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pubmed-article:15492122pubmed:abstractTextPlasma cells comprise a population of terminally differentiated B cells that are dependent on the transcriptional regulator B lymphocyte--induced maturation protein 1 (Blimp-1) for their development. We have introduced a gfp reporter into the Blimp-1 locus and shown that heterozygous mice express the green fluorescent protein in all antibody-secreting cells (ASCs) in vivo and in vitro. In vitro, these cells display considerable heterogeneity in surface phenotype, immunoglobulin secretion rate, and Blimp-1 expression levels. Importantly, analysis of in vivo ASCs induced by immunization reveals a developmental pathway in which increasing levels of Blimp-1 expression define developmental stages of plasma cell differentiation that have many phenotypic and molecular correlates. Thus, maturation from transient plasmablast to long-lived ASCs in bone marrow is predicated on quantitative increases in Blimp-1 expression.lld:pubmed
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pubmed-article:15492122pubmed:articleTitlePlasma cell ontogeny defined by quantitative changes in blimp-1 expression.lld:pubmed
pubmed-article:15492122pubmed:affiliationThe Walter and Eliza Hall Institute of Medical Research, 1G Royal Parade, Parkville, Victoria, 3050, Australia.lld:pubmed
pubmed-article:15492122pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:15492122pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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