Calcium concentration and movement in the diadic cleft space of the cardiac ventricular cell

被引:146
作者
Langer, GA
Peskoff, A
机构
[1] UNIV CALIF LOS ANGELES,SCH MED,DEPT MED,LOS ANGELES,CA 90095
[2] UNIV CALIF LOS ANGELES,SCH MED,DEPT PHYSIOL,LOS ANGELES,CA 90095
[3] UNIV CALIF LOS ANGELES,SCH MED,DEPT BIOMATH,LOS ANGELES,CA 90095
关键词
D O I
10.1016/S0006-3495(96)79677-7
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We model the space between the junctional sarcoplasmic reticulum (JSR) membrane and the inner leaflet of the transverse tubular (''T'') sarcolemmal (SL) membrane, the diadic cleft, with respect to calcium (Ca) concentration and movement, The model predicts the following: 1) Ca influx via the ''L'' channel increases [Ca] to 1 mu M within a distance of 50 nm from the channel mouth in <500 mu s. This is sufficient to trigger Ca release from a domain of 9 ''feet.'' 2) By contrast, ''reverse'' Na/Ca exchange will increase [Gal to similar to 0.5 mu M throughout the cleft space in 10 ms, sufficient to trigger Ca release, but clearly to a lesser extent and more slowly than the channel. 3) After a 20-ms JSR release into the cleft via the ''feet'' [Ca] peaks at 600 mu M (cleft center) to 100 mu M (cleft periphery) and then declines to diastolic level (100 nM) within 150 ms throughout the cleft. 4) The ratio of flux out of the cleft via Na/Ca exchange to flux out of the cleft to the cytosol varies inversely as JSR Ca release, 5) Removal of SL anionic Ca-binding sites from the model will cause [Ca] to fall to 100 nM throughout the cleft in <1 ms after JSR release ceases. This markedly reduces Na/Ca exchange. 6) Removal from or decreased concentration of Na/Ca exchangers in the cleft will cause [Ca] to fall too slowly after JSR release to permit triggered release upon subsequent excitation.
引用
收藏
页码:1169 / 1182
页数:14
相关论文
共 54 条
[1]   RELAXATION IN RABBIT AND RAT CARDIAC-CELLS - SPECIES-DEPENDENT DIFFERENCES IN CELLULAR MECHANISMS [J].
BASSANI, JWM ;
BASSANI, RA ;
BERS, DM .
JOURNAL OF PHYSIOLOGY-LONDON, 1994, 476 (02) :279-293
[2]  
BASSINGTHWAIGHT.JB, 1972, ELECTRICAL PHENOMENA, P353
[3]   CA2+ TRANSIENTS IN CARDIAC MYOCYTES MEASURED WITH HIGH AND LOW-AFFINITY CA2+ INDICATORS [J].
BERLIN, JR ;
KONISHI, M .
BIOPHYSICAL JOURNAL, 1993, 65 (04) :1632-1647
[4]   DIFFUSION AROUND A CARDIAC CALCIUM-CHANNEL AND THE ROLE OF SURFACE BOUND CALCIUM [J].
BERS, DM ;
PESKOFF, A .
BIOPHYSICAL JOURNAL, 1991, 59 (03) :703-721
[5]  
Bockris J.O., 1970, Modern Electrochemistry, V1, DOI DOI 10.1007/978-1-4615-8600-5
[6]  
BOHLE T, 1995, BIOPHYS J, V68, P121, DOI 10.1016/S0006-3495(95)80166-9
[7]   SPATIAL NONUNIFORMITIES IN [CA2+](I) DURING EXCITATION-CONTRACTION COUPLING IN CARDIAC MYOCYTES [J].
CANNELL, MB ;
CHENG, H ;
LEDERER, WJ .
BIOPHYSICAL JOURNAL, 1994, 67 (05) :1942-1956
[8]   A FUZZY SUBSARCOLEMMAL SPACE FOR INTRACELLULAR NA+ IN CARDIAC-CELLS [J].
CARMELIET, E .
CARDIOVASCULAR RESEARCH, 1992, 26 (05) :433-442
[9]  
Crank J, 1979, MATH DIFFUSION
[10]   CONTRACTIONS INDUCED BY A CALCIUM-TRIGGERED RELEASE OF CALCIUM FROM SARCOPLASMIC-RETICULUM OF SINGLE SKINNED CARDIAC CELLS [J].
FABIATO, A ;
FABIATO, F .
JOURNAL OF PHYSIOLOGY-LONDON, 1975, 249 (03) :469-495