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金属硫蛋白-III在中枢神经系统损伤后的作用。

Role of metallothionein-III following central nervous system damage.

作者信息

Carrasco Javier, Penkowa Milena, Giralt Mercedes, Camats Jordi, Molinero Amalia, Campbell Iain L, Palmiter Richard D, Hidalgo Juan

机构信息

Institute of Neurosciences and Department of Cellular Biology, Physiology and Immunology, Animal Physiology Unit, Faculty of Sciences, Autonomous University of Barcelona, Bellaterra, Barcelona, Spain 08193.

出版信息

Neurobiol Dis. 2003 Jun;13(1):22-36. doi: 10.1016/s0969-9961(03)00015-9.

Abstract

We evaluated the physiological relevance of metallothionein-III (MT-III) in the central nervous system following damage caused by a focal cryolesion onto the cortex by studying Mt3-null mice. In normal mice, dramatic astrogliosis and microgliosis and T-cell infiltration were observed in the area surrounding the lesioned tissue, along with signs of increased oxidative stress and apoptosis. There was also significant upregulation of cytokines/growth factors such as tumor necrosis factor-alpha, interleukin (IL)-1 alpha/beta, and IL-6 as measured by ribonuclease protection assay. Mt3-null mice did not differ from control mice in these responses, in sharp contrast to results obtained in Mt1- Mt2-null mice. In contrast, Mt3-null mice showed increased expression of several neurotrophins as well as of the neuronal sprouting factor GAP-43. Thus, unlike MT-I and MT-II, MT-III does not affect the inflammatory response elicited in the central nervous system by a cryoinjury, nor does it serve an important antioxidant role, but it may influence neuronal regeneration during the recovery process.

摘要

我们通过研究 Mt3 基因敲除小鼠,评估了局灶性冷冻损伤皮层后中枢神经系统中金属硫蛋白 III(MT-III)的生理相关性。在正常小鼠中,在损伤组织周围区域观察到显著的星形胶质细胞增生、小胶质细胞增生和 T 细胞浸润,同时伴有氧化应激增加和细胞凋亡的迹象。通过核糖核酸酶保护试验检测,细胞因子/生长因子如肿瘤坏死因子-α、白细胞介素(IL)-1α/β和 IL-6 也有显著上调。Mt3 基因敲除小鼠在这些反应中与对照小鼠没有差异,这与 Mt1-Mt2 基因敲除小鼠的结果形成鲜明对比。相比之下,Mt3 基因敲除小鼠显示出几种神经营养因子以及神经元发芽因子 GAP-43 的表达增加。因此,与 MT-I 和 MT-II 不同,MT-III 不影响冷冻损伤在中枢神经系统中引发的炎症反应,也不发挥重要的抗氧化作用,但它可能在恢复过程中影响神经元再生。

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