Anti-CACNA1G (internal region) polyclonal antibody

Low voltage-activated T-type calcium channels are encoded by a family of at least three genes, with additional diversity created by alternative splicing, This study describes the cloning of the human brain alpha 1G, which is a novel isoform, Ca(v)3.1c, Comparison of this sequence to genomic sequences deposited in the GenBank allowed us to identify the intron/exon boundaries of the human CACNA1G gene, A full-length cDNA mas constructed, then used to generate a stably-transfected mammalian cell line. The resulting currents were analyzed for their voltage- and time-dependent properties, These properties identify this gene as encoding a T-type Ca2+ channel. (C) 2000 Federation of European Biochemical Societies.

There has been a spectacular rise in the global prevalence of type 2 diabetes mellitus and cardiovascular complications are the major cause of morbidity and mortality in diabetic patients. The objective of the study was to investigate ventricular myocyte shortening, intracellular Ca2+ signalling and expression of genes encoding cardiac muscle proteins in the aged Zucker diabetic fatty (ZDF) rat. There was a fourfold elevation in non-fasting blood glucose in ZDF rats (478.43 +/- A 29.22 mg/dl) compared to controls (108.22 +/- A 2.52 mg/dl). Amplitude of shortening, time to peak (TPK) and time to half (THALF) relaxation of shortening were unaltered in ZDF myocytes compared to age-matched controls. Amplitude and THALF decay of the Ca2+ transient were unaltered; however, TPK Ca2+ transient was prolonged in ZDF myocytes (70.0 +/- A 3.2 ms) compared to controls (58.4 +/- A 2.3 ms). Amplitude of the L-type Ca2+ current was reduced across a wide range of test potentials (-30 to +40 mV) in ZDF myocytes compared to controls. Sarcoplasmic reticulum Ca2+ content was unaltered in ZDF myocytes compared to controls. Expression of genes encoding cardiac muscle proteins, membrane Ca2+ channels, and cell membrane ion transport and intracellular Ca2+ transport proteins were variously altered. Myh6, Tnnt2, Cacna2d3, Slc9a1, and Atp2a2 were downregulated while Myl2, Cacna1g, Cacna1h, and Atp2a1 were upregulated in ZDF ventricle compared to controls. The results of this study have demonstrated that preserved ventricular myocyte shortening is associated with altered mechanisms of Ca2+ transport and a changing pattern of genes encoding a variety of Ca2+ signalling and cardiac muscle proteins in aged ZDF rat.