Differential modulation of L-type Ca2+ current by SR Ca2+ release at the T-tubules and surface membrane of rat ventricular myocytes

被引:75
作者
Brette, F [1 ]
Sallé, L
Orchard, CH
机构
[1] Univ Leeds, Sch Biomed Sci, Leeds LS2 9JT, W Yorkshire, England
[2] Univ Caen, Lab Physiol Cellulaire, F-14032 Caen, France
关键词
transverse tubules; calcium channel; inactivation; facilitation;
D O I
10.1161/01.RES.0000135547.53927.F6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We have characterized modulation of I-Ca by Ca2+ at the t-tubules (ie, in control cells) and surface sarcolemma (ie, in detubulated cells) of cardiac ventricular myocytes, using the whole-cell patch clamp technique to record ICa. ICa inactivation was significantly slower in detubulated cells than in control cells (27.1 +/- 7.8 ms, n=22, versus 16.4 +/- 7.9 ms, n=22; P<0.05). In atrial myocytes, which lack t-tubules, I-Ca inactivation was not changed by the treatment used to produce detubulation. In the presence of ryanodine or BAPTA, or when Ba2+ was used as the charge carrier, the rate of inactivation was not significantly different in control and detubulated cells. Frequency-dependent facilitation occurred in control cells but not in detubulated cells, and was abolished by ryanodine. These results suggest that Ca2+ released from the SR has a greater effect on I-Ca in the t-tubules than at the surface sarcolemma. This does not appear to be due to differences in local Ca2+ release from the SR, because the gain of Ca2+ release was not significantly different in control and detubulated cells. These data suggest that the t-tubules are a key site for the regulation of transsarcolemmal Ca2+ flux by Ca2+ release from the SR; this could play a role in altered Ca2+ homeostasis in pathological conditions. The full text of this article is available online at http://circres.ahajournals.org.
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页码:E1 / U9
页数:16
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