Infrapatellar Fat Pad: An Alternative Source of Adipose-Derived Mesenchymal Stem Cells.

Arthritis Pub Date : 2016-01-01 Epub Date: 2016-04-26 DOI:10.1155/2016/4019873
P Tangchitphisut, N Srikaew, S Numhom, A Tangprasittipap, P Woratanarat, S Wongsak, C Kijkunasathian, S Hongeng, I R Murray, T Tawonsawatruk
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引用次数: 46

Abstract

Introduction. The Infrapatellar fat pad (IPFP) represents an emerging alternative source of adipose-derived mesenchymal stem cells (ASCs). We compared the characteristics and differentiation capacity of ASCs isolated from IPFP and SC. Materials and Methods. ASCs were harvested from either IPFP or SC. IPFPs were collected from patients undergoing total knee arthroplasty (TKA), whereas subcutaneous tissues were collected from patients undergoing lipoaspiration. Immunophenotypes of surface antigens were evaluated. Their ability to form colony-forming units (CFUs) and their differentiation potential were determined. The ASCs karyotype was evaluated. Results. There was no difference in the number of CFUs and size of CFUs between IPFP and SC sources. ASCs isolated from both sources had a normal karyotype. The mesenchymal stem cells (MSCs) markers on flow cytometry was equivalent. IPFP-ASCs demonstrated significantly higher expression of SOX-9 and RUNX-2 over ASCs isolated from SC (6.19 ± 5.56-, 0.47 ± 0.62-fold; p value = 0.047, and 17.33 ± 10.80-, 1.56 ± 1.31-fold; p value = 0.030, resp.). Discussion and Conclusion. CFU assay of IPFP-ASCs and SC-ASCs harvested by lipoaspiration technique was equivalent. The expression of key chondrogenic and osteogenic genes was increased in cells isolated from IPFP. IPFP should be considered a high quality alternative source of ASCs.

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Abstract Image

Abstract Image

髌下脂肪垫:脂肪来源间充质干细胞的替代来源。
介绍。髌下脂肪垫(IPFP)代表了一种新兴的脂肪源性间充质干细胞(ASCs)的替代来源。我们比较了从IPFP和SC分离的ASCs的特性和分化能力。从IPFP或SC中采集ASCs。IPFP采集自全膝关节置换术(TKA)患者,而皮下组织采集自抽脂术患者。评估表面抗原的免疫表型。测定了它们形成集落形成单位(cfu)的能力和分化潜力。评估ASCs的核型。结果。在IPFP和SC源之间,cfu的数量和大小没有差异。从两个来源分离的ASCs核型正常。流式细胞术显示间充质干细胞(MSCs)标记物相等。与SC分离的ASCs相比,IPFP-ASCs中SOX-9和RUNX-2的表达显著增加(分别为6.19±5.56、0.47±0.62倍);P值分别为0.047、17.33±10.80、1.56±1.31倍;P值= 0.030,resp.)。讨论与结论。脂吸法收获的IPFP-ASCs与SC-ASCs的CFU检测结果相当。从IPFP分离的细胞中,关键软骨和成骨基因的表达增加。指规数应被认为是一种高质量的可选择的辅助技术成分来源。
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