{"title":"兔正常再生胰腺提取物体外诱导大鼠骨髓间充质干细胞转化为胰岛样结构细胞","authors":"Huifeng Wang, Yichen Xu, Liqing Wu, Yali Kou, Zhuo Wu, Wen-hong Zhao, Y. Wei, Hongjing Liu, Weiping Chen","doi":"10.52274/ispmed20190908","DOIUrl":null,"url":null,"abstract":"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.","PeriodicalId":243745,"journal":{"name":"ISP Medicine","volume":"8 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Rabbit Normal Regenerating Pancreas Extract induces rat BM-MSCs into Pancreatic Islet-like Structure Cells in vitro\",\"authors\":\"Huifeng Wang, Yichen Xu, Liqing Wu, Yali Kou, Zhuo Wu, Wen-hong Zhao, Y. Wei, Hongjing Liu, Weiping Chen\",\"doi\":\"10.52274/ispmed20190908\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"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.\",\"PeriodicalId\":243745,\"journal\":{\"name\":\"ISP Medicine\",\"volume\":\"8 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1900-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ISP Medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.52274/ispmed20190908\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ISP Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.52274/ispmed20190908","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
摘要
骨髓间充质干细胞(Bone marrow mesenchymal stem cells, BM-MSCs)具有向胰岛素生成细胞(Insulin production cells, IPCs)分化的显著优势。本研究试图开发一种方法,可能能够使用正常再生胰腺提取物(N-RPE)培养基诱导BM-MSCs进入胰岛表型,在测试中评估该方法的有效性和简单复制的新条件培养基方案。从大鼠骨髓中分离纯化MSCs。将骨髓间充质干细胞分化为成脂型、成骨型和心肌型,并评估其多系潜能。大鼠脑间充质干细胞采用混合兔条件培养基N-RPE的胰岛分化培养基。15天后,通过谱系特异性形态学评估分化情况,可以观察到三个阶段:诱导细胞、胰岛样细胞(ILCs)和胰岛样结构(ILSs)。形态学、扫描电镜(SEM)、DTZ染色、Mallory染色、HE染色及葡萄糖刺激结果表明,N-RPE能刺激胰岛细胞向BM-MSCs分化提供适宜的发育微环境。此外,胰岛相关基因(ins/glu)和蛋白(胰岛素/胰高血糖素)的表达表明,培养兔N-RPE可提高大鼠BM-MSCs的转分化效率。来源于正常胰腺组织的N-RPE能够促进胰腺微环境的发育,显著增强BM-MSCs向ILSs的转分化。本研究结果将有助于优化骨髓间充质干细胞的培养条件,并为胰岛组织工程的发展提供新的策略。
Rabbit Normal Regenerating Pancreas Extract induces rat BM-MSCs into Pancreatic Islet-like Structure Cells in vitro
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.