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局部微环境通过局部调节雌激素受体 α 的活性来引发泌乳期和 involution 期间乳腺四肽重复结构域 9A 的调节。

The local microenvironment instigates the regulation of mammary tetratricopeptide repeat domain 9A during lactation and involution through local regulation of the activity of estrogen receptor α.

机构信息

School of Biological Sciences, Nanyang Technological University, Republic of Singapore.

出版信息

Biochem Biophys Res Commun. 2012 Sep 14;426(1):65-70. doi: 10.1016/j.bbrc.2012.08.036. Epub 2012 Aug 14.

DOI:10.1016/j.bbrc.2012.08.036
PMID:22917536
Abstract

Tetratricopeptide repeat domain 9A (TTC9A) belongs to a family of TTC9 proteins. Its induction by progesterone in breast cancer cells was associated with marked growth inhibition and induction of focal adhesion. TTC9A interacts specifically with actin-binding protein tropomyosin Tm5NM-1 which stabilizes actin filament and focal adhesion. However, the function of TTC9A is still obscure. This study exploited mice model to characterize the regulation of TTC9A gene expression during mammary development and explored possible mechanisms of TTC9A gene regulation. It was demonstrated that mammary TTC9A expression is distinctively down-regulated in gland undergoing functional differentiation (lactation) and up-regulated during involution. Furthermore, TTC9A expression during lactation and involution is regulated by the factors in the local microenvironment. This is illustrated with teat sealing model in which the teat sealed glands (undergoing involution) expressed significantly higher levels of TTC9A protein and mRNA than the contralateral non-sealed lactating glands. Importantly, this local induction of TTC9A expression upon involution coincided with the re-activation of estrogen receptor α (ERα). Together with the observation that TTC9A is a direct ERα target gene, we propose that the fall and rise of TTC9A levels during lactation and involution is caused by the changes of ERα activity that is in turn regulated by the factors in the microenvironment.

摘要

四肽重复结构域 9A(TTC9A)属于 TTC9 蛋白家族。孕激素诱导乳腺癌细胞中 TTC9A 的表达与明显的生长抑制和粘着斑形成有关。TTC9A 特异性地与肌动蛋白结合蛋白原肌球蛋白 Tm5NM-1 相互作用,稳定肌动蛋白丝和粘着斑。然而,TTC9A 的功能仍不清楚。本研究利用小鼠模型来研究 TTC9A 基因在乳腺发育过程中的表达调控,并探讨 TTC9A 基因调控的可能机制。研究表明,乳腺 TTC9A 的表达在功能分化(泌乳)的腺中明显下调,在退化过程中上调。此外,泌乳和退化过程中 TTC9A 的表达受局部微环境中的因素调节。这可以通过乳头发炎模型来证明,其中乳头发炎的乳腺(正在退化)表达的 TTC9A 蛋白和 mRNA 水平明显高于对侧未发炎的泌乳乳腺。重要的是,这种局部诱导的 TTC9A 在退化过程中的表达与雌激素受体α(ERα)的重新激活同时发生。结合 TTC9A 是 ERα 的直接靶基因这一观察结果,我们提出,泌乳和退化过程中 TTC9A 水平的下降和上升是由 ERα 活性的变化引起的,而 ERα 活性又受到微环境中因素的调节。

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