Expression of glypican-1, syndecan-1 and syndecan-4 mRNAs protein kinase C-regulated in rat immature Sertoli cells by semi-quantitative RT-PCR analysis

Citation
S. Brucato et al., Expression of glypican-1, syndecan-1 and syndecan-4 mRNAs protein kinase C-regulated in rat immature Sertoli cells by semi-quantitative RT-PCR analysis, BBA-GEN SUB, 1474(1), 2000, pp. 31-40
Citations number
56
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS
ISSN journal
03044165 → ACNP
Volume
1474
Issue
1
Year of publication
2000
Pages
31 - 40
Database
ISI
SICI code
0304-4165(20000306)1474:1<31:EOGSAS>2.0.ZU;2-L
Abstract
In seminiferous tubules, Sertoli cells provide structural and nutritional s upport for the developing germinal cells. Cell to cell signalization and ce ll adhesion require proteoglycans expressed at the cell membrane. A prelimi nary biochemical and structural approach indicated that cell surface proteo glycans are mostly heparan sulfate (HSPG) in immature rat Sertoli cells. Th e present study focused on the qualitative and quantitative expression of t hree membrane HSPG, syndecan-1, syndecan-4 and glypican-1 in Sertoli cells of 20-day-old rat. A semiquantitative multiplex RT-PCR strategy was develop ed to appreciate the effect of PKC activation on the mRNA expression of the three HSPG. Our data show that the syndecan-1 and glypican-1 mRNA expressi on is increased by the phorbol myristate acetate (PMA) suggesting a regulat ion of their expression by the phosphatidyl inositol pathway, as previously hypothesized (Fagen et al., Biochim. Biophys. Acta, 1472 (1999) 250-261). In addition, a physiological effector of the PKC as ATP gave similar effect s. Thus, this overexpression could be related with paracrine factors secret ed by germ cells. (C) 2000 Elsevier Science B.V. All rights reserved.