Increased serum IgA in Fcα/μR-deficient mice on the (129 x C57BL/6) F1 genetic background

被引:6
作者
Kurita, Naoki [1 ]
Honda, Shin-ichiro [1 ]
Shibuya, Akira [1 ]
机构
[1] Univ Tsukuba, Grad Sch Comprehens Human Sci, Inst Basic Med Sci, Dept Immunol, Tsukuba, Ibaraki 3058575, Japan
关键词
Fc alpha/mu R; IgA; Peyer's patches; FDC; Germinal center; POLYMERIC IMMUNOGLOBULIN RECEPTOR; MUCOSAL SURFACES; IMMUNE-RESPONSES; EPITHELIAL-CELLS; TISSUES; ABSENCE; APRIL; GUT;
D O I
10.1016/j.molimm.2014.09.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fc alpha/mu R (CD351) is an Fc receptor for both IgA and IgM, which is abundantly expressed in the small intestine. However, the role of Fc alpha/mu R in the intestinal tissue is largely unknown. Here, we found that Fc alpha/mu R is highly expressed on follicular dendritic cells (FDCs) in Peyer's patches (PP) in the small intestine. Fc alpha/mu R-deficient mice on the (129 x C57BL/6) F1 background showed increased serum, but not fecal, IgA level in response to gut-oriented antigens. IgA(+) B cells were increased in PP, but not in the lamina propria, of Fc alpha/mu R-deficient mice, which was attenuated after reduction of commensal microbiota by oral treatment with antibiotics. Analyses of bone marrow chimeric mice, in which either FDCs or blood cells or both lack the expression of Fc alpha/mu R, suggested that FDCs, but not blood cells, were responsible for the increased serum IgA concentration in Fc alpha/mu R-deficient mice. Moreover, Fc alpha/mu R-deficient mice showed enhanced germinal center formation against commensal microbiota in PP. Thus, serum IgA production against gut-oriented antigens is negatively regulated by Fc alpha/mu R on FDCs in the F1 mice. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:367 / 372
页数:6
相关论文
共 28 条
[11]   The polymeric immunoglobulin receptor: bridging innate and adaptive immune responses at mucosal surfaces [J].
Kaetzel, CS .
IMMUNOLOGICAL REVIEWS, 2005, 206 :83-99
[12]   STRUCTURE AND FUNCTION OF IMMUNOGLOBULIN-A RECEPTORS ON PHAGOCYTIC-CELLS [J].
KERR, MA ;
MAZENGERA, RL ;
STEWART, WW .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1990, 18 (02) :215-217
[13]   The genotype of mice influences the autoimmune response to spliceosome proteins induced by cytomegalovirus gB immunization [J].
Lipes, J ;
Skamene, E ;
Newkirk, MM .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2002, 129 (01) :19-26
[14]   DCs induce CD40-independent immunoglobulin class switching through BLyS and APRIL [J].
Litinskiy, MB ;
Nardelli, B ;
Hilbert, DM ;
He, B ;
Schaffer, A ;
Casali, P ;
Cerutti, A .
NATURE IMMUNOLOGY, 2002, 3 (09) :822-829
[15]   Homeland Security: IgA immunity at the frontiers of the body [J].
Macpherson, Andrew J. ;
Geuking, Markus B. ;
McCoy, Kathy D. .
TRENDS IN IMMUNOLOGY, 2012, 33 (04) :160-167
[16]   IgA Fc receptors [J].
Monteiro, RC ;
van de Winkel, JGJ .
ANNUAL REVIEW OF IMMUNOLOGY, 2003, 21 :177-204
[17]   Role of retinoic acid in the imprinting of gut-homing IgA-secreting cells [J].
Mora, J. Rodrigo ;
von Andrian, Ulrich H. .
SEMINARS IN IMMUNOLOGY, 2009, 21 (01) :28-35
[18]   Recognition of commensal microflora by toll-like receptors is required for intestinal homeostasis [J].
Rakoff-Nahoum, S ;
Paglino, J ;
Eslami-Varzaneh, F ;
Edberg, S ;
Medzhitov, R .
CELL, 2004, 118 (02) :229-241
[19]   Fc receptors [J].
Ravetch, JV .
CURRENT OPINION IN IMMUNOLOGY, 1997, 9 (01) :121-125
[20]  
Sakamoto N, 2001, EUR J IMMUNOL, V31, P1310, DOI 10.1002/1521-4141(200105)31:5<1310::AID-IMMU1310>3.0.CO