The role of extracellular matrix alterations in mediating astrocyte damage and pericyte dysfunction in Alzheimer's disease: A comprehensive review
- PMID: 34182602
- DOI: 10.1111/ejn.15372
The role of extracellular matrix alterations in mediating astrocyte damage and pericyte dysfunction in Alzheimer's disease: A comprehensive review
Abstract
The brain is a highly vascularized tissue protected by the blood-brain barrier (BBB), a complex structure allowing only necessary substances to pass through into the brain while limiting the entrance of harmful toxins. The BBB comprises several components, and the most prominent features are tight junctions between endothelial cells (ECs), which are further wrapped in a layer of pericytes. Pericytes are multitasked cells embedded in a thick basement membrane (BM) that consists of a fibrous extracellular matrix (ECM) and are surrounded by astrocytic endfeet. The primary function of astrocytes and pericytes is to provide essential blood supply and vital nutrients to the brain. In Alzheimer's disease (AD), long-term neuroinflammatory cascades associated with infiltration of harmful neurotoxic proteins may lead to BBB dysfunction and altered ECM components resulting in brain homeostatic imbalance, synaptic damage, and declined cognitive functions. Moreover, BBB structure and functional integrity may be lost due to induced ECM alterations, astrocyte damage, and pericytes dysfunction, leading to amyloid-beta (Aβ) hallmarks deposition in different brain regions. Herein, we highlight how BBB, ECM, astrocytes, and pericytes dysfunction can play a leading role in AD's pathogenesis and discuss their impact on brain functions.
Keywords: Alzheimer's disease; BBB dysfunction; astrocytes pericytes; basement membrane; extracellular matrix.
© 2021 Federation of European Neuroscience Societies and John Wiley & Sons Ltd.
References
REFERENCES
-
- Al'Qteishat, A., Gaffney, J., Krupinski, J., Rubio, F., West, D. C., Kumar, S., Kumar, P., Mitsios, N., & Slevin, M. (2006). Changes in hyaluronan production and metabolism following ischaemic stroke in man. Brain, 129, 2158-2176. https://doi.org/10.1093/brain/awl139
-
- Andrews, E. M., Richards, R. J., Yin, F. Q., Viapiano, M. S., & Jakeman, L. B. (2012). Alterations in chondroitin sulfate proteoglycan expression occur both at and far from the site of spinal contusion injury. Experimental neurology, 235, 174-187.
-
- Anwar, M. (2019). The effect of exaggerated induced inflammatory disorders and related disturbances in microglia-neuron homeostasis on the precipitation and remission of neurological disorders. IBRO Reports, 6, S493. https://doi.org/10.1016/j.ibror.2019.07.1547
-
- Anwar, M. M., Ali, O. S., Rashed, L. A., Badawi, A. M., & Eltablawy, N. A. (2018). Regulation of miRNA-124, nuclear factor-kappa B and β-catenin expression in response to novel therapeutic protocol in LPS induced Alzheimer's disease in rats. Research in Neuroscience, 7(1), 17. https://doi.org/10.5923/j.neuroscience.20180701.03
-
- Anwar, M. M., Ali, O. S., Rashed, L. A., Badawi, A. M., & Eltablawy, N. A. (2019a). The effect of using kefir grains and mesenchymal stem cells in LPS-induced Alzheimer's disease neuroinflammatory model. Revista eNeurobiología, 10(25), 23. Revista eNeurobiología 10(25):181219, 2019
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