1. ¹Department of Urology, University of Vienna, Wien, Austria
2. ²Department of Urology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA
3. ³Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA
4. ⁴Department of Reproductive Endocrinology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA

Correspondence: B Planz, Department of Urology, Friedrich-Laustr. 11, 40472 Düsseldorf, Germany. E-mail: bplanz@hotmail.com

Received 11 September 2003; Revised 10 November 2003; Accepted 19 November 2003.

Abstract

We established explant primary cultures in order to study the growth and hormone responsiveness, and the differentiation process of prostatic epithelial cells. Cell outgrowth was achieved from explant tissue by using a new DU145-cell-conditioned medium and special plastic coverslips. To define the present model, proliferation assays were tested by [³H]thymidine assay and planimetric analysis. Cells were analyzed using immunocytochemistry, light, phase contrast and electron microscopy, polymerase chain reaction, telomerase ELISA and immunoassay (PSA). Morphology and electron microscopy revealed typical epithelial differentiation. Immunocytochemistry showed the content of basal and secretory epithelial cells, endocrine paracrine cells and a high level of proliferation. With increasing culture time, mature epithelial differentiation (PSA) increases and the initial increase of -smooth muscle actin (-SMA) decreases again. After further passaging, -SMA expression is no longer detected and PSA expression decreases. Furthermore, epithelial cells showed both androgen responsiveness and androgen receptor expression. These findings show the presence of epithelial cells in a process of differentiation with endocrine paracrine cells and a high level of proliferation. This model may maintain the cellular and functional properties more closely related to the human prostate and may provide a valuable tool for studying stem cells and differentiation characteristics.