A Simple High Yield Technique for Isolation of Wharton's Jelly-derived Mesenchymal Stem Cell

Q3 Biochemistry, Genetics and Molecular Biology Avicenna journal of medical biotechnology Pub Date : 2024-02-06 DOI:10.18502/ajmb.v16i2.14860
Bahareh Niknam, Arezou Azizsoltani, Neda Heidari, S. Tokhanbigli, Helia Alavifard, Mahsa Haji Valili, D. Amani, H. A. Aghdaei, Seyed Mahmoud Hashemi, Kaveh Baghaei
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Abstract

Background: The isolation of Mesenchymal Stem Cells (MSCs) from various tissues is possible, with the umbilical cord emerging as a competitive alternative to bone marrow. In order to fulfill the demands of cell therapy, it is essential to generate stem cells on a clinical scale while minimizing time, cost, and contamination. Here is a simple and effective protocol for isolating MSC from Wharton's Jelly (WJ-MSC) using the explant method with various supplements. Methods: Utilizing the explant method, small fragments of Wharton's jelly from the human umbilical cord were cultured in a flask. The multipotency of the isolated cells, were confirmed by their differentiation ability to osteocyte and adipocyte. Additionally, the immunophenotyping of WJ-MSCs showed positive expression of CD73, CD90, and CD105, while remaining negative for hematopoietic markers CD34 and CD45, meeting the criteria for WJ-MSC identification. Following that, to evaluate cells' proliferative capacity, various supplements, including basic Fibroblast Growth Factor (bFGF), Non-Essential amino acids (NEA), and L-Glutamine (L-Gln) were added to either alpha-Minimal Essential Medium (α-MEM) or Dulbecco's Modified Eagle's Medium-F12 (DMEM-F12), as the basic culture media. Results: WJ-MSCs isolated by the explant method were removed from the tissue after seven days and transferred to the culture medium. These cells differentiated into adipocyte and osteocyte lineages, expressing CD73, CD90, and CD105 positively and CD34 and CD45 negatively. The results revealed that addition of bFGF to α-MEM or DMEM-F12 media significantly increased the proliferation of MSCs when compared to the control group. However, there were no significant differences observed when NEA or L-Gln were added. Conclusion: Although bFGF considerably enhances cell proliferation, our study de-monstrates that MSCs can grow and expand when properly prepared Wharton's jelly tissues of the human umbilical cord.
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分离沃顿果冻间充质干细胞的简单高产技术
背景:从各种组织中分离间充质干细胞(MSCs)是可能的,脐带成为替代骨髓的一种有竞争力的方法。为了满足细胞治疗的需求,必须在临床规模上生成干细胞,同时尽量减少时间、成本和污染。下面介绍一种简单有效的方案,利用外植法和各种补充剂从沃顿果冻中分离间充质干细胞(WJ-MSC)。方法:利用外植法,在烧瓶中培养取自人体脐带的小块沃顿果冻。分离细胞的多潜能性通过其向骨细胞和脂肪细胞的分化能力得到证实。此外,WJ-间充质干细胞的免疫分型显示 CD73、CD90 和 CD105 阳性表达,而造血标记 CD34 和 CD45 阴性,符合 WJ 间充质干细胞的鉴定标准。随后,为了评估细胞的增殖能力,在基本培养基α-MEM或Dulbecco改良老鹰培养基-F12(DMEM-F12)中加入了各种补充剂,包括碱性成纤维细胞生长因子(bFGF)、非必需氨基酸(NEA)和L-谷氨酰胺(L-Gln)。结果用外植法分离的 WJ 间充质干细胞在七天后从组织中取出并转移到培养基中。这些细胞分化为脂肪细胞系和骨细胞系,阳性表达 CD73、CD90 和 CD105,阴性表达 CD34 和 CD45。结果显示,与对照组相比,在 α-MEM 或 DMEM-F12 培养基中添加 bFGF 能显著增加间充质干细胞的增殖。然而,在添加 NEA 或 L-Gln 时没有观察到明显差异。结论虽然 bFGF 能明显增强细胞增殖,但我们的研究还是证明了间充质干细胞在适当制备人脐带的沃顿果冻组织后也能生长和扩增。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Avicenna journal of medical biotechnology
Avicenna journal of medical biotechnology Biochemistry, Genetics and Molecular Biology-Biotechnology
CiteScore
2.90
自引率
0.00%
发文量
43
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