Zhao Dan, Xue Changyue, Lin Shiyu, Shi Sirong, Li Qianshun, Liu Mengting, Cai Xiaoxiao, Lin Yunfeng
State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, P. R. China.
J Cell Physiol. 2017 Jun;232(6):1548-1558. doi: 10.1002/jcp.25681. Epub 2016 Nov 20.
This study aimed to investigate the role of Notch signaling pathway for angiogenesis in a three-dimensional (3D) collagen gel model with co-culture of adipose-derived stromal cells (ASCs) and endothelial cells (ECs). A 3D collagen gel model was established in vitro by implanting both ASCs from green fluorescent protein-labeled mouse and ECs from red fluorescent protein-labeled mouse, and the phenomena of angiogenesis with Notch signaling inducer Jagged1, inhibitor DAPT and PBS, respectively were observed by confocal laser scanning microscopy. Semi-quantitative PCR and immunofluorescent staining were conducted to detect expressions of angiogenesis-related genes and proteins. Angiogenesis in the co-culture gels was promoted by Jagged1 treatment while attenuated by DAPT treatment, compared to control group. In co-culture system of ASCs and ECs, the gene expressions of VEGFA, VEGFB, Notch1, Notch2, Hes1, Hey1, VEGFR1,and the protein expression of VEGFA, VEGFB, Notch1, Hes1, Hey1 were increased by Jagged1 treatment and decreased by DAPT treatment in ECs. And the result of VEGFR3 was the opposite. However, the same results did not appear completely in ASCs. These results revealed the VEGFA/B-Notch1/2-Hes1/Hey1- VEGFR1/3 signal axis played an important role in angiogenesis when ASCs and ECs were co-cultured in a 3D collagen gel model. J. Cell. Physiol. 232: 1548-1558, 2017. © 2016 Wiley Periodicals, Inc.
本研究旨在探讨Notch信号通路在脂肪来源基质细胞(ASC)与内皮细胞(EC)共培养的三维(3D)胶原凝胶模型中对血管生成的作用。通过植入绿色荧光蛋白标记小鼠的ASC和红色荧光蛋白标记小鼠的EC在体外建立3D胶原凝胶模型,并用共聚焦激光扫描显微镜分别观察Notch信号诱导剂Jagged1、抑制剂DAPT和PBS作用下的血管生成现象。进行半定量PCR和免疫荧光染色以检测血管生成相关基因和蛋白的表达。与对照组相比,Jagged1处理促进了共培养凝胶中的血管生成,而DAPT处理则使其减弱。在ASC与EC的共培养体系中,Jagged1处理使EC中VEGFA、VEGFB、Notch1、Notch2、Hes1、Hey1、VEGFR1的基因表达以及VEGFA、VEGFB、Notch1、Hes1、Hey1的蛋白表达增加,DAPT处理则使其降低。而VEGFR3的结果相反。然而,在ASC中并未完全出现相同的结果。这些结果表明,当ASC与EC在3D胶原凝胶模型中共培养时,VEGFA/B-Notch1/2-Hes1/Hey1-VEGFR1/3信号轴在血管生成中起重要作用。《细胞生理学杂志》2017年第232卷:1548 - 1558页。© 2016威利期刊公司