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来源于骨髓和滑液的间充质干细胞的细胞来源依赖性体外软骨形成分化潜能

Cell Source-Dependent In Vitro Chondrogenic Differentiation Potential of Mesenchymal Stem Cell Established from Bone Marrow and Synovial Fluid of .

作者信息

Son Young-Bum, Jeong Yeon Ik, Jeong Yeon Woo, Hossein Mohammad Shamim, Olsson Per Olof, Tinson Alex, Singh Kuhad Kuldip, Lee Sang-Yun, Hwang Woo Suk

机构信息

UAE Biotech Research Center, Abu Dhabi 30310, United Arab Emirates.

Hilli E.T. Cloning and Surgical Centre Presidential Camels and Camel Racing Affairs, Al-Ain 17292, United Arab Emirates.

出版信息

Animals (Basel). 2021 Jun 28;11(7):1918. doi: 10.3390/ani11071918.

Abstract

Mesenchymal stem cells (MSCs) are promising multipotent cells with applications for cartilage tissue regeneration in stem cell-based therapies. In cartilage regeneration, both bone marrow (BM-MSCs) and synovial fluid (SF-MSCs) are valuable sources. However, the cellular characteristics and chondrocyte differentiation potential were not reported in either of the camel stem cells. The in vitro chondrocyte differentiation competence of MSCs, from (BM and SF) sources of the same (camel) donor, was determined. Both MSCs were evaluated on pluripotent markers and proliferation capacity. After passage three, both MSCs showed fibroblast-like morphology. The proliferation capacity was significantly increased in SF-MSCs compared to BM-MSCs. Furthermore, SF-MSCs showed an enhanced expression of transcription factors than BM-MSCs. SF-MSCs exhibited lower differentiation potential toward adipocytes than BM-MSCs. However, the osteoblast differentiation potential was similar in MSCs from both sources. Chondrogenic pellets obtained from SF-MSCs revealed higher levels of chondrocyte-specific markers than those from BM-MSCs. Additionally, glycosaminoglycan (GAG) content was elevated in SF-MSCs related to BM-MSCs. This is, to our knowledge, the first study to establish BM-MSCs and SF-MSCs from the same donor and to demonstrate in vitro differentiation potential into chondrocytes in camels.

摘要

间充质干细胞(MSCs)是一种很有前景的多能细胞,在基于干细胞的疗法中可用于软骨组织再生。在软骨再生中,骨髓(BM-MSCs)和滑液(SF-MSCs)都是宝贵的来源。然而,关于骆驼干细胞的细胞特性和软骨细胞分化潜能均未见报道。本研究测定了来自同一(骆驼)供体的(骨髓和滑液)来源的MSCs的体外软骨细胞分化能力。对两种MSCs的多能性标志物和增殖能力进行了评估。传代三次后,两种MSCs均呈现成纤维细胞样形态。与BM-MSCs相比,SF-MSCs的增殖能力显著增强。此外,SF-MSCs转录因子的表达高于BM-MSCs。SF-MSCs向脂肪细胞的分化潜能低于BM-MSCs。然而,两种来源的MSCs向成骨细胞的分化潜能相似。从SF-MSCs获得的软骨形成微球中软骨细胞特异性标志物的水平高于BM-MSCs。此外,与BM-MSCs相比,SF-MSCs中糖胺聚糖(GAG)含量升高。据我们所知,这是第一项从同一供体建立BM-MSCs和SF-MSCs,并证明骆驼MSCs体外向软骨细胞分化潜能的研究。

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