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大鼠脂肪组织来源的基质细胞向雪旺样细胞分化的研究

[Study on differentiation of rat adipose tissue-derived stromal cells into Schwann-like cells].

作者信息

Ren Zhi-Wu, Zhao Zhe, Wang Yu, Chen Ji-Feng, Zhan Sheng-Feng, Liu Yan, Xu Wen-Jing, Zhang Li, Peng Jiang, Lu Shi-Bi

机构信息

Orthopaedic Research Institute of PLA General Hospital, Beijing 100853, China.

出版信息

Zhongguo Ying Yong Sheng Li Xue Za Zhi. 2011 Nov;27(4):385-8.

Abstract

OBJECTIVE

To investigate the phenotypic, molecular and biological characteristics of adipose tissue-derived stromal cells (ADSCs) differentiated alonely a Schwann cells (SCs) lineage and to provide a new cells' seed source for nerve tissue engineering or cell therapy.

METHODS

Cultured ADSCs were isolated from SD rats and the undifferentiated ADSCs were confirmed by detection of MSC-specific cell-surface markers. The ADSCs were differentiated along a glial cell lineage using an established cocktail of growth factors. Following differention, we used immunofluorescene staining and RT-PCR to evaluate the characteristics of differentiated WJMSCs.

RESULTS

ADSCs were successfully isolated from the rats' fat tissue. The isolated ADSCs expressed CD29, CD90 but not CD34, CD44 nor CD45. Osteogenic differentiation was detected by Alizarin red staining and adipogenic differentiation was comfirmed by Oil-red O staining. ADSCs treated with a mixture of glial growth factors adopted a spindle-like morphology similar to Schwann cells. Immunocytochemical staining and RT-PCR analysis revealed that the treated cells expressed the glial markers S100, P75 and glial fibrillary acidic protein indicative of differentiation.

CONCLUSION

ADSCs can be differentiated into cells that are Schwann-like in terms of morphologic features and phenotype and could be suitable Schwann-cell substitutes for nerve repair in clinical applications.

摘要

目的

研究脂肪组织来源的基质细胞(ADSCs)向施万细胞(SCs)谱系单独分化的表型、分子和生物学特性,为神经组织工程或细胞治疗提供一种新的细胞种子来源。

方法

从SD大鼠中分离培养ADSCs,并通过检测间充质干细胞特异性细胞表面标志物来确认未分化的ADSCs。使用既定的生长因子混合物使ADSCs沿神经胶质细胞谱系分化。分化后,我们使用免疫荧光染色和逆转录-聚合酶链反应(RT-PCR)来评估分化后的ADSCs的特性。

结果

成功从大鼠脂肪组织中分离出ADSCs。分离出的ADSCs表达CD29、CD90,但不表达CD34、CD44和CD45。通过茜素红染色检测到成骨分化,用油红O染色确认了脂肪生成分化。用神经胶质生长因子混合物处理的ADSCs呈现出类似于施万细胞的纺锤状形态。免疫细胞化学染色和RT-PCR分析表明,处理后的细胞表达了表明分化的神经胶质标志物S100、P75和神经胶质纤维酸性蛋白。

结论

ADSCs可以分化为在形态特征和表型方面类似于施万细胞的细胞,并且可能是临床应用中适合用于神经修复的施万细胞替代物。

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