cells. (B) Contour plots showing       affinity Abs were also decreased, suggesting that DOCK11
donor-derived NP-specific cells (B220+CD38+CD95–NP+Ly5.1–) among         expression after the B cell activation stage may contribute to
naive B cells from mice given transfers with B1-8 IgH-bearing B cells    the affinity maturation of Abs.
of the indicated Dock11 genotypes. Contour plots are gated on
B220+CD38+CD95– cells. Detailed gating strategies are shown in           Impact of the DOCK11 deficiency on the expansion of
Supplemental Fig. 3B. Numbers show the percentages of cells in each      Ag-specific populations among GC B cells
gate. (C) Frequencies of donor-derived NP-specific cells among           The specificities of GC B cells are assessed through competition
naive B cells in (B). Each symbol represents an individual mouse.        among B cell clones (3). Because DOCK11 appeared to contribute to
Horizontal lines represent means. Data are from four independent
experiments, using five or more mice per experimental group. (D)         independent experiments, using five mice per experimental group. (F)
Contour plots showing donor-derived NP-specific IgG1+ GC B cells         Frequencies of B cell clones carrying the indicated numbers of nucleotide
(B220+CD38–CD95+NP+IgG1+Ly5.2+Ly5.1–) from mice given the                mutations on the VH186.2 region among donor-derived NP-specific IgG1+
transfer with the B1-8 IgH-bearing B cells of the indicated Dock11       GC B cell clones in (E). Numbers in the centers represent the numbers of
genotypes, followed by an immunization with NP-CGG. Contour              clones sequenced. Means and SEM of the nucleotide mutations are shown
plots are gated on B220+CD38–CD95+NP+IgG1+ cells. Detailed gating        below the pie chart. p = 0.070 (Welch t test). (G) Frequencies of high-
strategies are shown in Supplemental Fig. 3C. Numbers show the per-      affinity clones carrying a W33L mutation among donor-derived NP-
centages of cells in each gate. (E) Frequencies of donor-derived cells   specific IgG1+ GC B cell clones in (E). Numbers in the centers represent
among NP-specific IgG1+ GC B cells in (D). Each symbol represents an     the numbers of clones sequenced. p = 0.38 (Fisher exact test). ***p , 0.001
individual mouse. Horizontal lines represent means. Data are from two    (Welch t test). WT, wild-type.

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ImmunoHorizons                                                             CONTRIBUTION OF DOCK11 TO Ag-SPECIFIC GC B CELLS                  525

the frequency of Ag-specific GC B cells, we examined the impact of           derived NP-specific IgG1+ GC B cells described above were single-
the DOCK11 deficiency on the competition among B cell clones. To             cell sorted, followed by sequencing of the VH186.2 region, a region
generate DOCK11-deficient B cells with specificity to NP, Dock11              corresponding to specificity to NP (42, 43). Although statistical
KO mice (28) were crossed with B1-8 IgH-carrying mice. As a                 significance was not identified (p = 0.070 in Welch t test), smaller
source of a DOCK11-sufficient control, B1-8 IgH-carrying mice                 numbers of mutations were accumulated among DOCK11-
were used. The numbers of NP-specific B cells were enumerated                deficient GC B cells (Fig. 4F). Similarly, smaller numbers of
by flow cytometry (Supplemental Fig. 3A). B cells from these mice,           high-affinity clones with a W33L mutation (42) were identified
including 1 3 105 of NP-specific cells, were transferred into                among DOCK11-deficient GC B cells, as compared with those
congenic wild-type mice (Fig. 4A). The resultant chimeras would             among DOCK11-sufficient counterparts (Fig. 4G). However, no
contain donor-derived NP-specific B cells with or without DOCK11             statistical significance was identified (p = 0.38 in Fisher exact test).
expression and endogenous DOCK11-sufficient B cells. NP-specific               Thus, the impact of the DOCK11 deficiency on somatic hyper-
B cells accounted for 0.06% of splenocytes, irrespective of DOCK11          mutations, if any, may be minor.
expression on the transferred cells (Fig. 4B, 4C, Supplemental
Fig. 3B). After immunization with NP-CGG, DOCK11-sufficient                   Impact of the DOCK11 deficiency on
donor cells accounted for 89% of NP-specific IgG1+ GC B cells                B cell–intrinsic signaling

