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Related Concept Videos

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Heterotrimeric G proteins are guanine nucleotide-binding proteins. As the name suggests, heterotrimeric G proteins are composed of three subunits: alpha, beta, and gamma. They remain GDP-bound or GTP-bound inside the cells and switch between inactive/active states. The Gα subunit possesses the nucleotide-binding pocket that binds guanine nucleotides and switches between GDP or GTP-bound states. In contrast, the Gꞵ and Gγ subunits are always bound together with high...
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In animal cells, the extracellular matrix allows cells within tissues to withstand external stresses and transmits signals from the outside of the cell to the inside. The extracellular matrix is extensive, and its composition varies between different types of tissues. For example, the reticular fibers and ground substance make up the ECM in loose connective tissue, while collagen and bone minerals make up the ECM of bone tissue. 
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Visualizing the mechanical activation of Src.

Yingxiao Wang1, Elliot L Botvinick, Yihua Zhao

  • 1Department of Bioengineering and the Whitaker Institute of Biomedical Engineering, La Jolla, California 92093, USA.

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|April 23, 2005
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Summary
This summary is machine-generated.

Mechanical forces trigger cell signaling through Src activation. A novel reporter reveals waves of Src activation propagating along cell membranes, guided by the cytoskeleton, offering insights into mechanotransduction.

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Area of Science:

  • Cellular mechanobiology
  • Biophysics
  • Molecular cell biology

Background:

  • Cellular functions are significantly influenced by mechanical cues.
  • The mechanisms of mechanical stimulus transduction into biochemical signals are not fully understood.
  • Src regulates integrin-cytoskeleton interactions, crucial for mechanical signal transduction.

Purpose of the Study:

  • To develop a tool for imaging and quantifying Src activation in live cells.
  • To investigate the spatio-temporal dynamics of Src activation in response to mechanical stimuli.
  • To elucidate the role of the cytoskeleton in transmitting mechanical signals.

Main Methods:

  • Development of a genetically encoded Src reporter using Förster resonance energy transfer (FRET).
  • Application of localized mechanical stimulation using laser-tweezer traction on human umbilical vein endothelial cells (HUVECs).
  • Imaging and quantification of Src activation dynamics in response to mechanical force.

Main Results:

  • Observed rapid, distal Src activation upon mechanical stimulation.
  • Detected a slower, directional wave propagation of Src activation along the plasma membrane at 18.1 nm/s.
  • Demonstrated that disruption of actin filaments or microtubules abolished force-induced Src activation.

Conclusions:

  • Mechanotransduction involves dynamic, cytoskeleton-mediated transmission of Src activation signals.
  • The developed Src reporter enables spatio-temporal characterization of mechanotransduction in live cells.
  • Mechanical forces direct biochemical signals through the cytoskeleton to specific cellular locations.