Hematopoietic Stem Cell Development by Isabelle Godin Ph.D, Ana Cumano M.D. (auth.)

By Isabelle Godin Ph.D, Ana Cumano M.D. (auth.)

Hematopoietic Stem Cells brings jointly articles protecting the biology of hematopoietic stem cells in the course of embryonic improvement, reporting specific points of fly, fish, avian and mammalian types. hence, this booklet permits a comparative assessment of hematopoietic stem phone new release within the assorted periods, emphasizing the conserved traits in improvement. This booklet culminates with state-of –the artwork wisdom on hematopoietic improvement in human species and discussions of the newest breakthroughs with relevance to either researchers and clinicians.

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Ann NY Acad Sci 2001 ; 938:96-107. 80. Bernex F, De Sepulveda P, Kress C er al, Spatial and temporal patterns of c-kir expressing cells in the WlacZ/+ and WlaczlWl acz mouse embryos. Development 1996; 122:3023-3033. 81. Drake CJ, Brandt SJ. Trusk TC et al. Tall/SCL is expressed in endothelial progenitor cellsl angioblasts and defines a dorsal-to-ventral gradient of vasculogenesis. Dev Bioi 1997 ; 192:17-30. 82. Iwarna A, Hamaguchi I. Hashiyma M et al, Molecular cloning and characterization of mouse TIE and TEK receptor tyrosine kinase genes and their expression in hematopoietic stem cells.

Science 2002; 297:99-102. CHAPTER 3 Extra- and Intraembryonic HSC Commitment in the Avian Model Thierry Jaffredo, Karine Bollerot, Krisztina Minko, Rodolphe Gautier, Stephane Romero and Cecile Drevon Introduction H ematopoietic stem cells (HSC) are at the basis of the hematopoietic system construction. In adult higher Vertebrates, HSC, defined by their multipotentiality and self-renewal capacity, settle in the bone marrow where they can differentiate into progenitors with more restricted lineage potential and generate all blood lineages via a cascade of commitment events.

6o In the next decades, classical tissue recombination studies sURjestedthat blood system formation requires diffusible signals from the adjacent endoderm. ' 3,51 ,62 Various growth factors may be responsible for this endodermal effect (notably bFGF and VEGF). i" VEGF is present in the mouse,7,22,42 avian,I,25 Xenopus '< and zebraflsh58 YS endoderm. In mouse VEGF Knock Out (KO), the loss of a single allele is sufficient to impair both HC and EC development lO,24 demonstrating that gene dosage is critical for these processes.

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