Aksu A Emre, Rubin J Peter, Dudas Jason R, Marra Kacey G
Division of Plastic and Reconstructive Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA 15261, USA.
Ann Plast Surg. 2008 Mar;60(3):306-22. doi: 10.1097/SAP.0b013e3180621ff0.
Adipose-derived stem cells (ASCs) display multilineage plasticity and, under appropriate conditions, can mineralize their extracellular matrix and undergo osteogenesis. The aims of this study are to examine in vitro osteogenic differentiation properties of ASCs to assess the role of gender, fat depot, and optimal duration as variables for differentiation. Human ASCs were isolated from superficial and deep adipose layers of the abdominoplasty specimens obtained from patients undergoing elective surgeries. ASCs were cultured in osteogenic media (OM). After 1, 2, and 4 weeks of differentiation, cultures were assessed for markers of osteogenesis. Alkaline phosphatase (AP), alizarin red (AR) and Masson trichrome (MT) stainings for osteoblastic transformation, matrix mineralization, and collagen production; enzyme-linked immunosorbent assay (ELISA) for Gla-osteocalcin; and Western blot analysis for osteonectin protein expression were performed. Osteogenic differentiation began as early as 1 week. Cells exhibited a vertical growth pattern, lacunae formed in the cultures, matrix volume increased, and mineralization was observed. Differences in AP staining were most evident during the first week. AR activity progressively increased over 4 weeks, and collagen was secreted only by differentiated ASCs. There was no significant difference in the degree of osteogenic differentiation between the ASCs from both depots in the female. In the male, the superficial depot ASCs differentiated faster and more efficiently than those of the deep depot. Male ASCs from both depots differentiated more effectively than female ASCs from both depots. We describe a hierarchy of osteogenic differentiation potential based on gender and anatomic harvest site by layering adipose tissues of the abdominal wall. ASCs derived from male superficial layer were most efficient in achieving osteogenesis. In future clinical applications using stem cells for osseous healing, these gender and depot differences will guide our clinical methods.
脂肪来源干细胞(ASCs)具有多向分化潜能,在适当条件下,能够使其细胞外基质矿化并进行成骨分化。本研究旨在检测ASCs的体外成骨分化特性,以评估性别、脂肪储存部位和最佳分化持续时间作为分化变量的作用。从接受择期手术患者的腹壁整形标本的浅、深脂肪层中分离出人ASCs。将ASCs培养于成骨培养基(OM)中。分化1、2和4周后,评估培养物的成骨标志物。进行碱性磷酸酶(AP)、茜素红(AR)和Masson三色(MT)染色以检测成骨细胞转化、基质矿化和胶原蛋白生成;采用酶联免疫吸附测定(ELISA)检测骨钙素;并进行骨连接蛋白蛋白表达的蛋白质印迹分析。成骨分化最早在1周开始。细胞呈现垂直生长模式,培养物中形成腔隙,基质体积增加,并观察到矿化现象。AP染色的差异在第一周最为明显。AR活性在4周内逐渐增加,且只有分化的ASCs分泌胶原蛋白。女性两个储存部位的ASCs在成骨分化程度上没有显著差异。在男性中,浅部储存部位的ASCs比深部储存部位的ASCs分化更快、更有效。来自两个储存部位的男性ASCs比来自两个储存部位的女性ASCs分化更有效。我们通过分层腹壁脂肪组织,描述了基于性别和解剖采集部位的成骨分化潜能等级。来自男性浅层的ASCs在实现成骨方面最有效。在未来使用干细胞进行骨愈合的临床应用中,这些性别和储存部位差异将指导我们的临床方法。