In an attempt to directly screen autophagy regulators, Arsham and Neufeld [1] combined standard mosaic analysis with live-cell imaging of LysoTracker Red and fixed-cell imaging of autophagy-specific fluorescent protein markers
In an attempt to directly screen autophagy regulators, Arsham and Neufeld [1] combined standard mosaic analysis with live-cell imaging of LysoTracker Red and fixed-cell imaging of autophagy-specific fluorescent protein markers. There are three morphologically distinct forms of autophagy in mammalian cells: macroautophagy, SJ 172550 microautophagy, and chaperone-mediated autophagy [13]. This…