Literature DB >> 8581921

Polarized epithelial cells of the hamster seminal vesicle in a serum-free bicameral culture system: evidence of secretory and endocytic activities.

G Rodrigues1, S Gulbenkian, L R Mata.   

Abstract

Primary cultures of epithelial cells from the hamster seminal vesicle were established in a chemically defined medium supplemented with hormones and growth factors. Epithelial cell clusters were prepared combining enzymatic dissociation and mechanical disaggregation and then seeded in bicameral systems equipped with collagen-membrane inserts. A growth curve was generated and the cells were characterized morphologically and morphometrically by light and electron microscopy. The immunocytochemical detection of cytokeratins and the measurement of transepithelial electrical resistance were also performed. The secretory activity was studied by fluorography using L-[35S]methionine as a precursor, and endocytosis was approached using horseradish peroxidase as a tracer. Our results show that epithelial cells of the seminal vesicle can be grown as a monolayer of morphological and functionally polarized cells which retain secretory and endocytic activities. These cell cultures might therefore prove useful to investigate further the regulation of secretion and endocytosis in the seminal vesicle and are a promising model to approach, in a broader scope, cell polarity and protein sorting and targeting.

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Year:  1995        PMID: 8581921     DOI: 10.1007/bf00319145

Source DB:  PubMed          Journal:  Cell Tissue Res        ISSN: 0302-766X            Impact factor:   5.249


  23 in total

1.  Redistribution and recycling of internalized membrane in seminal vesicle secretory cells.

Authors:  L R Mata; E I Christensen
Journal:  Biol Cell       Date:  1990       Impact factor: 4.458

2.  Dynamics of HRPase absorption in the epithelial cells of the hamster seminal vesicles.

Authors:  L R Mata
Journal:  J Microsc Biol Cell       Date:  1976-03

3.  Secretory cell activity in the hamster seminal vesicle following castration. A morphometric ultrastructural study.

Authors:  L R Mata; J F David-Ferreira
Journal:  Biol Cell       Date:  1985       Impact factor: 4.458

4.  Identification of two strains of MDCK cells which resemble separate nephron tubule segments.

Authors:  J C Richardson; V Scalera; N L Simmons
Journal:  Biochim Biophys Acta       Date:  1981-02-18

5.  In vitro propagation of seminal vesicle epithelial cells.

Authors:  M M Lieber; S S Barham; C M Veneziale
Journal:  Invest Urol       Date:  1980-01

6.  Testosterone interferes with the kinetics of endocytosis in the hamster seminal vesicle.

Authors:  L R Mata; J F David-Ferreira
Journal:  Biol Cell       Date:  1990       Impact factor: 4.458

7.  Occluding junctions and cell behavior in primary cultures of normal and neoplastic mammary gland cells.

Authors:  P B Pickett; D R Pitelka; S T Hamamoto; D S Misfeldt
Journal:  J Cell Biol       Date:  1975-08       Impact factor: 10.539

8.  Polarized monolayers formed by epithelial cells on a permeable and translucent support.

Authors:  M Cereijido; E S Robbins; W J Dolan; C A Rotunno; D D Sabatini
Journal:  J Cell Biol       Date:  1978-06       Impact factor: 10.539

9.  Glucocorticoids increase amylase mRNA levels, secretory organelles, and secretion in pancreatic acinar AR42J cells.

Authors:  C D Logsdon; J Moessner; J A Williams; I D Goldfine
Journal:  J Cell Biol       Date:  1985-04       Impact factor: 10.539

10.  Permeability of intestinal capillaries. Pathway followed by dextrans and glycogens.

Authors:  N Simionescu; M Simionescu; G E Palade
Journal:  J Cell Biol       Date:  1972-05       Impact factor: 10.539

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