| Literature DB >> 30999031 |
Masahito Nakazaki1, Masanori Sasaki2, Yuko Kataoka-Sasaki3, Shinichi Oka3, Junpei Suzuki3, Yuichi Sasaki3, Hiroshi Nagahama3, Kazuo Hashi3, Jeffery D Kocsis4, Osamu Honmou1.
Abstract
Cerebral small vessel disease (CSVD) is not only a cause of vascular dementia (VD) but also a contributing factor to Alzheimer's disease (AD). The essential pathological feature of CSVD is the disruption of blood-brain barrier (BBB). Dysfunction of BBB due to degeneration of both endothelial cells and pericytes in capillaries leads to neuronal damage and progressive brain atrophy. Moreover, deterioration of amyloid-β (Aβ) clearance due to the failure of the transvascular BBB transport system results in accumulation of Aβ in the brain. Intravenous infusion of mesenchymal stem cells (MSCs) elicits functional recovery in experimental models including stroke and spinal cord injury. One effect of MSCs is to restore disrupted BBB through remodeling of microvasculature. Using spontaneously hypertensive rats (stroke-prone) with impaired cognitive function as a CSVD model, we have shown that infused MSCs has a therapeutic effect for cognitive function. Restoration of BBB function via remodeling of microvasculature and inhibition of Aβ accumulation could inhibit progressive brain atrophy and lead to restore cognitive dysfunction. Gene expression analysis indicated that infused MSCs activates both transforming growth factor-β and angiopoietin 1 signaling pathways and promotes the remodeling of microvasculature. Thus, infused MSCs may represent a novel therapy for both VD and AD.Entities:
Keywords: blood–brain barrier; cellular therapy; cerebral small vessel disease; dementia; mesenchymal stem cell
Year: 2019 PMID: 30999031 DOI: 10.1016/j.neuroscience.2019.04.018
Source DB: PubMed Journal: Neuroscience ISSN: 0306-4522 Impact factor: 3.590