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在小鼠海马体中注射红藻氨酸后,组织纤溶酶原激活物-纤溶酶系统对神经元细胞粘附分子的蛋白水解作用。

Proteolysis of neuronal cell adhesion molecule by the tissue plasminogen activator-plasmin system after kainate injection in the mouse hippocampus.

作者信息

Endo A, Nagai N, Urano T, Takada Y, Hashimoto K, Takada A

机构信息

Department of Dentistry and Oral and Maxillofacial Surgery, Hamamatsu University School of Medicine, Japan.

出版信息

Neurosci Res. 1999 Jan;33(1):1-8. doi: 10.1016/s0168-0102(98)00105-9.

Abstract

Tissue plasminogen activator (tPA) is a serine protease that converts inactive plasminogen to the active protease plasmin and mediates extracellular metabolism. tPA is transcriptionally induced in the mouse hippocampus by pharmacological or electrical stimulation of neuronal activity and mediates excitotoxin-induced neuronal degeneration. Therefore, we hypothesized that tPA would be induced in the hippocampus after kainic acid (KA) injection into the lateral cerebral ventricle (LCV) and that the activated tPA-plasmin system would degrade the neuronal cell adhesion molecule (NCAM), which is a component of the extracellular matrix. In order to investigate this possibility, we first examined whether NCAM is a substrate for the tPA plasmin system by incubating mouse brain homogenates with tPA and plasminogen at 37 degrees C. Next, we examined the degradation of NCAM and the changes of tPA activity in the mouse hippocampus with immunohistochemical procedures and histological zymography after KA injection into both LCVs. As a result, we observed neuronal atrophy and a decrease of NCAM immunoreactivity along with an increase of tPA activity in the CA3 area of the hippocampus. These results suggest that activation of the tPA plasmin system after KA injection into the LCVs results in the degradation of NCAM in the CA3 area.

摘要

组织型纤溶酶原激活物(tPA)是一种丝氨酸蛋白酶,它能将无活性的纤溶酶原转化为活性蛋白酶纤溶酶,并介导细胞外代谢。tPA在小鼠海马体中通过药理学或电刺激神经元活动而被转录诱导,并介导兴奋性毒素诱导的神经元变性。因此,我们推测在向侧脑室(LCV)注射 kainic acid(KA)后,海马体中会诱导产生tPA,并且激活的tPA - 纤溶酶系统会降解神经元细胞粘附分子(NCAM),NCAM是细胞外基质的一个组成部分。为了研究这种可能性,我们首先通过在37℃下将小鼠脑匀浆与tPA和纤溶酶原一起孵育,来检测NCAM是否是tPA - 纤溶酶系统的底物。接下来,我们在向双侧LCV注射KA后,用免疫组织化学方法和组织学酶谱分析法检测小鼠海马体中NCAM的降解情况以及tPA活性的变化。结果,我们在海马体的CA3区域观察到神经元萎缩、NCAM免疫反应性降低以及tPA活性增加。这些结果表明,向LCV注射KA后tPA - 纤溶酶系统的激活导致了CA3区域中NCAM的降解。

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