1. TMBIM6 (transmembrane BAX inhibitor motif containing 6) enhances autophagy and reduces renal dysfunction in a cyclosporine A-induced nephrotoxicity model
- Author
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Kyung-Woon Kim, Geum Hwa Lee, Woo Ho Kim, Raj Kumar Yadav, Byung Hyun Park, Harun Or Rashid, Bo Li, Hyung Ryong Kim, Won Kim, Hwa-Young Lee, Han Eul Jung, Min Kyung Choi, Han-Jung Chae, Yong Chul Lee, and Binod Kumar Yadav
- Subjects
Autophagosome ,Basic Research Papers ,Apoptosis ,mTORC1 ,Kidney ,Lysosome ,Phagosomes ,medicine ,Autophagy ,Animals ,Humans ,Molecular Biology ,Mechanistic target of rapamycin ,Mice, Knockout ,Sirolimus ,biology ,Cell Biology ,Cell biology ,Transplantation ,Disease Models, Animal ,medicine.anatomical_structure ,biology.protein ,Cyclosporine ,TFEB ,Lysosomes ,Microtubule-Associated Proteins ,Immunosuppressive Agents ,medicine.drug - Abstract
Cyclosporine A (CsA) is widely used as an immunosuppressor in transplantation. Previous studies reported that CsA induces autophagy and that chronic treatment with CsA results in accumulation of autophagosomes and reduced autophagic clearance. Autophagy is a prosurvival process that promotes recovery from acute kidney injury by degrading misfolded proteins produced in the kidney. In the present study, we used TMBIM6-expressing HK-2, human kidney tubular cells (TMBIM6 cells) and Tmbim6 knockout (tmbim6−/-) mice. When exposed to CsA, the TMBIM6 cells maintained autophagy activity by preventing autophagosome accumulation. With regard to signaling, PRKKA/AMPK phosphorylation and mechanistic target of rapamycin (serine/threonine kinase) complex 1 (MTORC1) expression and its downstream target TFEB (transcription factor EB), a lysosome biogenesis factor, were regulated in the TMBIM6 cells. Lysosomal activity was highly increased or stably maintained in the presence of TMBIM6. In addition, treatment of tmbim6−/-mice with CsA resulted in increased autophagosome formation and decreased lysosome formation and activity. We also found that tmbim6−/-mice were susceptible to CsA-induced kidney injury. Taken together, these results indicate that TMBIM6 protects against CsA-induced nephrotoxicity both in vitro and in vivo by inducing autophagy and activating lysosomes.
- Published
- 2015