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PMID: 12543863 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

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

Blood ·Vol. 101 ·No. 10 ·2003-05-15 ·Pages 4013-21

Underhill GH, George D, Bremer EG, Kansas GS

Abstract

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 up-regulation, 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 down-regulation of several RNA polymerase I- related factors, consistent with terminal differentiation, and exhibited a down-regulation 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 up-regulation 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.

MeSH Terms
Animals Blotting, Western Cell Cycle/immunology Cell Cycle Proteins/genetics Cell Differentiation Cell Division Crosses, Genetic Gene Expression Profiling/methods Immunoglobulin M/genetics Mice Mice, Inbred C57BL Mice, Knockout Organ Specificity Plasma Cells/cytology,immunology,physiology Reelin Protein Reverse Transcriptase Polymerase Chain Reaction Transcription, Genetic
Chemicals
Cell Cycle Proteins Immunoglobulin M Reelin Protein Reln protein, mouse
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Underhill Gregory H
Department of Biomedical Engineering, Northwestern University, Evanston, IL, USA.
George David
Bremer Eric G
Kansas Geoffrey S
Article Info
Journal
Blood
Abbr.
Blood
ISSN
0006-4971
Published
2003-05-15
Epub
2003-00-23
Pages
4013-21
Language
English
Region
United States
NLM ID
7603509
Subset
IM
Grants
NHLBI NIH HHS · HL58710 · United States
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