Journal Article

FUNDC1 protects against doxorubicin-induced cardiomyocyte PANoptosis through stabilizing mtDNA via interaction with TUFM

Wang, Xiang, Ren, Jun, Ge, Junbo, Xu, Haixia, Zhu, Hong, Bi, Yaguang, Zhang, Yingmei

2022

Overview

Doxorubicin (DOX) is an effective anthracycline chemotherapeutic anticancer drug with its life-threatening cardiotoxicity severely limiting its clinical application. Mitochondrial damage-induced cardiomyocyte death is considered an essential cue for DOX cardiotoxicity. FUN14 domain containing 1 (FUNDC1) is a mitochondrial membrane protein participating in the regulation of mitochondrial integrity in multiple diseases although its role in DOX cardiomyopathy remains elusive. Here, we examined whether PANoptosis, a novel type of programmed cell death closely associated with mitochondrial damage, was involved in DOX-induced heart injury, and FUNDC1-mediated regulation of cardiomyocyte PANoptosis, if any. FUNDC1 was downregulated in heart tissues in patients with dilated cardiomyopathy (DCM) and DOX-challenged mice. FUNDC1 deficiency aggravated DOX-induced cardiac dysfunction, mitochondrial injury, and cardiomyocyte PANoptosis. Further examination revealed that FUNDC1 countered cytoplasmic release of mitochondrial DNA (mtDNA) and activation of PANoptosome through interaction with mitochondrial Tu translation elongation factor (TUFM), a key factor in the translational expression and repair of mitochondrial DNA, via its 96–133 amino acid domain. TUFM intervention reversed FUNDC1-elicited protection against DOX-induced mtDNA cytosolic release and cardiomyocyte PANoptosis. Our findings shed light toward a beneficial role of FUNDC1 in DOX cardiotoxicity and cardiomyocyte PANoptosis, thus offering therapeutic promises in DOX-induced cardiotoxicity.

• Publisher: Nature Publishing Group UK,Springer Nature B.V,Nature Publishing Group
• Subject: 101/28 / 13/1 / 13/109 / 13/95 / 14/19 / 14/34 / 38/1 / 38/22 / 38/77 / 631/443/592/75/74 / 692/699/75 / 82/58 / Amino acids / Animals / Anthracycline / Antibodies / Antitumor agents / Apoptosis / Biochemistry / Biomedical and Life Sciences / Cardiomyocytes / Cardiomyopathy / Cardiotoxicity / Cardiotoxicity - metabolism / Cell Biology / Cell Culture / Cell death / Chemotherapy / Dilated cardiomyopathy / DNA repair / DNA, Mitochondrial - genetics / Doxorubicin / Doxorubicin - metabolism / Doxorubicin - pharmacology / Immunology / Life Sciences / Membrane proteins / Membrane Proteins - metabolism / Mice / Mitochondria - metabolism / Mitochondrial DNA / Mitochondrial Proteins - metabolism / Myocytes, Cardiac - metabolism / Peptide Elongation Factor Tu - metabolism / Translation elongation