Persistent Na+ influx drives L-type channel resting Ca2+ entry in rat melanotrophs. (May 2019)
- Record Type:
- Journal Article
- Title:
- Persistent Na+ influx drives L-type channel resting Ca2+ entry in rat melanotrophs. (May 2019)
- Main Title:
- Persistent Na+ influx drives L-type channel resting Ca2+ entry in rat melanotrophs
- Authors:
- Kayano, Tomohiko
Sasaki, Yuto
Kitamura, Naoki
Harayama, Nobuya
Moriya, Taiki
Dayanithi, Govindan
Verkhratsky, Alexei
Shibuya, Izumi - Abstract:
- Graphical abstract: Highlights: The resting [Ca 2+ ]i of rat melanotrophs was reversibly suppressed by antagonists of L-type Ca 2+ channels. The resting [Ca 2+ ]I was also suppressed by a reduction in the extracellular Na + concentration. When cells were voltage-clamped at –80 mV, lowering the extracellular Na + caused a positive shift of the holding current. mRNAs of TRPV1, TRPV4, TRPC6, and TRPM3-5 were detected with RT-PCR. The TRPV channel blocker, ruthenium red, suppressed the holding current and significantly decreased the resting [Ca 2+ ]i . Abstract: Rat melanotrophs express several types of voltage-gated and ligand-gated calcium channels, although mechanisms involved in the maintenance of the resting intracellular Ca 2+ concentration ([Ca 2+ ]i ) remain unknown. We analyzed mechanisms regulating resting [Ca 2+ ]i in dissociated rat melanotrophs by Ca 2+ -imaging and patch-clamp techniques. Treatment with antagonists of L-type, but not N- or P/Q-type voltage-gated Ca 2+ channels (VGCCs) as well as removal of extracellular Ca 2+ resulted in a rapid and reversible decrease in [Ca 2+ ]i, indicating constitutive Ca 2+ influx through L-type VGCCs. Reduction of extracellular Na + concentration (replacement with NMDG + ) similarly decreased resting [Ca 2+ ]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 ofGraphical abstract: Highlights: The resting [Ca 2+ ]i of rat melanotrophs was reversibly suppressed by antagonists of L-type Ca 2+ channels. The resting [Ca 2+ ]I was also suppressed by a reduction in the extracellular Na + concentration. When cells were voltage-clamped at –80 mV, lowering the extracellular Na + caused a positive shift of the holding current. mRNAs of TRPV1, TRPV4, TRPC6, and TRPM3-5 were detected with RT-PCR. The TRPV channel blocker, ruthenium red, suppressed the holding current and significantly decreased the resting [Ca 2+ ]i . Abstract: Rat melanotrophs express several types of voltage-gated and ligand-gated calcium channels, although mechanisms involved in the maintenance of the resting intracellular Ca 2+ concentration ([Ca 2+ ]i ) remain unknown. We analyzed mechanisms regulating resting [Ca 2+ ]i in dissociated rat melanotrophs by Ca 2+ -imaging and patch-clamp techniques. Treatment with antagonists of L-type, but not N- or P/Q-type voltage-gated Ca 2+ channels (VGCCs) as well as removal of extracellular Ca 2+ resulted in a rapid and reversible decrease in [Ca 2+ ]i, indicating constitutive Ca 2+ influx through L-type VGCCs. Reduction of extracellular Na + concentration (replacement with NMDG + ) similarly decreased resting [Ca 2+ ]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, Ba 2+ 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 [Ca 2+ ]i . These results indicate operation of a constitutive cation conductance sensitive to ruthenium red, which regulates resting membrane potential and [Ca 2+ ]i in rat melanotrophs. … (more)
- Is Part Of:
- Cell calcium. Volume 79(2019)
- Journal:
- Cell calcium
- Issue:
- Volume 79(2019)
- Issue Display:
- Volume 79, Issue 2019 (2019)
- Year:
- 2019
- Volume:
- 79
- Issue:
- 2019
- Issue Sort Value:
- 2019-0079-2019-0000
- Page Start:
- 11
- Page End:
- 19
- Publication Date:
- 2019-05
- Subjects:
- Rat melanotrophs -- Cation conductance -- Voltage-gated calcium channels -- Patch-clamp, Ca2+ imaging, ruthenium red -- Ca2+ homeostasis
Calcium -- Metabolism -- Periodicals
Vertebrates -- Physiology -- Periodicals
Calcium -- Physiological effect -- Periodicals
Cell physiology -- Periodicals
Calcium in the body -- Periodicals
572.516 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01434160 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.ceca.2019.02.001 ↗
- Languages:
- English
- ISSNs:
- 0143-4160
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3097.724000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 9972.xml