Persistent Na+ influx drives L-type channel resting Ca2+ entry in rat melanotrophs
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
30772686
DOI
10.1016/j.ceca.2019.02.001
PII: S0143-4160(19)30004-1
Knihovny.cz E-resources
- Keywords
- Ca(2+) homeostasis, Cation conductance, Patch-clamp, Ca(2+) imaging, ruthenium red, Rat melanotrophs, Voltage-gated calcium channels,
- MeSH
- TRPV Cation Channels antagonists & inhibitors metabolism MeSH
- Rats MeSH
- Melanotrophs metabolism MeSH
- Patch-Clamp Techniques MeSH
- Rats, Wistar MeSH
- Ruthenium Red pharmacology MeSH
- Sodium metabolism MeSH
- Calcium metabolism MeSH
- Calcium Channels, L-Type metabolism MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- TRPV Cation Channels MeSH
- Ruthenium Red MeSH
- Sodium MeSH
- Calcium MeSH
- Calcium Channels, L-Type MeSH
Rat melanotrophs express several types of voltage-gated and ligand-gated calcium channels, although mechanisms involved in the maintenance of the resting intracellular Ca2+ concentration ([Ca2+]i) remain unknown. We analyzed mechanisms regulating resting [Ca2+]i in dissociated rat melanotrophs by Ca2+-imaging and patch-clamp techniques. Treatment with antagonists of L-type, but not N- or P/Q-type voltage-gated Ca2+ channels (VGCCs) as well as removal of extracellular Ca2+ resulted in a rapid and reversible decrease in [Ca2+]i, indicating constitutive Ca2+ influx through L-type VGCCs. Reduction of extracellular Na+ concentration (replacement with NMDG+) similarly decreased resting [Ca2+]i. When cells were champed at -80 mV, decrease in the extracellular Na+ resulted in a positive shift of the holding current. In cell-attached voltage-clamp and whole-cell current-clamp configurations, the reduction of extracellular Na+ caused hyperpolarisation. The holding current shifted in negative direction when extracellular K+ concentration was increased from 5 mM to 50 mM in the presence of K+ channel blockers, Ba2+ and TEA, indicating cation nature of persistent conductance. RT-PCR analyses of pars intermedia tissues detected mRNAs of TRPV1, TRPV4, TRPC6, and TRPM3-5. The TRPV channel blocker, ruthenium red, shifted the holding current in positive direction, and significantly decreased the resting [Ca2+]i. These results indicate operation of a constitutive cation conductance sensitive to ruthenium red, which regulates resting membrane potential and [Ca2+]i in rat melanotrophs.
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