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螺旋-环-螺旋蛋白Id-1对乳腺上皮细胞分化的抑制作用。

Suppression of mammary epithelial cell differentiation by the helix-loop-helix protein Id-1.

作者信息

Desprez P Y, Hara E, Bissell M J, Campisi J

机构信息

Department of Cancer Biology, Lawrence Berkeley Laboratory, University of California, Berkeley 94720, USA.

出版信息

Mol Cell Biol. 1995 Jun;15(6):3398-404. doi: 10.1128/MCB.15.6.3398.

Abstract

Cell proliferation and differentiation are precisely coordinated during the development and maturation of the mammary gland, and this balance invariably is disrupted during carcinogenesis. Little is known about the cell-specific transcription factors that regulate these processes in the mammary gland. The mouse mammary epithelial cell line SCp2 grows well under standard culture conditions but arrests growth, forms alveolus-like structures, and expresses beta-casein, a differentiation marker, 4 to 5 days after exposure to basement membrane and lactogenic hormones (differentiation signals). We show that this differentiation entails a marked decline in the expression of Id-1, a helix-loop-helix (HLH) protein that inactivates basic HLH transcription factors in other cell types. SCp2 cells stably transfected with an Id-1 expression vector grew more rapidly than control cells under standard conditions, but in response to differentiation signals, they arrested growth and formed three-dimensional structures similar to those of control cells. Id-1-expressing cells did not, however, express beta-casein. Moreover, 8 to 10 days after receiving differentiation signals, they lost three-dimensional organization, invaded the basement membrane, and then resumed growth. SCp2 cells expressing an Id-1 antisense vector grew more slowly than controls; in response to differentiation signals, they remained stably growth arrested and fully differentiated, as did control cells. We suggest that Id-1 renders cells refractory to differentiation signals and receptive to growth signals by inactivating one or more basic HLH proteins that coordinate growth and differentiation in the mammary epithelium.

摘要

在乳腺的发育和成熟过程中,细胞增殖和分化受到精确协调,而这种平衡在致癌过程中总是被打破。关于调节乳腺中这些过程的细胞特异性转录因子,我们所知甚少。小鼠乳腺上皮细胞系SCp2在标准培养条件下生长良好,但在接触基底膜和催乳激素(分化信号)后4至5天,会停止生长,形成肺泡样结构,并表达β-酪蛋白(一种分化标志物)。我们发现,这种分化伴随着Id-1表达的显著下降,Id-1是一种螺旋-环-螺旋(HLH)蛋白,在其他细胞类型中可使碱性HLH转录因子失活。用Id-1表达载体稳定转染的SCp2细胞在标准条件下比对照细胞生长得更快,但在对分化信号作出反应时,它们停止生长并形成与对照细胞相似的三维结构。然而,表达Id-1的细胞不表达β-酪蛋白。此外,在接受分化信号8至10天后,它们失去三维组织结构,侵入基底膜,然后恢复生长。表达Id-1反义载体的SCp2细胞比对照细胞生长得更慢;在对分化信号作出反应时,它们像对照细胞一样保持稳定的生长停滞并完全分化。我们认为,Id-1通过使一种或多种在乳腺上皮中协调生长和分化的碱性HLH蛋白失活,使细胞对分化信号产生抗性并对生长信号敏感。

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