The role of ADAM10 in astrocytes: Implications for Alzheimer’s disease

Richard J. Elsworthy*, Eric J. Hill, Connor Dunleavy, Sarah Aldred

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

Abstract

Much of the early research into AD relies on a neuron-centric view of the brain, however, evidence of multiple altered cellular interactions between glial cells and the vasculature early in AD has been demonstrated. As such, alterations in astrocyte function are widely recognized a contributing factor in the pathogenesis of AD. The processes by which astrocytes may be involved in AD make them an interesting target for therapeutic intervention, but in order for this to be most effective, there is a need for the specific mechanisms involving astrocyte dysfunction to be investigated. “α disintegrin and metalloproteinase” 10 (ADAM10) is capable of proteolytic cleavage of the amyloid precursor protein which prevents amyloid-β generation. As such ADAM10 has been identified as an interesting enzyme in AD pathology. ADAM10 is also known to play a role in a significant number of cellular processes, most notable in notch signaling and in inflammatory processes. There is a growing research base for the involvement of ADAM10 in regulating astrocytic function, primarily from an immune perspective. This review aims to bring together available evidence for ADAM10 activity in astrocytes, and how this relates to AD pathology.
Original languageEnglish
Article number1056507
Number of pages8
JournalFrontiers in Aging Neuroscience
Volume14
Early online date30 Nov 2022
DOIs
Publication statusPublished - 30 Nov 2022

Bibliographical note

© 2022 Elsworthy, Hill, Dunleavy and
Aldred. This is an open-access article
distributed under the terms of the Creative
Commons Attribution License (CC BY). The
use, distribution or reproduction in other
forums is permitted, provided the original
author(s) and the copyright owner(s) are
credited and that the original publication in
this journal is cited, in accordance with
accepted academic practice. No use,
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which does not comply with these terms.

Keywords

  • Aging Neuroscience
  • astrocyte
  • ADAM10 (a disintegrin and metalloprotease 10)
  • inflammation
  • Alzheimer’s disease
  • amyloid-beta

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