Control of lysosomal-mediated cell death by the pH-dependent calcium channel RECS1

• Published in: Science advances Vol. 7; no. 46; p. eabe5469
• Main Authors: Pihán, Philippe, Lisbona, Fernanda, Borgonovo, Janina, Edwards-Jorquera, Sandra, Nunes-Hasler, Paula, Castillo, Karen, Kepp, Oliver, Urra, Hery, Saarnio, Suvi, Vihinen, Helena, Carreras-Sureda, Amado, Forveille, Sabrina, Sauvat, Allan, De Giorgis, Daniela, Pupo, Amaury, Rodríguez, Diego A, Quarato, Giovanni, Sagredo, Alfredo, Lourido, Fernanda, Letai, Anthony, Latorre, Ramon, Kroemer, Guido, Demaurex, Nicolas, Jokitalo, Eija, Concha, Miguel L, Glavic, Álvaro, Green, Douglas R, Hetz, Claudio
• Format: Journal Article
• Language: English
• Published: United States American Association for the Advancement of Science (AAAS) 12.11.2021; American Association for the Advancement of Science
• Subjects: Biomedicine and Life Sciences; Cell Biology; Life Sciences; Medicin och hälsovetenskap; SciAdv r-articles
• ISSN: 2375-2548; 2375-2548
• DOI: 10.1126/sciadv.abe5469

Programmed cell death is regulated by the balance between activating and inhibitory signals. Here, we have identified RECS1 (responsive to centrifugal force and shear stress 1) [also known as TMBIM1 (transmembrane BAX inhibitor motif containing 1)] as a proapoptotic member of the TMBIM family. In contrast to other proteins of the TMBIM family, RECS1 expression induces cell death through the canonical mitochondrial apoptosis pathway. Unbiased screening indicated that RECS1 sensitizes cells to lysosomal perturbations. RECS1 localizes to lysosomes, where it regulates their acidification and calcium content, triggering lysosomal membrane permeabilization. Structural modeling and electrophysiological studies indicated that RECS1 is a pH-regulated calcium channel, an activity that is essential to trigger cell death. RECS1 also sensitizes whole animals to stress in vivo in and zebrafish models. Our results unveil an unanticipated function for RECS1 as a proapoptotic component of the TMBIM family that ignites cell death programs at lysosomes.