首页> 外文期刊>Journal of Neuroscience Research >Mice lacking tissue plasminogen activator and urokinase plasminogen activator genes show attenuated matrix metalloproteases activity after sciatic nerve crush.
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Mice lacking tissue plasminogen activator and urokinase plasminogen activator genes show attenuated matrix metalloproteases activity after sciatic nerve crush.

机译:缺乏组织纤溶酶原激活物和尿激酶纤溶酶原激活物基因的小鼠在坐骨神经挤压后表现出减弱的基质金属蛋白酶活性。

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摘要

Plasminogen activators (PAs), tissue PA (tPA) and urokinase PA (uPA), have been shown to be induced in sensory neurons after sciatic nerve crush. These findings suggested that PAs facilitate peripheral nerve regeneration by digesting adhesive cell contacts and by activation of other proteases, thereby initiating a proteolytic cascade. Both tPA and uPA activate some matrix metalloproteases (MMPs), indirectly via plasminogen activation or directly, such as the uPA activation of MMP-2. In this study, we demonstrated, by using tPA and uPA knockout mice, that a lack of a plasminogen activator affected MMP-9 and MMP-2 activity after crushing of the sciatic nerve. These findings show that the PAs are important for MMP-9 and MMP-2 activity at the crush site.
机译:坐骨神经挤压后,已在感觉神经元中诱导了纤溶酶原激活物(PAs),组织PA(tPA)和尿激酶PA(uPA)。这些发现表明,PAs通过消化粘附细胞接触和激活其他蛋白酶来促进周围神经再生,从而启动蛋白水解级联反应。 tPA和uPA都可以通过纤溶酶原激活或间接(例如MMP-2的uPA激活)间接激活某些基质金属蛋白酶(MMP)。在这项研究中,我们证明了通过使用tPA和uPA基因敲除小鼠,缺乏一种纤溶酶原激活剂会影响坐骨神经压伤后的MMP-9和MMP-2活性。这些发现表明,PA对粉碎部位的MMP-9和MMP-2活性很重要。

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