Peritoneal B-2 cells comprise a distinct B-2 cell population with B-1b-like characteristics

被引:55
作者
Hastings, William D.
Tumang, Joseph R.
Behrens, Timothy W.
Rothstein, Thomas L.
机构
[1] Boston Univ, Sch Med, Dept Microbiol, Boston, MA 02118 USA
[2] Boston Univ, Sch Med, Dept Med, Boston, MA 02118 USA
[3] Boston Univ, Med Ctr, Evans Mem Dept Clin Res, Immunobiol Unit, Boston, MA 02118 USA
[4] Univ Minnesota, Sch Med, Dept Med, Minneapolis, MN 55455 USA
[5] Univ Minnesota, Sch Med, Ctr Immunol, Minneapolis, MN 55455 USA
关键词
antibodies; B cells; cell differentiation; rodent;
D O I
10.1002/eji.200535142
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
B-1 and B-2 cells are lymphocyte populations that differ in development, surface marker expression, tissue localization, and function. Though mainly found in the spleen, lymph nodes, and circulation of mice, small numbers of B-2 cells are found in the peritoneal cavity, a site predominantly populated by B-1 cells. Here, we characterized peritoneal B-2 cells, and determined their relationship to B-1 cells. We found that peritoneal B-2 cells appear to be intermediate between splenic B-2 and peritoneal B-1 cells in terms of surface marker expression of B220, CD80, and CD43, expression of several marker genes, and in vitro viability and IgM secretion. Adoptive transfer of peritoneal B-2 cells into severe combined immunodeficiency mice resulted in the acquisition of a phenotype reminiscent of B-1b cells, as shown by up-regulation of Mac-1 and CD43, and downregulation of CD23. Moreover, adoptively transferred peritoneal B-2 cells recapitulated B-1 cell function by producing natural IgM in recipient mice. These data suggest that peritoneal B-2 cells express some characteristics of B-1b cells and that this similarity increases with additional time in the peritoneal cavity.
引用
收藏
页码:1114 / 1123
页数:10
相关论文
共 39 条
[1]   Identification of a precursor to phosphatidyl choline-specific B-1 cells suggesting that B-1 cells differentiate from splenic conventional B cells in vivo: Cyclosporin A blocks differentiation to B-1 [J].
Arnold, LW ;
McCray, SK ;
Tatu, C ;
Clarke, SH .
JOURNAL OF IMMUNOLOGY, 2000, 164 (06) :2924-2930
[2]   DEVELOPMENT OF B-1 CELLS - SEGREGATION OF PHOSPHATIDYL CHOLINE-SPECIFIC B-CELLS TO THE B-1 POPULATION OCCURS AFTER IMMUNOGLOBULIN GENE-EXPRESSION [J].
ARNOLD, LW ;
PENNELL, CA ;
MCCRAY, SK ;
CLARKE, SH .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (05) :1585-1595
[3]   B-1 and B-2 cell-derived immunoglobulin M antibodies are nonredundant components of the protective response to influenza virus infection [J].
Baumgarth, N ;
Herman, OC ;
Jager, GC ;
Brown, LE ;
Herzenberg, LA ;
Chen, JZ .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (02) :271-280
[4]  
BERLAND R, ANN REV IMMUNOL, V20, P253
[5]   A critical role of natural immunoglobulin M in immediate defense against systemic bacterial infection [J].
Boes, M ;
Prodeus, AP ;
Schmidt, T ;
Carroll, MC ;
Chen, JZ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (12) :2381-2386
[6]   A SEVERE COMBINED IMMUNODEFICIENCY MUTATION IN THE MOUSE [J].
BOSMA, GC ;
CUSTER, RP ;
BOSMA, MJ .
NATURE, 1983, 301 (5900) :527-530
[7]  
Casali P, 1996, CURR TOP MICROBIOL, V210, P167
[8]   B cell receptor signal strength determines B cell fate [J].
Casola, S ;
Otipoby, KL ;
Alimzhanov, M ;
Humme, S ;
Uyttersprot, N ;
Kutok, JL ;
Carroll, MC ;
Rajewsky, K .
NATURE IMMUNOLOGY, 2004, 5 (03) :317-327
[9]   A VH11Vκ9B cell antigen receptor drives generation of CD5+ B cells both in vivo and in vitro [J].
Chumley, MJ ;
Dal Porto, JM ;
Kawaguchi, S ;
Cambier, JC ;
Nemazee, D ;
Hardy, RR .
JOURNAL OF IMMUNOLOGY, 2000, 164 (09) :4586-4593
[10]   The unique antigen receptor signaling phenotype of B-1 cells is influenced by locale but induced by antigen [J].
Chumley, MJ ;
Dal Porto, JM ;
Cambier, JC .
JOURNAL OF IMMUNOLOGY, 2002, 169 (04) :1735-1743