Autophagy Induced by Deficiency of Sphingosine-1-phosphate Phosphohydrolase 1 Is Switched to Apoptosis by Calpain-mediated Autophagy-related Gene 5 (Atg5) Cleavage

• Published in: The Journal of biological chemistry Vol. 286; no. 52; pp. 44380 - 44390
• Main Authors: Lépine, Sandrine, Allegood, Jeremy C., Edmonds, Yvette, Milstien, Sheldon, Spiegel, Sarah
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 30.12.2011; American Society for Biochemistry and Molecular Biology
• Subjects: Activating Transcription Factor 6 - genetics; Activating Transcription Factor 6 - metabolism; Adenine - analogs & derivatives; Adenine - pharmacology; Antibiotics, Antineoplastic - pharmacology; Apoptosis; Apoptosis - drug effects; Apoptosis - physiology; Autophagy; Autophagy - drug effects; Autophagy - physiology; Autophagy-Related Protein 5; Calpain; Calpain - genetics; Calpain - metabolism; Cell Line, Tumor; Ceramide; Ceramides - biosynthesis; Ceramides - genetics; Down-Regulation - drug effects; Down-Regulation - physiology; Doxorubicin; Doxorubicin - pharmacology; eIF-2 Kinase - genetics; eIF-2 Kinase - metabolism; Endoribonucleases - genetics; Endoribonucleases - metabolism; ER Stress; Female; Gene Silencing; Humans; Lysophospholipids - genetics; Lysophospholipids - metabolism; Membrane Proteins - antagonists & inhibitors; Membrane Proteins - genetics; Membrane Proteins - metabolism; Microtubule-Associated Proteins - genetics; Microtubule-Associated Proteins - metabolism; Phosphoric Monoester Hydrolases - antagonists & inhibitors; Phosphoric Monoester Hydrolases - genetics; Phosphoric Monoester Hydrolases - metabolism; Protein-Serine-Threonine Kinases - genetics; Protein-Serine-Threonine Kinases - metabolism; Proteolysis; Signal Transduction; Sphingolipid; Sphingosine - analogs & derivatives; Sphingosine - genetics; Sphingosine - metabolism; Sphingosine 1-phosphate; SPP1; ER Stress; Sphingolipid; SPP1; Ceramide; Calpain; Autophagy; Doxorubicin; Apoptosis; Sphingosine 1-phosphate
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M111.257519

Sphingosine 1-phosphate (S1P) and ceramide have been implicated in both autophagy and apoptosis. However, the roles of these sphingolipid metabolites in the links between these two processes are not completely understood. Depletion of S1P phosphohydrolase-1 (SPP1), which degrades intracellular S1P, induces the unfolded protein response and endoplasmic reticulum stress-induced autophagy (Lépine, S., Allegood, J. C., Park, M., Dent, P., Milstien, S., and Spiegel, S. (2011) Cell Death Differ. 18, 350–361). Surprisingly, however, treatment with doxorubicin, which by itself also induced autophagy, markedly reduced the extent of autophagy mediated by depletion of SPP1. Concomitantly, doxorubicin-induced apoptosis was greatly enhanced by down-regulation of SPP1. Autophagy and apoptosis seemed to be sequentially linked because inhibiting autophagy with 3-methyladenine also markedly attenuated apoptosis. Moreover, silencing Atg5 or the three sensors of the unfolded protein response, IRE1α, ATF6, and PKR-like eIF2α kinase (PERK), significantly decreased both autophagy and apoptosis. Doxorubicin stimulated calpain activity and Atg5 cleavage, which were significantly enhanced in SPP1-depleted cells. Inhibition or depletion of calpain not only suppressed Atg5 cleavage, it also markedly decreased the robust apoptosis induced by doxorubicin in SPP1-deficient cells. Importantly, doxorubicin also increased de novo synthesis of the pro-apoptotic sphingolipid metabolite ceramide. Elevation of ceramide in turn stimulated calpain; conversely, inhibiting ceramide formation suppressed Atg5 cleavage and apoptosis. Hence, doxorubicin switches protective autophagy in SPP1-depleted cells to apoptosis by calpain-mediated Atg5 cleavage. The switch between autophagy and apoptosis is an important and complicated process that is not well understood. Doxorubicin treatment switches protective autophagy in sphingosine-1-phosphate phosphohydrolase-1 (SPP1)-depleted cells to apoptosis, increasing ceramide synthesis that enhances calpain activation and cleavage of pro-autophagic Atg5, generating a pro-apoptotic fragment. Depletion of SPP1 sensitizes cells to doxorubicin-induced apoptosis. Sphingolipid metabolites are involved in the cross-talk between autophagy and apoptosis.