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Vascular myocytes are central to brain aging. Small vessel disease (SVD; arteriolosclerosis) is a widespread cause of lacunar stroke and vascular dementia and is characterized by fibrosis and depletion of vascular myocytes in small penetrating arteries. Vascular endothelial growth factor (VEGF) is associated with brain aging, and Immunolabeling for vascular endothelial growth factor receptor 2 (VEGFR2) is a potent determinant of cell fate. Here, we tested whether VEGFR2 in vascular myocytes is associated with older age and SVD in human brain. Immunolabeling for VEGFR2 in deep gray matter was assessed in older people with or without moderate-severe SVD or in younger people without brain pathology or with a monogenic form of SVD (Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy). All cases were without Alzheimer's disease pathology. Myocyte VEGFR2 was associated with increasing age (p = 0.0026) but not with SVD pathology or with sclerotic index or blood vessel density. We conclude that VEGFR2 is consistently expressed in small artery myocytes of older people and may mediate effects of VEGF on brain vascular aging.

Original publication

DOI

10.1016/j.neurobiolaging.2016.03.002

Type

Journal article

Journal

Neurobiol Aging

Publication Date

06/2016

Volume

42

Pages

110 - 115

Keywords

Arteriolosclerosis, Flk-1, Small vessel disease, Vascular dementia, Vasculopathy, Aged, Aged, 80 and over, Aging, Arteriosclerosis, CADASIL, Cerebral Arteries, Female, Gene Expression, Humans, Male, Muscle Cells, Vascular Endothelial Growth Factor Receptor-2