ErbB4的细胞内结构域可诱导乳腺上皮细胞分化。
The intracellular domain of ErbB4 induces differentiation of mammary epithelial cells.
作者信息
Muraoka-Cook Rebecca S, Sandahl Melissa, Husted Carty, Hunter Debra, Miraglia Leah, Feng Shu-mang, Elenius Klaus, Earp H Shelton
机构信息
Lineberger Comprehensive Cancer Center and Departments of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
出版信息
Mol Biol Cell. 2006 Sep;17(9):4118-29. doi: 10.1091/mbc.e06-02-0101. Epub 2006 Jul 12.
Differentiation of mammary epithelium in vivo requires signaling through prolactin- and ErbB4/HER4-dependent mechanisms; how these pathways intersect is unknown. We show herein that HC11 mouse mammary cells undergo ErbB4-dependent lactational differentiation. Prolactin and the ErbB4 ligand HB-EGF each induced STAT5A activation, expression of lactogenic differentiation markers, and lumen formation in three-dimensional Matrigel cultures in HC11 cells. ErbB4 undergoes ligand-dependent transmembrane domain cleavage at Val-675, releasing a soluble 80-kDa intracellular domain (s80(HER4)) that localizes to nuclei; the physiological relevance of s80(HER4) is unknown. A HER4(V675A) mutant abolishing transmembrane cleavage impaired STAT5A activity, lactogenic gene expression, and lumen formation. Kinase-dead HER4(KD) was neither cleaved nor able to induce differentiation of HC11 cells. Without treating HC11 cells with prolactin or HB-EGF, s80(HER4) (expressed from a cDNA construct) localized to the nucleus, activated STAT5A, and induced three-dimensional lumen formation. Nuclear localization of exogenous s80(HER4) required intact kinase activity of s80(HER4), as did activation of STAT5A. In contrast, nuclear localization of s80(HER4) and STAT5A activation did not require the 16-amino acid region of the ErbB4 intracellular domain specific to the Cyt-1 isoform of ErbB4, and absent in the Cyt-2 isoform. These results suggest that s80(HER4) formation contributes to ErbB4-dependent differentiation of mammary epithelial cells.
体内乳腺上皮细胞的分化需要通过催乳素和依赖ErbB4/HER4的机制进行信号传导;这些途径如何交叉尚不清楚。我们在此表明,HC11小鼠乳腺细胞经历依赖ErbB4的泌乳分化。催乳素和ErbB4配体HB-EGF均可诱导HC11细胞中STAT5A激活、产乳分化标志物的表达以及在三维基质胶培养物中形成管腔。ErbB4在Val-675处发生依赖配体的跨膜结构域裂解,释放出定位于细胞核的可溶性80 kDa细胞内结构域(s80(HER4));s80(HER4)的生理相关性尚不清楚。消除跨膜裂解的HER4(V675A)突变体损害了STAT5A活性、产乳基因表达和管腔形成。激酶失活的HER4(KD)既不被裂解也不能诱导HC11细胞分化。在不使用催乳素或HB-EGF处理HC11细胞的情况下,(从cDNA构建体表达的)s80(HER4)定位于细胞核,激活STAT5A,并诱导三维管腔形成。外源性s80(HER4)的核定位需要s80(HER4)完整的激酶活性,STAT5A的激活也是如此。相比之下,s80(HER4)的核定位和STAT5A激活不需要ErbB4细胞内结构域中特定于ErbB4的Cyt-1异构体且在Cyt-2异构体中不存在的16个氨基酸区域。这些结果表明,s80(HER4)的形成有助于乳腺上皮细胞依赖ErbB4的分化。