|
|
||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Rapid Communication |
1 University of Tokyo Graduate School of Medicine
2 Keio University School of Medicine
* To whom correspondence should be addressed. E-mail: msata-circ{at}umin.ac.jp.
| Abstract |
|---|
In contrast to conventional assumption, recent reports proposed the possibility that hematopoietic stem cells (HSCs) may have broader potential to differentiate into various cell types. Here, we tested the pluripotency of HSCs by comparing vascular lesions induced by mechanical injury after bone marrow reconstitution with total bone marrow (TBM) cells, c-Kit+ Sca-1+ Lin- (KSL) cells, or a single HSC cell ("Tip"-SP CD34-KSL cell, CD34- c-Kit+ Sca-1+ Lin- cell with the strongest dye-efflux activity), harboring green fluorescent protein (GFP). The lesions contained a significant number of GFP-positive cells in the TBM and KSL groups, whereas GFP-positive cells were rarely detected in the HSC group. These results suggest that "transdifferentiation" of a highly purified HSC appears to be a rare event if it occurs at all, while bone marrow cells including the KSL fraction can give rise to vascular cells that substantially contribute to repair or lesion formation after mechanical injury.
Key Words. endothelial cells, hematopoietic stem cells, progenitor, smooth muscle cells, transdifferentiation
This article has been cited by other articles:
![]() |
H. Iwata and M. Sata Origin of Cells That Contribute to Neointima Growth Circulation, June 17, 2008; 117(24): 3060 - 3061. [Full Text] [PDF] |
||||
![]() |
Y. Diao, S. Guthrie, S.-L. Xia, X. Ouyang, L. Zhang, J. Xue, P. Lee, M. Grant, E. Scott, and M. S. Segal Long-Term Engraftment of Bone Marrow-Derived Cells in the Intimal Hyperplasia Lesion of Autologous Vein Grafts Am. J. Pathol., March 1, 2008; 172(3): 839 - 848. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Tanaka, M. Sata, T. Natori, J.-r. Kim-Kaneyama, K. Nose, M. Shibanuma, Y. Hirata, and R. Nagai Circulating progenitor cells contribute to neointimal formation in nonirradiated chimeric mice FASEB J, February 1, 2008; 22(2): 428 - 436. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Koide, S. Morikawa, Y. Mabuchi, Y. Muguruma, E. Hiratsu, K. Hasegawa, M. Kobayashi, K. Ando, K. Kinjo, H. Okano, et al. Two Distinct Stem Cell Lineages in Murine Bone Marrow Stem Cells, May 1, 2007; 25(5): 1213 - 1221. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Sumi, M. Sata, S.-i. Miura, K.-A. Rye, N. Toya, Y. Kanaoka, K. Yanaga, T. Ohki, K. Saku, and R. Nagai Reconstituted High-Density Lipoprotein Stimulates Differentiation of Endothelial Progenitor Cells and Enhances Ischemia-Induced Angiogenesis Arterioscler. Thromb. Vasc. Biol., April 1, 2007; 27(4): 813 - 818. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Sahara, M. Sata, T. Morita, K. Nakamura, Y. Hirata, and R. Nagai Diverse Contribution of Bone Marrow Derived Cells to Vascular Remodeling Associated With Pulmonary Arterial Hypertension and Arterial Neointimal Formation Circulation, January 30, 2007; 115(4): 509 - 517. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. I. Civin STEM CELLS' Impact Continues Its Ascent Stem Cells, September 1, 2006; 24(9): 1993 - 1994. [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH |
| STEM CELLS | THE ONCOLOGIST | CME | ALPHAMED PRESS JOURNALS |
