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Title:
Piezo1 is a mechanically activated ion channel and mediates pressure induced pancreatitis | Nature Communications
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Merely touching the pancreas can lead to premature zymogen activation and pancreatitis but the mechanism is not completely understood. Here we demonstrate that pancreatic acinar cells express the mechanoreceptor Piezo1 and application of pressure within the gland produces pancreatitis. To determine if this effect is through Piezo1 activation, we induce pancreatitis by intrapancreatic duct instillation of the Piezo1 agonist Yoda1. Pancreatitis induced by pressure within the gland is prevented by a Piezo1 antagonist. In pancreatic acinar cells, Yoda1 stimulates calcium influx and induces calcium-dependent pancreatic injury. Finally, selective acinar cell-specific genetic deletion of Piezo1 protects mice against pressure-induced pancreatitis. Thus, activation of Piezo1 in pancreatic acinar cells is a mechanism for pancreatitis and may explain why pancreatitis develops following pressure on the gland as in abdominal trauma, pancreatic duct obstruction, pancreatography, or pancreatic surgery. Piezo1 blockade may prevent pancreatitis when manipulation of the gland is anticipated. Manipulation of the pancreas during surgery can induce acute pancreatitis due to zymogen activation. Here the authors show that the mechanoreceptor Piezo1 is activated by pressure and its activation leads to calcium dependent pancreatic injury whereas its inhibition is protective against pancreatitis.
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piezo, pancreatic, pancreatitis, cells, pubmed, article, pressure, acinar, pancreas, mice, google, scholar, cas, yoda, duct, cell, fig, activation, min, nature, acute, gsmtx, calcium, acini, piezoaci, ion, channel, channels, tissue, central, number, supplementary, saline, solution, mpo, data, mechanically, activated, mechanical, effects, analyzed, experiments, catalog, analysis, intracellular, expressed, performed, genetic, deletion, chronic,
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nature portfolio ion channel partnerships privacy policy thermo scientific kit advertising ca2+release-activated ca2+channel blockade open allowing cations reprints nature 554 nature 527 nature 515 nature subjecting tamoxifen-treated ptf1a-creer calcium-dependent enzyme activation cryo-electron microscopy revealed quantitative reverse transcription-pcr pressure-activated ion channels glass coverslips pre-treated store-operated entry pathways34 buffered saline solutions injury-induced facultative restoration piezo1-facilitated calcium entry single-cell transcriptome analysis called low-pressure input piezo1-mediated mechanism wild-type littermates lacking permissions mediating pressure-induced pancreatitis mechanosensitive ion channels c57bl/6j male mice representative live-cell imaging real-time pcr procedures test solutions live-cell imaging studies cell death induced real-time rt-pcr multiple comparison post-test calcium-apoptosis link piezo1fl/fl animals lacking dmem/f12 media gsmtx4 pre-treatment indicating endoscopic retrograde cholangiopancreatography supplementary movie 1 supplementary movie 2 supplementary movie 3 provided critical review specific piezo1 agonist12 toxic ca2+signal generation vascular development cation channel piezo1
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headline:Piezo1 is a mechanically activated ion channel and mediates pressure induced pancreatitis
description:Merely touching the pancreas can lead to premature zymogen activation and pancreatitis but the mechanism is not completely understood. Here we demonstrate that pancreatic acinar cells express the mechanoreceptor Piezo1 and application of pressure within the gland produces pancreatitis. To determine if this effect is through Piezo1 activation, we induce pancreatitis by intrapancreatic duct instillation of the Piezo1 agonist Yoda1. Pancreatitis induced by pressure within the gland is prevented by a Piezo1 antagonist. In pancreatic acinar cells, Yoda1 stimulates calcium influx and induces calcium-dependent pancreatic injury. Finally, selective acinar cell-specific genetic deletion of Piezo1 protects mice against pressure-induced pancreatitis. Thus, activation of Piezo1 in pancreatic acinar cells is a mechanism for pancreatitis and may explain why pancreatitis develops following pressure on the gland as in abdominal trauma, pancreatic duct obstruction, pancreatography, or pancreatic surgery. Piezo1 blockade may prevent pancreatitis when manipulation of the gland is anticipated. Manipulation of the pancreas during surgery can induce acute pancreatitis due to zymogen activation. Here the authors show that the mechanoreceptor Piezo1 is activated by pressure and its activation leads to calcium dependent pancreatic injury whereas its inhibition is protective against pancreatitis.
datePublished:2018-04-30T00:00:00Z
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headline:Piezo1 is a mechanically activated ion channel and mediates pressure induced pancreatitis
description:Merely touching the pancreas can lead to premature zymogen activation and pancreatitis but the mechanism is not completely understood. Here we demonstrate that pancreatic acinar cells express the mechanoreceptor Piezo1 and application of pressure within the gland produces pancreatitis. To determine if this effect is through Piezo1 activation, we induce pancreatitis by intrapancreatic duct instillation of the Piezo1 agonist Yoda1. Pancreatitis induced by pressure within the gland is prevented by a Piezo1 antagonist. In pancreatic acinar cells, Yoda1 stimulates calcium influx and induces calcium-dependent pancreatic injury. Finally, selective acinar cell-specific genetic deletion of Piezo1 protects mice against pressure-induced pancreatitis. Thus, activation of Piezo1 in pancreatic acinar cells is a mechanism for pancreatitis and may explain why pancreatitis develops following pressure on the gland as in abdominal trauma, pancreatic duct obstruction, pancreatography, or pancreatic surgery. Piezo1 blockade may prevent pancreatitis when manipulation of the gland is anticipated. Manipulation of the pancreas during surgery can induce acute pancreatitis due to zymogen activation. Here the authors show that the mechanoreceptor Piezo1 is activated by pressure and its activation leads to calcium dependent pancreatic injury whereas its inhibition is protective against pancreatitis.
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