The Potential Role of Integrin Signaling in Memory and Cognitive Impairment

Biomolecules. 2023 Jan 5;13(1):108. doi: 10.3390/biom13010108.

Abstract

Dementia currently has no cure and, due to the increased prevalence and associated economic and personal burden of this condition, current research efforts for the development of potential therapies have intensified. Recently, targeting integrins as a strategy to ameliorate dementia and other forms of cognitive impairment has begun to gain traction. Integrins are major bidirectional signaling receptors in mammalian cells, mediating various physiological processes such as cell-cell interaction and cell adhesion, and are also known to bind to the extracellular matrix. In particular, integrins play a critical role in the synaptic transmission of signals, hence their potential contribution to memory formation and significance in cognitive impairment. In this review, we describe the physiological roles that integrins play in the blood-brain barrier (BBB) and in the formation of memories. We also provide a clear overview of how integrins are implicated in BBB disruption following cerebral pathology. Given that vascular contributions to cognitive impairment and dementia and Alzheimer's' disease are prominent forms of dementia that involve BBB disruption, as well as chronic inflammation, we present current approaches shown to improve dementia-like conditions with integrins as a central focus. We conclude that integrins are vital in memory formation and that their disruption could lead to various forms of cognitive impairment. While further research to understand the relationships between integrins and memory is needed, we propose that the translational relevance of research efforts in this area could be improved through the use of appropriately aged, comorbid, male and female animals.

Keywords: and blood–brain barrier; dementia; extracellular matrix; integrins.

Publication types

  • Review

MeSH terms

  • Alzheimer Disease* / metabolism
  • Blood-Brain Barrier / metabolism
  • Cognitive Dysfunction* / metabolism
  • Humans
  • Inflammation / metabolism
  • Integrins / metabolism

Substances

  • Integrins

Grants and funding

This research received no external funding.