Manganese Exposure Enhances the Release of Misfolded α-Synuclein via Exosomes by Impairing Endosomal Trafficking and Protein Degradation Mechanisms

• Published in: International journal of molecular sciences Vol. 25; no. 22; p. 12207
• Main Authors: Rokad, Dharmin, Harischandra, Dilshan S., Samidurai, Manikandan, Chang, Yuan-Teng, Luo, Jie, Lawana, Vivek, Sarkar, Souvarish, Palanisamy, Bharathi N., Manne, Sireesha, Kim, Dongsuk, Zenitsky, Gary, Jin, Huajun, Anantharam, Vellareddy, Willette, Auriel, Kanthasamy, Arthi, Kanthasamy, Anumantha G.
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 14-11-2024; MDPI
• Subjects: Disease; Pesticides; Plasma; Protein expression; Proteins
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms252212207

Excessive exposure to manganese (Mn) increases the risk of chronic neurological diseases, including Parkinson’s disease (PD) and other related Parkinsonisms. Aggregated α-synuclein (αSyn), a hallmark of PD, can spread to neighboring cells by exosomal release from neurons. We previously discovered that Mn enhances its spread, triggering neuroinflammatory and neurodegenerative processes. To better understand the Mn-induced release of exosomal αSyn, we examined the effect of Mn on endosomal trafficking and misfolded protein degradation. Exposing MN9D dopaminergic neuronal cells stably expressing human wild-type (WT) αSyn to 300 μM Mn for 24 h significantly suppressed protein and mRNA expression of Rab11a, thereby downregulating endosomal recycling, forcing late endosomes to mature into multivesicular bodies (MVBs). Ectopic expression of WT Rab11a significantly mitigated exosome release, whereas ectopic mutant Rab11a (S25N) increased it. Our in vitro and in vivo studies reveal that Mn exposure upregulated (1) mRNA and protein levels of endosomal Rab27a, which mediates the fusion of MVBs with the plasma membrane; and (2) expression of the autophagosomal markers Beclin-1 and p62, but downregulated the lysosomal marker LAMP2, thereby impairing autophagolysosome formation as confirmed by LysoTracker, cathepsin, and acridine orange assays. Our novel findings demonstrate that Mn promotes the exosomal release of misfolded αSyn by impairing endosomal trafficking and protein degradation.