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2000
Volume 9, Issue 2
  • ISSN: 1567-2050
  • E-ISSN: 1875-5828

Abstract

The Notch pathway is a critical mediator of short-range cell-cell communication that is reiteratively used to regulate a diverse array of cellular processes during embryonic development and the renewal and maintenance of adult tissues. Most Notch-dependent processes utilize a core signaling mechanism that is dependent on regulated intramembrane proteolysis: Upon ligand binding, Notch receptors undergo ectodomain shedding by ADAM metalloproteases, followed by γ-secretase-mediated intramembrane proteolysis. This releases the Notch intracellular domain, which translocates to the nucleus to activate transcription. In this review, we highlight the roles of Notch signaling particularly in self-renewing tissues in adults and several human diseases and raise some key considerations when targeting ADAMs and γ-secretase as disease-modifying strategies for Alzheimer's Disease.

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/content/journals/car/10.2174/156720512799361600
2012-02-01
2025-04-23
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/content/journals/car/10.2174/156720512799361600
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  • Article Type:
    Research Article
Keyword(s): -secretase; ADAM; CADASIL; multiple sclerosis; Notch; stem cell; T-ALL; tissue renewal
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