Lee Tet Woo, Tsang Vicky W K, Birch Nigel P
School of Biological Sciences and Centre for Brain Research, University of Auckland Auckland, New Zealand.
School of Biological Sciences and Centre for Brain Research, University of Auckland Auckland, New Zealand ; Brain Research New Zealand, Rangahau Roro Aotearoa Auckland, New Zealand.
Front Cell Neurosci. 2015 Oct 13;9:396. doi: 10.3389/fncel.2015.00396. eCollection 2015.
Although its roles in the vascular space are most well-known, tissue plasminogen activator (tPA) is widely expressed in the developing and adult nervous system, where its activity is believed to be regulated by neuroserpin, a predominantly brain-specific member of the serpin family of protease inhibitors. In the normal physiological state, tPA has been shown to play roles in the development and plasticity of the nervous system. Ischemic damage, however, may lead to excess tPA activity in the brain and this is believed to contribute to neurodegeneration. In this article, we briefly review the physiological and pathological roles of tPA in the nervous system, which includes neuronal migration, axonal growth, synaptic plasticity, neuroprotection and neurodegeneration, as well as a contribution to neurological disease. We summarize tPA's multiple mechanisms of action and also highlight the contributions of the inhibitor neuroserpin to these processes.
尽管组织型纤溶酶原激活剂(tPA)在血管系统中的作用最为人熟知,但它在发育中的和成年的神经系统中广泛表达,据信其活性受神经丝氨酸蛋白酶抑制因子调节,神经丝氨酸蛋白酶抑制因子是丝氨酸蛋白酶抑制剂丝氨酸蛋白酶抑制剂家族中主要存在于大脑的成员。在正常生理状态下,tPA已被证明在神经系统的发育和可塑性中发挥作用。然而,缺血性损伤可能导致大脑中tPA活性过高,据信这会导致神经退行性变。在本文中,我们简要回顾了tPA在神经系统中的生理和病理作用,包括神经元迁移、轴突生长、突触可塑性、神经保护和神经退行性变,以及对神经疾病的影响。我们总结了tPA的多种作用机制,并强调了抑制剂神经丝氨酸蛋白酶抑制因子对这些过程的贡献。