RRC ID 88379
Author Clayton EL, Milioto C, Muralidharan B, Norona FE, Edgar JR, Soriano A, Jafar-Nejad P, Rigo F, Collinge J, Isaacs AM.
Title Frontotemporal dementia causative CHMP2B impairs neuronal endolysosomal traffic-rescue by TMEM106B knockdown.
Journal Brain
Abstract Mutations in the endosome-associated protein CHMP2B cause frontotemporal dementia and lead to lysosomal storage pathology in neurons. We here report that physiological levels of mutant CHMP2B causes reduced numbers and significantly impaired trafficking of endolysosomes within neuronal dendrites, accompanied by increased dendritic branching. Mechanistically, this is due to the stable incorporation of mutant CHMP2B onto neuronal endolysosomes, which we show renders them unable to traffic within dendrites. This defect is due to the inability of mutant CHMP2B to recruit the ATPase VPS4, which is required for release of CHMP2B from endosomal membranes. Strikingly, both impaired trafficking and the increased dendritic branching were rescued by treatment with antisense oligonucleotides targeting the well validated frontotemporal dementia risk factor TMEM106B, which encodes an endolysosomal protein. This indicates that reducing TMEM106B levels can restore endosomal health in frontotemporal dementia. As TMEM106B is a risk factor for frontotemporal dementia caused by both C9orf72 and progranulin mutations, and antisense oligonucleotides are showing promise as therapeutics for neurodegenerative diseases, our data suggests a potential new strategy for treating the wide range of frontotemporal dementias associated with endolysosomal dysfunction.
Volume 141(12)
Pages 3428-3442
Published 2018-12-1
DOI 10.1093/brain/awy284
PII 5212875
PMID 30496365
PMC PMC6262218
MeSH Animals Brain / metabolism Cells, Cultured Dendrites / metabolism* Endosomal Sorting Complexes Required for Transport / metabolism* Endosomes / metabolism* Female Frontotemporal Dementia / metabolism* Gene Knockdown Techniques Lysosomes / metabolism* Male Membrane Proteins / genetics* Mice, Inbred C57BL Mice, Transgenic Nerve Tissue Proteins / genetics Nerve Tissue Proteins / metabolism* Neuronal Plasticity
IF 11.337
Resource
Mice RBRC00806