Expression of MT-3 protein in the human kidney

被引:79
作者
Garrett, SH [1 ]
Sens, MA [1 ]
Todd, JH [1 ]
Somji, S [1 ]
Sens, DA [1 ]
机构
[1] W Virginia Univ, Dept Pathol, Robert C Byrd Hlth Sci Ctr, Morgantown, WV 26506 USA
关键词
proximal tubule; metallothionein; kidney; immunohistochemistry; MT-3; metals; nephrotoxicity;
D O I
10.1016/S0378-4274(99)00003-X
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The objective of the present study was to determine the expression of MT-3 in the human kidney. To accomplish this, an antibody was generated against a unique 8 amino acid sequence present in MT-3 that is not shared by any other MT family member. Western analysis demonstrated that the resulting antibody reacted with a protein band of approximately 6 kDa, corresponding to the known molecular weight of MT-3. Immunohistochemical staining using this antibody demonstrated reactivity with several epithelial components of the nephron. In the glomerulus, moderate intensity was demonstrated in parietal epithelial cells of Bowman's capsule and in visceral epithelial cells of the glomerular tuft. Proximal convoluted tubule cells exhibited moderate cytoplasmic MT-3 reactivity. Distal tubules showed strong cytoplasmic staining for MT-3, particularly in the medullary rays. In the medulla, MT-3 staining was the most variable, with weak to moderate staining in the medullary collecting ducts and a general absence of staining in the thin loops of Henle and in the transitional epithelium of the renal pelvis. The finding that MT-3 is constitutively expressed in several glomerular and tubular epithelial elements of the human kidney warrants consideration of an expanded role for this protein family in maintaining renal homeostasis. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:207 / 214
页数:8
相关论文
共 27 条
  • [1] MODULATION OF METALLOTHIONEIN-III MESSENGER-RNA CONTENT AND GROWTH-RATE OF RAT C6-GLIAL CELLS BY TRANSFECTION WITH HUMAN 5-HT1D RECEPTOR GENES
    AMOUREUX, MC
    WURCH, T
    PAUWELS, PJ
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 214 (02) : 639 - 645
  • [2] METALLOTHIONEIN - ASPECTS RELATED TO COPPER AND ZINC-METABOLISM
    COUSINS, RJ
    [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 1983, 6 : 15 - 21
  • [3] ENHANCED NEUROTROPHIC ACTIVITY IN ALZHEIMERS-DISEASE CORTEX IS NOT ASSOCIATED WITH DOWN-REGULATION OF METALLOTHIONEIN-III (GIF)
    ERICKSON, JC
    SEWELL, AK
    JENSEN, LT
    WINGE, DR
    PALMITER, RD
    [J]. BRAIN RESEARCH, 1994, 649 (1-2) : 297 - 304
  • [4] ALTERED SUBCELLULAR-DISTRIBUTION OF CADMIUM FOLLOWING CADMIUM PRETREATMENT - POSSIBLE MECHANISM OF TOLERANCE TO CADMIUM-INDUCED LETHALITY
    GOERING, PL
    KLAASSEN, CD
    [J]. TOXICOLOGY AND APPLIED PHARMACOLOGY, 1983, 70 (02) : 195 - 203
  • [5] METALLOTHIONEIN
    HAMER, DH
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 1986, 55 : 913 - 951
  • [6] Expression of MT-3 mRNA in human kidney, proximal tubule cell cultures, and renal cell carcinoma
    Hoey, JG
    Garrett, SH
    Sens, MA
    Todd, JH
    Sens, DA
    [J]. TOXICOLOGY LETTERS, 1997, 92 (02) : 149 - 160
  • [7] Effect of several metallothionein inducers on oxidative stress defense mechanisms in rats
    Iszard, MB
    Liu, J
    Klassen, CD
    [J]. TOXICOLOGY, 1995, 104 (1-3) : 25 - 33
  • [8] Kagi J H, 1987, Experientia Suppl, V52, P25
  • [9] Kagi J. H. R., 1993, METALLOTHIONEIN, P29
  • [10] MAMMALIAN METALLOTHIONEIN
    KAGI, JHR
    HUNZIKER, P
    [J]. BIOLOGICAL TRACE ELEMENT RESEARCH, 1989, 21 : 111 - 118