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Permanent URL to this publication: http://dx.doi.org/10.5167/uzh-34627

Manso, Y; Serra, M; Comes, G; Giralt, M; Carrasco, J; Cols, N; Vasák, M; González-Duarte, P; Hidalgo, J (2010). The comparison of mouse full metallothionein-1 versus alpha and beta domains and metallothionein-1-to-3 mutation following traumatic brain injury reveals different biological motifs. Journal of Neuroscience Research, 88(8):1708-1718.

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Abstract

Traumatic injury to the brain is one of the leading causes of injury-related death or disability, but current therapies are limited. Previously it has been shown that the antioxidant proteins metallothioneins (MTs) are potent neuroprotective factors in animal models of brain injury. The exogenous administration of MTs causes effects consistent with the roles proposed from studies in knock-out mice. We herewith report the results comparing full mouse MT-1 with the independent alpha and beta domains, alone or together, in a cryoinjury model. The lesion of the cortex caused the mice to perform worse in the horizontal ladder beam and the rota-rod tests; all the proteins showed a modest effect in the former test, while only full MT-1 improved the performance of animals in the rota-rod, and the alpha domain showed a rather detrimental effect. Gene expression analysis by RNA protection assay demonstrated that all proteins may alter the expression of host-response genes such as GFAP, Mac1 and ICAM, in some cases being the beta domain more effective than the alpha domain or even the full MT-1. A MT-1-to-MT-3 mutation blunted some but not all the effects caused by the normal MT-1, and in some cases increased its potency. Thus, splitting the two MT-1 domains do not seem to eliminate all MT functions but certainly modifies them, and different motifs seem to be present in the protein underlying such functions.

Item Type:Journal Article, refereed, original work
Communities & Collections:04 Faculty of Medicine > Department of Biochemistry
07 Faculty of Science > Department of Biochemistry
DDC:570 Life sciences; biology
Language:English
Date:June 2010
Deposited On:06 Jul 2010 08:27
Last Modified:21 Dec 2013 10:37
Publisher:Wiley-Blackwell
ISSN:0360-4012
Publisher DOI:10.1002/jnr.22342
PubMed ID:20127815
Citations:Web of Science®. Times Cited: 4
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Scopus®. Citation Count: 5

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