Lysosomal dysfunction and overload of nucleosides in thymidine phosphorylase deficiency of MNGIE.

Abstract

Inherited deficiency of thymidine phosphorylase (TP), encoded by TYMP, leads to a rare disease with multiple mitochondrial DNA (mtDNA) abnormalities, mitochondrial neurogastrointestinal encephalomyopathy (MNGIE). However, the impact of TP deficiency on lysosomes remains unclear, which are important for mitochondrial quality control and nucleic acid metabolism. Muscle biopsy tissue and skin fibroblasts from MNGIE patients, patients with m.3243 A > G mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) and healthy controls (HC) were collected to perform mitochondrial and lysosomal functional analyses. In addition to mtDNA abnormalities, compared to controls distinctively reduced expression of LAMP1 and increased mitochondrial content were detected in the muscle tissue of MNGIE patients. Skin fibroblasts from MNGIE patients showed decreased expression of LAMP2, lowered lysosomal acidity, reduced enzyme activity and impaired protein degradation ability. TYMP knockout or TP inhibition in cells can also induce the similar lysosomal dysfunction. Using lysosome immunoprecipitation (Lyso- IP), increased mitochondrial proteins, decreased vesicular proteins and V-ATPase enzymes, and accumulation of various nucleosides were detected in lysosomes with TP deficiency. Treatment of cells with high concentrations of dThd and dUrd also triggers lysosomal dysfunction and disruption of mitochondrial homeostasis. Therefore, the results provided evidence that TP deficiency leads to nucleoside accumulation in lysosomes and lysosomal dysfunction, revealing the widespread disruption of organelles underlying MNGIE.

• Authors: Jixiang Du, Fuchen Liu, Xihan Liu, Dandan Zhao, Dongdong Wang, Hongsheng Sun, Chuanzhu Yan, Yuying Zhao
• Journal: Journal of translational medicine (J Transl Med) Vol. 22 Issue 1 Pg. 449 (May 13 2024) ISSN: 1479-5876 [Electronic] England
• PMID: 38741129 (Publication Type: Journal Article)
• Copyright: © 2024. The Author(s).

Chemical References

• Thymidine Phosphorylase
• DNA, Mitochondrial
• Nucleosides
• Lysosomal-Associated Membrane Protein 2

Topics

• Humans
• Lysosomes (metabolism)
• Thymidine Phosphorylase (metabolism, deficiency, genetics)
• Mitochondrial Encephalomyopathies (metabolism, pathology, genetics)
• Fibroblasts (metabolism, pathology)
• DNA, Mitochondrial (genetics, metabolism)
• Mitochondria (metabolism)
• Nucleosides (metabolism)
• Intestinal Pseudo-Obstruction (metabolism, pathology, enzymology, genetics)
• Ophthalmoplegia (metabolism, pathology, congenital)
• Muscular Dystrophy, Oculopharyngeal (metabolism, pathology)
• Male
• Female
• Skin (pathology, metabolism)
• Lysosomal-Associated Membrane Protein 2 (metabolism)