VOLTAGE-DEPENDENT INSP3- INSENSITIVE CALCIUM CHANNELS IN MEMBRANES OF PANCREATIC ENDOPLASMIC-RETICULUM VESICLES

被引:83
作者
SCHMID, A
DEHLINGERKREMER, M
SCHULZ, I
GOGELEIN, H
机构
[1] Max-Planck-Institut für Biophysik, D-6000 Frankfurt (Main) 70
关键词
D O I
10.1038/346374a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
STIMULUS-SECRETION coupling in exocrine glands involves Ca2+ release from intracellular stores1,2. In endoplasmic reticulum vesicle preparations from rat exocrine pancreas, an inositol 1,4,5-trisphosphate(InsP3)-sensitive, as well as an InsP3-insensitive, Ca2+ pool has been characterized3. But Ca2+ channels in the endoplasmic reticulum of rat exocrine pancreas have not been demonstrated at the level of single-channel current. We have now used the patch-clamp technique on endoplasmic reticulum vesicles fused by means of the dehydration-rehydration method4-6. In excised patches, single Ba2+- and Ca2+-selective channels were recorded. The channel activity was markedly voltage-dependent. Caffeine increased channel open-state probability, whereas ruthenium red and Cd2+ blocked single-channel currents. Ryanodine, nifedipine and heparin had no effect on channel activity. The channel activity was not dependent on the free Ca2+ concentration, the presence of InsP3, or pH. We conclude that this calcium channel mediates Ca2+ release from an intracellular store through an InsP3-insensitive mechanism. © 1990 Nature Publishing Group.
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页码:374 / 376
页数:3
相关论文
共 25 条
[1]   CHARACTERIZATION OF CALCIUM-UPTAKE INTO ROUGH ENDOPLASMIC-RETICULUM OF RAT PANCREAS [J].
BAYERDORFFER, E ;
STREB, H ;
ECKHARDT, L ;
HAASE, W ;
SCHULZ, I .
JOURNAL OF MEMBRANE BIOLOGY, 1984, 81 (01) :69-82
[2]   A MEMBRANE-FUSION STRATEGY FOR SINGLE-CHANNEL RECORDINGS OF MEMBRANES USUALLY NON-ACCESSIBLE TO PATCH-CLAMPPIPETTE ELECTRODES [J].
CRIADO, M ;
KELLER, BU .
FEBS LETTERS, 1987, 224 (01) :172-176
[3]   INOSITOL 1,4,5-TRISPHOSPHATE ACTIVATES A CHANNEL FROM SMOOTH-MUSCLE SARCOPLASMIC-RETICULUM [J].
EHRLICH, BE ;
WATRAS, J .
NATURE, 1988, 336 (6199) :583-586
[4]   GTP-ACTIVATED COMMUNICATION BETWEEN DISTINCT INOSITOL 1,4,5-TRISPHOSPHATE-SENSITIVE AND 1,4,5-TRISPHOSPHATE-INSENSITIVE CALCIUM POOLS [J].
GHOSH, TK ;
MULLANEY, JM ;
TARAZI, FI ;
GILL, DL .
NATURE, 1989, 340 (6230) :236-239
[5]   CALCIUM SIGNALING MECHANISMS IN ENDOPLASMIC-RETICULUM ACTIVATED BY INOSITOL 1,4,5-TRISPHOSPHATE AND GTP [J].
GILL, DL ;
GHOSH, TK ;
MULLANEY, JM .
CELL CALCIUM, 1989, 10 (05) :363-374
[6]   PROPERTIES OF SINGLE K+ CHANNELS IN THE BASOLATERAL MEMBRANE OF RABBIT PROXIMAL STRAIGHT TUBULES [J].
GOGELEIN, H ;
GREGER, R .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1987, 410 (03) :288-295
[7]   CALCIUM CHANNELS - MOLECULAR PHARMACOLOGY, STRUCTURE AND REGULATION [J].
HOSEY, MM ;
LAZDUNSKI, M .
JOURNAL OF MEMBRANE BIOLOGY, 1988, 104 (02) :81-105
[8]  
KEMMER TP, 1987, J BIOL CHEM, V262, P13758
[9]   CYTOPLASMIC FREE CA IN ISOLATED SNAIL NEURONS AS REVEALED BY FLUORESCENT-PROBE FURA-2 - MECHANISMS OF CA RECOVERY AFTER CA LOAD AND CA RELEASE FROM INTRACELLULAR STORES [J].
KOSTYUK, PG ;
MIRONOV, SL ;
TEPIKIN, AV ;
BELAN, PV .
JOURNAL OF MEMBRANE BIOLOGY, 1989, 110 (01) :11-18
[10]   HIGH SELECTIVITY OF CALCIUM CHANNELS IN SINGLE DIALYZED HEART-CELLS OF THE GUINEA-PIG [J].
LEE, KS ;
TSIEN, RW .
JOURNAL OF PHYSIOLOGY-LONDON, 1984, 354 (SEP) :253-272