Abstract

Mechanosensitive ion channels rely on membrane composition to transduce physical stimuli into electrical signals. The Piezo1 channel mediates mechanoelectrical transduction and regulates crucial physiological processes, including vascular architecture and remodeling, cell migration, and erythrocyte volume. The identity of the membrane components that modulate Piezo1 function remain largely unknown. Using lipid profiling analyses, we here identify dietary fatty acids that tune Piezo1 mechanical response. We find that margaric acid, a saturated fatty acid present in dairy products and fish, inhibits Piezo1 activation and polyunsaturated fatty acids (PUFAs), present in fish oils, modulate channel inactivation. Force measurements reveal that margaric acid increases membrane bending stiffness, whereas PUFAs decrease it. We use fatty acid supplementation to abrogate the phenotype of gain-of-function Piezo1 mutations causing human dehydrated hereditary stomatocytosis. Beyond Piezo1, our findings demonstrate that cell-intrinsic lipid profile and changes in the fatty acid metabolism can dictate the cell’s response to mechanical cues.

Highlights

  • Mechanosensitive ion channels rely on membrane composition to transduce physical stimuli into electrical signals

  • We find that when part of the plasma membrane, the saturated fatty acid margaric acid (MA; C17) inhibits Piezo[1] currents, whereas C20 and C22 polyunsaturated fatty acids (PUFAs) regulates inactivation

  • We demonstrate here that culturing N2A cells with a fatty acid enriched in human microvascular endothelial cells (HMVEC) changes Piezo[1] to feature currents similar to the ones found in HMVEC

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Summary

Introduction

Mechanosensitive ion channels rely on membrane composition to transduce physical stimuli into electrical signals. The Piezo[1] channel mediates mechanoelectrical transduction and regulates crucial physiological processes, including vascular architecture and remodeling, cell migration, and erythrocyte volume. The Piezo[1] mechanosensitive cation channel has been shown to mediate crucial physiological processes that include, but are not limited to, blood pressure regulation[1,2,3], vascular architecture and remodeling[4,5], erythrocyte volume regulation[6], chondrocyte mechanotransduction[7,8], lineage choice in neural stem cells[9], and association of neurons with astrocytes[10]. The most common fatty acids in membrane lipids have 14–22 carbon atoms and carry one unsaturation (e.g., oleic acid), and in some cases as many as six double bonds[29] These chemical features confer cells the capacity to control membrane thickness and fluidity in different physiological contexts. We find that when part of the plasma membrane, the saturated fatty acid margaric acid (MA; C17) inhibits Piezo[1] currents, whereas C20 (arachidonic acid [AA] and EPA) and C22

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