Aging of neural stem cells and vascular dysfunction: mechanisms, interconnection, and therapeutic perspectives
- PMID: 41170303
- PMCID: PMC12569804
- DOI: 10.1016/j.cccb.2025.100402
Aging of neural stem cells and vascular dysfunction: mechanisms, interconnection, and therapeutic perspectives
Abstract
Background: Aging of the central nervous system is accompanied by a progressive decline in neuroplasticity, regenerative capacity, and vascular integrity. Neural stem cells (NSCs) and cerebral vasculature are both critically involved in maintaining homeostasis, and their age-related dysfunction contributes to neurodegenerative and cerebrovascular diseases.
Objective: This article explores the mechanisms underlying NSC aging and vascular deterioration, their mutual interconnection, and the implications for brain health in aging populations.
Methods: We review current evidence on molecular and cellular pathways affecting neurogenesis and cerebral perfusion, including dysregulation of BDNF, VEGF, mTOR, AMPK, and the effects of oxidative stress and chronic inflammation. We also highlight emerging biomarkers and therapeutic targets.
Results: Aging disrupts the neurovascular unit, impairing both neurogenesis and vascular support systems. Chronic inflammation and oxidative stress exacerbate these processes, forming a self-perpetuating degenerative cycle. Antioxidant and anti-inflammatory therapies, along with stem cell-based interventions such as mesenchymal stem cells (MSCs) and induced pluripotent stem cells (iPSCs), show promise for restoring neural and vascular function.
Conclusion: Addressing both NSC and vascular aging is essential for developing effective interventions against cognitive decline and cerebrovascular pathology. Integrative and personalized therapeutic strategies targeting shared molecular pathways hold great promise for future clinical applications.
Keywords: Blood–brain barrier (BBB); Cerebrovascular aging; Chronic inflammation; Mesenchymal stem cells (MSCs); Neural stem cells (NSCs); Neurovascular unit; Oxidative stress; Vascular dysfunction.
© 2025 The Author(s).
Conflict of interest statement
The authors declare no conflict of interest.
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