Robinson Gertraud W, Pacher-Zavisin Margit, Zhu Bing Mei, Yoshimura Akihiko, Hennighausen Lothar
Laboratory of Genetics and Physiology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892-0822, USA.
Dev Dyn. 2007 Mar;236(3):654-61. doi: 10.1002/dvdy.21058.
Signal transducer and activator of transcription 5 and 3 (Stat5 and Stat3) control pregnancy-mediated mammary development and involution-dependent remodeling, respectively. Suppressor of cytokine signaling 3 (Socs3) has been implicated in the modulation of both Stat3 and Stat5 activity. To explore the biology of Socs3 in mammary tissue, the gene was deleted using Cre-mediated recombination. Deletion of the Socs3 gene from mammary stem or early progenitor cells did not grossly alter pregnancy-mediated mammary development but resulted in impaired lactation due to attenuated proliferation. Loss of Socs3 from differentiated luminal cells did not interfere with glandular function during lactation, but resulted in accelerated tissue remodeling upon weaning. Loss of Socs3 led to enhanced and precocious Stat3 activation. Thus, Socs3 serves as a modulator of Stat3 activity to ensure controlled proliferation and apoptosis in pregnancy and involution, respectively.
信号转导及转录激活因子5和3(Stat5和Stat3)分别控制妊娠介导的乳腺发育和 involution 依赖性重塑。细胞因子信号转导抑制因子3(Socs3)参与了对Stat3和Stat5活性的调节。为了探究Socs3在乳腺组织中的生物学功能,利用Cre介导的重组技术删除了该基因。从乳腺干细胞或早期祖细胞中删除Socs3基因并未显著改变妊娠介导的乳腺发育,但由于增殖减弱导致泌乳受损。从分化的腔上皮细胞中缺失Socs3并不影响泌乳期间的腺体功能,但在断奶后导致组织重塑加速。Socs3的缺失导致Stat3激活增强和早熟。因此,Socs3作为Stat3活性的调节剂,分别确保在妊娠和 involution 过程中增殖和凋亡得到控制。