| Literature DB >> 27247394 |
Mark D Levin1, Gautam K Singh1, Hai Xia Zhang2, Keita Uchida2, Beth A Kozel1, Phyllis K Stein3, Atilla Kovacs3, Ruth E Westenbroek4, William A Catterall5, Dorothy Katherine Grange1, Colin G Nichols6.
Abstract
Cantu syndrome (CS) is caused by gain-of-function (GOF) mutations in genes encoding pore-forming (Kir6.1, KCNJ8) and accessory (SUR2, ABCC9) KATP channel subunits. We show that patients with CS, as well as mice with constitutive (cGOF) or tamoxifen-induced (icGOF) cardiac-specific Kir6.1 GOF subunit expression, have enlarged hearts, with increased ejection fraction and increased contractility. Whole-cell voltage-clamp recordings from cGOF or icGOF ventricular myocytes (VM) show increased basal L-type Ca(2+) current (LTCC), comparable to that seen in WT VM treated with isoproterenol. Mice with vascular-specific expression (vGOF) show left ventricular dilation as well as less-markedly increased LTCC. Increased LTCC in KATP GOF models is paralleled by changes in phosphorylation of the pore-forming α1 subunit of the cardiac voltage-gated calcium channel Cav1.2 at Ser1928, suggesting enhanced protein kinase activity as a potential link between increased KATP current and CS cardiac pathophysiology.Entities:
Keywords: KATP; KCNJ8; Kir6.1; cardiovascular system; transgenic
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Year: 2016 PMID: 27247394 PMCID: PMC4914204 DOI: 10.1073/pnas.1606465113
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205