Zhang Lan, Wang Jing-Miao, Wang Ling, Zheng Shuyu, Bai Yueyue, Fu Jia-Ling, Wang Yan, Zhang Jian-Ping, Xiao Yuan, Hou Min, Nie Qian, Gan Yu-Wen, Liang Xing-Miao, Hu Xue-Bin, Li David Wan-Cheng
The State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, Guangdong, China.
The State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, Guangdong, China.
J Biol Chem. 2025 Jan;301(1):108064. doi: 10.1016/j.jbc.2024.108064. Epub 2024 Dec 9.
Epithelial mesenchymal transition (EMT) of lens epithelial cells (LECs) is one of the most important pathogenic mechanisms in lens fibrotic disorders, and the regulatory mechanisms of EMT have not been fully understood. Here, we demonstrate that the cAMP-response element binding protein (CREB) can regulate lens EMT in a phosphorylation-dependent and phosphorylation-independent manners with dual mechanisms. First, CREB-S133 phosphorylation is implicated in TGFβ-induced EMT of mouse LECs and also in injury-induced mouse anterior subcapsular cataract model. The interaction between CREB and p300 is necessary for CREB regulation of TGFβ-induced EMT, since inhibition of CREB-p300 interaction and p300 knockdown led to attenuated expression of mesenchymal genes. Second, S133A-CREB, a mutant mimicking constant dephosphorylation at S133, exhibits notable occupancy in the enhancers of mesenchymal genes and confers robust transcription activity on EMT genes. Introduction of R314A mutation in S133A-CREB, which abolishes the interaction between S133A-CREB and its co-activator, cAMP-regulated transcriptional co-activators led to substantial suppression of mesenchymal gene expression in mouse LECs. Taken together, our results showed that CREB regulates lens EMT in dual mechanisms and that the S133A-CREB acts as a novel transcription factor. Mechanistically, CREB interacts with p300 in a S133 phosphorylation-dependent manner to positively regulate lens EMT genes. In contrast, S133A-CREB interacts with cAMP-regulated transcriptional co-activators to confer a robust activation of lens EMT genes.
晶状体上皮细胞(LECs)的上皮-间质转化(EMT)是晶状体纤维化疾病中最重要的致病机制之一,而EMT的调控机制尚未完全明确。在此,我们证明环磷酸腺苷反应元件结合蛋白(CREB)可通过双重机制以磷酸化依赖和非依赖方式调节晶状体EMT。首先,CREB-S133磷酸化参与了转化生长因子β(TGFβ)诱导的小鼠LECs的EMT过程,在损伤诱导的小鼠前囊下白内障模型中也发挥作用。CREB与p300之间的相互作用对于CREB调节TGFβ诱导的EMT是必需的,因为抑制CREB-p300相互作用和敲低p300会导致间充质基因表达减弱。其次,S133A-CREB是一种模拟S133位点持续去磷酸化的突变体,在间充质基因的增强子中表现出显著的占据,并赋予EMT基因强大的转录活性。在S133A-CREB中引入R314A突变,该突变消除了S133A-CREB与其共激活因子环磷酸腺苷调节的转录共激活因子之间的相互作用,导致小鼠LECs中间充质基因表达大幅抑制。综上所述,我们的结果表明CREB通过双重机制调节晶状体EMT,且S133A-CREB作为一种新型转录因子发挥作用。从机制上讲,CREB以S133磷酸化依赖的方式与p300相互作用,正向调节晶状体EMT基因。相反,S133A-CREB与环磷酸腺苷调节的转录共激活因子相互作用,赋予晶状体EMT基因强大的激活作用。