内科学
血管性痴呆
内分泌学
促炎细胞因子
医学
CD14型
神经退行性变
神经炎症
炎症
痴呆
受体
疾病
作者
Chengyun Tang,Emily Burns,Jane J. Border,David Bunn,Cameron Cantwell,Andrew Gregory,Claire Johnson,Yanbin Dong,Richard J. Roman,David L. Mattson,Fan Fan
摘要
Abstract Background Hypertension is a leading risk factor for the development of Alzheimer’s disease and Alzheimer’s disease‐related dementia (AD/ADRD), which is closely linked with cerebral vascular inflammation and dysfunction. We previously found that high‐salt‐treated Dahl Salt‐Sensitive (SS) rats displayed blood‐brain barrier (BBB) leakage, astrocyte activation, neurodegeneration, and cognitive impairments. CD14 functions in the Toll‐like receptor 4 (TLR4) complex to initiate proinflammatory signaling events in response to LPS. CD14 levels were elevated in the brains of human and animal AD/ADRD models. This study aims to explore the vascular contribution of CD14 to AD/ADRD. Method The expression of Cd14 was assessed through RT‐PCR in primary cerebral vascular smooth muscle cells (VSMCs) isolated from TgF344‐AD rats, and the results were compared to cells from control rats. The myogenic response of the middle cerebral artery (MCA) was compared between SS (SS CD14+/+ ), SS CD14‐/‐ , and SD rats with and without the induction of hypertension with 4% NaCl diets. BBB function was detected by the leakage of injected Evans blue and fibrinogen. Brain cytokine levels were detected with Bio‐Plex Rat Cytokine 23‐Plex Assay. Result Cd14 emerged as one of the significantly upregulated top genes in high‐salt‐fed SS CD14+/+ rats, with a subsequent three‐fold increase observed specifically in cerebral VSMCs of AD compared with control rats. Hypertensive SS CD14+/+ rats exhibited an impaired myogenic response of the MCA compared to normotensive SS CD14+/+ rats and SD rats fed with both high‐ and low‐salt diets. Notably, the deletion of CD14 demonstrated a remarkable trend in enhancing the myogenic response of the MCA in female SS CD14‐/‐ rats. Furthermore, high salt‐fed 24‐week SS CD14+/+ rats displayed BBB dysfunction. An augmented pan‐cytokine panel was observed in low salt‐fed 12‐week SS CD14+/+ rats, and this effect was magnified in high salt‐fed 24‐week SS CD14+/+ rats. Conclusion These results collectively point to the potential role of CD14 in influencing vascular and immune responses, suggesting a link between CD14, hypertension, and cerebrovascular pathologies, particularly in the context of AD. Additional investigations are warranted to delve into the underlying mechanisms and ascertain whether CD14 exhibits a sex‐specific role in AD/ADRD.
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