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细胞在微图案上的黏附重排受 Piezo1 通道调控。

Adherent cell remodeling on micropatterns is modulated by Piezo1 channels.

机构信息

Department of Mechanical and Aerospace Engineering, University at Buffalo, Buffalo, NY, 14260, USA.

Department of Physiology and Biophysics, University at Buffalo, Buffalo, NY, 14260, USA.

出版信息

Sci Rep. 2021 Mar 3;11(1):5088. doi: 10.1038/s41598-021-84427-y.

Abstract

Adherent cells utilize local environmental cues to make decisions on their growth and movement. We have previously shown that HEK293 cells grown on the fibronectin stripe patterns were elongated. Here we show that Piezo1 function is involved in cell spreading. Piezo1 expressing HEK cells plated on fibronectin stripes elongated, while a knockout of Piezo1 eliminated elongation. Inhibiting Piezo1 conductance using GsMTx4 or Gd blocked cell spreading, but the cells grew thin tail-like extensions along the patterns. Images of GFP-tagged Piezo1 showed plaques of Piezo1 moving to the extrusion edges, co-localized with focal adhesions. Surprisingly, in non-spreading cells Piezo1 was located primarily on the nuclear envelope. Inhibiting the Rho-ROCK pathway also reversibly inhibited cell extension indicating that myosin contractility is involved. The growth of thin extrusion tails did not occur in Piezo1 knockout cells suggesting that Piezo1 may have functions besides acting as a cation channel.

摘要

贴壁细胞利用局部环境线索来决定其生长和运动。我们之前已经表明,在纤连蛋白条带图案上生长的 HEK293 细胞会伸长。在这里,我们显示 Piezo1 功能参与细胞扩展。在纤连蛋白条带上培养的表达 Piezo1 的 HEK 细胞伸长,而 Piezo1 的敲除消除了伸长。使用 GsMTx4 或 Gd 抑制 Piezo1 电导会阻止细胞扩展,但细胞会沿着图案生长出细的尾状延伸。GFP 标记的 Piezo1 的图像显示 Piezo1 斑块移动到挤出边缘,与焦点粘连共定位。令人惊讶的是,在非扩展细胞中,Piezo1 主要位于核膜上。抑制 Rho-ROCK 途径也可逆地抑制细胞延伸,表明肌球蛋白收缩性参与其中。在 Piezo1 敲除细胞中不会发生细挤出尾巴的生长,这表明 Piezo1 可能除了作为阳离子通道之外还有其他功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5984/7930019/ccff1dac4238/41598_2021_84427_Fig1_HTML.jpg

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