首页> 外文期刊>The Journal of general physiology >Calcium buffering properties of sarcoplasmic reticulum and calcium-induced Ca2+ release during the quasi-steady level of release in twitch fibers from frog skeletal muscle
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Calcium buffering properties of sarcoplasmic reticulum and calcium-induced Ca2+ release during the quasi-steady level of release in twitch fibers from frog skeletal muscle

机译:蛙骨骼肌抽搐纤维准稳态释放过程中肌浆网的钙缓冲特性和钙诱导的Ca2 +释放

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Experiments were performed to characterize the properties of the intrinsic Ca2+ buffers in the sarcoplasmic reticulum (SR) of cut fibers from frog twitch muscle. The concentrations of total and free calcium ions within the SR ([CaT]SR and [Ca2+]SR) were measured, respectively, with the EGTA/phenol red method and tetramethylmurexide (a low affinity Ca2+ indicator). Results indicate SR Ca2+ buffering was consistent with a single cooperative-binding component or a combination of a cooperative-binding component and a linear binding component accounting for 20% or less of the bound Ca2+. Under the assumption of a single cooperative-binding component, the most likely resting values of [Ca2+]SR and [CaT]SR are 0.67 and 17.1 mM, respectively, and the dissociation constant, Hill coefficient, and concentration of the Ca-binding sites are 0.78 mM, 3.0, and 44 mM, respectively. This information can be used to calculate a variable proportional to the Ca2+ permeability of the SR, namely d[CaT]SR/dt ÷ [Ca2+]SR (denoted release permeability), in experiments in which only [CaT]SR or [Ca2+]SR is measured. In response to a voltage-clamp step to ?20 mV at 15°C, the release permeability reaches an early peak followed by a rapid decline to a quasi-steady level that lasts ~50 ms, followed by a slower decline during which the release permeability decreases by at least threefold. During the quasi-steady level of release, the release amplitude is 3.3-fold greater than expected from voltage activation alone, a result consistent with the recruitment by Ca-induced Ca2+ release of 2.3 SR Ca2+ release channels neighboring each channel activated by its associated voltage sensor. Release permeability at ?60 mV increases as [CaT]SR decreases from its resting physiological level to ~0.1 of this level. This result argues against a release termination mechanism proposed in mammalian muscle fibers in which a luminal sensor of [Ca2+]SR inhibits release when [CaT]SR declines to a low level.
机译:进行实验以表征青蛙抽搐肌肉切纤维的肌浆网(SR)中内在Ca2 +缓冲液的特性。用EGTA /酚红法和四甲基默雷西德(低亲和性Ca2 +指示剂)分别测量了SR([CaT] SR和[Ca2 +] SR)中总钙离子和游离钙离子的浓度。结果表明,SR Ca2 +缓冲与单个合作结合成分或合作结合成分与线性结合成分的组合一致,占结合Ca2 +的20%或更少。在单个协作结合成分的假设下,[Ca2 +] SR和[CaT] SR的最可能静止值分别为0.67和17.1 mM,并且解离常数,Hill系数和Ca结合位点的浓度分别为0.78 mM,3.0和44 mM。在仅使用[CaT] SR或[Ca2 +]的实验中,此信息可用于计算与SR的Ca2 +渗透率成比例的变量,即d [CaT] SR / dt÷[Ca2 +] SR(表示释放渗透率)。 SR被测量。响应电压钳制步骤,在15°C时达到20 mV,释放磁导率达到一个早期峰值,随后迅速下降至持续约50 ms的准稳态水平,随后缓慢下降,在此期间释放渗透率至少降低三倍。在准稳定水平的释放过程中,释放幅度比单独的电压激活所预期的要大3.3倍,这一结果与Ca诱导的Ca 2+释放募集到2.3 SR Ca 2+释放通道(与每个由其相关电压激活的通道相邻)一致传感器。当[CaT] SR从其静止的生理水平降低至该水平的〜0.1时,释放通透性在60 mV时增加。该结果与哺乳动物肌肉纤维中提出的释放终止机制相矛盾,在该机制中,当[CaT] SR降低至较低水平时,[Ca2 +] SR的腔传感器会抑制释放。

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