Expansion of specialized epidermis induced by hormonal state and mechanical strain. (May 2015)

• Record Type: Journal Article
• Authors: Wu, Hsin-Jung; Easwaran, Teresa; Offutt, Carlos D.; Elgar, Richard Levi; Spandau, Dan F.; Koyama, Sachiko; Foley, John
• Is Part Of: Mechanisms of development. Volume 136(2015)
• Page Start: 73
• Page End: 86
• Publication Date: 2015-05
• Subjects: Nipple -- Areola -- Lactation -- Pregnancy -- Hormones -- Mechanical strain; Developmental biology -- Periodicals; Molecular biology -- Periodicals; Developmental Biology -- Periodicals; Molecular Biology -- Periodicals; Biologie du développement -- Périodiques; Biologie moléculaire -- Périodiques; Developmental biology; Molecular biology; Periodicals; Electronic journals; 571.8
• DOI: 10.1016/j.mod.2015.01.002
• Languages: English
• ISSNs: 0925-4773

Abstract

Highlights: During lactation, murine nipple specialized epidermis expands to form an areola. Areola formation is associated with increased extracellular matrix remodeling. Nipple fibroblasts express estrogen, progesterone, relaxin and oxytocin receptors. Areola formation requires hormones, as well as the mechanical strain of nursing. Abstract: In mammals, some sites of specialized skin such as the palms, soles, and lips grow proportionally with the animal. However, other types of specialized skin such as the nipple and anal/genital region are dramatically altered with changes of reproductive status. The specific cell types that mediate the growth of these sites have not been identified. In the mouse, we observed a dramatic expansion of the specialized epidermis of the nipple, coupled to changes in connective tissue and hair shaft density, which we designate as areola formation. During this process thymidine analog uptake was elevated in the epidermis and hair follicles. Although there were no changes in connective tissue cell proliferation, we did observe an altered expression of extracellular matrix genes. In addition, the fibroblasts of the virgin nipple areola and region showed increased transcript and protein levels for estrogen, progesterone, relaxin, and oxytocin relative to those of ventral skin. To determine the role of pregnancy, lactation hormonal milieu, and localized mechanical strain on areola formation, we created models that separated these stimuli and evaluated changes in gross structure, proliferation and protein expression. While modest increases of epidermal proliferation and remodeling of connective tissue occurred as a result of individual stimuli, areola formation required exposure to pregnancy hormones, as well as mechanical strain.