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模拟微重力条件下脂肪来源干细胞神经元分化过程中神经营养因子及其受体的表达模式

Expression pattern of neurotrophins and their receptors during neuronal differentiation of adipose-derived stem cells in simulated microgravity condition.

作者信息

Zarrinpour Vajiheh, Hajebrahimi Zahra, Jafarinia Mojtaba

机构信息

Department of Biology, Fars Science and Research Branch, Islamic Azad University, Marvdasht, Iran; Department of Biology, Marvdasht Branch, Islamic Azad University, Marvdasht, Iran.

Aerospace Research Institute, Ministry of Science Research and Technology, Tehran, Iran.

出版信息

Iran J Basic Med Sci. 2017 Feb;20(2):178-186. doi: 10.22038/ijbms.2017.8244.

DOI:10.22038/ijbms.2017.8244
PMID:28293395
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5339659/
Abstract

OBJECTIVES

Studies have confirmed that microgravity, as a mechanical factor, influences both differentiation and function of mesenchymal stem cells. Here we investigated the effects of simulated microgravity on neural differentiation of human adipose-derived stem cells (ADSCs).

MATERIALS AND METHODS

We have used a fast rotating clinostat (clinorotation) to simulate microgravity condition. Real-time PCR and flow cytometry analysis were used to evaluate the regulation of neurotrophins, their receptors, and neural markers by simulated microgravity and their impact on neural differentiation of cells.

RESULTS

Our data revealed that simulation microgravity up-regulated the expression of MAP-2, BDNF, TrkB, NT-3, and TrkC both before and after neural differentiation. Also, the neural cells derived from ADSCs in microgravity condition expressed more MAP-2, GFAP, and synaptophysin protein in comparison to the 1G control.

CONCLUSION

We showed that simulated microgravity can enhance the differentiation of mesenchymal stem cells into neurons. Our findings provide a new strategy for differentiation of ADSCs to neural-like cells and probably other cell lineages. Meanwhile, microgravity simulation had no adverse effects on the viability of the cells and could be used as a new environment to successfully manipulate cells.

摘要

目的

研究已证实,微重力作为一种机械因素,会影响间充质干细胞的分化和功能。在此,我们研究了模拟微重力对人脂肪来源干细胞(ADSCs)神经分化的影响。

材料与方法

我们使用快速旋转的回转器(clinorotation)来模拟微重力条件。采用实时定量聚合酶链反应(Real-time PCR)和流式细胞术分析,以评估模拟微重力对神经营养因子、其受体和神经标志物的调控作用,以及对细胞神经分化的影响。

结果

我们的数据显示,在神经分化前后,模拟微重力均上调了微管相关蛋白2(MAP-2)、脑源性神经营养因子(BDNF)、酪氨酸激酶受体B(TrkB)、神经营养因子3(NT-3)和酪氨酸激酶受体C(TrkC)的表达。此外,与1G对照组相比,微重力条件下源自ADSCs的神经细胞表达更多的MAP-2、胶质纤维酸性蛋白(GFAP)和突触素蛋白。

结论

我们表明,模拟微重力可增强间充质干细胞向神经元的分化。我们的研究结果为将ADSCs分化为神经样细胞以及可能的其他细胞谱系提供了一种新策略。同时,微重力模拟对细胞活力没有不利影响,可作为成功操控细胞的新环境。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b839/5339659/2bc50a12447a/IJBMS-20-178-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b839/5339659/e37bbd007e09/IJBMS-20-178-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b839/5339659/2bc50a12447a/IJBMS-20-178-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b839/5339659/e37bbd007e09/IJBMS-20-178-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b839/5339659/2bc50a12447a/IJBMS-20-178-g002.jpg

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