Lysosphingomyelin-elicited Ca2+ mobilization from rat brain microsomes

Shigeki Furuya , Sadamu Kurono , Yoshio Hirabayashi
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引用次数: 12

Abstract

We have examined the Ca2+ release activity of sphingolipid-derivatives from rat brain microsomes using a Fura-2 cytofluorometric assay. Sphingosylphosphorylcholine, lysosphingomyelin, elicited a rapid Ca2+ release from both cerebral and cerebellar microsomes. Other compounds including sphingosine and sphingosine-1-phosphate were incapable of causing the Ca2+ release. The pharmacological properties suggest that the sphingosylphosphorylcholine-elicited Ca2+ mobilization is not mediated by inositol 1,4,5-triphosphate receptors. Immunocytochemical study showed the occurrence of sphingomyelin, a putative precursor for sphingosylphosphorylcholine, in the somatodendritic membrane domains of cerebellar neurons. These observations imply that sphingosylphosphorylcholine is a potent Ca2+ releaser in brain neurons.

溶鞘磷脂诱导大鼠脑微粒体Ca2+动员
我们使用Fura-2细胞荧光法检测了大鼠脑微粒体鞘脂衍生物的Ca2+释放活性。鞘氨磷胆碱,溶鞘磷脂,诱导Ca2+从大脑和小脑微粒体快速释放。其他化合物包括鞘氨醇和鞘氨醇-1-磷酸不能引起Ca2+释放。药理学性质表明鞘氨酰磷胆碱诱导的Ca2+动员不是由肌醇1,4,5-三磷酸受体介导的。免疫细胞化学研究表明,在小脑神经元的体树突膜域存在鞘磷脂,鞘磷脂被认为是鞘磷脂的前体。这些观察结果表明,鞘甲磷胆碱是脑神经元中有效的Ca2+释放剂。
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