| Literature DB >> 23733396 |
Hal E Broxmeyer1, Nirit Mor-Vaknin, Ferdinand Kappes, Maureen Legendre, Anjan K Saha, Xuan Ou, Heather O'Leary, Maegan Capitano, Scott Cooper, David M Markovitz.
Abstract
Understanding the factors that regulate hematopoiesis opens up the possibility of modifying these factors and their actions for clinical benefit. DEK, a non-histone nuclear phosphoprotein initially identified as a putative proto-oncogene, has recently been linked to regulate hematopoiesis. DEK has myelosuppressive activity in vitro on proliferation of human and mouse hematopoietic progenitor cells and enhancing activity on engraftment of long-term marrow repopulating mouse stem cells, has been linked in coordinate regulation with the transcription factor C/EBPα, for differentiation of myeloid cells, and apparently targets a long-term repopulating hematopoietic stem cell for leukemic transformation. This review covers the uniqueness of DEK, what is known about how it now functions as a nuclear protein and also as a secreted molecule that can act in paracrine fashion, and how it may be regulated in part by dipeptidylpeptidase 4, an enzyme known to truncate and modify a number of proteins involved in activities on hematopoietic cells. Examples are provided of possible future areas of investigation needed to better understand how DEK may be regulated and function as a regulator of hematopoiesis, information possibly translatable to other normal and diseased immature cell systems.Entities:
Keywords: Chromatin; DEK; Dipeptidylpeptidase IV; Hematopoietic progenitor cells; Hematopoietic stem cells; Receptors
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Year: 2013 PMID: 23733396 PMCID: PMC3814160 DOI: 10.1002/stem.1443
Source DB: PubMed Journal: Stem Cells ISSN: 1066-5099 Impact factor: 6.277