Prolactin Controls Mammary Gland Development via Direct and Indirect Mechanisms
Identifieur interne : 00D463 ( Main/Merge ); précédent : 00D462; suivant : 00D464Prolactin Controls Mammary Gland Development via Direct and Indirect Mechanisms
Auteurs : Cathrin Brisken ; Sarabjeet Kaur [Australie] ; Tony E. Chavarria ; Nadine Binart [France] ; Robert L. Sutherland [Australie] ; Robert A. Weinberg ; Paul A. Kelly [France] ; Christopher J. Ormandy [Australie]Source :
- Developmental Biology [ 0012-1606 ] ; 1999.
Descripteurs français
- Wicri :
- topic : Droit d'auteur, Histologie.
English descriptors
- KwdEn :
- Academic press, Alveolar buds, Alveolar development, Alveolus, Breast cancer, Brisken, Copyright, Duct, Ductal, Ductal development, Ductal elongation, Ductal side, Ductal termini, Endocrinology, Endogenous, Endogenous epithelium, Epithelial, Epithelial cells, Epithelium, Functional differentiation, Gland, Gland development, Growth hormone, Heterozygous, Histology, Kelly, Knockout, Knockout animals, Knockout epithelium, Knockout females, Knockout mice, Knockout transplants, Lobule, Lobuloalveolar, Lobuloalveolar development, Mammary, Mammary development, Mammary epithelial cells, Mammary epithelium, Mammary gland, Mammary gland development, Mammary glands, Nandi, Ormandy, Postpartum, Prlr, Prlr mice, Progesterone, Progesterone receptor, Prolactin, Prolactin receptor, Prolactin receptor gene, Rag1, Receptor, Tebs, Transplant, Whole mounts, development, mammary gland, prolactin, prolactin receptor, tissue recombination.
- Teeft :
- Academic press, Alveolar buds, Alveolar development, Alveolus, Breast cancer, Brisken, Copyright, Duct, Ductal, Ductal development, Ductal elongation, Ductal side, Ductal termini, Endocrinology, Endogenous, Endogenous epithelium, Epithelial, Epithelial cells, Epithelium, Functional differentiation, Gland, Gland development, Growth hormone, Heterozygous, Histology, Kelly, Knockout, Knockout animals, Knockout epithelium, Knockout females, Knockout mice, Knockout transplants, Lobule, Lobuloalveolar, Lobuloalveolar development, Mammary, Mammary development, Mammary epithelial cells, Mammary epithelium, Mammary gland, Mammary gland development, Mammary glands, Nandi, Ormandy, Postpartum, Prlr, Prlr mice, Progesterone, Progesterone receptor, Prolactin, Prolactin receptor, Prolactin receptor gene, Rag1, Receptor, Tebs, Transplant, Whole mounts.
Abstract
Abstract: The inactivation of the prolactin receptor gene by homologous recombination has made it possible to investigate the role of prolactin signaling in mammary gland development without resort to ablative surgery of the endocrine glands. In knockout mice lacking the prolactin receptor, mammary development is normal up to puberty. Subsequently, the ducts branch less frequently than those of wild-type animals. While terminal end buds differentiate to alveolar buds in wild-type females by the end of puberty, in knockout females terminal end bud-like structures persist at the ductal ends. To distinguish between the developmental defects that are intrinsic to the epithelium and those that result from systemic endocrine alterations in prolactin receptor knockout mice, mammary epithelium from prolactin receptor knockouts was transplanted into mammary fat pads of wild-type mice. In virgin mice, the knockout epithelial transplants developed normally at puberty, indicating an indirect effect of prolactin on ductal development. Prolactin receptor knockout females are infertile due to multiple reproductive defects, but epithelial transplants allowed us to assess the extent to which the absence of prolactin receptor is limiting, under systemic conditions that allow full mammary gland development. During pregnancy, the prolactin receptor knockout transplants showed normal side branching and the formation of alveolar buds, but no lobuloalveolar development. Thus, prolactin affects mammary morphogenesis in two different ways: it controls ductal side branching and terminal end bud regression in virgin animals via indirect mechanisms, but acts directly on the mammary epithelium to produce lobuloalveolar development during pregnancy.
Url:
DOI: 10.1006/dbio.1999.9271
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<front><div type="abstract" xml:lang="en">Abstract: The inactivation of the prolactin receptor gene by homologous recombination has made it possible to investigate the role of prolactin signaling in mammary gland development without resort to ablative surgery of the endocrine glands. In knockout mice lacking the prolactin receptor, mammary development is normal up to puberty. Subsequently, the ducts branch less frequently than those of wild-type animals. While terminal end buds differentiate to alveolar buds in wild-type females by the end of puberty, in knockout females terminal end bud-like structures persist at the ductal ends. To distinguish between the developmental defects that are intrinsic to the epithelium and those that result from systemic endocrine alterations in prolactin receptor knockout mice, mammary epithelium from prolactin receptor knockouts was transplanted into mammary fat pads of wild-type mice. In virgin mice, the knockout epithelial transplants developed normally at puberty, indicating an indirect effect of prolactin on ductal development. Prolactin receptor knockout females are infertile due to multiple reproductive defects, but epithelial transplants allowed us to assess the extent to which the absence of prolactin receptor is limiting, under systemic conditions that allow full mammary gland development. During pregnancy, the prolactin receptor knockout transplants showed normal side branching and the formation of alveolar buds, but no lobuloalveolar development. Thus, prolactin affects mammary morphogenesis in two different ways: it controls ductal side branching and terminal end bud regression in virgin animals via indirect mechanisms, but acts directly on the mammary epithelium to produce lobuloalveolar development during pregnancy.</div>
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