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膜去极化诱导组织型纤溶酶原激活物的钙依赖性分泌。

Membrane depolarization induces calcium-dependent secretion of tissue plasminogen activator.

作者信息

Gualandris A, Jones T E, Strickland S, Tsirka S E

机构信息

Department of Pharmacology, University Medical Center at Stony Brook, New York 11794-8651, USA.

出版信息

J Neurosci. 1996 Apr 1;16(7):2220-5. doi: 10.1523/JNEUROSCI.16-07-02220.1996.

Abstract

Tissue plasminogen activator (tPA), a serine protease that converts inactive plasminogen to active plasmin, is produced in the rat and mouse hippocampus and participates in neuronal plasticity. To help define the role of tPA in the nervous system, we have analyzed the regulation of its expression in the neuronal cell line PC12. In control cultures, tPA activity is exclusively cell-associated, and no activity is measurable in the culture medium. When the cells are treated with depolarizing agents, such as KCI, tPA activity becomes detectable in the medium. The increased secreted tPA activity is not accompanied by an increase in tPA mRNA levels, and it is not blocked by protein synthesis inhibitors. In contrast, tPA release is abolished by Ca2+ channel blockers, suggesting that chemically induced membrane depolarization stimulates the secretion of preformed enzyme. Moreover, KCI has a similar effect in vivo when administered to the murine brain via an osmotic pump: tPA activity increases along the CA2-CA3 regions and dentate gyrus of the hippocampal formation. These results demonstrate a neuronal activity-dependent secretory mechanism that can rapidly increase the amount of tPA in neuronal tissue.

摘要

组织型纤溶酶原激活剂(tPA)是一种丝氨酸蛋白酶,可将无活性的纤溶酶原转化为有活性的纤溶酶,在大鼠和小鼠海马体中产生并参与神经元可塑性。为了帮助确定tPA在神经系统中的作用,我们分析了其在神经元细胞系PC12中的表达调控。在对照培养物中,tPA活性仅与细胞相关,培养基中无法检测到活性。当用去极化剂(如氯化钾)处理细胞时,培养基中可检测到tPA活性。分泌的tPA活性增加并不伴随着tPA mRNA水平的增加,且不受蛋白质合成抑制剂的阻断。相反,Ca2+通道阻滞剂可消除tPA的释放,表明化学诱导的膜去极化刺激了预先形成的酶的分泌。此外,通过渗透泵将氯化钾注入小鼠脑内时,在体内也有类似的效果:tPA活性沿海马结构的CA2-CA3区域和齿状回增加。这些结果证明了一种神经元活动依赖性分泌机制,该机制可迅速增加神经元组织中tPA的量。

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