Gene expression profiling reveals a highly specialized genetic program of plasma cells

被引:74
作者
Underhill, GH
George, D
Bremer, EG
Kansas, GS
机构
[1] Northwestern Univ, Dept Immunol Microbiol, Chicago, IL 60611 USA
[2] Northwestern Univ, Dept Biomed Engn, Evanston, IL 60208 USA
[3] Northwestern Univ, Sch Med, Dept Neurol Surg, Pediat Brain Tumor Res Program, Chicago, IL 60611 USA
[4] Childrens Mem Inst Educ & Res, Chicago, IL USA
[5] Northwestern Univ, Sch Med, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
关键词
D O I
10.1182/blood-2002-08-2673
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The formation of terminally differentiated plasma cells represents the critical final step in B-cell differentiation. In this study, utilizing oligonucleotide microarray analysis, we describe the highly specialized genetic profile exhibited by terminally differentiated plasma cells. A total of 1476 known genes were differentially expressed by plasma cells compared with B cells. Plasma cells displayed an upregulation, induction, or a selective retention of a unique constellation of transcription factors, including members of the AP-1, nuclear factor-kappaB (NF-kappaB), nuclear factor of activated T cells (NFAT), and octamer binding factor families. Interestingly, plasma cells also displayed a downregulation of several RNA polymerase I-related factors, consistent with terminal differentiation, and exhibited a downregulation of the TATA box binding protein. Furthermore, plasma cells displayed alterations in multiple components of the Wnt and Notch signaling pathways and showed a unique pattern of apoptosis and proliferation-associated genes. Unexpectedly, plasma cells displayed an upregulation of 2 factors normally associated with microenvironmental positioning of neuronal cells, reelin and neuropilin-1. These results supply insight into the developmental genetics of plasma cell differentiation and provide a foundation for further analysis of plasma cell biology. (C) 2003 by The American Society of Hematology.
引用
收藏
页码:4013 / 4021
页数:9
相关论文
共 65 条
[1]   beta-catenin is a target for the ubiquitin-proteasome pathway [J].
Aberle, H ;
Bauer, A ;
Stappert, J ;
Kispert, A ;
Kemler, R .
EMBO JOURNAL, 1997, 16 (13) :3797-3804
[2]   An invitation to T and more: Notch signaling in lymphopoiesis [J].
Allman, D ;
Punt, JA ;
Izon, DJ ;
Aster, JC ;
Pear, WS .
CELL, 2002, 109 :S1-S11
[3]   Regulation of RNA polymerase I transcription in response to F9 embryonal carcinoma stem cell differentiation [J].
Alzuherri, HM ;
White, RJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (07) :4328-4334
[4]   Commitment of B lymphocytes to a plasma cell fate is associated with Blimp-1 expression in vivo [J].
Angelin-Duclos, C ;
Cattoretti, G ;
Lin, KI ;
Calame, K .
JOURNAL OF IMMUNOLOGY, 2000, 165 (10) :5462-5471
[5]   Glycosyltransferase activity of fringe modulates notch-delta interactions [J].
Brückner, K ;
Perez, L ;
Clausen, H ;
Cohen, S .
NATURE, 2000, 406 (6794) :411-415
[6]   Infectious susceptibility and severe deficiency of leukocyte rolling and recruitment in E-selectin and P-selectin double mutant mice [J].
Bullard, DC ;
Kunkel, EJ ;
Kubo, H ;
Hicks, MJ ;
Lorenzo, I ;
Doyle, NA ;
Doerschuk, CM ;
Ley, K ;
Beaudet, AL .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (05) :2329-2336
[7]   Plasma cells: finding new light at the end of B cell development [J].
Calame, KL .
NATURE IMMUNOLOGY, 2001, 2 (12) :1103-1108
[8]   Interleukin-6 inhibits Fas-induced apoptosis and stress-activated protein kinase activation in multiple myeloma cells [J].
Chauhan, D ;
Kharbanda, S ;
Ogata, A ;
Urashima, M ;
Teoh, G ;
Robertson, M ;
Kufe, DW ;
Anderson, KC .
BLOOD, 1997, 89 (01) :227-234
[9]   OCT-2 IS REQUIRED EARLY IN T-CELL-INDEPENDENT B-CELL ACTIVATION FOR G1 PROGRESSION AND FOR PROLIFERATION [J].
CORCORAN, LM ;
KARVELAS, M .
IMMUNITY, 1994, 1 (08) :635-645
[10]   Mutational switch of an IL-6 response to an interferon-γ-like response [J].
Costa-Pereira, AP ;
Tininini, S ;
Strobl, B ;
Alonzi, T ;
Schlaak, JF ;
Is'harc, H ;
Gesualdo, I ;
Newman, SJ ;
Kerr, IM ;
Poli, V .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (12) :8043-8047