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CCAAT/增强子结合蛋白β(C/EBPβ)的肝细胞核因子激活蛋白(LAP)和肝细胞核因子抑制蛋白(LIP)亚型在小鼠乳腺、肿瘤及培养的乳腺上皮细胞中的表达与功能

Expression and function of CCAAT/enhancer binding proteinbeta (C/EBPbeta) LAP and LIP isoforms in mouse mammary gland, tumors and cultured mammary epithelial cells.

作者信息

Dearth L R, Hutt J, Sattler A, Gigliotti A, DeWille J

机构信息

Molecular, Cellular and Developmental Biology Program, Department of Veterinary Biosciences, Ohio State University Comprehensive Cancer Center, Ohio State University, Columbus, Ohio 43210, USA.

出版信息

J Cell Biochem. 2001;82(3):357-70. doi: 10.1002/jcb.1167.

Abstract

CCAAT/Enhancer binding proteins (C/EBPs) play important roles in the regulation of cell growth and differentiation. This study investigated the expression and function of C/EBPbeta isoforms in the mouse mammary gland, mammary tumors, and a nontransformed mouse mammary epithelial cell line (HC11). C/EBPbeta mRNA levels are 2-5-fold higher in mouse mammary tumors derived from MMTV/c-neu transgenic mice compared with lactating and involuting mouse mammary gland. The "full-length" 38 kd C/EBPbeta LAP ("Liver-enriched Activator Protein") isoform is the predominant C/EBPbeta protein isoform in mammary tumor whole cell lysates, however, the truncated 20 kd C/EBPbeta LIP ("Liver-enriched Inhibitory Protein") isoform is also present at detectable levels (mean LAP:LIP ratio 5.3:1). The mammary tumor C/EBPbeta LAP:LIP ratio decreases 70% (from 5.3:1 to 1.6:1) when lysate preparation is switched from a rapid whole cell lysis protocol to a multistep nuclear/cytoplasmic fractionation protocol. In contrast to mammary tumors, only the C/EBPbeta LAP isoform is detectable in the mammary gland whole cell and nuclear lysates; the truncated "LIP" isoform is undetectable regardless of isolation protocol. Ectopic over expression of C/EBPbeta LIP or C/EBPbeta LAP did not alter HC11 growth rates. However, C/EBPbeta LIP over expressing HC11 cells (LAP:LIP ratio of approximately 1:1) exhibited a consistent 2-4 h delay in G(0)/S phase transition. C/EBPbeta LIP overexpressing HC11 cells did not express beta-casein mRNA (mammary epithelial cell differentiation marker) in response to lactogenic hormones. This defect in beta-casein expression was not corrected by carrying out the differentiation protocol in the presence of an artificial extracellular matrix. These results demonstrate that the "full-length" C/EBPbeta LAP isoform is the predominant C/EBPbeta protein isoform expressed in mouse mammary gland in vivo and mouse mammary epithelial cell cultures in vitro. C/EBPbeta LIP detected in mammary tumor lysates may result from in vivo production or ex vivo isolation-induced proteolysis of C/EBPbeta LAP. Ectopic overexpression of C/EBPbeta LIP (LAP:LIP ratio of approximately 1:1) inhibits mammary epithelial cell differentiation (beta-casein expression).

摘要

CCAAT/增强子结合蛋白(C/EBPs)在细胞生长和分化的调控中发挥着重要作用。本研究调查了C/EBPβ亚型在小鼠乳腺、乳腺肿瘤以及一种未转化的小鼠乳腺上皮细胞系(HC11)中的表达和功能。与泌乳期和退化期的小鼠乳腺相比,源自MMTV/c-neu转基因小鼠的小鼠乳腺肿瘤中C/EBPβ mRNA水平高2至5倍。“全长”38kd的C/EBPβ LAP(“肝脏富集激活蛋白”)亚型是乳腺肿瘤全细胞裂解物中主要的C/EBPβ蛋白亚型,然而,截短的20kd C/EBPβ LIP(“肝脏富集抑制蛋白”)亚型也以可检测水平存在(平均LAP:LIP比率为5.3:1)。当裂解物制备从快速全细胞裂解方案转换为多步核/细胞质分级分离方案时,乳腺肿瘤C/EBPβ LAP:LIP比率降低70%(从5.3:1降至1.6:1)。与乳腺肿瘤不同,在乳腺全细胞和核裂解物中仅可检测到C/EBPβ LAP亚型;无论分离方案如何,截短的“LIP”亚型均不可检测。异位过表达C/EBPβ LIP或C/EBPβ LAP不会改变HC11的生长速率。然而,过表达C/EBPβ LIP的HC11细胞(LAP:LIP比率约为1:1)在G(0)/S期转换中表现出持续2至4小时的延迟。过表达C/EBPβ LIP的HC11细胞在催乳激素刺激下不表达β-酪蛋白mRNA(乳腺上皮细胞分化标志物)。在人工细胞外基质存在的情况下进行分化方案并不能纠正β-酪蛋白表达的这种缺陷。这些结果表明,“全长”C/EBPβ LAP亚型是在体内小鼠乳腺和体外小鼠乳腺上皮细胞培养物中表达的主要C/EBPβ蛋白亚型。在乳腺肿瘤裂解物中检测到的C/EBPβ LIP可能是由于C/EBPβ LAP的体内产生或离体分离诱导的蛋白水解所致。异位过表达C/EBPβ LIP(LAP:LIP比率约为1:1)会抑制乳腺上皮细胞分化(β-酪蛋白表达)。

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