Mitochondrial impairment: A common motif in neuropsychiatric presentation? The link to the tryptophan–kynurenine metabolic system

M Tanaka, Á Szabó, E Spekker, H Polyák, F Tóth… - Cells, 2022 - mdpi.com
Nearly half a century has passed since the discovery of cytoplasmic inheritance of human
chloramphenicol resistance. The inheritance was then revealed to take place maternally by …

Mitochondrial dysfunction in Parkinson's disease–a key disease hallmark with therapeutic potential

MT Henrich, WH Oertel, DJ Surmeier… - Molecular …, 2023 - Springer
Mitochondrial dysfunction is strongly implicated in the etiology of idiopathic and genetic
Parkinson's disease (PD). However, strategies aimed at ameliorating mitochondrial …

INPP5D regulates inflammasome activation in human microglia

V Chou, RV Pearse, AJ Aylward, N Ashour… - Nature …, 2023 - nature.com
Microglia and neuroinflammation play an important role in the development and progression
of Alzheimer's disease (AD). Inositol polyphosphate-5-phosphatase D (INPP5D/SHIP1) is a …

The relationship of alpha-synuclein to mitochondrial dynamics and quality control

NJ Thorne, DA Tumbarello - Frontiers in molecular neuroscience, 2022 - frontiersin.org
Maintenance of mitochondrial health is essential for neuronal survival and relies upon
dynamic changes in the mitochondrial network and effective mitochondrial quality control …

Intrinsically disordered proteins and proteins with intrinsically disordered regions in neurodegenerative diseases

O Coskuner-Weber, O Mirzanli, VN Uversky - Biophysical Reviews, 2022 - Springer
Many different intrinsically disordered proteins and proteins with intrinsically disordered
regions are associated with neurodegenerative diseases. These types of proteins including …

[HTML][HTML] Increased CHCHD2 expression promotes liver fibrosis in nonalcoholic steatohepatitis via Notch/osteopontin signaling

Y Li, W Xiu, J Xu, X Chen, G Wang, J Duan, L Sun… - JCI insight, 2022 - ncbi.nlm.nih.gov
Nonalcoholic steatohepatitis (NASH) is closely related to liver fibrosis. The role of coiled-coil-
helix-coiled-coil-helix domain-containing 2 (CHCHD2) in NASH remains unknown …

Single-cell transcriptomics of human iPSC differentiation dynamics reveal a core molecular network of Parkinson's disease

G Novak, D Kyriakis, K Grzyb, M Bernini… - Communications …, 2022 - nature.com
Parkinson's disease (PD) is the second-most prevalent neurodegenerative disorder,
characterized by the loss of dopaminergic neurons (mDA) in the midbrain. The underlying …

CHCHD2 p. Thr61Ile knock‐in mice exhibit motor defects and neuropathological features of Parkinson's disease

L Fan, S Zhang, X Li, Z Hu, J Yang, S Zhang… - Brain …, 2023 - Wiley Online Library
Abstract The p. Thr61Ile (p. T61I) mutation in coiled‐coil‐helix–coiled‐coil‐helix domain
containing 2 (CHCHD2) was deemed a causative factor in Parkinson's disease (PD) …

Involvement of casein kinase 1 epsilon/delta (Csnk1e/d) in the pathogenesis of familial Parkinson's disease caused by CHCHD2

S Torii, S Arakawa, S Sato, K Ishikawa… - EMBO Molecular …, 2023 - embopress.org
Parkinson's disease (PD) is a common neurodegenerative disorder that results from the loss
of dopaminergic neurons. Mutations in coiled‐coil‐helix‐coiled‐coil‐helix domain …

Site-specific mitochondrial dysfunction in neurodegeneration

A Vodičková, SA Koren, AP Wojtovich - Mitochondrion, 2022 - Elsevier
Mitochondria are essential for neuronal survival and mitochondrial dysfunction is a hallmark
of neurodegeneration. The loss in mitochondrial energy production, oxidative stress, and …