PARTICIPATION OF TRANSIENT-TYPE CA-2+ CHANNELS IN THE SUSTAINED INCREASE OF CA-2+ LEVEL IN GH3 CELLS

被引:24
作者
SUZUKI, N
KUDO, Y
TAKAGI, H
YOSHIOKA, T
TANAKADATE, A
KANO, M
机构
[1] KITASATO UNIV,SCH MED,FACIL MED ENGN,SAGAMIHARA,KANAGAWA 228,JAPAN
[2] MITSUBISHI KASEI INST LIFE SCI,DEPT NEUROSCI,MACHIDA,TOKYO 194,JAPAN
[3] WASEDA UNIV,SCH SCI & ENGN,DEPT PHYS,SHINJU KU,TOKYO 169,JAPAN
[4] WASEDA UNIV,SCH HUMAN SCI,DEPT BASIC SCI,SAITAMA 359,JAPAN
关键词
D O I
10.1002/jcp.1041440109
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Participation of two types of Ca2+ channels (T‐ and L‐types) in the sustained increase of cytosolic‐free Ca2+ concentration ([Ca2+]i) was studied in thyrotropin‐releasing hormone (TRH)‐stimulated clonal GH3 pituitary cells. The effects of Ca2+ channel blockers were analyzed by measuring Ca2+ channel current and [Ca2+]i, using whole‐cell voltage‐clamp and Fura‐2 fluorometry, respectively. Phenytoin (100 μM) and Ni2+ (100 μM) selectively blocked T‐type Ca2+ channels and suppressed the TRH‐induced sustained [Ca2+]i increase in single cells. Synthetic ω‐conotoxin (ω‐CgTX, 2 μM) preferentially blocked L‐type Ca2+ channels, but it did not suppress the TRH‐induced sustained [Ca2+]i increase. The present results suggest that the sustained elevations of [Ca2+]i triggered by TRH may be mediated by T‐type Ca2+ channels in GH3 cells. Copyright © 1990 Wiley‐Liss, Inc.
引用
收藏
页码:62 / 68
页数:7
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