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CaV 3.1 and CaV 3.3 account for T-type Ca2+ current in GH3 cells
Mudado, M. A; Rodrigues, A. L; Prado, V. F; Beirão, P. S. L; Cruz, J. S.
Affiliation
  • Mudado, M. A; Universidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Bioquímica e Imunologia. Laboratório de Membranas Excitáveis. Belo Horizonte. BR
  • Rodrigues, A. L; Universidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Bioquímica e Imunologia. Laboratório de Membranas Excitáveis. Belo Horizonte. BR
  • Prado, V. F; Universidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Bioquímica e Imunologia. Laboratório de Neurobiologia Molecular. Belo Horizonte. BR
  • Beirão, P. S. L; Universidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Bioquímica e Imunologia. Laboratório de Membranas Excitáveis. Belo Horizonte. BR
  • Cruz, J. S; Universidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Bioquímica e Imunologia. Laboratório de Membranas Excitáveis. Belo Horizonte. BR
Braz. j. med. biol. res ; 37(6): 929-935, Jun. 2004. ilus, tab, graf
Article de En | LILACS | ID: lil-359901
Bibliothèque responsable: BR1.1
RESUMO
T-type Ca2+ channels are important for cell signaling by a variety of cells. We report here the electrophysiological and molecular characteristics of the whole-cell Ca2+ current in GH3 clonal pituitary cells. The current inactivation at 0 mV was described by a single exponential function with a time constant of 18.32 ñ 1.87 ms (N = 16). The I-V relationship measured with Ca2+ as a charge carrier was shifted to the left when we applied a conditioning pre-pulse of up to -120 mV, indicating that a low voltage-activated current may be present in GH3 cells. Transient currents were first activated at -50 mV and peaked around -20 mV. The half-maximal voltage activation and the slope factors for the two conditions are -35.02 ñ 2.4 and 6.7 ñ 0.3 mV (pre-pulse of -120 mV, N = 15), and -27.0 ñ 0.97 and 7.5 ñ 0.7 mV (pre-pulse of -40 mV, N = 9). The 8-mV shift in the activation mid-point was statistically significant (P < 0.05). The tail currents decayed bi-exponentially suggesting two different T-type Ca2+ channel populations. RT-PCR revealed the presence of a1G (CaV3.1) and a1I (CaV3.3) T-type Ca2+ channel mRNA transcripts.
Sujet(s)
Texte intégral: 1 Indice: LILACS Sujet Principal: Hypophyse / Canaux calciques de type T Limites du sujet: Humans langue: En Texte intégral: Braz. j. med. biol. res Thème du journal: BIOLOGIA / MEDICINA Année: 2004 Type: Article / Project document
Texte intégral: 1 Indice: LILACS Sujet Principal: Hypophyse / Canaux calciques de type T Limites du sujet: Humans langue: En Texte intégral: Braz. j. med. biol. res Thème du journal: BIOLOGIA / MEDICINA Année: 2004 Type: Article / Project document