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细胞外基质通过抑制小鼠乳腺上皮细胞中的转化生长因子-α来调节乳清酸性蛋白基因表达:体外培养和转基因小鼠研究

Extracellular matrix regulates whey acidic protein gene expression by suppression of TGF-alpha in mouse mammary epithelial cells: studies in culture and in transgenic mice.

作者信息

Lin C Q, Dempsey P J, Coffey R J, Bissell M J

机构信息

Life Science Division, Lawrence Berkeley Laboratories, Berkeley, California 94720, USA.

出版信息

J Cell Biol. 1995 May;129(4):1115-26. doi: 10.1083/jcb.129.4.1115.

Abstract

Whey acidic protein (WAP) is an abundant rodent milk protein. Its expression in mouse mammary epithelial cell cultures was previously found to require the formation of an extracellular matrix (ECM)-induced three-dimensional alveolar structure. In the absence of such structures, cells were shown to secrete diffusible factors leading to suppression of WAP expression. We demonstrate here that (a) TGF-alpha production and secretion by mammary cells is downregulated by the basement membrane-dependent alveolar structure, and (b) compared with beta-casein, WAP expression is preferentially inhibited both in culture and in transgenic mice when TGF-alpha is added or overexpressed. Thus, (c) the enhanced TGF-alpha production when cells are not in three-dimensional structures largely accounts for the WAP-inhibitory activity found in the conditioned medium. Since this activity can be abolished by incubating the conditioned medium with a function blocking antibody to TGF-alpha. The data suggest that ECM upregulates WAP by downregulating TGF-alpha production. We also propose that changes in TGF-alpha activity during mouse gestation and lactation could contribute to the pattern of temporal expression of WAP in the gland. These results provide a clear example of cooperation among lactogenic hormones, ECM, and locally acting growth factors in regulation of tissue-specific gene expression.

摘要

乳清酸性蛋白(WAP)是一种丰富的啮齿动物乳蛋白。先前发现,其在小鼠乳腺上皮细胞培养物中的表达需要形成细胞外基质(ECM)诱导的三维肺泡结构。在缺乏此类结构的情况下,细胞会分泌可扩散因子,导致WAP表达受到抑制。我们在此证明:(a)乳腺细胞产生和分泌的转化生长因子α(TGF-α)受基底膜依赖性肺泡结构的下调;(b)与β-酪蛋白相比,当添加或过表达TGF-α时,WAP表达在培养物和转基因小鼠中均优先受到抑制。因此,(c)当细胞处于非三维结构时TGF-α产生的增加在很大程度上解释了条件培养基中发现的WAP抑制活性。因为这种活性可以通过用针对TGF-α的功能阻断抗体孵育条件培养基来消除。这些数据表明,ECM通过下调TGF-α的产生来上调WAP。我们还提出,小鼠妊娠和哺乳期TGF-α活性的变化可能有助于乳腺中WAP的时间表达模式。这些结果提供了一个明确的例子,说明催乳激素、ECM和局部作用的生长因子在调节组织特异性基因表达中的协同作用。

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