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全器官培养中小鼠乳腺的退化:一种研究程序性细胞死亡的模型

Involution of mouse mammary glands in whole organ culture: a model for studying programmed cell death.

作者信息

Atwood C S, Ikeda M, Vonderhaar B K

机构信息

Laboratory of Tumor Immunology and Biology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892-1402.

出版信息

Biochem Biophys Res Commun. 1995 Feb 15;207(2):860-7. doi: 10.1006/bbrc.1995.1265.

Abstract

The DNA fragmentation and gene expression patterns of involuting mouse mammary glands were compared to mammary glands in whole organ culture induced to involute by the withdrawal of lactogenic hormones. Non-random DNA degradation was observed both in vivo and in vitro, indicating that the withdrawal of lactogenic hormones triggers a program of epithelial cell death. Similar patterns of gene expression for the milk protein beta-casein and the apoptosis associated factors TGF-beta 1, TGF-beta 2 and TGF-beta 3 were observed in vivo and in vitro. These results indicate that the withdrawal of lactogenic hormones is responsible for decreased milk synthesis, epithelial cell death and tissue restructuring and that whole organ culture of mouse mammary glands is a useful model for studying the molecular events involved in these processes during involution.

摘要

将退化期小鼠乳腺的DNA片段化和基因表达模式,与在全器官培养中因去除泌乳激素而诱导退化的乳腺进行了比较。在体内和体外均观察到非随机DNA降解,这表明泌乳激素的去除触发了上皮细胞死亡程序。在体内和体外观察到乳蛋白β-酪蛋白以及与细胞凋亡相关的因子TGF-β1、TGF-β2和TGF-β3的相似基因表达模式。这些结果表明,泌乳激素的去除导致乳汁合成减少、上皮细胞死亡和组织重塑,并且小鼠乳腺的全器官培养是研究退化过程中涉及这些过程的分子事件的有用模型。

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