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定义激活整合素和 Notch 信号所需的单个分子力。

Defining single molecular forces required to activate integrin and notch signaling.

机构信息

Department of Physics, Center for the Physics of Living Cells and Institute for Genomic Biology University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.

出版信息

Science. 2013 May 24;340(6135):991-4. doi: 10.1126/science.1231041.

Abstract

Cell-cell and cell-matrix mechanical interactions through membrane receptors direct a wide range of cellular functions and orchestrate the development of multicellular organisms. To define the single molecular forces required to activate signaling through a ligand-receptor bond, we developed the tension gauge tether (TGT) approach in which the ligand is immobilized to a surface through a rupturable tether before receptor engagement. TGT serves as an autonomous gauge to restrict the receptor-ligand tension. Using a range of tethers with tunable tension tolerances, we show that cells apply a universal peak tension of about 40 piconewtons (pN) to single integrin-ligand bonds during initial adhesion. We find that less than 12 pN is required to activate Notch receptors. TGT can also provide a defined molecular mechanical cue to regulate cellular functions.

摘要

细胞膜受体介导的细胞-细胞和细胞-基质相互作用可以指导广泛的细胞功能,并协调多细胞生物的发育。为了定义激活配体-受体键合信号所需的单个分子力,我们开发了张力计系绳(TGT)方法,其中在受体结合之前,通过可断裂的系绳将配体固定在表面上。TGT 作为一个自主的测量仪,限制了受体-配体的张力。我们使用一系列具有可调张力容限的系绳,表明细胞在初始黏附过程中对单个整合素-配体键施加约 40 皮牛顿(pN)的通用峰值张力。我们发现,激活 Notch 受体所需的张力小于 12 pN。TGT 还可以提供定义明确的分子力学线索来调节细胞功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09d4/3710701/3652b185fe09/nihms-487887-f0001.jpg

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