Identification of metallothionein receptors in human astrocytes

被引:31
作者
ElRefaey, H
Ebadi, M
Kuszynski, CA
Sweeney, J
Hamada, FM
Hamed, A
机构
[1] UNIV NEBRASKA, COLL MED, DEPT PHARMACOL, OMAHA, NE 68198 USA
[2] UNIV NEBRASKA, COLL MED, DEPT PATHOL, OMAHA, NE 68198 USA
[3] UNIV NEBRASKA, COLL MED, DEPT MICROBIOL, OMAHA, NE 68198 USA
关键词
metallothionein; glutathione; metallothionein receptors; oxidative stress;
D O I
10.1016/S0304-3940(97)00548-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Metallothionein (MT) isoforms are low molecular weight (6000-7000 Da) zinc binding proteins containing 60-68 amino acid residues, 25-30% cysteine, no aromatic amino acids, and binding between 5-7 g zinc/mol of protein. Since the synthesis of MT is induced by endotoxin, cytokines, and gIucocorticoids, MT is now considered to be an acute phase protein protecting against oxygen radicals and oxidative damages caused by inflammation, tissue injury, and stress to the central nervous system. By postulating that a specific mechanism must exist to foster the induction of MTs I and Il by numerous and diversified factors, we searched for and identified for the first time, MT receptors on U373MG cell membrane preparations, by using fluoresceinated MT I isoform probe; and by employing cysteine, glutathione, and four MT isoforns to determine high affinity and specific binding. MT receptors revealed a K-d value of 0.84 nM and a B-max of 99.82 fmol/mg protein. Moreover, MT receptors were found in greater density on the surface of aggregated astrocytes. We postulate that conditions or agents generating reactive oxygen species may influence the expression of MT receptors. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:131 / 134
页数:4
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