By Anthony Ho; Ronald Hoffman; Esmail D Zanjani
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Additional info for Stem cell transplantation : biology, processing, and therapy
On the other hand, the hematopoietic microenvironment in vivo allows sustenance of lifelong hematopoiesis by promoting a self-renewal type of HSC divisions. Following HSC transplantation, the reconstitution of a myeloablated host support the view that a limited number of HSC can divide and reconstitute a myeloablated host and create a HSC pool large enough to sustain long-term donor-derived hematopoiesis [16–19]. 1 The fate of a hematopoietic stem cell (HSC) division: HSC expansion, HSC maintenance and HSC extinction.
Regulation of hematopoiesis through adhesion receptors. J Leukocyte Biol 69: 307–316. 74. Punzel M, Gupta P, Verfaillie CM (2002). The microenvironment of AFT024 cells maintains primitive human hematopoiesis by counteracting contact mediated inhibition of proliferation. Cell Commun Adhes 9: 149–159. 75. Fruehauf S, Srbic K, Seggewiss R, et al. (2002). Functional characterization of podia formation in normal and malignant hematopoeitic cells. J Leukocyte Biol 71: 425–432. 76. Wagner W, Saffrich R, Wirkner U, Eckstein V, Blake J, Ansorge A, Schwager C, Wein F, Miesala K, Ansorge W, Ho AD (2005).
There is evidence that early HSC express a promiscuous set of transcription factors  and an open chromatin structure required to maintain their multipotentiality, which is quenched progressively as these cells progress down a particular lineage of differentiation . The mechanisms that govern these stem cell fate decisions are likely under tight control, but remain potentially alterable. Although the global gene expression profiles for HSC have recently been described, very little is known regarding the dynamics of gene expression necessary for HSC fate decisions [11–13].