Cell & Bioscience (May 2024)

Methylmalonic acidemia triggers lysosomal-autophagy dysfunctions

  • Michele Costanzo,
  • Armando Cevenini,
  • Laxmikanth Kollipara,
  • Marianna Caterino,
  • Sabrina Bianco,
  • Francesca Pirozzi,
  • Gianluca Scerra,
  • Massimo D’Agostino,
  • Luigi Michele Pavone,
  • Albert Sickmann,
  • Margherita Ruoppolo

DOI
https://doi.org/10.1186/s13578-024-01245-1
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 18

Abstract

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Abstract Background Methylmalonic acidemia (MMA) is a rare inborn error of propionate metabolism caused by deficiency of the mitochondrial methylmalonyl-CoA mutase (MUT) enzyme. As matter of fact, MMA patients manifest impairment of the primary metabolic network with profound damages that involve several cell components, many of which have not been discovered yet. We employed cellular models and patients-derived fibroblasts to refine and uncover new pathologic mechanisms connected with MUT deficiency through the combination of multi-proteomics and bioinformatics approaches. Results Our data show that MUT deficiency is connected with profound proteome dysregulations, revealing molecular actors involved in lysosome and autophagy functioning. To elucidate the effects of defective MUT on lysosomal and autophagy regulation, we analyzed the morphology and functionality of MMA-lysosomes that showed deep alterations, thus corroborating omics data. Lysosomes of MMA cells present as enlarged vacuoles with low degradative capabilities. Notwithstanding, treatment with an anti-propionigenic drug is capable of totally rescuing lysosomal morphology and functional activity in MUT-deficient cells. These results indicate a strict connection between MUT deficiency and lysosomal-autophagy dysfunction, providing promising therapeutic perspectives for MMA. Conclusions Defective homeostatic mechanisms in the regulation of autophagy and lysosome functions have been demonstrated in MUT-deficient cells. Our data prove that MMA triggers such dysfunctions impacting on autophagosome-lysosome fusion and lysosomal activity.

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