{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,29]],"date-time":"2026-09-29T17:16:22Z","timestamp":1790702182554,"version":"4.1.0"},"reference-count":61,"publisher":"American Physiological Society","issue":"2","funder":[{"DOI":"10.13039\/100015627","name":"QUEST Diagnostics","doi-asserted-by":"crossref","award":["NA"],"award-info":[{"award-number":["NA"]}],"id":[{"id":"10.13039\/100015627","id-type":"DOI","asserted-by":"crossref"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["American Journal of Physiology-Cell Physiology"],"published-print":{"date-parts":[[2019,8,1]]},"abstract":"<jats:p> Hereditary xerocytosis (HX) is caused by missense mutations in either the mechanosensitive cation channel PIEZO1 or the Ca<jats:sup>2+<\/jats:sup>-activated K<jats:sup>+<\/jats:sup> channel KCNN4. All HX-associated KCNN4 mutants studied to date have revealed increased current magnitude and red cell dehydration. Baseline KCNN4 activity was increased in HX red cells heterozygous for KCNN4 mutant V282M. However, HX red cells maximally stimulated by Ca<jats:sup>2+<\/jats:sup> ionophore A23187 or by PMCA Ca<jats:sup>2+<\/jats:sup>-ATPase inhibitor orthovanadate displayed paradoxically reduced KCNN4 activity. This reduced Ca<jats:sup>2+<\/jats:sup>-stimulated mutant KCNN4 activity in HX red cells was associated with unchanged sensitivity to KCNN4 inhibitor senicapoc and KCNN4 activator Ca<jats:sup>2+<\/jats:sup>, with slightly elevated Ca<jats:sup>2+<\/jats:sup> uptake and reduced PMCA activity, and with decreased KCNN4 activation by calpain inhibitor PD150606. The altered intracellular monovalent cation content of HX red cells prompted experimental nystatin manipulation of red cell Na and K contents. Nystatin-mediated reduction of intracellular K<jats:sup>+<\/jats:sup> with corresponding increase in intracellular Na<jats:sup>+<\/jats:sup> in wild-type cells to mimic conditions of HX greatly suppressed vanadate-stimulated and A23187 -stimulated KCNN4 activity in those wild-type cells. However, conferral of wild-type cation contents on HX red cells failed to restore wild-type-stimulated KCNN4 activity to those HX cells. The phenotype of reduced, maximally stimulated KCNN4 activity was shared by HX erythrocytes expressing heterozygous PIEZO1 mutants R2488Q and V598M, but not by HX erythrocytes expressing heterozygous KCNN4 mutant R352H or PIEZO1 mutant R2456H. Our data suggest that chronic KCNN4-driven red cell dehydration and intracellular cation imbalance can lead to reduced KCNN4 activity in HX and wild-type red cells. <\/jats:p>","DOI":"10.1152\/ajpcell.00074.2019","type":"journal-article","created":{"date-parts":[[2019,5,15]],"date-time":"2019-05-15T19:14:02Z","timestamp":1557947642000},"page":"C287-C302","source":"Crossref","is-referenced-by-count":17,"title":["Erythrocyte ion content and dehydration modulate maximal Gardos channel activity in KCNN4 V282M\/+ hereditary xerocytosis red cells"],"prefix":"10.1152","volume":"317","author":[{"given":"Alicia","family":"Rivera","sequence":"first","affiliation":[{"name":"Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David H.","family":"Vandorpe","sequence":"additional","affiliation":[{"name":"Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Boris E.","family":"Shmukler","sequence":"additional","affiliation":[{"name":"Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Immacolata","family":"Andolfo","sequence":"additional","affiliation":[{"name":"Department of Molecular Medicine and Medical Biotechnologies, \u201cFederico II\u201d University of Naples, CEINGE Biotecnologie Avanzate, Naples, Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Achille","family":"Iolascon","sequence":"additional","affiliation":[{"name":"Department of Molecular Medicine and Medical Biotechnologies, \u201cFederico II\u201d University of Naples, CEINGE Biotecnologie Avanzate, Naples, Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Natasha M.","family":"Archer","sequence":"additional","affiliation":[{"name":"Division of Hematology and Oncology, Boston Children\u2019s Hospital, Dana-Farber Cancer Center, Department of Pediatrics, Harvard Medical School, Boston, Massachusetts"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Estela","family":"Shabani","sequence":"additional","affiliation":[{"name":"Department of Immunology and Infectious Diseases, Harvard T. 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