Prolactin and mammary gland development

被引:110
作者
Horseman, ND [1 ]
机构
[1] Univ Cincinnati, Coll Med, Dept Mol & Cellular Physiol, Cincinnati, OH 45267 USA
关键词
prolactin; dual-functioning somatolactotrophs; secretagogues;
D O I
10.1023/A:1018708704335
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Prolactin (PRL) regulates the development of the mammary gland at three stages in the reproductive life history of females. The first stage is mammary gland organogenesis, during which PRL contributes to the maturation of the mammary glands from a primary ductal system, which grows from terminal end buds, to the fully mature nonpregnant gland. The mature mammary gland is characterized by an absence of terminal end buds, and the development of a highly branched architecture, which is decorated by lobular buds. During pregnancy PRL, placental lactogens, and progesterone stimulate the expansion and physiological differentiation of the lobuloalveolar system from the lobular buds. After delivery PRL, in the context of falling progesterone, stimulates the final induction of milk protein gene expression acid lactation. PRL acts directly on the mammary epithelium, and indirectly by stimulating luteal progesterone secretion in rodents. Disruption of the genes for PRL and the PRL receptor, as well as those for transcription factors important in mammary gland regulation (Stat proteins), have provided a new set of animal models with which to study normal mammary gland development and the relationships of PRL to breast carcinogenesis. Two major deficiencies in our current knowledge of PRL actions are our understanding of the role of epithelial-stromal interactions in PRL-induced mammary morphogenesis. and the identity of developmentally important genes that are regulated by PRL during normal mammary gland organogenesis.
引用
收藏
页码:79 / 88
页数:10
相关论文
共 63 条
[31]   Stat5a is mandatory for adult mammary gland development and lactogenesis [J].
Liu, XW ;
Robinson, GW ;
Wagner, KU ;
Garrett, L ;
WynshawBoris, A ;
Hennighausen, L .
GENES & DEVELOPMENT, 1997, 11 (02) :179-186
[32]   MICE LACKING PROGESTERONE-RECEPTOR EXHIBIT PLEIOTROPIC REPRODUCTIVE ABNORMALITIES [J].
LYDON, JP ;
DEMAYO, FJ ;
FUNK, CR ;
MANI, SK ;
HUGHES, AR ;
MONTGOMERY, CA ;
SHYAMALA, G ;
CONNEELY, OM ;
OMALLEY, BW .
GENES & DEVELOPMENT, 1995, 9 (18) :2266-2278
[33]  
LYONS WR, 1958, RECENT PROG HORM RES, V14, P219
[34]   NEU DIFFERENTIATION FACTOR HEREGULIN MODULATES GROWTH AND DIFFERENTIATION OF HC11 MAMMARY EPITHELIAL-CELLS [J].
MARTE, BM ;
JESCHKE, M ;
GRAUSPORTA, D ;
TAVERNA, D ;
HOFER, P ;
GRONER, B ;
YARDEN, Y ;
HYNES, NE .
MOLECULAR ENDOCRINOLOGY, 1995, 9 (01) :14-23
[35]  
NICOLL CS, 1980, FED PROC, V39, P2561
[36]   MECHANISMS OF PROLACTIN RECEPTOR REGULATION IN MAMMARY-GLAND [J].
ORMANDY, CJ ;
SUTHERLAND, RL .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1993, 91 (1-2) :C1-C6
[37]   Null mutation of the prolactin receptor gene produces multiple reproductive defects in the mouse [J].
Ormandy, CJ ;
Camus, A ;
Barra, J ;
Damotte, JD ;
Lucas, B ;
Buteau, H ;
Edery, M ;
Brousse, N ;
Babinet, C ;
Binart, N ;
Kelly, PA .
GENES & DEVELOPMENT, 1997, 11 (02) :167-178
[38]   THE EFFECT OF PROGESTINS ON PROLACTIN RECEPTOR GENE-TRANSCRIPTION IN HUMAN BREAST-CANCER CELLS [J].
ORMANDY, CJ ;
GRAHAM, J ;
KELLY, PA ;
CLARKE, CL ;
SUTHERLAND, RL .
DNA AND CELL BIOLOGY, 1992, 11 (10) :721-726
[39]   RAS MEDIATES SRC BUT NOT EPIDERMAL GROWTH FACTOR-RECEPTOR TYROSINE KINASE SIGNALING PATHWAYS IN GH(4) NEUROENDOCRINE CELLS [J].
PICKETT, CA ;
GUTIERREZHARTMANN, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (18) :8612-8616
[40]   STIMULATION OF LACTOTROPE DIFFERENTIATION IN-VITRO BY FIBROBLAST GROWTH-FACTOR [J].
PORTER, TE ;
WILES, CD ;
FRAWLEY, LS .
ENDOCRINOLOGY, 1994, 134 (01) :164-168