Seagroves T N, Krnacik S, Raught B, Gay J, Burgess-Beusse B, Darlington G J, Rosen J M
Department of Cell Biology, Baylor College of Medicine, Houston, Texas 77030, USA.
Genes Dev. 1998 Jun 15;12(12):1917-28. doi: 10.1101/gad.12.12.1917.
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.
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。