Nakorn Thanyaphong Na, Miyamoto Toshihiro, Weissman Irving L
Department of Pathology and Developmental Biology, Stanford University School of Medicine, CA 94305, USA.
Proc Natl Acad Sci U S A. 2003 Jan 7;100(1):205-10. doi: 10.1073/pnas.262655099. Epub 2002 Dec 18.
Although it has been shown that unfractionated bone marrow, hematopoietic stem cells, common myeloid progenitors, and bipotent megakaryocyteerythrocyte progenitors can give rise to megakaryocyte colonies in culture, monopotent megakaryocyte-committed progenitors (MKP) have never been prospectively isolated from the bone marrow of adult mice. Here, we use a monoclonal antibody to the megakaryocyte-associated surface protein, CD9, to purify MKPs from the c-kit(+)Sca-1(-)IL7Ralpha(-)Thy1.1(-)Lin(-) fraction of adult C57BLKa-Thy1.1 bone marrow. The CD9(+) fraction contained a subset of CD41(+)FcgammaR(lo)CD34(+)CD38(+) cells that represent approximately 0.01% of the total nucleated bone marrow cells. They give rise mainly to colony-forming unit-megakaryocytes and occasionally burst-forming unit-megakaryocytes, with a plating efficiency >60% at the single-cell level. In vivo, MKPs do not have spleen colony-forming activity nor do they contribute to long-term multilineage hematopoiesis; they give rise only to platelets for approximately 3 weeks. Common myeloid progenitors and megakaryocyteerythrocyte progenitors can differentiate into MKPs after 72 h in stromal cultures, indicating that MKPs are downstream of these two progenitors. These isolatable MKPs will be very useful for further studies of megakaryopoiesis as well as the elucidation of their gene expression patterns.
尽管已有研究表明,未分级的骨髓、造血干细胞、常见髓系祖细胞以及双能巨核细胞 - 红细胞祖细胞在培养中能够产生巨核细胞集落,但单能巨核细胞定向祖细胞(MKP)从未在成年小鼠骨髓中被前瞻性地分离出来。在此,我们使用针对巨核细胞相关表面蛋白CD9的单克隆抗体,从成年C57BLKa-Thy1.1小鼠骨髓的c-kit(+)Sca-1(-)IL7Ralpha(-)Thy1.1(-)Lin(-)组分中纯化MKP。CD9(+)组分包含一个CD41(+)FcgammaR(lo)CD34(+)CD38(+)细胞亚群,其约占骨髓有核细胞总数的0.01%。它们主要产生巨核细胞集落形成单位,偶尔产生巨核细胞爆式集落形成单位,在单细胞水平上接种效率>60%。在体内,MKP不具有脾集落形成活性,也不参与长期多系造血;它们仅在约3周内产生血小板。常见髓系祖细胞和巨核细胞 - 红细胞祖细胞在基质培养72小时后可分化为MKP,这表明MKP位于这两种祖细胞的下游。这些可分离的MKP对于巨核细胞生成的进一步研究以及其基因表达模式的阐明将非常有用。