1. Academic Validation
  2. In vivo functions of p75NTR: challenges and opportunities for an emerging therapeutic target

In vivo functions of p75NTR: challenges and opportunities for an emerging therapeutic target

  • Trends Pharmacol Sci. 2021 Sep;42(9):772-788. doi: 10.1016/j.tips.2021.06.006.
Subash C Malik 1 Elif G Sozmen 2 Bernat Baeza-Raja 3 Natacha Le Moan 3 Katerina Akassoglou 2 Christian Schachtrup 4
Affiliations

Affiliations

  • 1 Institute of Anatomy and Cell Biology, Faculty of Medicine, University of Freiburg, Freiburg, Germany; Faculty of Biology, University of Freiburg, Freiburg, Germany.
  • 2 Center for Neurovascular Brain Immunology at Gladstone and UCSF; Gladstone Institutes, San Francisco, CA, USA; Department of Neurology and Weill Institute for Neurosciences, University of California San Francisco, San Francisco, CA, USA.
  • 3 Gladstone Institutes, San Francisco, CA, USA.
  • 4 Institute of Anatomy and Cell Biology, Faculty of Medicine, University of Freiburg, Freiburg, Germany; Center for Basics in NeuroModulation (NeuroModul Basics), Faculty of Medicine, University of Freiburg, Freiburg, Germany. Electronic address: [email protected].
Abstract

The p75 neurotrophin receptor (p75NTR) functions at the molecular nexus of cell death, survival, and differentiation. In addition to its contribution to neurodegenerative diseases and nervous system injuries, recent studies have revealed unanticipated roles of p75NTR in liver repair, fibrinolysis, lung fibrosis, muscle regeneration, and metabolism. Linking these various p75NTR functions more precisely to specific mechanisms marks p75NTR as an emerging candidate for therapeutic intervention in a wide range of disorders. Indeed, small molecule inhibitors of p75NTR binding to neurotrophins have shown efficacy in models of Alzheimer's disease (AD) and neurodegeneration. Here, we outline recent advances in understanding p75NTR pleiotropic functions in vivo, and propose an integrated view of p75NTR and its challenges and opportunities as a pharmacological target.

Keywords

Alzheimer’s disease; fibrinolysis; neurodegenerative diseases; neurotrophin receptors; small molecule inhibitors.

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