Hydrogen peroxide induces Arl1 degradation and impairs Golgi-mediated trafficking.

Mol Biol Cell

Department of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, MI 48109-1085.

Published: August 2020

Reactive oxygen species (ROS)-induced oxidative stress has been associated with diseases such as amyotrophic lateral sclerosis, stroke, and cancer. While the effect of ROS on mitochondria and endoplasmic reticulum (ER) has been well documented, its consequence on the Golgi apparatus is less well understood. In this study, we characterized the Golgi structure and function in HeLa cells after exposure to hydrogen peroxide (HO), a reagent commonly used to introduce ROS to cells. Treatment of cells with 1 mM HO for 10 min resulted in the degradation of Arl1 and dissociation of GRIP domain-containing proteins Golgin-97 and Golgin-245 from the -Golgi. This effect could be rescued by treatment of cells with a ROS scavenger -acetyl cysteine or protease inhibitors. Structurally, HO treatment reduced the number of cisternal membranes per Golgi stack, suggesting a loss of -Golgi cisternae. Functionally, HO treatment inhibited both anterograde and retrograde protein transport, consistent with the loss of membrane tethers on the -Golgi cisternae. This study revealed membrane tethers at the -Golgi as novel specific targets of ROS in cells.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7525819PMC
http://dx.doi.org/10.1091/mbc.E20-01-0063DOI Listing

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