Skip Navigation
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Your Environment. Your Health.

Publication Detail

Title: Roles of the metallothionein family of proteins in the central nervous system.

Authors: Hidalgo, J; Aschner, M; Zatta, P; Vasák, M

Published In Brain Res Bull, (2001 May 15)

Abstract: Metallothioneins (MTs) constitute a family of proteins characterized by a high heavy metal [Zn(II), Cu(I)] content and also by an unusual cysteine abundance. Mammalian MTs are comprised of four major isoforms designated MT-1 trough MT-4. MT-1 and MT-2 are expressed in most tissues including the brain, whereas MT-3 (also called growth inhibitory factor) and MT-4 are expressed predominantly in the central nervous system and in keratinizing epithelia, respectively. All MT isoforms have been implicated in disparate physiological functions, such as zinc and copper metabolism, protection against reactive oxygen species, or adaptation to stress. In the case of MT-3, an additional involvement of this isoform in neuromodulatory events and in the pathogenesis of Alzheimer's disease has also been suggested. It is essential to gain insight into how MTs are regulated in the brain in order to characterize MT functions, both in normal brain physiology, as well as in pathophysiological states. The focus of this review concerns the biology of the MT family in the context of their expression and functional roles in the central nervous system.

PubMed ID: 11470309 Exiting the NIEHS site

MeSH Terms: Animals; Central Nervous System/cytology; Central Nervous System/metabolism*; Copper/metabolism; Humans; Metallothionein/genetics; Metallothionein/metabolism*; Neurodegenerative Diseases/metabolism; Neurodegenerative Diseases/physiopathology; Oxidative Stress/physiology; Protein Isoforms/genetics; Protein Isoforms/metabolism*; Zinc/metabolism

Back
to Top