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α-拉托毒素与大鼠脑突触体及PC12细胞相互作用的表征

Characterization of alpha-latrotoxin interaction with rat brain synaptosomes and PC12 cells.

作者信息

Grasso A, Pelliccia M, Alemà S

出版信息

Toxicon. 1982;20(1):149-56. doi: 10.1016/0041-0101(82)90184-2.

Abstract

alpha-latrotoxin, a polypeptide neurotoxin purified from the venom of the spider Latrodectus mactans tredecimguttatus, induces a massive release of a variety of neurotransmitters from rat brain synaptosomes and a clonal pheochromocytoma cell line (PC12 cells). In both systems secretion of catecholamines is dose- and calcium-dependent. Efflux of catecholamines is coupled with a substantial release of intracellular ATP. Independent of alpha-latrotoxin with PC12 cells is followed by a rapid influx of calcium and sodium ions, the rate being dependent on toxin and calcium concentrations. By reductive methylation it is possible to radioactively label alpha-latrotoxin without appreciable loss of neurotoxicity. A sensitive binding assay in vitro allows the identification of a limited number of specific binding sites in central nervous system synaptic membranes and PC12 cells, for which tritiated alpha-latrotoxin displays nanomolar affinity.

摘要

α-拉托毒素是一种从红斑寇蛛毒液中纯化得到的多肽神经毒素,它能诱导大鼠脑突触体和克隆性嗜铬细胞瘤细胞系(PC12细胞)大量释放多种神经递质。在这两种系统中,儿茶酚胺的分泌均呈剂量和钙依赖性。儿茶酚胺的外流与细胞内ATP的大量释放相关联。在PC12细胞中,α-拉托毒素独立作用后会伴随钙离子和钠离子的快速内流,其速率取决于毒素和钙的浓度。通过还原甲基化作用,可以对α-拉托毒素进行放射性标记,而不会明显丧失其神经毒性。体外敏感的结合测定法能够鉴定中枢神经系统突触膜和PC12细胞中有限数量的特异性结合位点,氚标记的α-拉托毒素对这些位点具有纳摩尔级的亲和力。

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