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半月板碎片来源间充质干细胞的分离、鉴定及多能分化

Isolation, Characterization, and Multipotent Differentiation of Mesenchymal Stem Cells Derived from Meniscal Debris.

作者信息

Fu Weili, Xie Xing, Li Qi, Chen Gang, Zhang Chenghao, Tang Xin, Li Jian

机构信息

Department of Orthopedics, West China Hospital, Sichuan University, Chengdu, China; Department of Orthopedic Surgery, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Institute of Sports Medicine, Peking University Third Hospital, Beijing, China.

出版信息

Stem Cells Int. 2016;2016:5093725. doi: 10.1155/2016/5093725. Epub 2016 Dec 4.

Abstract

This study aimed to culture and characterize mesenchymal stem cells derived from meniscal debris. Cells in meniscal debris from patients with meniscal injury were isolated by enzymatic digestion, cultured in vitro to the third passage, and analyzed by light microscopy to observe morphology and growth. Third-passage cultures were also analyzed for immunophenotype and ability to differentiate into osteogenic, adipogenic, and chondrogenic lineages. After 4-5 days in culture, cells showed a long fusiform shape and adhered to the plastic walls. After 10-12 days, cell clusters and colonies were observed. Third-passage cells showed uniform morphology and good proliferation. They expressed CD44, CD90, and CD105 but were negative for CD34 and CD45. Cultures induced to differentiate via osteogenesis became positive for Alizarin Red staining as well as alkaline phosphatase activity. Cultures induced to undergo adipogenesis were positive for Oil Red O staining. Cultures induced to undergo chondrogenesis were positive for staining with Toluidine Blue, Alcian Blue, and type II collagen immunohistochemistry, indicating cartilage-specific matrix. These results indicate that the cells we cultured from meniscal debris are mesenchymal stem cells capable of differentiating along three lineages. These stem cells may be valuable source for meniscal regeneration.

摘要

本研究旨在培养和鉴定源自半月板碎片的间充质干细胞。通过酶消化法分离半月板损伤患者半月板碎片中的细胞,体外培养至第三代,并通过光学显微镜分析以观察形态和生长情况。对第三代培养物还进行了免疫表型分析以及向成骨、成脂和成软骨谱系分化能力的分析。培养4 - 5天后,细胞呈长梭形并贴附于塑料壁上。10 - 12天后,观察到细胞簇和集落。第三代细胞形态均匀且增殖良好。它们表达CD44、CD90和CD105,但CD34和CD45呈阴性。诱导成骨分化的培养物茜素红染色及碱性磷酸酶活性呈阳性。诱导成脂分化的培养物油红O染色呈阳性。诱导成软骨分化的培养物甲苯胺蓝、阿尔辛蓝染色及II型胶原免疫组化呈阳性,表明存在软骨特异性基质。这些结果表明,我们从半月板碎片中培养的细胞是能够沿三个谱系分化的间充质干细胞。这些干细胞可能是半月板再生的宝贵来源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a40/5164906/7d3f0874a37a/SCI2016-5093725.001.jpg

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