| Literature DB >> 26488117 |
Alexandra Bortnick1, Cornelis Murre1.
Abstract
Plasma cells are terminally differentiated B cells responsible for maintaining protective serum antibody titers. Despite their clinical importance, our understanding of the linear genomic features and chromatin structure of plasma cells is incomplete. The plasma cell differentiation program can be triggered by different signals and in multiple, diverse peripheral B cell subsets. This heterogeneity raises questions about the gene regulatory circuits required for plasma cell specification. Recently, new regulators of plasma cell differentiation have been identified and the enhancer landscapes of naïve B cells have been described. Other studies have revealed that the bone marrow niche harbors heterogeneous plasma cell subsets. Still undefined are the minimal requirements to become a plasma cell and what molecular features make peripheral B cell subsets competent to become antibody-secreting plasma cells. New technologies promise to reveal underlying chromatin configurations that promote efficient antibody secretion. For further resources related to this article, please visit the WIREs website.Entities:
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Year: 2015 PMID: 26488117 PMCID: PMC4761274 DOI: 10.1002/wdev.213
Source DB: PubMed Journal: Wiley Interdiscip Rev Dev Biol ISSN: 1759-7684 Impact factor: 5.814