Brain PathologyNeurosciencePeer-reviewed journal article
TMCC2 Associates with Alzheimer's Disease Pathology in the Human Brain
Paul C.R. HopkinsiD, Claire TroakesiD, Andrew KingiD, Guy TeariD
Abstract
Transmembrane and Coiled-Coil 2 (TMCC2) is a protein that forms complexes with both apolipoprotein E (apoE) and the amyloid protein precursor (APP), two proteins central to the etiology of Alzheimers disease (AD). Here we have carried out the first investigation of TMCC2 expression in the human brain, where TMCC2 immunoreactivity is primarily neuronal. We also examined TMCC2 localization in late onset AD brains,early onset AD cases bearing a mutation in APP, and in Down syndrome cases. TMCC2 immunoreactivity is closely associated with APP immunoreactivity in both control and AD cases. In all AD cases examined, TMCC2 associated with dense core senile plaques and adjacent dystrophic neurites, but not with amyloid surrounding the core, nor with diffuse amyloid plaques or neurofibrillary tangles. In Down syndrome, we found dystrophic neurites in senile plaques that were positive for amyloid and TMCC2, but not for APP, in addition to the APP- and TMCC2-positive dense cores. Western blot analysis revealed TMCC2 exists as at least three protein isoforms. The relative abundance of the isoforms varies in the temporal gyrus and cerebellum, the relative proportions of which were influenced by APOE and/or dementia status. Taken together, these observations are consistent with the evolutionarily conserved interactions between APP and TMCC2 and suggest cooperation betweenTMCC2 and APP in the normal and AD brain. These findings thus support a role for TMCC2 as a mediator of the impact of apoE on AD pathogenesis.
- organism: human
- assay: protein structure
- research focus: cell type annotation
- research focus: differential expression
- research focus: gene regulatory network inference
- research focus: protein structure prediction
- approach: statistical model
- approach: experimental assay
- Citations
- 0
- FWCI
- 0.00
- Field percentile
- 15th percentile
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Tau-tubulin kinase 1 and amyloid-β peptide induce phosphorylation of collapsin response mediator protein-2 and enhance neurite degeneration in Alzheimer disease mouse models
Seiko Ikezu, Kaitlin L. Ingraham Dixie, … Tsuneya Ikezu·Acta Neuropathologica CommunicationsPeer-reviewed·Feb 4, 2020
- Loss of TREM2 exacerbates parenchymal amyloid pathology but diminishes CAA in Tg-SwDI mice
Rui Zhong, Yingzheng Xu, … Ling Li·bioRxiv·Nov 4, 2023
- Amyloid accumulation drives proteome-wide alterations in mouse models of Alzheimers disease like pathology
Jeffrey N. Savas, Yizhi Wang, … John R. Yates·Cell ReportsPeer-reviewed·Nov 1, 2017
- Aβ Amyloid Scaffolds the Accumulation of Matrisome and Additional Proteins in Alzheimer's Disease
Yona Levites, Eric B. Dammer, … Todd Eliot Golde·Cell Reports MedicinePeer-reviewed·Aug 1, 2024
- TREM2 deficiency causes region-specific brain effects in a mouse model of cerebral amyloid angiopathy
Constanza Mercado, Armando Amaro, … Cristian A. Lasagna‐Reeves·Journal of NeuroinflammationPeer-reviewed·Sep 26, 2026
- Protein phosphatase 2A, complement component 4, and APOE genotype linked to Alzheimer disease using a systems biology approach
Gyungah Jun, Yang You, … Lindsay A. Farrer·Alzheimer s & DementiaPeer-reviewed·Feb 9, 2022