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PI3K/Akt信号通路小分子抑制剂促进在电纺聚己内酯/胶原蛋白生物复合支架上培养的人子宫内膜干细胞向运动神经元分化。

Inhibitor of PI3K/Akt Signaling Pathway Small Molecule Promotes Motor Neuron Differentiation of Human Endometrial Stem Cells Cultured on Electrospun Biocomposite Polycaprolactone/Collagen Scaffolds.

作者信息

Ebrahimi-Barough Somayeh, Hoveizi Elham, Yazdankhah Meysam, Ai Jafar, Khakbiz Mehrdad, Faghihi Faezeh, Tajerian Roksana, Bayat Neda

机构信息

Department of Tissue Engineering and Applied Cell Sciences, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.

Department of Biology, Faculty of Sciences, Shahid Chamran University , Ahvaz, Iran.

出版信息

Mol Neurobiol. 2017 May;54(4):2547-2554. doi: 10.1007/s12035-016-9828-z. Epub 2016 Mar 18.

Abstract

Small molecules as useful chemical tools can affect cell differentiation and even change cell fate. It is demonstrated that LY294002, a small molecule inhibitor of phosphatidylinositol 3-kinase (PI3K)/Akt signal pathway, can inhibit proliferation and promote neuronal differentiation of mesenchymal stem cells (MSCs). The purpose of this study was to investigate the differentiation effect of Ly294002 small molecule on the human endometrial stem cells (hEnSCs) into motor neuron-like cells on polycaprolactone (PCL)/collagen scaffolds. hEnSCs were cultured in a neurogenic inductive medium containing 1 μM LY294002 on the surface of PCL/collagen electrospun fibrous scaffolds. Cell attachment and viability of cells on scaffolds were characterized by scanning electron microscope (SEM) and 3-(4,5-dimethylthiazoyl-2-yl)2,5-diphenyltetrazolium bromide (MTT) assay. The expression of neuron-specific markers was assayed by real-time PCR and immunocytochemistry analysis after 15 days post induction. Results showed that attachment and differentiation of hEnSCs into motor neuron-like cells on the scaffolds with Ly294002 small molecule were higher than that of the cells on tissue culture plates as control group. In conclusion, PCL/collagen electrospun scaffolds with Ly294002 have potential for being used in neural tissue engineering because of its bioactive and three-dimensional structure which enhances viability and differentiation of hEnSCs into neurons through inhibition of the PI3K/Akt pathway. Thus, manipulation of this pathway by small molecules can enhance neural differentiation.

摘要

小分子作为有用的化学工具,可以影响细胞分化甚至改变细胞命运。已证明,磷脂酰肌醇3激酶(PI3K)/Akt信号通路的小分子抑制剂LY294002可抑制间充质干细胞(MSC)的增殖并促进其向神经元分化。本研究的目的是探讨LY294002小分子对人子宫内膜干细胞(hEnSC)在聚己内酯(PCL)/胶原蛋白支架上分化为运动神经元样细胞的作用。将hEnSC培养在PCL/胶原蛋白电纺纤维支架表面含1μM LY294002的神经诱导培养基中。通过扫描电子显微镜(SEM)和3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)法对支架上细胞的附着和活力进行表征。诱导后15天,通过实时PCR和免疫细胞化学分析检测神经元特异性标志物的表达。结果显示,与作为对照组的组织培养板上的细胞相比,hEnSC在含有LY294002小分子的支架上向运动神经元样细胞的附着和分化更高。总之,含有LY294002的PCL/胶原蛋白电纺支架因其生物活性和三维结构而具有用于神经组织工程的潜力,该结构通过抑制PI3K/Akt途径增强hEnSC向神经元的活力和分化。因此,通过小分子操纵该途径可增强神经分化。

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