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1.
Biocell ; 30(3): 431-438, dec. 2006. ilus
Article in English | LILACS | ID: lil-491542

ABSTRACT

Caveolin-1, the first member of caveolin family reported, is recognized as the structural component of caveola, a plasma membrane invagination or vesicles that are a subcompartment distinct from clathrin-coated pits. This protein is also known to be involved in cholesterol trafficking. The aim of this study was to determine the expression of caveolin-1 in adult rat Leydig cells. Testis sections incubated with an antibody to caveolin-1 showed, by immunohistochemistry, a moderate number of Leydig cells with different degrees of immunoreaction and a strong reaction in endothelial cells and in the lamina propia of seminiferous tubules.Caveolin- 1 was detected in the cell cytoplasm with a granular pattern and on the cell surface of Leydig cells cultured 24 h on uncoated, laminin-1 or type IV collagen coated coverslips. We also observed a milder reaction in 3 h cultures. Immunoreaction was also detected in Leydig cells with an antibody to tyrosine-phosphorylated caveolin-1. By double immunofluorescent technique, we observed co-localization of caveolin- I and 313-hydroxysteroid dehydrogenase. Western blot analysis revealed a band of about 22 kDa molecular weight that was recognized with both caveolin-1 and tyrosine-phosphocaveolin-1 antibodies. Caveolin-l is one of a few proteins with ademonstrated ability to bind cholesterol in vivo. In this context, the presence of caveolin- in Leydig cells may be related to cholesterol traffic--a rate limiting step in steroid biosynthesis.


Subject(s)
Animals , Male , Rats , /analysis , Blotting, Western , Caveolin 1/analysis , Caveolin 1/metabolism , Leydig Cells/metabolism , Leydig Cells/chemistry , Cholesterol/metabolism , Cells, Cultured , Cytoplasm , Rats, Sprague-Dawley , Testis/cytology
2.
Journal of Veterinary Science ; : 101-104, 2006.
Article in English | WPRIM | ID: wpr-32321

ABSTRACT

The expression of caveolin-1 and -2 in the retina was examined; Western blot analysis showed that both were present. Immunohistochemistry indicated that caveolin-1 was expressed in the majority of retinal layers, including the ganglion cell layer, inner plexiform layer, outer plexiform layer, and in the vascular endothelial cells of the retina. Caveolin-2 was primarily immunostained in the vessels, but in a few other elements as well. This is the first demonstration of caveolin differential expression in the retina of rats, and suggests that caveolin plays an important role in signal transduction in glial cells and neuronal cells.


Subject(s)
Animals , Male , Rats , Caveolin 1/analysis , Caveolin 2/analysis , Gene Expression Regulation , Immunohistochemistry , Rats, Sprague-Dawley , Retina/chemistry
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