Medical Journals

Different Kinetics of Blimp-1 Induction in B Cell Subsets Revealed by Reporter Gene.

Authors:
  • Fairfax Kirsten A
  • Corcoran Lynn M
  • Pridans Clare
  • Huntington Nicholas D
  • Kallies Axel
  • Nutt Stephen L
  • Tarlinton David M

From: Immunology Division, Walter and Eliza Hall Institute of Medical Research, 1G Royal Parade, Parkville, Victoria, Australia.

Journal of immunology (Baltimore, Md. : 1950)

  • Publish Date: Apr 2007
  • ISSN: 0022-1767
  • Volume: 178
  • Issue: 7
  • Pages: 4104-11
  • Medium: Print
  • Language: English
  • Citation (JAMA): Fairfax Kirsten A, Corcoran Lynn M, Pridans Clare, et al. Different Kinetics of Blimp-1 Induction in B Cell Subsets Revealed by Reporter Gene.. J. Immunol. Apr 2007;178:4104-11

Abstract

The transcriptional repressor Blimp-1 (B lymphocyte-induced maturation protein 1) has been described as a “master regulator” of B cell differentiation into Ab-secreting cells (ASCs). Although there is mounting evidence for the importance and necessity of Blimp-1 in plasma cell development, there is uncertainty as to the role it plays in B cell differentiation of B cell subsets and the way in which it may interact with other transcription factors such as Pax5 and Bcl6 during ASC differentiation. Using a mouse expressing GFP under the control of the Blimp-1 regulatory elements (Blimp-1(GFP/+)), we examined the kinetics of Blimp-1 up-regulation in purified B cell subsets following activation. B1 cells showed the most rapid and pronounced up-regulation of Blimp-1 in response to the mitogens tested, followed by marginal zone B cells and then conventional B2 cells. Interestingly, only B1 cells substantially up-regulated Blimp-1 expression in response to CpG. B1 cells secreted negligible Ig upon isolation but were able to up-regulate Blimp-1 and initiate Ig secretion within 28 h of stimulation. Also of interest, B1 cells have a transcriptional factor profile that is intermediate between a naive B cell and an ASC, indicative of the semiactivated state of B1 cells. Transferred naive Blimp-1(GFP/+) B1 and B2 cells both gave rise to ASCs in the bone marrow, suggesting no intrinsic barriers to B1 cell entry into the long-lived ASC compartment.

Mesh Headings (Keywords): Animals, B-Cell-Specific Activator Protein, B-Lymphocyte Subsets, Bone Marrow, Cell Differentiation, DNA-Binding Proteins, Genes, Reporter, Green Fluorescent Proteins, Immunoglobulins, Kinetics, Lymphocyte Activation, Mice, Mice, Mutant Strains, Regulatory Elements, Transcriptional, Repressor Proteins, Transcription Factors, Up-Regulation


Check for Full Text / PubMed Unique Identifier (PMID): 17371965


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

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The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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