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老年髋部骨折患者循环中的塑料黏附间充质干细胞。

Circulating plastic adherent mesenchymal stem cells in aged hip fracture patients.

机构信息

Orthopaedic Research Unit, Department of Orthopaedic Research and Traumatology, Turku University Hospital and University of Turku, Turku, Finland.

出版信息

J Orthop Res. 2010 Dec;28(12):1634-42. doi: 10.1002/jor.21167.

Abstract

We examined the presence of circulating plastic adherent multipotent mesenchymal stem cells (MSCs) in fracture patients. Three patient groups (n = 10-18) were evaluated, including elderly females with a femoral neck fracture treated with cemented hemiarthroplasty, an age- and sex-matched group with hip osteoarthritis (OA) treated with cemented total hip arthroplasty (THA), and younger adults with surgically treated lower extremity fractures. The presence of circulating MSCs pre- and postoperatively was compared to bone marrow (BM) MSCs from the same subjects. Criteria for identifying MSCs included cell surface markers (CD105+, CD73+, CD90+, CD45-, CD14-), proliferation through several passages as well as osteogenic, chondrogenic, and adipogenic differentiation. Plastic adherent MSCs were found in peripheral blood (PB) from 22% of hip fracture patients, 46% of younger fracture patients, and in none of 63 pre- and postmenopausal women with hip OA. When detectable, circulating MSCs appeared between 39 and 101 h after fracture. PB derived MSCs did not differ from BM derived MSCs, except for a small population (<15%) of CD34+ cells among PB derived MSCs. This initial study indicates mobilization of MSCs into the circulation in response to fracture, even in very old patients, while circulating MSCs were not detectable before or after elective THA.

摘要

我们研究了骨折患者循环中黏附的多能间充质干细胞(MSCs)的存在情况。评估了三组患者(n=10-18),包括接受骨水泥半髋关节置换术治疗的股骨颈骨折老年女性、接受骨水泥全髋关节置换术(THA)治疗的年龄和性别匹配的髋关节炎(OA)组,以及接受手术治疗的下肢骨折的年轻成年人。比较了术前和术后循环 MSCs 与同一受试者骨髓(BM)MSCs 的存在情况。鉴定 MSC 的标准包括细胞表面标志物(CD105+、CD73+、CD90+、CD45-、CD14-)、通过多个传代的增殖能力以及成骨、成软骨和脂肪分化能力。22%的髋部骨折患者、46%的年轻骨折患者外周血(PB)中可检测到黏附性 MSC,而 63 名绝经前和绝经后髋 OA 女性中均未检测到。当可检测到时,循环 MSC 出现在骨折后 39-101 小时之间。PB 衍生的 MSC 与 BM 衍生的 MSC 没有区别,除了 PB 衍生的 MSC 中有一小部分(<15%)CD34+细胞。这项初步研究表明,MSCs 动员到循环中以响应骨折,即使是非常年老的患者,而在择期 THA 前后均无法检测到循环 MSC。

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