Hematopoietic reconstitution by multipotent adult progenitor cells: precursors to long-term hematopoietic stem cells

被引:82
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. [1 ]
机构
[1] Univ Minnesota, Stem Cell Inst, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Ctr Canc, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Dept Pediat, Div Hematol Oncol, Blood & Marrow Transplant Program, Minneapolis, MN 55455 USA
[4] Stanford Univ, Sch Med, Dept Pathol, Inst Stem Cell Biol & Regenerat Med, Stanford, CA 94305 USA
[5] Katholieke Univ Leuven, Stamcel Inst Louvain, Dept Med, B-3000 Louvain, Belgium
关键词
D O I
10.1084/jem.20061115
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:129 / 139
页数:11
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