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1
C/EBPbeta, but not C/EBPalpha, is essential for ductal morphogenesis, lobuloalveolar proliferation, and functional differentiation in the mouse mammary gland.在小鼠乳腺中,C/EBPβ而非C/EBPα对于导管形态发生、小叶腺泡增殖及功能分化至关重要。
Genes Dev. 1998 Jun 15;12(12):1917-28. doi: 10.1101/gad.12.12.1917.
2
The C/EBPbeta transcription factor regulates epithelial cell proliferation and differentiation in the mammary gland.C/EBPβ转录因子调节乳腺上皮细胞的增殖和分化。
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3
Disruption of steroid and prolactin receptor patterning in the mammary gland correlates with a block in lobuloalveolar development.乳腺中类固醇和催乳素受体模式的破坏与小叶腺泡发育受阻相关。
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4
Expression and function of CCAAT/enhancer binding proteinbeta (C/EBPbeta) LAP and LIP isoforms in mouse mammary gland, tumors and cultured mammary epithelial cells.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
J Cell Biochem. 2001;82(3):357-70. doi: 10.1002/jcb.1167.
5
C/EBPbeta (CCAAT/enhancer binding protein) controls cell fate determination during mammary gland development.C/EBPβ(CCAAT/增强子结合蛋白)在乳腺发育过程中控制细胞命运的决定。
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6
Lactogenic hormones and tenascin-C regulate C/EBPalpha and beta in mammary epithelial cells.催乳激素和腱生蛋白-C调节乳腺上皮细胞中的C/EBPα和C/EBPβ。
J Cell Biochem. 2000 Jan;76(3):394-403. doi: 10.1002/(sici)1097-4644(20000301)76:3<394::aid-jcb7>3.0.co;2-b.
7
Effect of exogenous epidermal-like growth factors on mammary gland development and differentiation in the estrogen receptor-alpha knockout (ERKO) mouse.外源性表皮生长因子对雌激素受体α基因敲除(ERKO)小鼠乳腺发育和分化的影响。
Breast Cancer Res Treat. 2003 May;79(2):161-73. doi: 10.1023/a:1023938510508.
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Estrogen receptor-alpha expression in the mammary epithelium is required for ductal and alveolar morphogenesis in mice.乳腺上皮中雌激素受体α的表达是小鼠导管和腺泡形态发生所必需的。
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Expression and transactivating functions of the bZIP transcription factor GADD153 in mammary epithelial cells.bZIP转录因子GADD153在乳腺上皮细胞中的表达及反式激活功能
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Expression of CCAAT/enhancer binding proteins (C/EBP) is associated with squamous differentiation in epidermis and isolated primary keratinocytes and is altered in skin neoplasms.CCAAT/增强子结合蛋白(C/EBP)的表达与表皮及分离的原代角质形成细胞中的鳞状分化相关,且在皮肤肿瘤中发生改变。
J Invest Dermatol. 1998 Jun;110(6):939-45. doi: 10.1046/j.1523-1747.1998.00199.x.

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本文引用的文献

1
Development of mammary tumors from hyperplastic alveolar nodules transplanted into gland-free mammary fat pads of female C3H mice.将增生性肺泡结节移植到雌性C3H小鼠无腺体的乳腺脂肪垫中后乳腺肿瘤的发生情况。
Cancer Res. 1959 Jun;19(5):515-20.
2
The C/EBPbeta transcription factor regulates epithelial cell proliferation and differentiation in the mammary gland.C/EBPβ转录因子调节乳腺上皮细胞的增殖和分化。
Genes Dev. 1998 Jun 15;12(12):1907-16. doi: 10.1101/gad.12.12.1907.
3
Composite response elements mediate hormonal and developmental regulation of milk protein gene expression.复合反应元件介导乳蛋白基因表达的激素和发育调控。
Biochem Soc Symp. 1998;63:101-13.
4
Think globally, act locally: the making of a mouse mammary gland.全球思考,本地行动:小鼠乳腺的形成
Genes Dev. 1998 Feb 15;12(4):449-55. doi: 10.1101/gad.12.4.449.
5
Lactation status influences expression of CCAAT/enhancer binding protein isoform mRNA in the mouse mammary gland.泌乳状态影响小鼠乳腺中CCAAT/增强子结合蛋白异构体mRNA的表达。
J Cell Physiol. 1998 Feb;174(2):232-9. doi: 10.1002/(SICI)1097-4652(199802)174:2<232::AID-JCP10>3.0.CO;2-E.
6
Overexpression of C/EBPbeta-LIP, a naturally occurring, dominant-negative transcription factor, in human breast cancer.C/EBPβ-LIP(一种天然存在的显性负性转录因子)在人类乳腺癌中的过表达。
J Natl Cancer Inst. 1997 Dec 17;89(24):1887-91. doi: 10.1093/jnci/89.24.1887.
7
Defective adipocyte differentiation in mice lacking the C/EBPbeta and/or C/EBPdelta gene.缺乏C/EBPβ和/或C/EBPδ基因的小鼠脂肪细胞分化存在缺陷。
EMBO J. 1997 Dec 15;16(24):7432-43. doi: 10.1093/emboj/16.24.7432.
8
CCAAT/enhancer binding protein alpha regulates p21 protein and hepatocyte proliferation in newborn mice.CCAAT/增强子结合蛋白α调节新生小鼠的p21蛋白和肝细胞增殖。
Mol Cell Biol. 1997 Dec;17(12):7353-61. doi: 10.1128/MCB.17.12.7353.
9
An essential role for C/EBPbeta in female reproduction.C/EBPβ在雌性生殖中的重要作用。
Genes Dev. 1997 Sep 1;11(17):2153-62. doi: 10.1101/gad.11.17.2153.
10
Requirement of STAT5b for sexual dimorphism of body growth rates and liver gene expression.身体生长速率和肝脏基因表达的性别二态性对STAT5b的需求。
Proc Natl Acad Sci U S A. 1997 Jul 8;94(14):7239-44. doi: 10.1073/pnas.94.14.7239.

