Pubertal exposure to high fat diet causes mouse strain-dependent alterations in mammary gland development and estrogen responsiveness

被引:60
作者
Olson, L. K. [1 ,2 ]
Tan, Y. [1 ,2 ]
Zhao, Y. [1 ,2 ]
Aupperlee, M. D. [1 ,2 ]
Haslam, S. Z. [1 ,2 ]
机构
[1] Michigan State Univ, Dept Physiol, E Lansing, MI 48824 USA
[2] Michigan State Univ, Breast Canc & Environm Res Ctr, E Lansing, MI 48824 USA
基金
美国国家卫生研究院;
关键词
mammary gland; puberty; estrogen; amphiregulin; BREAST-CANCER RISK; OBESITY; PATTERNS; GROWTH; CHILDHOOD; LEPTIN; AMPHIREGULIN; ADOLESCENCE; MODULATION; C57BL/6J;
D O I
10.1038/ijo.2010.51
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Increased adolescent obesity rates in the United States are a significant public health concern. Obesity or increased adiposity during puberty in girls, an important period of breast development and a window of exposure sensitivity, may influence breast development and cancer risk. The purpose of this study was to investigate the impact of a high fat diet (HFD) on mammary gland development in obesity-susceptible C57BL/6 and obesity-resistant BALB/c mice. Design: Pubertal or adult C57BL/6 and BALB/c mice were fed an HFD or control diet (CD) from 3 to 7 weeks of age or from 10 to 14 weeks of age, respectively. The effects of HFD diet on body weight, adiposity, mammary gland development, and mammary gland response to estrogen were evaluated. Results: Pubertal C57BL/6 mice fed the HFD had a significant increase in body weight and adiposity, and this was accompanied by stunted mammary duct elongation and reduced mammary epithelial cell proliferation. Ovariectomy and estrogen (17-beta-estradiol, E) treatment of pubertal HFD-fed C57BL/6 mice showed decreased mammary gland stimulation by E. Amphiregulin, a downstream mediator of pubertal E action, was reduced in mammary glands of HFD-fed C57BL/6 mice. Weight loss and reduced adiposity initiated by switching C57BL/6 mice from HFD to CD restored ductal elongation. Pubertal BALB/c mice fed the HFD did not exhibit a significant increase in body weight or adiposity; HFD caused increased mammary epithelial cell proliferation and had no effect on response to E. HFD had no effect on body weight or the mammary glands of adult mice. Conclusions: HFD during puberty had a profound strain-specific effect on murine mammary gland development. Obesity and increased adiposity were associated with reduced responsiveness to estrogen and stunted ductal growth. Importantly, the effect of diet and adiposity on the mammary gland was specific to the pubertal period of development. International Journal of Obesity (2010) 34, 1415-1426; doi: 10.1038/ijo.2010.51; published online 16 March 2010
引用
收藏
页码:1415 / 1426
页数:12
相关论文
共 52 条
[1]   Growth patterns and the risk of breast cancer in women [J].
Ahlgren, M ;
Melbye, M ;
Wohlfahrt, J ;
Sorensen, TIA .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (16) :1619-1626
[2]   Differential hormonal regulation and function of progesterone receptor isoforms in normal adult mouse mammary gland [J].
Aupperlee, Mark D. ;
Haslam, Sandra Z. .
ENDOCRINOLOGY, 2007, 148 (05) :2290-2300
[3]   Strain-Specific Differences in the Mechanisms of Progesterone Regulation of Murine Mammary Gland Development [J].
Aupperlee, Mark D. ;
Drolet, Alexis A. ;
Durairaj, Srinivasan ;
Wang, Weizhong ;
Schwartz, Richard C. ;
Haslam, Sandra Z. .
ENDOCRINOLOGY, 2009, 150 (03) :1485-1494
[4]   Progesterone receptor isoforms A and B: Temporal and spatial differences in expression during murine mammary gland development [J].
Aupperlee, MD ;
Smith, KT ;
Kariagina, A ;
Haslam, SZ .
ENDOCRINOLOGY, 2005, 146 (08) :3577-3588
[5]   Body fatness during childhood and adolescence and incidence of breast cancer in premenopausal women: a prospective cohort study [J].
Baer, HJ ;
Colditz, GA ;
Rosner, B ;
Michels, KB ;
Rich-Edwards, JW ;
Hunter, DJ ;
Willett, WC .
BREAST CANCER RESEARCH, 2005, 7 (03) :R314-R325
[6]  
BANERJEE M R, 1976, TCA (Tissue Culture Association) Manual, V2, P457, DOI 10.1007/BF00918341
[7]   Leptin is a metabolic signal to the reproductive system [J].
Barash, IA ;
Cheung, CC ;
Weigle, DS ;
Ren, HP ;
Kabigting, EB ;
Kuijper, JL ;
Clifton, DK ;
Steiner, RA .
ENDOCRINOLOGY, 1996, 137 (07) :3144-3147
[8]  
Berkey CS, 1999, CANCER-AM CANCER SOC, V85, P2400, DOI 10.1002/(SICI)1097-0142(19990601)85:11<2400::AID-CNCR15>3.0.CO
[9]  
2-O
[10]   Amphiregulin is an essential mediator of estrogen receptor α function in mammary gland development [J].
Ciarloni, Laura ;
Mallepell, Sonia ;
Brisken, Cathrin .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (13) :5455-5460