Regulation and activation of focal adhesion kinase and paxillin during the adhesion, proliferation, and differentiation of prostatic epithelial cells in vitro and in vivo

• Published in: Molecular endocrinology (Baltimore, Md.) Md.), 1996-08, Vol.10 (8), p.1010-1020
• Main Authors: Tremblay, L, Hauck, W, Nguyen, L T, Allard, P, Landry, F, Chapdelaine, A, Chevalier, S
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Animals; Cell Adhesion; Cell Adhesion Molecules - chemistry; Cell Adhesion Molecules - genetics; Cell Adhesion Molecules - metabolism; Cell Differentiation; Cell Division; Cells, Cultured; Cytoskeletal Proteins - metabolism; Dogs; Epithelial Cells; Epithelium - metabolism; Extracellular Matrix - physiology; Focal Adhesion Kinase 1; Focal Adhesion Protein-Tyrosine Kinases; Gonadal Steroid Hormones - pharmacology; Humans; Male; Molecular Sequence Data; Paxillin; Phosphoproteins - metabolism; Prostate - cytology; Prostate - drug effects; Prostate - metabolism; Protein-Tyrosine Kinases - chemistry; Protein-Tyrosine Kinases - genetics; Protein-Tyrosine Kinases - metabolism; RNA, Messenger - metabolism; Sequence Homology; Vitronectin - pharmacology
• ISSN: 0888-8809
• DOI: 10.1210/me.10.8.1010

Focal adhesion kinase (pp125FAK) is a nonreceptor protein tyrosine kinase transducing signals initiated through integrin activation triggered by cell/extracellular matrix (ECM) interactions. To examine its role in epithelial cell adhesion, proliferation, and differentiation, we have studied pp125FAK expression, activity, and association with paxillin in two canine prostate models in which these functions can be selectively regulated: in vitro by vitronectin (VN) and serum factors, and in vivo by sex steroids. Kinetic studies revealed that the adhesion and spreading of prostatic epithelial cells in primary culture was regulated by serum VN and a natural ECM containing VN produced by prostate cells. While barely detectable in freshly isolated prostate cells, proliferating cells, after 72 h in culture, expressed higher levels of FAK mRNA (8-fold), pp125FAK (50-fold), and paxillin (50-fold). In prostate cells with a reduced growth rate after 2 weeks in culture, we observed a decrease in pp125FAK (4-fold) and its transcript (3-fold), but no change in paxillin. In vivo, both proteins were undetectable in normal and hyperplastic glands composed of a well differentiated epithelium, and in prostates restored by androgen supplementation. In contrast, pp125FAK and paxillin were up-regulated by androgen deprivation (castration) and further increased by estrogen treatment, which yielded metaplastic prostates mostly composed of proliferating basal epithelial cells. Moreover, both proteins were constitutively phosphorylated on tyrosine in the metaplastic prostate, as well as in proliferating cultured cells. Together, these results demonstrate that pp125FAK expression is regulated at the protein and mRNA levels and forms active signaling complexes with paxillin when epithelial cells in contact with ECM proteins are induced to proliferate in vivo and in vitro.