For decades, in vitro expansion of transplantable hematopoietic stem cells (HSCs) has been an elusive goal. Here, we demonstrate that multipotent adult progenitor cells (MAPCs), isolated from green fluorescent protein (GFP)-transgenic mice and expanded in vitro for >40-80 population doublings, are capable of multilineage hematopoietic engraftment of immunodeficient mice. Among MAPC-derived GFP+CD45.2+ cells in the bone marrow of engrafted mice, HSCs were present that could radioprotect and reconstitute multilineage hematopoiesis in secondary and tertiary recipients, as well as myeloid and lymphoid hematopoietic progenitor subsets and functional GFP+ MAPC-derived lymphocytes that were functional. Although hematopoietic contribution by MAPCs was comparable to control KTLS HSCs, approximately 10(3)-fold more MAPCs were required for efficient engraftment. Because GFP+ host-derived CD45.1+ cells were not observed, fusion is not likely to account for the generation of HSCs by MAPCs.
Hematopoietic reconstitution by multipotent adult progenitor cells: precursors to long-term hematopoietic stem cells.
利用多能成体祖细胞进行造血重建:长期造血干细胞的前体
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作者:Serafini Marta, Dylla Scott J, Oki Masayuki, Heremans Yves, Tolar Jakub, Jiang Yuehua, Buckley Shannon M, Pelacho Beatriz, Burns Terry C, Frommer Sarah, Rossi Derrick J, Bryder David, Panoskaltsis-Mortari Angela, O'Shaughnessy Matthew J, Nelson-Holte Molly, Fine Gabriel C, Weissman Irving L, Blazar Bruce R, Verfaillie Catherine M
| 期刊: | Journal of Experimental Medicine | 影响因子: | 10.600 |
| 时间: | 2007 | 起止号: | 2007 Jan 22; 204(1):129-39 |
| doi: | 10.1084/jem.20061115 | 研究方向: | 发育与干细胞、细胞生物学 |
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