4.8 Article

Piezo1 Response to Shear Stress Is Controlled by the Components of the Extracellular Matrix

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume -, Issue -, Pages -

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.2c09169

Keywords

Piezo1; shear stress; mechanotransduction; extracellular matrix; integrins

Funding

  1. Australian Government Research Training Program Scholarship
  2. Australian Research Council (ARC) [LP190100728, DP200101248]
  3. NHMRC [GNT1174098]
  4. Australian Research Council [LP190100728] Funding Source: Australian Research Council

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This study investigates the influence of extracellular matrix (ECM) composition on the mechanosensitivity of the Piezo1 ion channel in response to hemodynamic forces. The presence of ECM proteins does not affect the sensitivity of Piezo1 to shear stress, but different ECM proteins regulate Piezo1 sensitivity depending on the shear stress level. These findings demonstrate that ECM/integrin interactions play a role in Piezo1 mechanosensitivity and provide new insights into how Piezo1 senses shear stress.
Piezo1 is a recently discovered Ca2+ permeable ion channel that has emerged as an integral sensor of hemodynamic forces within the cardiovascular system, contributing to vascular development and blood pressure regulation. However, how the composition of the extracellular matrix (ECM) affects the mechanosensitivity of Piezo1 in response to hemodynamic forces remains poorly understood. Using a combination of microfluidics and calcium imaging techniques, we probe the shear stress sensitivity of single HEK293T cells engineered to stably express Piezo1 in the presence of different ECM proteins. Our experiments show that Piezo1 sensitivity to shear stress is not dependent on the presence of ECM proteins. However, different ECM proteins regulate the sensitivity of Piezo1 depending on the shear stress level. Under high shear stress, fibronectin sensitizes Piezo1 response to shear, while under low shear stress, Piezo1 mechanosensitivity is improved in the presence of collagen types I and IV and laminin. Moreover, we report that alpha 5#1 and alpha v#3 integrins are involved in Piezo1 sensitivity at high shear, while alpha v#3 and alpha v#5 integrins are involved in regulating the Piezo1 response at low shear stress. These results demonstrate that the ECM/integrin interactions influence Piezo1 mechanosensitivity and could represent a mechanism whereby extracellular forces are transmitted to Piezo1 channels, providing new insights into the mechanism by which Piezo1 senses shear stress.

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