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模拟微重力会引发人角质细胞的上皮间质转化。

Simulated microgravity triggers epithelial mesenchymal transition in human keratinocytes.

机构信息

Dipartimento di Medicina Clinica e Molecolare, Sapienza Università di Roma, Rome, Italy.

Dipartimento di Medicina Sperimentale, Seconda Università di Napoli, Napoli, Italy.

出版信息

Sci Rep. 2017 Apr 3;7(1):538. doi: 10.1038/s41598-017-00602-0.

Abstract

The microgravitational environment is known to affect the cellular behaviour inducing modulation of gene expression and enzymatic activities, epigenetic modifications and alterations of the structural organization. Simulated microgravity, obtained in the laboratory setting through the use of a Random Positioning Machine (RPM), represents a well recognized and useful tool for the experimental studies of the cellular adaptations and molecular changes in response to weightlessness. Short exposure of cultured human keratinocytes to the RPM microgravity influences the cellular circadian clock oscillation. Therefore, here we searched for changes on the regenerative ability and response to tissue damage of human epidermal cells through the analysis of the effects of the simulated microgravity on the re-epithelialization phase of the repair and wound healing process. Combining morphological, biochemical and molecular approaches, we found that the simulated microgravity exposure of human keratinocytes promotes a migratory behavior and triggers the epithelial-mesenchymal transition (EMT) through expression of the typical EMT transcription factors and markers, such as Snail1, Snail2 and ZEB2, metalloproteases, mesenchymal adhesion molecules and cytoskeletal components.

摘要

微重力环境已知会影响细胞行为,诱导基因表达和酶活性的调节、表观遗传修饰以及结构组织的改变。通过使用随机定位机(RPM)在实验室环境中模拟微重力,是研究细胞适应和分子变化以应对失重的一种公认且有用的工具。培养的人角质形成细胞短暂暴露于 RPM 微重力会影响细胞的昼夜节律振荡。因此,在这里,我们通过分析模拟微重力对修复和伤口愈合过程中再上皮化阶段的影响,寻找对人表皮细胞再生能力和对组织损伤反应的变化。通过结合形态学、生化和分子方法,我们发现人角质形成细胞的模拟微重力暴露促进迁移行为,并通过表达典型的 EMT 转录因子和标志物(如 Snail1、Snail2 和 ZEB2)、金属蛋白酶、间充质黏附分子和细胞骨架成分触发上皮-间充质转化(EMT)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b9c/5428850/a2f8e4181315/41598_2017_602_Fig1_HTML.jpg

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