粒体自噬                        
                
                                
                        
                            自噬                        
                
                                
                        
                            生物                        
                
                                
                        
                            自噬体                        
                
                                
                        
                            线粒体                        
                
                                
                        
                            细胞生物学                        
                
                                
                        
                            细胞内                        
                
                                
                        
                            细胞凋亡                        
                
                                
                        
                            生物化学                        
                
                        
                    
            作者
            
                Katharina C. Lorentzen,Alan R. Prescott,Ian G. Ganley            
         
                    
            出处
            
                                    期刊:Autophagy
                                                         [Taylor & Francis]
                                                        日期:2024-08-23
                                                        卷期号:: 1-23
                                                        被引量:1
                                 
         
        
    
            
            标识
            
                                    DOI:10.1080/15548627.2024.2395149
                                    
                                
                                 
         
        
                
            摘要
            
            Macroautophagy/autophagy enables lysosomal degradation of a diverse array of intracellular material. This process is essential for normal cellular function and its dysregulation is implicated in many diseases. Given this, there is much interest in understanding autophagic mechanisms of action in order to determine how it can be best targeted therapeutically. In mitophagy, the selective degradation of mitochondria via autophagy, mitochondria first need to be primed with signals that allow the recruitment of the core autophagy machinery to drive the local formation of an autophagosome around the target mitochondrion. To determine how the recruitment of different core autophagy components can drive mitophagy, we took advantage of the
         
            
 
                 
                
                    
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