Abstract

In order to reduce cellular complexity in the study of the controls of the biochemical differentiation of mammary gland epithelium, approximately 100-fold purified epithelial cells from the mammary glands of virgin BALB/c mice were grown in three-dimensional collagen gels, and formed colonies that resembled mammary ductules. Here we report the induction of a biochemical differentiation in these purified epithelial cells in response to appropriate hormonal signals, starting from the state in the virgin mammary gland and ending with the stage characteristic of lactation. Induction of the synthesis of caseins was examined as a marker of mammary functional differentiation using sensitive immunologic autoradiography. The cells were maximally induced by the combination of the hormones, insulin, prolactin, aldosterone, and hydrocortisone, in both serum-containing and essentially serum-free media. The induction required insulin and prolactin, and was enhanced by the presence of the steroids. The cellular distribution of the induction was general, inasmuch as three-quarters of the hormone-stimulated cells were casein-positive according to immunocytochemistry. In order to assess the role of the three-dimensional conformation in the induction process, the purified mammary epithelial cells were grown as monolayers on plastic and collagen-coated surfaces. In these two-dimensional cultures, the synthesis of casein was not induced, suggesting that cell shape, orientation, and multicellular organization are important parameters in the hormonal induction of the biochemical differentiation. The finding of the induction of differentiation-specific proteins in cultures of purified epithelial cells from virgin glands allows examination of the molecular mechanisms involved in the complete induction process in the virtual absence of fat cells, fibroblasts, and the complex assortment of biochemical constituents of the mammary fat pad.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call