Local environmental factors determine hematopoietic differentiation of neural stem cells
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.
Grant support
HL61750
NHLBI NIH HHS - United States
- MeSH
- Colony-Forming Units Assay MeSH
- beta-Galactosidase metabolism MeSH
- Cell Differentiation * MeSH
- Bone Marrow Cells cytology MeSH
- Galactosides metabolism MeSH
- Hematopoietic Stem Cells cytology MeSH
- Hematopoietic System MeSH
- Hematopoiesis MeSH
- Immunohistochemistry MeSH
- Indoles metabolism MeSH
- Stem Cells cytology metabolism MeSH
- Culture Media MeSH
- Mice MeSH
- Neurons cytology MeSH
- Spleen cytology surgery MeSH
- Stem Cell Transplantation MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, U.S. Gov't, P.H.S. MeSH
- Names of Substances
- 5-bromo-4-chloro-3-indolyl beta-galactoside MeSH Browser
- beta-Galactosidase MeSH
- Galactosides MeSH
- Indoles MeSH
- Culture Media MeSH
Stem cells exhibit unique properties and hold high therapeutic promise, but factors influencing their differentiation after transplantation need to be recognized and defined for this promise to be fully met. Here, we demonstrate that endogenous colony-forming unit spleen (CFU-S) colonies are not generated in lethally irradiated mice transplanted with neural stem cells obtained from brain tissue of syngeneic donors. We investigated the proportion of transplanted neural stem cells that contributed to hematopoietic reconstitution and compared the distribution of transplanted cells in nonsplenectomized to that of splenectomized mice following sublethal whole-body irradiation. We also used clonogenic assays, colony assays, and histochemical analyses to explore conditions under which transplanted, beta-galactosidase-tagged neural stem cells underwent hematopoietic differentiation. Our results suggest that neural stem cells do undergo extramedullary hematopoiesis, even while no endogenous hematopoietic colonies develop in the spleen. Furthermore, we found that neural stem cells effectively colonized the bone marrow of splectomized recipients. We conclude that the hematopoietic differentiation of neural stem cells is highly dependent on the extramedullary environment. We also conclude that the bone marrow does not provide an environment supportive of hematopoietic differentiation by neural stem cells.
References provided by Crossref.org
Issues in stem cell plasticity