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(Fig. 4D, Supplemental Fig. 3C). In contrast, DOCK11-deficient               DOCK11 was found to contribute to the expansion of Ag-specific
counterparts accounted for only 15% of NP-specific IgG1+ GC                  populations among GC B cells in a cell-intrinsic manner. To
B cells (Fig. 4E). Thus, DOCK11-deficient clones were outcompeted            examine the impact of the DOCK11 deficiency on B cell–intrinsic
by endogenous DOCK11-sufficient clones in a B cell–intrinsic manner.          signaling (44), splenic B cells were isolated from B1-8 IgH-carrying
    Ig genes are somatically hypermutated in GCs, contributing to           naive mice or DOCK11-deficient counterparts, followed by stimula-
the generation of high-affinity B cell clones. To examine the impact          tion with T cell–independent type II Ag NP-Ficoll. In DOCK11-
of the DOCK11 deficiency on somatic hypermutations, the donor-               sufficient B cells, the stimulation induced the phosphorylation of

FIGURE 5. Impact of the DOCK11 deficiency on B cell–intrinsic signaling.
(A) Histograms of B1-8 IgH-bearing B cells (wild type [WT]) or DOCK11-deficient counterparts (KO) expressing the indicated phosphorylated (p)
kinases after the stimulation with or without NP-Ficoll for 5 min. Histograms are gated on B220+Igk– cells. (B) Mean fluorescence intensity (MFI) for
the indicated phosphorylated kinases after the stimulation with NP-Ficoll in (A). Each symbol represents an individual mouse from which B cells
were isolated. Horizontal lines represent means. Data are pooled from two independent experiments, using six or more mice per experimental
group. (C) Gating strategies for NP-specific B cells with GC phenotypes. The left contour plot is gated on CD19+ cells. Numbers show the
percentages of cells in each gate. (D and E) Numbers of NP-specific GC-like B cells (D) and frequencies of GC-like cells among NP-specific B cells
(E) in spleens from B1-8 IgH-carrying mice (WT) or DOCK11-deficient counterparts (KO) 7 d postimmunization with NP-Ficoll. Each symbol
represents an individual mouse. Horizontal lines represent geometric means (D) and means (E). Data are pooled from two independent experiments,
using six to seven mice per experimental group. **p , 0.01, *p , 0.05 (Welch t test).

https://doi.org/10.4049/immunohorizons.2000048
526       CONTRIBUTION OF DOCK11 TO Ag-SPECIFIC GC B CELLS                                                                             ImmunoHorizons

kinases, including SYK and BTK (Fig. 5A, 5B). In contrast, the                    in DOCK11-deficient mice. Collectively, DOCK11 may contribute to
phosphorylation of these kinases was suppressed in DOCK11-                        B cell–intrinsic signaling in vitro and in vivo.
deficient B cells. Thus, the DOCK11 deficiency appeared to
suppress B cell–intrinsic signaling in vitro.                                     Contribution of DOCK11 expression by B cells to the
    The impact of the DOCK11 deficiency was then examined in                       induction of Tfh cells
vivo. B1-8 IgH-carrying mice or DOCK11-deficient counterparts                      B cell–intrinsic signaling appeared to be responsible for the
were i.p. immunized with NP-Ficoll. As previously reported (45),                  impaired expansion of Ag-specific populations among GC B cells in
NP-specific B cells with GC phenotypes were induced in the                         DOCK11-deficient mice. However, the selection of GC B cells is
spleens of DOCK11-sufficient mice (Fig. 5C–E). However, the                         generally dependent on help from Tfh cells (46–48). Therefore, we
numbers and frequencies of these GC-like B cells were decreased                   examined the impact of the DOCK11 deficiency on the induction of
                                                                                  Tfh cells. B cell–specific DOCK11-deficient mice and Cd19-Cre
                                                                                  mice as a control were immunized with NP-CGG. The numbers of
                                                                                  Tfh cells were enumerated in the spleens of these mice (Fig. 6A).
                                                                                  The numbers (Fig. 6B) and frequencies of Tfh cells (Fig. 6C) were
                                                                                  both lower in DOCK11-deficient mice than in Cd19-Cre mice. In

