Electrophysiological Recordings of Single-cell Ion Currents Under Well-defined Shear Stress.

J Vis Exp

Department of Medicine, Division of Pulmonary, Critical Care, Sleep and Allergy, University of Illinois at Chicago.

Published: August 2019

AI Article Synopsis

  • Fluid shear stress significantly influences endothelial function, promoting vasodilation in response to increased blood flow and highlighting the role of shear patterns in atherosclerosis development, with laminar stress being protective while disturbed stress is harmful.
  • Mechanosensitive ion channels are crucial for translating mechanical shear stress into cellular responses that regulate the production of vasoactive substances, with specific channels linked to vasodilation and vasoconstriction.
  • Research is challenged by the difficulty of recording real-time activation of these ion channels under shear stress, and a new modified parallel plate flow chamber protocol aims to overcome this obstacle for better understanding endothelial dysfunction and atherogenesis.

Article Abstract

Fluid shear stress is well known to play a major role in endothelial function. In most vascular beds, elevated shear stress from acute increases in blood flow triggers a signaling cascade resulting in vasodilation thereby alleviating mechanical stress on the vascular wall. The pattern of shear stress is also well known to be a critical factor in the development of atherosclerosis with laminar shear stress being atheroprotective and disturbed shear stress being pro-atherogenic. While we have a detailed understanding of the various intermediate cell signaling pathways, the receptors that first translate the mechanical stimulus into chemical mediators are not completely understood. Mechanosensitive ion channels are critical to the response to shear and regulate shear-induced cell signaling thereby controlling the production of vasoactive mediators. These channels are among the earliest activated signaling components to shear and have been linked to shear-induced vasodilation through promoting nitric oxide production (e.g., inwardly rectifying K [Kir] and transient receptor potential [TRP] channels) and endothelium hyperpolarizing factor (e.g., Kir and calcium-activated K [KCa] channels) and shear-induced vasoconstriction through an undetermined mechanism that involves piezo channels. Understanding the biophysical mechanism by which these channels are activated by shear forces (i.e., directly or through a primary mechano-receptor) could provide potential new targets to resolve the pathophysiology associated with endothelial dysfunction and atherogenesis. It is still a major challenge to record flow-induced activation of ion channels in real time using electrophysiology. The standard methods to expose cells to well-defined shear stress, such as the cone and plate rheometer and closed parallel plate flow chamber do not allow real time study of ion channel activation. The goal of this protocol is to describe a modified parallel plate flow chamber that allows real time electrophysiological recording of mechanosensitive ion channels under well-defined shear stress.

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Source
http://dx.doi.org/10.3791/59776DOI Listing

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