FACS-Free isolation and purification protocol of mouse prostate epithelial cells for organoid primary culture
Lilianne Frégeau-Proulx,
Aurélie Lacouture,
Cindy Weidmann,
Cynthia Jobin,
Étienne Audet-Walsh
Affiliations
Lilianne Frégeau-Proulx
Endocrinology - Nephrology Research Axis, CHU de Québec – Université Laval Research Center, Québec, QC, Canada; Department of molecular medicine, Faculty of Medicine, Université Laval, Québec, QC, Canada; Centre de recherche sur le cancer de l'Université Laval, Québec, QC, Canada
Aurélie Lacouture
Endocrinology - Nephrology Research Axis, CHU de Québec – Université Laval Research Center, Québec, QC, Canada; Department of molecular medicine, Faculty of Medicine, Université Laval, Québec, QC, Canada; Centre de recherche sur le cancer de l'Université Laval, Québec, QC, Canada
Cindy Weidmann
Endocrinology - Nephrology Research Axis, CHU de Québec – Université Laval Research Center, Québec, QC, Canada; Centre de recherche sur le cancer de l'Université Laval, Québec, QC, Canada
Cynthia Jobin
Endocrinology - Nephrology Research Axis, CHU de Québec – Université Laval Research Center, Québec, QC, Canada; Department of molecular medicine, Faculty of Medicine, Université Laval, Québec, QC, Canada; Centre de recherche sur le cancer de l'Université Laval, Québec, QC, Canada
Étienne Audet-Walsh
Endocrinology - Nephrology Research Axis, CHU de Québec – Université Laval Research Center, Québec, QC, Canada; Department of molecular medicine, Faculty of Medicine, Université Laval, Québec, QC, Canada; Centre de recherche sur le cancer de l'Université Laval, Québec, QC, Canada; Corresponding author.
The prostate is a gland that contributes to men's fertility. It is highly responsive to androgens and is often the site of carcinogenesis, as prostate cancer is the most frequent cancer in men in over a hundred countries. To study the normal prostate, few in vitro models exist, and most of them do not express the androgen receptor (AR). To overcome this issue, prostate epithelial cells can be grown in primary culture ex vivo in 2- and 3-dimensional culture (organoids). However, methods to purify these cells often require flow cytometry, thus necessitating specialized instruments and expertise. Herein, we present a detailed protocol for the harvest, purification, and primary culture of mouse prostate epithelial cells to grow prostate organoids ex vivo. This protocol does not require flow cytometry approaches, facilitating its implementation in most research laboratories, and organoids grown with this protocol are highly responsive to androgens. In summary, we present a new simple method that can be used to grow prostate organoids that recapitulate the androgen response of this gland in vivo.