Rhythms in barriers and fluids: Circadian clock regulation in the aging neurovascular unit

被引:9
|
作者
Skapetze, Lea [1 ,4 ]
Owino, Sharon [2 ]
Lo, Eng H. [3 ,4 ]
Arai, Ken [3 ]
Merrow, Martha [1 ,4 ]
Harrington, Mary [2 ,4 ]
机构
[1] Ludwig Maximilians Univ Munchen, Inst Med Psychol, Fac Med, Munich, Germany
[2] Smith Coll, Neurosci Program, Northampton, MA 01060 USA
[3] Harvard Med Sch, Massachusetts Gen Hosp, Neuroprotect Res Labs, Boston, MA USA
[4] Consortium Int Rech Circadienne AVC CIRCA, Munich, Germany
关键词
Circadian clock; Aging; Neurovascular unit; Neurodegeneration; Chaperone -mediated autophagy; Oligodendrocyte precursor cells; BLOOD-BRAIN-BARRIER; CHAPERONE-MEDIATED AUTOPHAGY; TUMOR-NECROSIS-FACTOR; AGE-RELATED DECLINE; REV-ERB-ALPHA; CEREBROSPINAL-FLUID; SUPRACHIASMATIC NUCLEUS; EXTRACELLULAR-MATRIX; LOCOMOTOR-ACTIVITY; PROSTAGLANDIN D-2;
D O I
10.1016/j.nbd.2023.106120
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The neurovascular unit is where two very distinct physiological systems meet: The central nervous system (CNS) and the blood. The permeability of the barriers separating these systems is regulated by time, including both the 24 h circadian clock and the longer processes of aging. An endogenous circadian rhythm regulates the transport of molecules across the blood-brain barrier and the circulation of the cerebrospinal fluid and the glymphatic system. These fluid dynamics change with time of day, and with age, and especially in the context of neurodegeneration. Factors may differ depending on brain region, as can be highlighted by consideration of circadian regulation of the neurovascular niche in white matter. As an example of a potential target for clinical applications, we highlight chaperone-mediated autophagy as one mechanism at the intersection of circadian dysregulation, aging and neurodegenerative disease. In this review we emphasize key areas for future research.
引用
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页数:13
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