Role of metallothionein-III following central nervous system damage

被引:57
作者
Carrasco, J
Penkowa, M
Giralt, M
Camats, J
Molinero, A
Campbell, IL
Palmiter, RD
Hidalgo, J [1 ]
机构
[1] Univ Autonoma Barcelona, Fac Ciencias, Unidad Fisiol Animal, Dept Biol Celular Fisiol & Inmunol, Bellaterra 08193, Barcelona, Spain
[2] Univ Autonoma Barcelona, Inst Neurosci, Bellaterra 08193, Barcelona, Spain
[3] Univ Copenhagen, Panum Inst, Dept Medt Anat, DK-2200 Copenhagen, Denmark
[4] Scripps Res Inst, Dept Neuropharmacol, La Jolla, CA 92037 USA
[5] Univ Washington, Dept Biochem, Howard Hughes Med Inst, Seattle, WA 98195 USA
关键词
D O I
10.1016/S0969-9961(03)00015-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We evaluated the physiological relevance of metallothionein-Ill (NIT-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. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:22 / 36
页数:15
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