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在患有脂肪营养不良的Bscl2(-/-)雌性小鼠中,青春期前暴露于染料木黄酮对乳腺发育和阴道开口的分离反应。

Segregated responses of mammary gland development and vaginal opening to prepubertal genistein exposure in Bscl2(-/-) female mice with lipodystrophy.

作者信息

Li Rong, El Zowalaty Ahmed E, Chen Weiqin, Dudley Elizabeth A, Ye Xiaoqin

机构信息

Department of Physiology and Pharmacology, College of Veterinary Medicine, University of Georgia, Athens, GA 30602, USA; Interdisciplinary Toxicology Program, University of Georgia, Athens, GA 30602, USA.

Department of Physiology, Georgia Regents University, Augusta, GA 30912, USA.

出版信息

Reprod Toxicol. 2015 Jul;54:76-83. doi: 10.1016/j.reprotox.2014.10.023. Epub 2014 Nov 5.

Abstract

Berardinelli-Seip congenital lipodystrophy 2-deficient (Bscl2(-/-)) mice recapitulate human BSCL2 disease with lipodystrophy. Bscl2-encoded seipin is detected in adipocytes and epithelium of mammary gland. Postnatal mammary gland growth spurt and vaginal opening signify pubertal onset in female mice. Bscl2(-/-) females have longer and dilated mammary gland ducts at 5-week old and delayed vaginal opening. Prepubertal exposure to 500ppm genistein diet increases mammary gland area and accelerates vaginal opening in both control and Bscl2(-/-) females. However, genistein treatment increases ductal length in control but not Bscl2(-/-) females. Neither prepubertal genistein treatment nor Bscl2-deficiency affects phospho-estrogen receptor α or progesterone receptor expression patterns in 5-week old mammary gland. Interestingly, Bscl2-deficiency specifically reduces estrogen receptor β expression in mammary gland ductal epithelium. In summary, Bscl2(-/-) females have accelerated postnatal mammary ductal development but delayed vaginal opening; they display segregated responses in mammary gland development and vaginal opening to prepubertal genistein treatment.

摘要

贝拉尔迪内利-塞普先天性脂肪营养不良2缺陷(Bscl2(-/-))小鼠重现了人类伴有脂肪营养不良的BSCL2疾病。在脂肪细胞和乳腺上皮中可检测到Bscl2编码的丝蛋白。产后乳腺生长突增和阴道开口标志着雌性小鼠青春期开始。5周龄的Bscl2(-/-)雌性小鼠乳腺导管更长且扩张,阴道开口延迟。青春期前暴露于500ppm染料木黄酮饮食会增加对照和Bscl2(-/-)雌性小鼠的乳腺面积并加速阴道开口。然而,染料木黄酮处理增加了对照雌性小鼠的导管长度,但对Bscl2(-/-)雌性小鼠无效。青春期前的染料木黄酮处理和Bscl2缺陷均不影响5周龄乳腺中磷酸化雌激素受体α或孕激素受体的表达模式。有趣的是,Bscl2缺陷特异性降低了乳腺导管上皮中雌激素受体β的表达。总之,Bscl2(-/-)雌性小鼠产后乳腺导管发育加速但阴道开口延迟;它们在乳腺发育和阴道开口方面对青春期前染料木黄酮处理表现出不同的反应。

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