Biology Direct (Oct 2023)

Identification of RNA reads encoding different channels in isolated rat ventricular myocytes and the effect of cell stretching on L-type Ca 2+ current

  • Andre G. Kamkin,
  • Olga V. Kamkina,
  • Viktor E. Kazansky,
  • Vadim M. Mitrokhin,
  • Andrey Bilichenko,
  • Elizaveta A. Nasedkina,
  • Stanislav A. Shileiko,
  • Anastasia S. Rodina,
  • Alexandra D. Zolotareva,
  • Valentin I. Zolotarev,
  • Pavel V. Sutyagin,
  • Mitko I. Mladenov

DOI
https://doi.org/10.1186/s13062-023-00427-0
Journal volume & issue
Vol. 18, no. 1
pp. 1 – 23

Abstract

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Abstract Background The study aimed to identify transcripts of specific ion channels in rat ventricular cardiomyocytes and determine their potential role in the regulation of ionic currents in response to mechanical stimulation. The gene expression levels of various ion channels in freshly isolated rat ventricular cardiomyocytes were investigated using the RNA-seq technique. We also measured changes in current through CaV1.2 channels under cell stretching using the whole-cell patch-clamp method. Results Among channels that showed mechanosensitivity, significant amounts of TRPM7, TRPC1, and TRPM4 transcripts were found. We suppose that the recorded L-type Ca 2+ current is probably expressed through CaV1.2. Furthermore, stretching cells by 6, 8, and 10 μm, which increases I SAC through the TRPM7, TRPC1, and TRPM4 channels, also decreased I Ca,L through the CaV1.2 channels in K+ in/K+ out, Cs+ in/K+ out, K+ in/Cs+ out, and Cs+ in/Cs+ out solutions. The application of a nonspecific I SAC blocker, Gd3+, during cell stretching eliminated I SAC through nonselective cation channels and I Ca,L through CaV1.2 channels. Since the response to Gd3+ was maintained in Cs+ in/Cs+ out solutions, we suggest that voltage-gated CaV1.2 channels in the ventricular myocytes of adult rats also exhibit mechanosensitive properties. Conclusions Our findings suggest that TRPM7, TRPC1, and TRPM4 channels represent stretch-activated nonselective cation channels in rat ventricular myocytes. Probably the CaV1.2 channels in these cells exhibit mechanosensitive properties. Our results provide insight into the molecular mechanisms underlying stretch-induced responses in rat ventricular myocytes, which may have implications for understanding cardiac physiology and pathophysiology.

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