Ghobadi Farnaz, Rahmanifar Farhad, Mehrabani Davood, Tamadon Amin, Dianatpour Mehdi, Zare Shahrokh, Razeghian Jahromi Iman
Stem Cells Technology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Department of Basic Sciences, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.
Int J Reprod Biomed. 2018 Feb;16(2):83-92.
Endometrial mesenchymal stem stromal cells (EnMSCs) are critical for uterine function, repair, and regeneration.
This study introduced isolation technique of EnMSCs and compared the characteristics of EnMSCs in mature and immature ewes.
Endometrial tissue samples from the uterus of 10 ewes were collected from the slaughterhouse. Endometrial cells were isolated from tissue using cold incubation and then chopping and treating was performed with collagenase type I. Isolated cells were cultured in cell culture medium and then attached cells to flasks were harvested as EnMSCs and subcultured. To enumerate the cells, the population doubling time (PDT) was determined and 2.2×10 cells in passage 4 were seeded into 24-well culture plates to compare the growth curves of isolated cells. Reverse transcription polymerase chain reaction (RT-PCR) was performed for detection of CD34 and CD73 markers. The osteogenic and adipogenic potential of isolated cells were determined using differentiation tests.
EnMSCs adhered to the flasks and displayed spindle-shape. Based on findings of the cell count and the growth curves, the EnMSCs growth was significantly more prominent in immature ewes in comparison to mature sheep. The PDT of EnMSCs in immature ewes was about 21 hr whereas this time period was two times higher (45 hr) in mature sheep. RT-PCR analyses of EnMSCs were positive for CD73 and negative for CD34. EnMSCs were differentiated into osteoblasts and adipocytes
Based on mesenchymal stem cells characters confirmed in EnMSCs, they can be a candidate for cell therapy and regenerative medicine.
子宫内膜间充质干/基质细胞(EnMSCs)对子宫功能、修复和再生至关重要。
本研究介绍了EnMSCs的分离技术,并比较了成熟和未成熟母羊中EnMSCs的特征。
从屠宰场收集10只母羊子宫的子宫内膜组织样本。采用冷孵育从组织中分离子宫内膜细胞,然后用I型胶原酶进行切碎和处理。将分离的细胞培养于细胞培养基中,然后收获贴壁于培养瓶的细胞作为EnMSCs并进行传代培养。为了对细胞进行计数,测定群体倍增时间(PDT),并将第4代的2.2×10个细胞接种到24孔培养板中,以比较分离细胞的生长曲线。进行逆转录聚合酶链反应(RT-PCR)检测CD34和CD73标志物。使用分化试验确定分离细胞的成骨和成脂潜能。
EnMSCs贴壁于培养瓶并呈纺锤形。根据细胞计数和生长曲线的结果,与成熟母羊相比,未成熟母羊中EnMSCs的生长明显更突出。未成熟母羊中EnMSCs的PDT约为21小时,而成熟母羊中这一时间段则高出两倍(45小时)。EnMSCs的RT-PCR分析显示CD73呈阳性,CD34呈阴性。EnMSCs可分化为成骨细胞和脂肪细胞。
基于在EnMSCs中证实的间充质干细胞特征,它们可成为细胞治疗和再生医学的候选者。