在小鼠乳腺中,C/EBPβ而非C/EBPα对于导管形态发生、小叶腺泡增殖及功能分化至关重要。

C/EBPbeta, but not C/EBPalpha, is essential for ductal morphogenesis, lobuloalveolar proliferation, and functional differentiation in the mouse mammary gland.

作者信息

Seagroves T N, Krnacik S, Raught B, Gay J, Burgess-Beusse B, Darlington G J, Rosen J M

机构信息

Department of Cell Biology, Baylor College of Medicine, Houston, Texas 77030, USA.

出版信息

Genes Dev. 1998 Jun 15;12(12):1917-28. doi: 10.1101/gad.12.12.1917.

DOI:10.1101/gad.12.12.1917
PMID:9637692
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC316914/
Abstract

The CCAAT/enhancer binding proteins (C/EBPs) are differentially expressed throughout mammary gland development and interact with binding sites within the promoter of a milk protein gene, beta-casein. The specific roles of C/EBPbeta and C/EBPalpha in mouse mammary gland development and differentiation have been investigated in mice that carry targeted deletions of these genes. C/EBPbeta-/- virgin mice exhibited cystic, enlarged mammary ducts with decreased secondary branching. Transplantation of C/EBPbeta-/- mammary epithelium into the cleared mammary fat pads of nude mice confirmed that this defect in ductal morphogenesis was intrinsic to the epithelium. When treated with estrogen/progesterone (E+P) to simulate pregnancy, C/EBPbeta-/- mammary glands displayed only limited lobuloalveolar development and ductal side branching. Primary mammary epithelial cells obtained from E+P-treated C/EBPbeta-/- mice that were cultured on extracellular matrix gels did not functionally differentiate in response to lactogenic hormones despite their organization into three-dimensional structures. Expression of beta-casein protein was inhibited 85%-100% and whey acidic protein (WAP) was undetectable. In contrast, no detectable alterations in mammary development or beta-casein expression were observed in mammary outgrowths derived from newborn C/EBPalpha-/- mammary epithelium transplanted into the cleared mammary fat pads of syngeneic hosts. These results demonstrate that C/EBPbeta, but not C/EBPalpha, is required for ductal morphogenesis, lobuloalveolar development, and functional differentiation of mammary epithelial cells.

摘要

CCAAT/增强子结合蛋白(C/EBPs)在乳腺发育过程中呈差异表达,并与乳蛋白基因β-酪蛋白启动子内的结合位点相互作用。在携带这些基因靶向缺失的小鼠中,已对C/EBPβ和C/EBPα在小鼠乳腺发育和分化中的具体作用进行了研究。C/EBPβ基因敲除的处女小鼠表现出囊性、扩张的乳腺导管,二级分支减少。将C/EBPβ基因敲除的乳腺上皮移植到裸鼠清除后的乳腺脂肪垫中,证实导管形态发生的这种缺陷是上皮细胞固有的。用雌激素/孕酮(E+P)处理以模拟怀孕时,C/EBPβ基因敲除的乳腺仅表现出有限的小叶腺泡发育和导管侧支分支。从经E+P处理的C/EBPβ基因敲除小鼠获得的原代乳腺上皮细胞,尽管它们组织成三维结构,但在体外基质凝胶上培养时,对催乳激素没有功能性分化反应。β-酪蛋白的表达被抑制了85%-100%,且未检测到乳清酸性蛋白(WAP)。相比之下,将新生C/EBPα基因敲除的乳腺上皮移植到同基因宿主清除后的乳腺脂肪垫中,在乳腺生长中未观察到乳腺发育或β-酪蛋白表达的可检测变化。这些结果表明,乳腺上皮细胞的导管形态发生、小叶腺泡发育和功能分化需要C/EBPβ,而不是C/EBPα。