Literature DB >> 11535666

E(f)-current contributes to whole-cell calcium current in low calcium in frog sympathetic neurons.

H Liang1, K S Elmslie.   

Abstract

Because Ca(2+) plays diverse roles in intracellular signaling in neurons, several types of calcium channels are employed to control Ca(2+) influx in these cells. Our experiments focus on resolving the paradox of why whole-cell current has not been observed under typical recording conditions for one type of calcium channel that is highly expressed in frog sympathetic neurons. These channels, referred to as E(f)-channels, are present in the membrane at a density greater than the channels that carry approximately 90% of whole-cell current in low Ba(2+); but, E(f)-current has not been detected in low Ba(2+). Using Ca(2+) instead of Ba(2+) as the charge carrier, we recorded a possible E-type current in frog sympathetic neurons. The current was resistant to specific blockers of N-, L-, and P/Q-type calcium channels but was more sensitive to Ni(2+) block than was N- or L-current. Current amplitude in Ca(2+) is slightly greater than that in Ba(2+). In 3 mM Ca(2+), the current contributed approximately 12% of total current at peak voltage and increased at voltages more hyperpolarized to the peak, reaching approximately 40% at -30 mV, where whole-cell current starts to activate. The presence of E(f)-current in 3 mM Ca(2+) suggests a potential role for E(f)-channels in regulating calcium influx into sympathetic neurons.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11535666     DOI: 10.1152/jn.2001.86.3.1156

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  7 in total

1.  Single channel measurements demonstrate the voltage dependence of permeation through N-type and L-type CaV channels.

Authors:  Zafir Buraei; Hye Kyung Lee; Keith S Elmslie
Journal:  Channels (Austin)       Date:  2015       Impact factor: 2.581

2.  Identification of CaV channel types expressed in muscle afferent neurons.

Authors:  Renuka Ramachandra; Bassil Hassan; Stephanie G McGrew; James Dompor; Mohamed Farrag; Victor Ruiz-Velasco; Keith S Elmslie
Journal:  J Neurophysiol       Date:  2013-07-10       Impact factor: 2.714

3.  NaV1.9 channels in muscle afferent neurons and axons.

Authors:  Tyler L Marler; Andrew B Wright; Kristina L Elmslie; Ankeeta K Heier; Ethan Remily; Jeong Sook Kim-Han; Renuka Ramachandra; Keith S Elmslie
Journal:  J Neurophysiol       Date:  2018-05-30       Impact factor: 2.714

4.  Domain III regulates N-type (CaV2.2) calcium channel closing kinetics.

Authors:  Viktor Yarotskyy; Guofeng Gao; Blaise Z Peterson; Keith S Elmslie
Journal:  J Neurophysiol       Date:  2011-12-28       Impact factor: 2.714

5.  Slowed N-type calcium channel (CaV2.2) deactivation by the cyclin-dependent kinase inhibitor roscovitine.

Authors:  Zafir Buraei; Mircea Anghelescu; Keith S Elmslie
Journal:  Biophys J       Date:  2005-06-10       Impact factor: 4.033

6.  Rapid and reversible block of N-type calcium channels (CaV 2.2) by omega-conotoxin GVIA in the absence of divalent cations.

Authors:  Haoya Liang; Keith S Elmslie
Journal:  J Neurosci       Date:  2002-10-15       Impact factor: 6.167

7.  Voltage control of Ca²⁺ permeation through N-type calcium (Ca(V)2.2) channels.

Authors:  Zafir Buraei; Haoya Liang; Keith S Elmslie
Journal:  J Gen Physiol       Date:  2014-08-11       Impact factor: 4.086

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.