PLATELET-DERIVED GROWTH-FACTOR EFFECTS ON PURIFIED TESTICULAR PERITUBULAR MYOID CELLS - BINDING, CYTOSOLIC CA2-MATRIX PRODUCTION ENHANCEMENT( INCREASE, MITOGENIC ACTIVITY, AND EXTRACELLULAR)

Citation
L. Gnessi et al., PLATELET-DERIVED GROWTH-FACTOR EFFECTS ON PURIFIED TESTICULAR PERITUBULAR MYOID CELLS - BINDING, CYTOSOLIC CA2-MATRIX PRODUCTION ENHANCEMENT( INCREASE, MITOGENIC ACTIVITY, AND EXTRACELLULAR), Endocrinology, 133(4), 1993, pp. 1880-1890
Citations number
65
Categorie Soggetti
Endocrynology & Metabolism
Journal title
ISSN journal
00137227
Volume
133
Issue
4
Year of publication
1993
Pages
1880 - 1890
Database
ISI
SICI code
0013-7227(1993)133:4<1880:PGEOPT>2.0.ZU;2-6
Abstract
The response of purified rat testicular peritubular myoid cells (PMC) to platelet-derived growth factor (PDGF) was studied. Freshly isolated PMC were devoid of measurable amounts of PDGF-binding sites. However, after 1 day in culture in serum-free conditions, specific high affini ty receptors were detected. The estimated binding sites per cell revea led that PMC express more receptors for PDGF-BB, followed by PDGF-AB a nd PDGF-AA. PDGF treatment of cultured PMC increased the cytosolic Ca2 + concentration, showing a rank order of potencies with PDGF-BB > PDGF -AB > PDGF-AA. PMC proliferation, as measured by direct cell counting, was also stimulated by all three PDGF isoforms, with the same order o f potencies observed for the increase in intracellular Ca2+. This effe ct was inhibited by antibodies to PDGF. Moreover, PDGF treatment incre ased the release of type IV collagen and fibronectin, and induced the release of type V collagen and laminin. These results demonstrate that testicular PMC are induced to express functionally active PDGF recept ors in response to cell culturing. These data suggest that PMC may be a target for PDGF and that PDGF-mediated effects in vivo are dependent on factors regulating the expression of the receptors. The role that PDGF may play in normal and pathological testicular processes is discu ssed.