» Articles » PMID: 2000969

Removal of Sialic Acid Alters Both T- and L-type Calcium Currents in Cardiac Myocytes

Overview
Journal Am J Physiol
Specialty Physiology
Date 1991 Mar 1
PMID 2000969
Citations 17
Authors
Affiliations
Soon will be listed here.
Abstract

The whole cell configuration of the patch-clamp technique was used to test the hypothesis that the presence of sialic acid residues influences both T- and L-type Ca2+ currents (ICa,T and ICa,L) in cultured pacemaker cells isolated from the rabbit sinoatrial node. Removal of these anionic sugar moieties by neuraminidase (1.0 U/ml for 5-20 min) increased ICa,T in five of nine cells (by a factor of 2.2-5.1) and ICa,L in three of six cells (by a factor of 1.2-1.6). In cells that did not exhibit such an increase, the enzyme reduced ICa,T but had no significant effect on ICa,L. In cells that exhibited an increase in ICa,T, exposure to neuraminidase also shifted the activation curve to more negative potentials and increased the slope of the inactivation curve. The enzyme did not influence the gating of ICa,L or the rates of inactivation of either ICa,T or ICa,L. The enhancement of ICa,T and ICa,L could not be mimicked by including neuraminidase in the patch pipette or by adding a contaminant of the enzyme preparation, phospholipase C, to the bath. When external Ca2+ was replaced by Ba2+, neither ICa,T nor ICa,L was increased significantly by neuraminidase. It is proposed that by removing sialic acid residues neuraminidase might directly alter the gating of T-type Ca2+ channels. On the other hand, the increased amplitudes of ICa,T and ICa,L might be due to a rise in intracellular Ca2+.

Citing Articles

Neuraminidase-induced externalization of phosphatidylserine activates ADAM17 and impairs insulin signaling in endothelial cells.

Ferreira-Santos L, Ramirez-Perez F, Foote C, Augenreich M, McMillan N, Williams M Am J Physiol Heart Circ Physiol. 2023; 326(1):H270-H277.

PMID: 37999645 PMC: 11219045. DOI: 10.1152/ajpheart.00638.2023.


Models of the cardiac L-type calcium current: A quantitative review.

Agrawal A, Wang K, Polonchuk L, Cooper J, Hendrix M, Gavaghan D WIREs Mech Dis. 2022; 15(1):e1581.

PMID: 36028219 PMC: 10078428. DOI: 10.1002/wsbm.1581.


Neuraminidase-1 promotes heart failure after ischemia/reperfusion injury by affecting cardiomyocytes and invading monocytes/macrophages.

Heimerl M, Sieve I, Ricke-Hoch M, Erschow S, Battmer K, Scherr M Basic Res Cardiol. 2020; 115(6):62.

PMID: 32975669 PMC: 7519006. DOI: 10.1007/s00395-020-00821-z.


Modelling inherited cardiac disease using human induced pluripotent stem cell-derived cardiomyocytes: progress, pitfalls, and potential.

van Mil A, Balk G, Neef K, Buikema J, Asselbergs F, Wu S Cardiovasc Res. 2018; 114(14):1828-1842.

PMID: 30169602 PMC: 6887927. DOI: 10.1093/cvr/cvy208.


Reduced myocyte complex N-glycosylation causes dilated cardiomyopathy.

Ednie A, Deng W, Yip K, Bennett E FASEB J. 2018; 33(1):1248-1261.

PMID: 30138037 PMC: 6355090. DOI: 10.1096/fj.201801057R.