Autophagy eliminates cytoplasmic beta-catenin and NICD to promote the cardiac differentiation of P19CL6 cells

作者：Jia Zhuqing; Wang Jiaji; Wang Weiping; Tian Yuyao; XiangWei Wenshu; Chen Ping; Ma Kangtao; Zhou Chunyan^*

来源：Cellular Signalling, 2014, 26(11): 2299-2305.

DOI：10.1016/j.cellsig.2014.07.028

• Autophagy
• Atg7
• Atg5
• Wnt
• Notch
• Cardiomyocyte differentiation

Autophagy plays important roles in adipogenesis and neuron development. However, how autophagy contributes to cardiac development is not well understood. The main aim of our study was to determine the association between autophagy and myocardial differentiation and its roles in this process. Using a well-established in vitro cardiomyocyte differentiation system, P19CL6 cells, we found that autophagy occurred from the early stage of cardiac differentiation. Blocking autophagy by knocking-down of autophagy-related gene Atg7 or Atg5 inhibited the cardiac differentiation of P19CL6 cells. Further investigation demonstrated that LO and P62 could form a complex with S-catenin and NICD, respectively, and promoted the degradation of beta-catenin and NICD. Enhancing autophagy promoted the formation of complex, whereas blocking autophagy attenuated the degradation of beta-catenin and NICD. Taken together, autophagy could facilitate P19CL6 cells to complete the cardiac differentiation process through blocking Wnt and Notch signaling pathways.

• 出版日期2014-11
• 单位北京大学