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Histol Histopathol ; 22(7): 719-28, 2007 07.
Article in English | MEDLINE | ID: mdl-17455146

ABSTRACT

Metallothioneins (MT) were localized by immunochemistry in different organs and cell compartments of turbot exposed to sublethal concentrations (100 ppb) of Cd for 7 days. The polyclonal rabbit anti-cod MT antibody (NIVA, Norway) applied herein exhibited positive cross-reactivity with turbot MTs. Immunoreactive MTs were localized in the branchial epithelium, in the liver and in the kidney of turbot. In Cd exposed fishes MTs were demonstrated mainly in branchial chloride cells (CC) and to a lesser extend in the area where progenitor cells are located and in the cells of the respiratory epithelium (secondary lamellae). A higher staining intensity for MTs was observed in CC of the interlamellar space of the main branchial epithelium in comparison with control CC. MT-staining was also observed in the chondroblasts of the cartilage and in the erythrocytes within blood vessels both in control and Cd-exposed specimens. MT immunoreaction was high in the liver hepatocytes and weak in the epithelium of the proximal portion of the kidney in exposed turbot. The tegument, spleen and muscle were devoid of any immunolabelling in both treatments. Ultrastructural studies at the transmission electron microscope revealed that Cd-induced MTs were mainly located in the cytoplasm of gill CC, the lysosomes and the cytoplasm of hepatocytes and in the basal labyrinth of kidney proximal nephrocytes. The differential localization/induction of MTs in different cell types described hereby suggests that the quantification of the specific expression of MT may be used in biomonitoring programs as a biomarker of Cd exposure in aquatic environments.


Subject(s)
Cadmium Chloride/pharmacology , Fish Proteins/biosynthesis , Flatfishes/metabolism , Metallothionein/biosynthesis , Animals , Biomarkers/metabolism , Blotting, Western , Environmental Monitoring/methods , Gills/drug effects , Gills/metabolism , Gills/ultrastructure , Immunohistochemistry , Kidney/drug effects , Kidney/metabolism , Kidney/ultrastructure , Liver/drug effects , Liver/metabolism , Liver/ultrastructure , Microscopy, Electron, Transmission , Muscles/drug effects , Muscles/metabolism , Polarography , Spleen/drug effects , Spleen/metabolism , Time Factors , Up-Regulation/drug effects
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