By J. -P. Lévesque, I. G. Winkler, S. R. Larsen, J. E. J. Rasko (auth.), Katalin Kauser MD, PhD, DSc, Andreas-Michael Zeiher MD (eds.)
There is pleasure generated virtually day-by-day in regards to the attainable makes use of of stem cells to regard human disease.
The skill of stem cells to procure assorted wanted phenotypes has opened the door for a brand new self-discipline: regenerative drugs. a lot of the curiosity for this goal is generated by way of embryonic stem cells, yet their use remains to be arguable for ethical purposes in addition to scientifically. much less debatable and available are the grownup bone marrow-derived progenitors together with hematopoietic stem cells, endothelial progenitors and mesenchymal stem cells.
The formidable aim of this quantity is to supply a complete evaluate of the at the moment to be had details regarding the healing application of grownup bone marrow-derived cells. each one bankruptcy has been written via an comprehensive specialist within the box, making this a highly priceless source for someone searching for an up to the moment overview of present perform in grownup bone marrow-derived cellphone therapy.
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Additional info for Bone Marrow-Derived Progenitors
2006). Additionally, these MSCs were strongly attracted by CXCL12 and hepatocyte growth factor gradients in vitro, providing evidence that such receptor–ligand interactions, along with MMPs, may be involved in trafﬁcking of MSCs. 2 Mesenchymal Stem Cells Are Present in Circulating Human Blood During Gestation MSCs are present in circulating human blood during the ﬁrst trimester (Campagnoli et al. 2001; Gotherstrom et al. 2004; Chan et al. 2005). These cells are abundant from at least 7 weeks of gestation, and they persist until approximately 12 weeks gestation, at which time they decline and almost disappear from the fetal circulation.
Exp Hematol 6:590–594 Mobilization of Bone Marrow-Derived Progenitors 29 Barry F, Boynton R, Murphy M, et al (2001) The SH-3 and SH-4 antibodies recognize distinct epitopes on CD73 from human mesenchymal stem cells. Biochem Biophys Res Commun 289:519–524 Barry FP, Boynton RE, Haynesworth S, et al (1999) The monoclonal antibody SH-2, raised against human mesenchymal stem cells, recognizes an epitope on endoglin (CD105). Biochem Biophys Res Commun 265:134–139 Bensaid W, Trifﬁtt JT, Blanchat C, et al (2003) A biodegradable ﬁbrin scaffold for mesenchymal stem cell transplantation.
Impaired BMDPC mobilization has also been described in matrix metalloproteinase-9 knockout (MMP-9-KO) mice (Heissig et al. 2002). Both in eNOSKO and MMP-9-KO mice postischemic injury, VEGF-induced BMDPC mobilization was impaired. eNOS-KO mice showed a decreased level of preMMP-9 in the bone marrow, suggesting an important role for MMP-9 as a downstream effector of this pathway (Aicher et al. 2003). eNOS likely plays a critical role in the bone marrow compartment. Bone marrow osteoblastic cells as well as stromal cells express eNOS, which may also contribute to the proper maturation and differentiation of different lineage bone marrow cells (Ozuyaman et al.