Cat amniotic membrane multipotent cells are nontumorigenic and are safe for use in cell transplantation.

IF 1.7 Q4 CELL BIOLOGY Stem Cells and Cloning-Advances and Applications Pub Date : 2014-08-27 eCollection Date: 2014-01-01 DOI:10.2147/SCCAA.S67790
Atanasio S Vidane, Aline F Souza, Rafael V Sampaio, Fabiana F Bressan, Naira C Pieri, Daniele S Martins, Flavio V Meirelles, Maria A Miglino, Carlos E Ambrósio
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引用次数: 44

Abstract

Amnion-derived mesenchymal stem cells (AMSCs) are multipotent cells with an enhanced ability to differentiate into multiple lineages. AMSCs can be acquired through noninvasive methods, and therefore are exempt from the typical ethical issues surrounding stem cell use. The objective of this study was to isolate and characterize AMSCs from a cat amniotic membrane for future application in regenerative medicine. The cat AMSCs were harvested after mechanical and enzymatic digestion of amnion. In culture medium, the cat AMSCs adhered to a plastic culture dish and displayed a fibroblast-like morphology. Immunophenotyping assays were positive for the mesenchymal stem cell-specific markers CD73 and CD90 but not the hematopoietic markers CD34, CD45, and CD79. Under appropriate conditions, the cat AMSCs differentiated into osteogenic, chondrogenic, and adipogenic cell lineages. One advantage of cat AMSCs was nonteratogenicity, assessed 4 weeks post injection of undifferentiated AMSCs into immunodeficient mice. These findings suggest that cat amniotic membranes may be an important and useful source of mesenchymal stem cells for clinical applications, especially for cell or tissue replacement in chronic and degenerative diseases.

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猫羊膜多能细胞是非致瘤性的,用于细胞移植是安全的。
羊膜来源的间充质干细胞(AMSCs)是一种多能细胞,具有向多个谱系分化的增强能力。AMSCs可以通过非侵入性方法获得,因此可以免于围绕干细胞使用的典型伦理问题。本研究的目的是从猫羊膜中分离和表征AMSCs,为未来在再生医学中的应用奠定基础。机械和酶消化羊膜后收获猫AMSCs。在培养基中,猫AMSCs粘附在塑料培养皿上,呈现成纤维细胞样形态。免疫表型分析显示间充质干细胞特异性标记CD73和CD90阳性,但造血标记CD34、CD45和CD79不阳性。在适当的条件下,cat AMSCs分化为成骨细胞、软骨细胞和脂肪细胞系。猫AMSCs的一个优点是无致畸性,在将未分化的AMSCs注射到免疫缺陷小鼠体内4周后进行了评估。这些发现表明猫羊膜可能是临床应用间充质干细胞的重要和有用的来源,特别是在慢性和退行性疾病的细胞或组织替代方面。
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来源期刊
CiteScore
6.50
自引率
0.00%
发文量
10
审稿时长
16 weeks
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