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海马体中组织型纤溶酶原激活剂 - 纤溶酶系统的定位与调节

Localization and regulation of the tissue plasminogen activator-plasmin system in the hippocampus.

作者信息

Salles Fernando J, Strickland Sidney

机构信息

Laboratory of Neurobiology and Genetics, The Rockefeller University, New York, New York 10021, USA.

出版信息

J Neurosci. 2002 Mar 15;22(6):2125-34. doi: 10.1523/JNEUROSCI.22-06-02125.2002.

Abstract

The extracellular protease cascade of tissue plasminogen activator (tPA) and plasminogen has been implicated in neuronal plasticity and degeneration. We show here that unstimulated expression of tPA in the mouse hippocampus is concentrated in the mossy fiber pathway, with little or no expression within the perforant path, the Schaffer collaterals, or neuronal cell bodies. tPA protein is also expressed in vascular endothelial cells throughout the brain parenchyma. Four hours after excitotoxic injury, tPA protein is transiently induced within CA1 pyramidal neurons. The induced CA1 tPA is localized to neurons that survive the injury and is enzymatically active. Within the mossy fiber pathway, injury resulted in decreased tPA protein. In contrast, mossy fiber tPA activity displayed a biphasic character: transient increase at 8 hr, then a decrease by 24 hr after injury. Analysis of plasminogen activator inhibitor-1 (PAI-1) expression showed that PAI-1 antigen is upregulated by 24 hr and could account for the tPA activity downregulation seen at this time point. Plasminogen immunohistochemistry suggested an increase within the mossy fiber pathway after injury. Finally, hippocampal tPA expression among various mammalian species was strikingly different. These results indicate a complex control of tPA protein and enzymatic activity in the hippocampus that may help regulate neuronal plasticity.

摘要

组织型纤溶酶原激活物(tPA)和纤溶酶原的细胞外蛋白酶级联反应与神经元可塑性和变性有关。我们在此表明,小鼠海马体中未受刺激的tPA表达集中在苔藓纤维通路,在穿通通路、海马体联合纤维或神经元细胞体内几乎没有或没有表达。tPA蛋白也在整个脑实质的血管内皮细胞中表达。兴奋性毒性损伤4小时后,CA1锥体神经元内短暂诱导出tPA蛋白。诱导的CA1 tPA定位于在损伤中存活的神经元,并且具有酶活性。在苔藓纤维通路中,损伤导致tPA蛋白减少。相比之下,苔藓纤维tPA活性呈现双相特征:损伤后8小时短暂增加,然后在24小时时下降。对纤溶酶原激活物抑制剂-1(PAI-1)表达的分析表明,PAI-1抗原在24小时时上调,这可以解释在这个时间点观察到的tPA活性下调。纤溶酶原免疫组织化学表明损伤后苔藓纤维通路内增加。最后,不同哺乳动物物种之间海马体tPA表达存在显著差异。这些结果表明海马体中tPA蛋白和酶活性受到复杂调控,这可能有助于调节神经元可塑性。

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