Aging drives cerebrovascular network remodeling and functional changes in the mouse brain

被引:23
作者
Bennett, Hannah C. [1 ]
Zhang, Qingguang [2 ,3 ]
Wu, Yuan-ting [1 ,5 ]
Manjila, Steffy B. [1 ]
Chon, Uree [1 ,6 ]
Shin, Donghui [1 ]
Vanselow, Daniel J. [1 ]
Pi, Hyun-Jae [1 ]
Drew, Patrick J. [2 ,4 ]
Kim, Yongsoo [1 ,2 ]
机构
[1] Penn State Univ, Dept Neural & Behav Sci, Hershey, PA 17033 USA
[2] Penn State Univ, Ctr Neural Engn, Dept Engn Sci & Mech, University Pk, PA 16802 USA
[3] Michigan State Univ, Dept Physiol, E Lansing, MI 48824 USA
[4] Penn State Univ, Dept Biomed Engn Biol & Neurosurg, University Pk, PA 16802 USA
[5] Cedars Sinai Med Ctr, Dept Neurosurg, Dept Computat Biomed, Los Angeles, CA 90048 USA
[6] Stanford Univ, Neurosci Grad Program, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
CORTICAL BLOOD-FLOW; COGNITIVE IMPAIRMENT; CHOLINERGIC CIRCUITS; HEMODYNAMIC SIGNALS; PERICYTE LOSS; LAYER; 6B; CORTEX; MICE; BARRIER; AGE;
D O I
10.1038/s41467-024-50559-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Aging is frequently associated with compromised cerebrovasculature and pericytes. However, we do not know how normal aging differentially impacts vascular structure and function in different brain areas. Here we utilize mesoscale microscopy methods and in vivo imaging to determine detailed changes in aged murine cerebrovascular networks. Whole-brain vascular tracing shows an overall similar to 10% decrease in vascular length and branching density with similar to 7% increase in vascular radii in aged brains. Light sheet imaging with 3D immunolabeling reveals increased arteriole tortuosity of aged brains. Notably, vasculature and pericyte densities show selective and significant reductions in the deep cortical layers, hippocampal network, and basal forebrain areas. We find increased blood extravasation, implying compromised blood-brain barrier function in aged brains. Moreover, in vivo imaging in awake mice demonstrates reduced baseline and on-demand blood oxygenation despite relatively intact neurovascular coupling. Collectively, we uncover regional vulnerabilities of cerebrovascular network and physiological changes that can mediate cognitive decline in normal aging.
引用
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页数:20
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