Molecular Pharmacology Laboratory, Institute of Molecular Medicine, Peking University, 100871, Beijing, China; Translational and Regenerative Medicine Centre, Aston Medical School, Aston University, Birmingham, B4 7ET, UK.
Molecular Pharmacology Laboratory, Institute of Molecular Medicine, Peking University, 100871, Beijing, China.
Biochem Biophys Res Commun. 2021 Jan 1;534:1020-1025. doi: 10.1016/j.bbrc.2020.10.046. Epub 2020 Oct 31.
Significant cellular morphology changes in renal tubules were observed in diabetes patients and animal models. However, the interaction between insulin and tubular epithelial cells microvillar structure remains obscure. To understand microvillar dynamics, we used Scanning Ion Conductance Microscope to visualize microvillar in the living cell. Here, we found two layers of microvilli on the tubular epithelial cell surface: short compact microvilli and netlike long microvilli. Insulin treatment could increase microvilli length and density. This process was mediated by the PIK/PLCγ signaling pathway, other than the PIK/Arp2/3 signal pathway. In conclusion, our findings present a novel insulin signaling transduction mechanism, which contributes to understanding renal tubular epithelial cell microvilli dynamic regulation.
在糖尿病患者和动物模型中观察到肾小管细胞形态发生显著变化。然而,胰岛素与肾小管上皮细胞微绒毛结构之间的相互作用仍不清楚。为了了解微绒毛的动力学,我们使用扫描离子电导显微镜来观察活细胞中的微绒毛。在这里,我们发现肾小管上皮细胞表面有两层微绒毛:短而紧凑的微绒毛和网状长微绒毛。胰岛素处理可以增加微绒毛的长度和密度。这个过程是由 PIK/PLCγ 信号通路介导的,而不是 PIK/Arp2/3 信号通路。总之,我们的发现提出了一种新的胰岛素信号转导机制,有助于理解肾小管上皮细胞微绒毛的动态调节。