Genetic programs regulating HSC specification, maintenance and expansion.

Abstract:

:All mature blood cells originate from a small population of self-renewing pluripotent hematopoietic stem cells (HSCs). The capacity to self-renew characterizes all stem cells, whether normal or neoplastic. Interestingly, recent studies suggest that self-renewal is essential for tumor cell maintenance, implicating that this process has therapeutic relevance. Unfortunately, the molecular bases for self-renewal of vertebrate cells remain poorly defined. This article will focus on the developmental mechanisms underlying fetal and adult HSC homeostasis. Specifically, distinctions between genetic programs regulating HSC specification (identity), self-renewal (in both fetal and adult) and differentiation/commitment will be discussed with a special emphasis on transcriptional and chromatin regulators.

journal_name

Oncogene

journal_title

Oncogene

authors

Lessard J,Faubert A,Sauvageau G

doi

10.1038/sj.onc.1207940

subject

Has Abstract

pub_date

2004-09-20 00:00:00

pages

7199-209

issue

43

eissn

0950-9232

issn

1476-5594

pii

1207940

journal_volume

23

pub_type

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