转分化
间充质干细胞
小岛
胰腺
骨髓
细胞生物学
生物
细胞分化
脂肪生成
胰岛素
干细胞
内分泌学
免疫学
生物化学
基因
作者
Huifeng Wang,Yichen Xu,Liqing Wu,Yali Kou,Zhuo Wu,Wenjing Zhao,Yashu Wei,Hongjing Liu,Weiping Chen
出处
期刊:ISP medicine
[I-Scientific Publication]
日期:2019-01-01
卷期号:3 (1): 1-12
被引量:1
标识
DOI:10.52274/ispmed20190908
摘要
Bone marrow mesenchymal stem cells (BM-MSCs) could differentiate into Insulin Producing Cells(IPCs) with notable advantages. The present study tried to develop a method may be able to use a normal regenerating pancreas extract(N-RPE) medium to induce BM-MSCs into islet phenotype, in tests to assess how efficient method and simple duplicate the novel condition medium protocol is. Isolate and purify MSCs from rat bone marrow. BM-MSCs were differentiated into Adipogenic, Osteogenic and Myocardium and the lineages were assessed its multi-lineage potential. Islet differentiation medium, blending rabbit conditioned medium N-RPE, was administered to rat BM-MSCs. After 15 days, differentiation was evaluated by lineage-specific morphology and three stages could be observed: induced cells, islet like cells(ILCs) and islet like structures(ILSs). The morphology, SEM, DTZ staining, Mallory staining, HE staining and glucose stimulation demonstrated that the N-RPE could stimulate suitable development microenvironment to supply the islet differentiate from BM-MSCs. In addition, islet-related genes (ins/glu) expression and proteins(insulin/glucagon) expression suggested that culture medium rabbit N-RPE enhanced the rat BM-MSCs transdifferentiation efficiency. N-RPE derived from normal pancreas tissue could promote pancreas development of microenvironment and significantly enhance the transdifferentiation of BM-MSCs into ILSs. Results from this work will contribute to optimize the conditions of BM-MSCs and supply a new strategy for the development of islet tissue engineering.
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