Splenic and peritoneal B-1 cells differ in terms of transcriptional and proliferative features that separate peritoneal B-1 from splenic B-2 cells

被引:32
作者
Fischer, GM
Solt, LA
Hastings, WD
Yang, KJ
Gerstein, RM
Nikolajczyk, BS
Clarke, SH
Rothstein, TL
机构
[1] Boston Univ, Med Ctr, Dept Microbiol, Boston, MA 02118 USA
[2] Boston Univ, Med Ctr, Dept Med, Boston, MA 02118 USA
[3] Boston Univ, Med Ctr, Evans Mem Dept Clin Res, Boston, MA 02118 USA
[4] Univ Massachusetts, Sch Med, Dept Mol Genet & Microbiol, Worcester, MA 01655 USA
[5] Univ N Carolina, Dept Microbiol & Immunol, Chapel Hill, NC 27599 USA
关键词
B lymphocytes; CD5; transcription factors; cytokines; cellular proliferation;
D O I
10.1006/cimm.2001.1860
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
B-1 cells constitute a distinct B cell subset with characteristic phenotypic and functional features. B-1 cells are highly represented among peritoneal lymphocytes; substantial numbers of B-1 cells are also located within splenic tissue. Here a number of differences in transcription factor and gene expression were identified that separate peritoneal B-1 and splenic B-2 cells, and then splenic B-1 cells obtained from immunoglobulin transgenic mice were tested for these parameters. Splenic B-1 cells resembled splenic B-2 cells rather than peritoneal B-1 cells in terms of nuclear expression of DNA-binding STAT3, CREB, and PU.1, with respect to transcriptional activation of IL-10, and in the failure to enter cell cycle in response to PMA. Splenic B-1 cells (B-1S) appear to constitute a unique population of B-1 cells, which, while sharing with peritoneal B-1 cells (B-1P) certain phenotypic features, differ from them in transcription factor and gene expression and in signaling for cell cycle progression. (C) 2001 Elsevier Science.
引用
收藏
页码:62 / 71
页数:10
相关论文
共 79 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]   Role of Stat3 in lipopolysaccharide-induced IL-10 gene expression [J].
Benkhart, EM ;
Siedlar, M ;
Wedel, A ;
Werner, T ;
Ziegler-Heitbrock, HWL .
JOURNAL OF IMMUNOLOGY, 2000, 165 (03) :1612-1617
[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]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[7]   B-LYL CELLS - IMMORTAL LY-1+ LYMPHOCYTE-B CELL-LINES SPONTANEOUSLY ARISING IN MURINE SPLENIC CULTURES [J].
BRAUN, J ;
CITRI, Y ;
BALTIMORE, D ;
FOROUZANPOUR, F ;
KING, L ;
TEHERANIZADEH, K ;
BRAY, M ;
KLIEWER, S .
IMMUNOLOGICAL REVIEWS, 1986, 93 :5-21
[8]   ANTI-PHOSPHORYLCHOLINE ANTIBODIES OF THE T15 IDIOTYPE ARE OPTIMALLY PROTECTIVE AGAINST STREPTOCOCCUS-PNEUMONIAE [J].
BRILES, DE ;
FORMAN, C ;
HUDAK, S ;
CLAFLIN, JL .
JOURNAL OF EXPERIMENTAL MEDICINE, 1982, 156 (04) :1177-1185
[9]   Stat3 as an oncogene [J].
Bromberg, JF ;
Wrzeszczynska, MH ;
Devgan, G ;
Zhao, YX ;
Pestell, RG ;
Albanese, C ;
Darnell, JE .
CELL, 1999, 98 (03) :295-303
[10]   Stat3 activation is required for cellular transformation by v-src [J].
Bromberg, JF ;
Horvath, CM ;
Besser, D ;
Lathem, WW ;
Darnell, JE .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (05) :2553-2558