Kelley S J, Thomas R, Dunham P B
Department of Biology, Syracuse University, Syracuse, NY 13244, USA.
J Membr Biol. 2000 Nov 1;178(1):31-41. doi: 10.1007/s002320010012.
K-Cl cotransport, KCC, is activated by swelling in many cells types, and promotes volume regulation by a KCl efflux osmotically coupled to water efflux. KCC is probably activated by swelling-inhibition of a kinase, permitting dephosphorylation, and activation of the cotransporter by a phosphatase. The myosin light chain kinase (MLCK) inhibitor ML-7 inhibits transporters activated by shrinkage. In red blood cells from three mammalian species, ML-7 stimulated KCC in a volume-dependent manner. Relative stimulation was greatest in more shrunken cells. Stimulation was reduced by moderate cell swelling and abolished by further swelling. The half-maximal stimulation is at approximately 20 microm ML-7, 50-fold greater than the IC(50) for inhibition of MLCK in vitro. Stimulation of KCC by ML-7 did not require cell Ca, while MLCK does. Therefore the target of ML-7 in stimulating KCC in red cells is probably not MLCK. The evidence favors stimulation of KCC by ML-7 by inhibiting the volume-sensitive kinase. Qualitatively similar effects of ML-7 on KCC in red cells from three mammalian species suggest a general mechanism.
钾氯共转运体(KCC)在多种细胞类型中可被肿胀激活,并通过与水外流渗透偶联的氯化钾外流促进体积调节。KCC可能是通过激酶的肿胀抑制作用而被激活,从而允许去磷酸化,并由磷酸酶激活共转运体。肌球蛋白轻链激酶(MLCK)抑制剂ML-7可抑制因细胞收缩而激活的转运体。在三种哺乳动物的红细胞中,ML-7以体积依赖性方式刺激KCC。在收缩程度更高的细胞中,相对刺激作用最大。适度的细胞肿胀会降低刺激作用,进一步肿胀则会消除刺激作用。刺激作用的半数最大值出现在约20微摩尔的ML-7浓度下,这比体外抑制MLCK的IC50值大50倍。ML-7对KCC的刺激作用不需要细胞内的钙离子,而MLCK则需要。因此,ML-7在红细胞中刺激KCC的靶点可能不是MLCK。有证据表明,ML-7通过抑制体积敏感性激酶来刺激KCC。ML-7对三种哺乳动物红细胞中KCC产生的定性相似效应提示了一种普遍机制。