LYST deficiency impairs autophagic lysosome reformation in neurons and alters lysosome number and size

• DOI: 10.1007/s00018-023-04695-x
• Publication Date: 2023-01-28T04:01:52Z
• Authors: Jenny Serra-Vinar...; Maxwell B. Sandler; Raffaella De Pace; Javier Manzella-L...; Antony Cougnoux; Keyvan Keyvanfar; Wendy J. Introne; Joseph A. Brzosto...; Michael E. Ward; William A. Gahl; Prashant Sharma; May Christine V. ...
• Keywords: Organelles; Neurons; 0301 basic medicine; 03 medical and health sciences; Vesicular Transport Proteins; Autophagy; Humans; Lysosomes; Chediak-Higashi Syndrome

Chediak-Higashi syndrome (CHS) is a rare, autosomal recessive disorder caused by biallelic mutations in the lysosomal trafficking regulator (LYST) gene. Even though enlarged lysosomes and/or lysosome-related organelles (LROs) are the typical cellular hallmarks of CHS, they have not been investigated in human neuronal models. Moreover, how and why the loss of LYST function causes a lysosome phenotype in cells has not been elucidated. We report that the LYST-deficient human neuronal model exhibits lysosome depletion accompanied by hyperelongated tubules extruding from enlarged autolysosomes. These results have also been recapitulated in neurons differentiated from CHS patients' induced pluripotent stem cells (iPSCs), validating our model system. We propose that LYST ensures the correct fission/scission of the autolysosome tubules during autophagic lysosome reformation (ALR), a crucial process to restore the number of free lysosomes after autophagy. We further demonstrate that LYST is recruited to the lysosome membrane, likely to facilitate the fission of autolysosome tubules. Together, our results highlight the key role of LYST in maintaining lysosomal homeostasis following autophagy and suggest that ALR dysregulation is likely associated with the neurodegenerative CHS phenotype.