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Complementary regulation of early B-lymphoid differentiation by genetic and epigenetic mechanisms. | LitMetric

AI Article Synopsis

  • B lymphopoiesis, the process of B cell development from hematopoietic stem cells (HSCs), is well-defined but still lacks comprehensive understanding of its early regulatory mechanisms.
  • Recent advancements in techniques for sorting progenitor cells and studying their epigenetic features have revealed that even the enriched HSCs vary in their potential to develop into B cells.
  • The differentiation involves complex interactions among transcription factors and significant epigenetic regulation, highlighting the coordinated impact of genetic and epigenetic mechanisms in early B-lineage development.

Article Abstract

Although B lymphopoiesis is one of the best-defined paradigms in cell differentiation, our knowledge of the regulatory mechanisms underlying its earliest processes, in which hematopoietic stem cells (HSCs) enter the B lineage, is limited. However, recent methodological advances in sorting progenitor cells and monitoring their epigenetic features have increased our understanding of HSC activities. It is now known that even the highly enriched HSC fraction is heterogeneous in terms of lymphopoietic potential. While surface markers and reporter proteins provide information on the sequential differentiation of B-lineage progenitors, complex interactions between transcription factors have also been shown to play a major role in this process. Epigenetic regulation of histones, nucleosomes, and chromatin appears to play a crucial background role in this elaborate transcription network. In this review, we summarize recent findings on the physiological processes of early B-lineage differentiation, which provides a new paradigm for understanding the harmonious action of genetic and epigenetic mechanisms.

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Source
http://dx.doi.org/10.1007/s12185-013-1424-7DOI Listing

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