Astrocytic reactivity triggered by defective autophagy and metabolic failure causes neurotoxicity in frontotemporal dementia type 3

Stem Cell Reports. 2021 Nov 9;16(11):2736-2751. doi: 10.1016/j.stemcr.2021.09.013. Epub 2021 Oct 21.


Frontotemporal dementia type 3 (FTD3), caused by a point mutation in the charged multivesicular body protein 2B (CHMP2B), affects mitochondrial ultrastructure and the endolysosomal pathway in neurons. To dissect the astrocyte-specific impact of mutant CHMP2B expression, we generated astrocytes from human induced pluripotent stem cells (hiPSCs) and confirmed our findings in CHMP2B mutant mice. Our data provide mechanistic insights into how defective autophagy causes perturbed mitochondrial dynamics with impaired glycolysis, increased reactive oxygen species, and elongated mitochondrial morphology, indicating increased mitochondrial fusion in FTD3 astrocytes. This shift in astrocyte homeostasis triggers a reactive astrocyte phenotype and increased release of toxic cytokines, which accumulate in nuclear factor kappa b (NF-κB) pathway activation with increased production of CHF, LCN2, and C3 causing neurodegeneration.

Keywords: CHMP2B; FTD3; NF-kB; autophagy; complement 3; cytokines; hiPSC-derived astrocytes; mitochondria; reactive astrocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Astrocytes / cytology
  • Astrocytes / metabolism*
  • Autophagy / genetics*
  • Cell Differentiation / genetics
  • Cells, Cultured
  • Endosomal Sorting Complexes Required for Transport / genetics*
  • Endosomal Sorting Complexes Required for Transport / metabolism
  • Frontotemporal Dementia / genetics*
  • Frontotemporal Dementia / metabolism
  • Gene Expression Profiling / methods
  • Genetic Predisposition to Disease / genetics*
  • Glycolysis / genetics
  • Homeostasis / genetics
  • Humans
  • Induced Pluripotent Stem Cells / metabolism
  • Mice
  • Mitochondria / genetics
  • Mitochondria / metabolism
  • Mutation*
  • RNA-Seq / methods
  • Signal Transduction / genetics


  • CHMP2B protein, human
  • Endosomal Sorting Complexes Required for Transport