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多能成体祖细胞介导的造血重建:长期造血干细胞的前体细胞

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

作者信息

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

机构信息

Stem Cell Institute and Cancer Center and Department of Pediatrics, Division of Hematology, Oncology, Blood and Marrow Transplant Program, University of Minnesota, Minneapolis, MN 55455, USA.

出版信息

J Exp Med. 2007 Jan 22;204(1):129-39. doi: 10.1084/jem.20061115. Epub 2007 Jan 16.

Abstract

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.

摘要

几十年来,可移植造血干细胞(HSC)的体外扩增一直是一个难以实现的目标。在此,我们证明,从绿色荧光蛋白(GFP)转基因小鼠中分离并在体外扩增超过40 - 80个群体倍增的多能成体祖细胞(MAPC),能够在免疫缺陷小鼠中进行多谱系造血植入。在移植小鼠骨髓中源自MAPC的GFP + CD45.2 +细胞中,存在能够对二级和三级受体进行辐射防护并重建多谱系造血的HSC,以及髓系和淋巴系造血祖细胞亚群和具有功能的源自MAPC的GFP +淋巴细胞。尽管MAPC的造血贡献与对照KTLS HSC相当,但高效植入需要的MAPC数量大约多10³倍。由于未观察到源自宿主的GFP + CD45.1 +细胞,融合不太可能是MAPC产生HSC的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cb/2118428/c6f3aafb053d/jem2040129f01.jpg

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