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                                                                                  contrast, similar numbers and frequencies of CD4+ effector T cells
                                                                                  were identified in these mice (Supplemental Fig. 4). These results
                                                                                  suggest that DOCK11 expression by B cells is required for the
                                                                                  differentiation of Tfh cells among Th cells.
                                                                                      To further examine at which stage the induction of Tfh cells
                                                                                  was influenced, mice lacking DOCK11 expression by Cg1-Cre
                                                                                  recombinase were used. As mentioned above, DOCK11 expression
                                                                                  would start to be deleted at the B cell activation stage (31). Cg1-Cre
                                                                                  mice were used as a control. After immunization with NP-CGG,
                                                                                  Tfh cells were similarly formed in these mice (Fig. 6D, 6E). Given
                                                                                  the timing of the induction of Cg1-Cre recombinase (31), these
                                                                                  results indicate that DOCK11 expression by B cells is required for
                                                                                  the induction of Tfh cells at the early stages of immune responses.

                                                                                  Impact of decreased Tfh cells on the expansion of
                                                                                  Ag-specific GC B cells
                                                                                  Because the induction of Tfh cells was suppressed in DOCK11-
                                                                                  deficient mice, we examined the competition of GC B cell clones in
                                                                                  these mice. B cell–specific DOCK11-deficient mice and Cd19-Cre
                                                                                  mice as a control were immunized with alum-precipitated CGG,
                                                                                  followed by the transfer of naive B cells from B1-8 IgH-carrying
                                                                                  congenic mice (Fig. 7A). Before secondary immunization, 3–4% of
                                                                                  NP-specific cells were identified among the transferred cells (Fig.
                                                                                  7B, 7C). Because GCs are an open structure (49, 50), Ag-specific
                                                                                  naive B cells potently participate in ongoing GC reactions (51).
                                                                                  After the secondary immunization of Cd19-Cre recipients with
                                                                                  NP-CGG, NP-specific cells accounted for 87% of donor-derived
                                                                                  IgG1+ GC B cells (Fig. 7D, 7E). Although the frequencies of
FIGURE 6. Contribution of DOCK11 expression by B cells on the                     NP-specific cells were significantly decreased to 79% in DOCK11-
induction of Tfh cells.                                                           deficient recipients, the difference may be minor. Thus, although
(A) Gating strategies for Tfh cells (CD4+CD44+CD62L–CXCR5+FoxP3–)                 the induction of Tfh cells was suppressed in DOCK11-deficient
or PD1+BCL6high    (hi)
                          Tfh cells. The leftmost contour plots are gated on      mice (Fig. 6B, 6C), the impact on the competition of GC B cell
      +
CD4 cells. Numbers show the percentages of cells in each gate. (B and             clones, if any, appeared to be minor.
D) Numbers of Tfh and PD1+BCL6hi Tfh cells in the spleens of the                      High-affinity B cell clones are selectively expanded with help
indicated strains 14 d postimmunization with NP-CGG. Each symbol                  from limited numbers of Tfh cells (46–48). Because the formation
represents an individual mouse. Horizontal lines represent geometric              of Tfh cells was suppressed in DOCK11-deficient mice, the expansion
means. Data are pooled from three independent experiments, using                  of B cell clones was examined in these mice. The donor-derived NP-
three or more mice per experimental group. (C and E) Frequencies                  specific IgG1+ GC B cells described above were single-cell sorted,
of Tfh and PD1+BCL6hi Tfh cells among CD4+ T cells in (B) and (D).                followed by sequencing of the VH186.2 region. Although slightly
**p , 0.01, *p , 0.05 (Welch t test). cKO, conditional KO; i.c., intracellular.   smaller numbers of mutations accumulated in donor-derived GC

                                                                                                           https://doi.org/10.4049/immunohorizons.2000048
ImmunoHorizons                                                             CONTRIBUTION OF DOCK11 TO Ag-SPECIFIC GC B CELLS                 527

