Suppr超能文献

FBP17介导的正常细胞与RasV12转化细胞之间细胞竞争中的指状膜突起。

FBP17-mediated finger-like membrane protrusions in cell competition between normal and RasV12-transformed cells.

作者信息

Kamasaki Tomoko, Miyazaki Yumi, Ishikawa Susumu, Hoshiba Kazuya, Kuromiya Keisuke, Tanimura Nobuyuki, Mori Yusuke, Tsutsumi Motosuke, Nemoto Tomomi, Uehara Ryota, Suetsugu Shiro, Itoh Toshiki, Fujita Yasuyuki

机构信息

Division of Molecular Oncology, Institute for Genetic Medicine, Hokkaido University Graduate School of Chemical Sciences and Engineering, Sapporo, Hokkaido 060-0815, Japan.

Faculty of Advanced Life Science, Hokkaido University, Sapporo, Hokkaido 001-0021, Japan.

出版信息

iScience. 2021 Aug 18;24(9):102994. doi: 10.1016/j.isci.2021.102994. eCollection 2021 Sep 24.

Abstract

At the initial stage of carcinogenesis, cell competition often occurs between newly emerging transformed cells and the neighboring normal cells, leading to the elimination of transformed cells from the epithelial layer. For instance, when RasV12-transformed cells are surrounded by normal cells, RasV12 cells are apically extruded from the epithelium. However, the underlying mechanisms of this tumor-suppressive process still remain enigmatic. We first show by electron microscopic analysis that characteristic finger-like membrane protrusions are projected from both normal and RasV12 cells at their interface. In addition, FBP17, a member of the F-BAR proteins, accumulates in RasV12 cells, as well as surrounding normal cells, which plays a positive role in the formation of finger-like protrusions and apical elimination of RasV12 cells. Furthermore, cdc42 acts upstream of these processes. These results suggest that the cdc42/FBP17 pathway is a crucial trigger of cell competition, inducing "protrusion to protrusion response" between normal and RasV12-transformed cells.

摘要

在癌变的初始阶段,新出现的转化细胞与相邻的正常细胞之间经常发生细胞竞争,导致转化细胞从上皮层中被清除。例如,当RasV12转化细胞被正常细胞包围时,RasV12细胞会从上皮顶端被挤出。然而,这种肿瘤抑制过程的潜在机制仍然不明。我们首先通过电子显微镜分析表明,在正常细胞和RasV12细胞的界面处,两者都会伸出特征性的手指状膜突起。此外,F-BAR蛋白家族成员FBP17在RasV12细胞以及周围的正常细胞中积累,它在手指状突起的形成和RasV12细胞的顶端清除中发挥积极作用。此外,cdc42在这些过程的上游起作用。这些结果表明,cdc42/FBP17通路是细胞竞争的关键触发因素,诱导正常细胞与RasV12转化细胞之间的“突起对突起反应”。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0c8/8405961/9a63d5a98b28/fx1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验