Fas‐apoptotic inhibitory molecule 2 localizes to the lysosome and facilitates autophagosome‐lysosome fusion through the LC3 interaction region motif–dependent interaction with LC3. Issue 1 (20th November 2019)

• Record Type: Journal Article
• Authors: Hong, Caroline Jeeyeon; Yeon, Jihye; Yeo, Bo Kyoung; Woo, Hanwoong; An, Hyun‐Kyu; Heo, Woojung; Kim, Kyuhyung; Yu, Seong‐Woon
• Is Part Of: FASEB journal. Volume 34:Issue 1(2020)
• Page Start: 161
• Page End: 179
• Publication Date: 2019-11-20
• Subjects: autolysosome -- autophagosome maturation -- FAIM2 -- LIR -- MAP1LC3B -- xbx‐6; Biology -- Periodicals; Biology, Experimental -- Periodicals; 570
• DOI: 10.1096/fj.201901626R
• Languages: English
• ISSNs: 0892-6638

Abstract

Abstract: Fas‐apoptotic inhibitory molecule 2 (FAIM2) is a member of the transmembrane BAX inhibitor motif–containing (TMBIM) family. TMBIM family is comprised of six anti‐apoptotic proteins that suppress cell death by regulating endoplasmic reticulum Ca 2+ homeostasis. Recent studies have implicated two TMBIM proteins, GRINA and BAX Inhibitor‐1, in mediating cytoprotection via autophagy. However, whether FAIM2 plays a role in autophagy has been unknown. Here we show that FAIM2 localizes to the lysosomes at basal state and facilitates autophagy through interaction with microtubule‐associated protein 1 light chain 3 proteins in human neuroblastoma SH‐SY5Y cells. FAIM2 overexpression increased autophagy flux, while autophagy flux was impaired in shRNA‐mediated knockdown (sh FAIM2 ) cells, and the impairment was more evident in the presence of rapamycin. In sh FAIM2 cells, autophagosome maturation through fusion with lysosomes was impaired, leading to accumulation of autophagosomes. A functional LC3‐interacting region motif within FAIM2 was essential for the interaction with LC3 and rescue of autophagy flux in sh FAIM2 cells while LC3‐binding property of FAIM2 was dispensable for the anti‐apoptotic function in response to Fas receptor‐mediated apoptosis. Suppression of autophagosome maturation was also observed in a null mutant of Caenorhabditis elegans lacking xbx‐6, the ortholog of FAIM2 . Our study suggests that FAIM2 is a novel regulator of autophagy mediating autophagosome maturation through the interaction with LC3.