Effects of repeated sleep deprivation on brain pericytes in mice

• Published in: Scientific reports 2023-08, Vol.13 (1), p.12760-12760, Article 12760
• Main Authors: Wu, Yan, Li, Pengfei, Bhat, Narayan, Fan, Hongkuan, Liu, Meng
• Format: Article
• Language: English
• Subjects: 631/378; 631/378/1341; 631/378/1385; 631/378/2607; Animals; Annexin V; Apoptosis; Blood-brain barrier; Blood-Brain Barrier - metabolism; Brain - metabolism; Brain Injuries - metabolism; Brain injury; Caspase-3; Cerebrospinal fluid; Hippocampus; Humanities and Social Sciences; Mice; multidisciplinary; Parenchyma; Pericytes; Pericytes - metabolism; Platelet-derived growth factor; Platelet-derived growth factor receptors; Receptor, Platelet-Derived Growth Factor beta - metabolism; Science; Science (multidisciplinary); Sleep deprivation; Sleep Deprivation - metabolism
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-023-40138-0

The damaging effects of sleep deprivation (SD) on brain parenchyma have been extensively studied. However, the specific influence of SD on brain pericytes, a primary component of the blood–brain barrier (BBB) and the neurovascular unit (NVU), is still unclear. The present study examined how acute or repeated SD impairs brain pericytes by measuring the cerebrospinal fluid (CSF) levels of soluble platelet-derived growth factor receptor beta (sPDGFRβ) and quantifying pericyte density in the cortex, hippocampus, and subcortical area of the PDGFRβ-P2A-CreER T2 /tdTomato mice, which predominantly express the reporter tdTomato in vascular pericytes. Our results showed that a one-time 4 h SD did not significantly change the CSF sPDGFRβ level. In contrast, repeated SD (4 h/day for 10 consecutive days) significantly elevated the CSF sPDGFRβ level, implying explicit pericyte damages due to repeated SD. Furthermore, repeated SD significantly decreased the pericyte densities in the cortex and hippocampus, though the pericyte apoptosis status remained unchanged as measured with Annexin V-affinity assay and active Caspase-3 staining. These results suggest that repeated SD causes brain pericyte damage and loss via non-apoptosis pathways. These changes to pericytes may contribute to SD-induced BBB and NVU dysfunctions. The reversibility of this process implies that sleep improvement may have a protective effect on brain pericytes.