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内皮细胞对骨髓基质细胞成骨潜能的调节作用。

Endothelial cell modulation of bone marrow stromal cell osteogenic potential.

作者信息

Kaigler Darnell, Krebsbach Paul H, West Erin R, Horger Kim, Huang Yen-Chen, Mooney David J

机构信息

Department of Biologic and Materials Sciences, University of Michigan, Ann Arbor, Michigan, USA.

出版信息

FASEB J. 2005 Apr;19(6):665-7. doi: 10.1096/fj.04-2529fje. Epub 2005 Jan 27.

DOI:10.1096/fj.04-2529fje
PMID:15677693
Abstract

In the context of bone development and regeneration, the intimate association of the vascular endothelium with osteogenic cells suggests that endothelial cells (ECs) may directly regulate the differentiation of osteoprogenitor cells. To investigate this question, bone marrow stromal cells (BMSCs) were cultured: in the presence of EC-conditioned medium, on EC extracellular matrix, and in EC cocultures with and without cell contact. RNA and protein were isolated from ECs and analyzed by reverse transcriptase-polymerase chain reaction and Western blotting, respectively, for expression of bone morphogenetic protein 2 (BMP-2). In animal studies, BMSCs and ECs were cotransplanted into severe combined immunodeficient mice on biodegradable polymer matrices, and histomorphometric analysis was performed to determine the extent of new bone and blood vessel formation. ECs significantly increased BMSC osteogenic differentiation in vitro only when cultured in direct contact. ECs expressed BMP-2, and experiments employing interfering RNA inhibition confirmed its production as contributing to the increased BMSC osteogenic differentiation. In vivo, cotransplantation of ECs with BMSCs resulted in greater bone formation than did transplantation of BMSCs alone. These data suggest that ECs function not only to form the microvasculature that delivers nutrients to developing bone but also to modulate the differentiation of osteoprogenitor cells in vitro and in vivo.

摘要

在骨骼发育和再生的背景下,血管内皮细胞与成骨细胞的密切关联表明内皮细胞(ECs)可能直接调节骨祖细胞的分化。为了研究这个问题,培养了骨髓间充质干细胞(BMSCs):在EC条件培养基存在下、在EC细胞外基质上以及在有或无细胞接触的EC共培养物中。从ECs中分离出RNA和蛋白质,分别通过逆转录-聚合酶链反应和蛋白质免疫印迹法分析骨形态发生蛋白2(BMP-2)的表达。在动物研究中,将BMSCs和ECs共移植到严重联合免疫缺陷小鼠的可生物降解聚合物基质上,并进行组织形态计量分析以确定新骨和血管形成的程度。仅在直接接触培养时,ECs才显著增加体外BMSC的成骨分化。ECs表达BMP-2,采用干扰RNA抑制的实验证实其产生有助于增加BMSC的成骨分化。在体内,ECs与BMSCs共移植比单独移植BMSCs导致更多的骨形成。这些数据表明,ECs不仅起到形成向发育中的骨骼输送营养物质的微血管的作用,而且在体外和体内调节骨祖细胞的分化。

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