Cited by 3Alzheimer's disease research and treatmentsCellular transport and secretionNeuroinflammation and Neurodegeneration Mechanisms

Alzheimer mutant speeds APP transport

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Gandy, Sam, Ehrlich, Michelle E.·2021·Journal of Experimental Medicine

Abstract

APPS198P segregates with rare familial forms of Alzheimer’s disease and resides within exon 5, unlike 27 other mutations that reside in exons 16 or 17. In this issue, Zhang et al. (2021. J. Exp. Med.https://doi.org/10.1084/jem.20210313) show that the brains of APPS198P transgenic mice accumulate excess levels of Aβ. In cultured cells, APPS198P undergoes accelerated ER folding, leading to early arrival in late vesicular compartments, thereby enhancing generation of Aβ.

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References 20 · Cited by 3

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Authors
Gandy, S., & Ehrlich, M. E.
Affiliations
  • James J. Peters VA Medical Center (US)
  • Icahn School of Medicine at Mount Sinai (US)
Corresponding author
  • Gandy, Sam
  • Ehrlich, Michelle E.
Venue
Journal of Experimental Medicine
Published
2021-05-14
Volume
218
Issue
6
ISSN
  • 0022-1007 (ISSN-L)
  • 1540-9538
OpenAlex
W3160141476
Cited by
3
References
20
Citations by year
2024: 1 · 2022: 2
FWCI
0.47
Type
journal article
Language
en
Open access
Locations
  • The Journal of Experimental Medicine (publishedVersion, cc-by-nc-sa)
  • PubMed Central (publishedVersion, cc-by-nc-sa)
  • PubMed (publishedVersion)
Funders
  • National Institute on Aging (MPI U01 AG046170, R01 AG057907, MPI RF1 AG058469, MPI RF1 AG059319, MPI R01 AG061894)
  • NIA-Designated Mount Sinai Alzheimer’s Disease Research Center (P30 AG066514)
  • The Sara and Gideon Gartner Foundation
  • The Louis B. Mayer Foundation
  • The Linda Wachner Foundation
Topics
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
  • Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
Keywords
Alzheimer's disease, amyloid-beta deposition, late endosomes, familial Alzheimer's disease, transgenic mice
MeSH terms
Alzheimer Disease, Animals, Brain, Exons, Mice, Transgenic, Amyloid beta-Peptides, Mice

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