Cao Baihui, Chen Xiaotong, Li Yubin, Zhou Tian, Chen Nuo, Guo Yaxin, Zhao Ming, Guo Chun, Shi Yongyu, Wang Qun, Du Xuexiang, Zhang Lining, Li Yan
Department of Immunology, School of Basic Medical Science, Cheeloo College of Medicine, Shandong University, Jinan, China.
Department of Immunology, School of Clinical and Basic Medical Sciences, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan, China.
NPJ Parkinsons Dis. 2024 Aug 6;10(1):146. doi: 10.1038/s41531-024-00760-9.
TFE3 and TFEB, as the master regulators of lysosome biogenesis and autophagy, are well characterized to enhance the synaptic protein α-synuclein degradation in protecting against Parkinson's disease (PD) and their levels are significantly decreased in the brain of PD patients. However, how TFE3 and TFEB are regulated during PD pathogenesis remains largely vague. Herein, we identified that programmed cell death 4 (PDCD4) promoted pathologic α-synuclein accumulation to facilitate PD development via suppressing both TFE3 and TFEB translation. Conversely, PDCD4 deficiency significantly augmented global and nuclear TFE3 and TFEB distributions to alleviate neurodegeneration in a mouse model of PD with overexpressing α-synuclein in the striatum. Mechanistically, like TFEB as we reported before, PDCD4 also suppressed TFE3 translation, rather than influencing its transcription and protein stability, to restrain its nuclear translocation and lysosomal functions, eventually leading to α-synuclein aggregation. We proved that the two MA3 domains of PDCD4 mediated the translational suppression of TFE3 through binding to its 5'-UTR of mRNA in an eIF-4A dependent manner. Based on this, we developed a blood-brain barrier penetrating RVG polypeptide modified small RNA drug against pdcd4 to efficiently prevent α-synuclein neurodegeneration in improving PD symptoms by intraperitoneal injections. Together, we suggest PDCD4 as a PD-risk protein to facilitate α-synuclein neurodegeneration via suppressing TFE3 and TFEB translation and further provide a potential small RNA drug against pdcd4 to treat PD by intraperitoneal injections.
作为溶酶体生物合成和自噬的主要调节因子,转录因子E3(TFE3)和转录因子EB(TFEB)在保护免受帕金森病(PD)侵害方面增强突触蛋白α-突触核蛋白降解的作用已得到充分表征,且它们在PD患者大脑中的水平显著降低。然而,在PD发病机制中TFE3和TFEB是如何被调控的仍很大程度上不清楚。在此,我们发现程序性细胞死亡4(PDCD4)通过抑制TFE3和TFEB的翻译促进病理性α-突触核蛋白积累以推动PD发展。相反,在纹状体中过表达α-突触核蛋白的PD小鼠模型中,PDCD4缺陷显著增加了TFE3和TFEB在整体和细胞核中的分布以减轻神经退行性变。机制上,与我们之前报道的TFEB一样,PDCD4也抑制TFE3的翻译,而非影响其转录和蛋白质稳定性,以限制其核转位和溶酶体功能,最终导致α-突触核蛋白聚集。我们证明PDCD4的两个MA3结构域通过以依赖真核翻译起始因子4A(eIF-4A)的方式结合到TFE3 mRNA的5'-非翻译区(5'-UTR)介导对TFE3的翻译抑制。基于此,我们开发了一种血脑屏障穿透性经狂犬病毒糖蛋白(RVG)多肽修饰的针对pdcd4的小RNA药物,通过腹腔注射有效预防α-突触核蛋白神经退行性变以改善PD症状。总之,我们提出PDCD4作为一种PD风险蛋白,通过抑制TFE3和TFEB翻译促进α-突触核蛋白神经退行性变,并进一步提供了一种潜在的针对pdcd4的小RNA药物通过腹腔注射治疗PD。