                         A                                                  B

                         C                       E

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                         D                                                                      F

                                                                                                G

FIGURE 7. Impact of decreased Tfh cells on the expansion of Ag-specific GC B cells.
(A) Experimental outline to examine the impact of decreased Tfh cells in DOCK11-deficient mice on the selection of Ag-specific cells among
transferred congenic B cells. (B) Gating strategies for NP-specific cells (B220+CD95–Ly5.1+NP+IgG1–) among transferred B cells. The left contour
plot is gated on B220+ cells. Numbers show the percentages of cells in each gate. (C) Frequencies of NP-specific cells among transferred B cells 1 d
posttransfer into the indicated recipients that were immunized with alum-precipitated CGG 14 d before. Each symbol represents an individual
mouse. Horizontal lines represent means. Data are pooled from three independent experiments, using five mice per experimental group. (D) Gating
strategies for NP-specific IgG1+ GC B cells derived from transferred B cells (B220+CD95+Ly5.1+NP+IgG1+). The leftmost contour plot is gated on
B220+ cells. Numbers show the percentages of cells in each gate. (E) Frequencies of NP-specific cells among donor-derived IgG1+ GC B cells 7 d
postsecondary immunization of the indicated recipients with NP-CGG. Each symbol represents an individual mouse. Horizontal lines represent
means. Data are pooled from two independent experiments, using six mice per experimental group. (F) Frequencies of B cell clones carrying the
indicated numbers of nucleotide mutations on the VH186.2 region among donor-derived NP-specific IgG1+ GC B cell clones in (E). Numbers in the
centers represent the numbers of clones sequenced. Means and SEM of the nucleotide mutations are shown below the pie chart. p = 0.42 (Welch
t test). (G) Frequencies of high-affinity clones carrying a W33L mutation among donor-derived NP-specific IgG1+ GC B cell clones in (E). Numbers
in the centers represent the numbers of clones sequenced. p = 0.90 (Fisher exact test). **p , 0.01 (Welch t test).

B cells from DOCK11-deficient recipients (Fig. 7F), similar changes          appeared to be required for the survival of Ag-specific GC B cells.
did not always occur in the frequency of high-affinity clones with the        Through adoptive transfer experiments, DOCK11 was found to
W33L mutation (42) (Fig. 7G). Thus, although the induction of Tfh           contribute to the expansion of Ag-specific populations among
cells was suppressed in DOCK11-deficient mice, the maturation of             GC B cells in a cell-intrinsic manner. The DOCK11 deficiency
GC B cells was not affected as much as originally expected.                  resulted in the suppression of B cell–intrinsic signaling in vitro
                                                                            and in vivo. Although DOCK11 expression by B cells was required
DISCUSSION                                                                  for the induction of Tfh cells at the early stages of immune
                                                                            responses, minor impacts were identified on the expansion of
In this study, we examined the contribution of DOCK11 to                    Ag-specific populations among GC B cells. Thus, DOCK11 may
the expansion of Ag-specific populations among GC B cells.                   contribute to the expansion of Ag-specific populations among
Immunization of conditional KO strains revealed that DOCK11                 GC B cells through the stimulation of B cell–intrinsic signaling.

https://doi.org/10.4049/immunohorizons.2000048
528    CONTRIBUTION OF DOCK11 TO Ag-SPECIFIC GC B CELLS                                                                              ImmunoHorizons

    Although DOCK11 was originally isolated from GC B cells (12),        (Wakayama Medical University), A. Takaoka (Hokkaido University), T. Yasuda
DOCK11 expression was rather downregulated in GC B cells as              (Hiroshima University), and A. Nishikimi (National Center for Geriatrics and
                                                                         Gerontology) for helpful comments and discussion; and N. Ogiso, A. Furio,
compared with that in naive follicular B cells. In our previous
                                                                         H. Kawasaki, S. Matsubara (National Center for Geriatrics and Gerontology),
finding, the expression levels of DOCK11 in GC B cells were               and our colleagues for technical assistance.
higher than those in non-GC B cells from immunized mice (12).
Under this condition, non-GC B cells are comprised of varied
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