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Updated: Oct 11, 2026

Isolation of Human Atrial Myocytes for Simultaneous Measurements of Ca2+ Transients and Membrane Currents
Published on: July 3, 2013
T-type calcium currents in rat cardiomyocytes during postnatal development: contribution to hormone secretion
V Leuranguer1, A Monteil, E Bourinet
1Physiopathologie des Canaux Ioniques, Institut de Génétique Humaine-Centre National de la Recherche Scientifique (CNRS) UPR 1142, 34396 Montpellier cedex 05, France.
Abstract:
T-type Ca(2+) channels have been suggested to play a role in cardiac automaticity, cell growth, and cardiovascular remodeling. Although three genes encoding for a T-type Ca(2+) channel have been identified, the nature of the isoform(s) supporting the cardiac T-type Ca(2+) current (I(Ca,T)) has not yet been determined. We describe the postnatal evolution of I(Ca,T) density in freshly dissociated rat atrial and ventricular myocytes and its functional properties at peak current density in young atrial myocytes. I(Ca,T) displays a classical low activation threshold, rapid inactivation kinetics, negative steady-state inactivation, slow deactivation, and the presence of a window current. Interestingly, I(Ca,T) is poorly sensitive to Ni(2+) and insensitive to R-type current toxin SNX-482. RT-PCR experiments and comparison of functional properties with recombinant Ca(2+) channel subtypes suggest that neonatal I(Ca,T) is related to the alpha(1G)-subunit. Atrial natriuretic factor (ANF) secretion was measured using peptide radioimmunoassays in atrial tissue. Pharmacological dissection of ANF secretion indicates an important contribution of I(Ca,T) to Ca(2+) signaling during the neonatal period.
Insights
Neonatal T-type calcium channels (I(Ca,T)) in rat hearts are primarily linked to the alpha(1G)-subunit. These channels significantly influence atrial natriuretic factor secretion and calcium signaling in early development.
Area of Science:
- Cardiovascular Physiology
- Molecular Cardiology
- Ion Channel Biology
Background:
- T-type Ca(2+) channels are implicated in cardiac functions like automaticity and remodeling.
- The specific isoforms responsible for cardiac T-type Ca(2+) current (I(Ca,T)) remain unidentified.
Purpose of the Study:
- To characterize the postnatal development and functional properties of cardiac I(Ca,T).
- To identify the molecular correlate of I(Ca,T) in neonatal rat cardiomyocytes.
- To investigate the role of I(Ca,T) in atrial natriuretic factor (ANF) secretion.
Main Methods:
- Patch-clamp electrophysiology on freshly dissociated rat atrial and ventricular myocytes.
- RT-PCR to analyze gene expression of Ca(2+) channel subtypes.
- Measurement of ANF secretion using peptide radioimmunoassays.
Main Results:
- I(Ca,T) density evolves postnatally in rat atrial and ventricular myocytes.
- Neonatal I(Ca,T) exhibits characteristic kinetics and is poorly sensitive to Ni(2+).
- Functional properties and RT-PCR suggest neonatal I(Ca,T) involves the alpha(1G)-subunit.
- I(Ca,T) significantly contributes to ANF secretion and Ca(2+) signaling in neonates.
Conclusions:
- The alpha(1G)-subunit is likely the primary component of cardiac I(Ca,T) during the neonatal period.
- Cardiac I(Ca,T) plays a crucial role in neonatal atrial function and calcium signaling pathways.
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