Jianing Song, Haolin Zhang, Xingyu Cao, Zizhang Ren, Chao Tian, Miao Jia, Meiling Wu, Xiaoli Wang, Juan Wang
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引用次数: 0
摘要
自噬对维持细胞稳态至关重要,并与多种疾病有关。在酿酒酵母中,Polymyxin B Sensitivity 2 (Pbs2)蛋白是丝裂原活化蛋白激酶(MAPK)家族的一员,在丝裂自噬中起作用。为了探索Pbs2在巨噬中的潜在作用,我们利用质粒构建和酵母转化技术设计了野生型和Pbs2缺陷型细胞,然后进行了一系列的自噬实验。首先,在氮饥饿后,采用经典的GFP-Atg8裂解法和Pho8Δ60活性法测定不同时间点的自噬活性水平。删除PBS2可显著降低GFP-Atg8蛋白切割和Pho8Δ60活性,表明PBS2对巨噬至关重要。此外,Pbs2对巨噬的影响与已知的Pbs2下游因子Hog1无关。其次,Atg8脂化实验表明,PBS2缺失后Atg8脂化水平升高,表明PBS2在Atg8脂化后起作用。第三,蛋白酶K保护实验表明,PBS2的缺失导致闭合的自噬体比例更高,这意味着PBS2影响自噬体关闭后的大自噬后期。综上所述,Pbs2调控氮饥饿诱导的巨噬后期。
Pbs2 regulates late-stage macroautophagy in Saccharomyces cerevisiae.
Autophagy is crucial for maintaining cellular homeostasis and is linked to various diseases. In Saccharomyces cerevisiae, the Polymyxin B Sensitivity 2 (Pbs2) protein is a member of the mitogen-activated protein kinase (MAPK) family and plays a role in mitophagy. To explore the potential role of Pbs2 in macroautophagy, we engineered wild-type and PBS2-deficient cells using plasmid construction and yeast transformation techniques, followed by a series of autophagy assays. First, after nitrogen starvation, the levels of autophagic activity were evaluated with the classical GFP-Atg8 cleavage assay and the Pho8Δ60 activity assay at different time points. Deleting PBS2 significantly decreased both GFP-Atg8 protein cleavage and Pho8Δ60 activity, indicating that Pbs2 is essential for macroautophagy. Furthermore, the influence of Pbs2 on macroautophagy was shown to be independent of Hog1, a well-known downstream factor of Pbs2. Second, the Atg8 lipidation assay demonstrated that Atg8 lipidation levels increased upon PBS2 deletion, suggesting that Pbs2 acts after Atg8 lipidation. Third, the proteinase K protection assay indicated that the loss of PBS2 led to a higher proportion of closed autophagosomes, implying that Pbs2 impacts the later stages of macroautophagy following autophagosome closure. In conclusion, Pbs2 regulates the late stages of macroautophagy induced by nitrogen starvation.