Activation of transposable elements is linked to a region- and cell type-specific interferon response in Parkinson's disease

Summary

Parkinson's disease (PD) is a neurodegenerative disorder involving a neuroinflammatory response, the cause of which remains unclear. Transposable elements (TEs) have been linked to inflammation, but their potential role in PD remains unexplored. Using bulk- and single-nuclei RNA-seq of postmortem brain tissue from four brain regions, we studied TE transcription and its correlation with PD neuroinflammation. Over a thousand TEs, including LINE-1 s and ERVs, were expressed in a cell type- and region-specific manner in the human brain. Increased TE expression was found in microglia and neurons in the substantia nigra and putamen of PD brains, but not amygdala or prefrontal cortex, compared to controls. This TE activation correlated with an innate immune response in the same brain regions. The link between an interferon response and TE activation was mechanistically confirmed using human pluripotent stem cell-derived microglia and neurons. Our findings provide insights into TE transcription in the PD brain and suggest that TEs may contribute to neuroinflammation and pathological progression in PD.

Authors Garza R, Adami A, Thiruvalluvan A, Wijesinghe S, Curle A, Tam O, Forcier T, Lagka DA, Kazakou NL, Atacho DAM, Sharma Y, Horvath V, Bermudez S, Johansson J, Rainbow DB, Castilla-Vallmanya L, Jones JL, Quaegebeur A, Hammell MG, Kirkeby A, Barker RA, Jakobsson J
Journal Science advances
Publication Date 2026 Sep 4;12(36):eaed2952
PubMed 42685224
PubMed Central PMC13537272
DOI 10.1126/sciadv.aed2952

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