Murayama Takashi, Ogawa Yasuo
Department of Pharmacology, Juntendo University School of Medicine, Tokyo, Japan.
Trends Cardiovasc Med. 2002 Oct;12(7):305-11. doi: 10.1016/s1050-1738(02)00179-2.
Ryanodine receptor (RyR) is a Ca(2)(+) release channel in the sarcoplasmic reticulum and plays an important role in excitation-contraction coupling in skeletal muscle. The Ca(2)(+) release through the RyR channel can be gated by two distinct modes: depolarization-induced Ca(2)(+) release (DICR) and Ca(2)(+)-induced Ca(2)(+) release (CICR). Two different RyR isoforms, RyR1 (or alpha-RyR) and RyR3 (or beta-RyR), have been found to be expressed in skeletal muscle. Most adult mammalian muscles express primarily RyR1, whereas almost equal amounts of the two RyR isoforms exist in many nonmammalian vertebrate muscles. RyR1 is believed to be responsible for both DICR and CICR, whereas RyR3 may function as the CICR channel. Recent findings demonstrate that alpha-RyR is selectively and markedly suppressed in CICR activity in frog skeletal muscle. This selective suppression of RyR1, although to a lesser extent, also was found to occur in mammalian skeletal muscle. This short review describes the biological meanings of this selective suppression and discusses physiological roles and significance of the two RyR isoforms in vertebrate skeletal muscle.
雷诺丁受体(RyR)是肌浆网中的一种Ca(2)(+)释放通道,在骨骼肌的兴奋-收缩偶联中起重要作用。通过RyR通道的Ca(2)(+)释放可由两种不同模式控制:去极化诱导的Ca(2)(+)释放(DICR)和Ca(2)(+)-诱导的Ca(2)(+)释放(CICR)。已发现两种不同的RyR亚型,即RyR1(或α-RyR)和RyR3(或β-RyR)在骨骼肌中表达。大多数成年哺乳动物肌肉主要表达RyR1,而在许多非哺乳动物脊椎动物肌肉中,两种RyR亚型的含量几乎相等。据信RyR1负责DICR和CICR,而RyR3可能作为CICR通道发挥作用。最近的研究结果表明,α-RyR在青蛙骨骼肌的CICR活性中被选择性地显著抑制。这种对RyR1的选择性抑制在哺乳动物骨骼肌中也有发现,尽管程度较轻。这篇简短的综述描述了这种选择性抑制的生物学意义,并讨论了两种RyR亚型在脊椎动物骨骼肌中的生理作用和意义。