下丘脑室旁核中的小胶质细胞感知血液动力学紊乱并促进高血压患者的交感神经兴奋

IF 25.5 1区 医学 Q1 IMMUNOLOGY
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引用次数: 0

摘要

高血压通常伴有交感神经强直性增高,但交感神经亢进是如何引发的尚不清楚。最近的研究发现,以小胶质细胞为中心的神经炎症导致了高血压的交感神经兴奋。在这项研究中,我们从形态学和转录组水平对小胶质细胞进行了时空分析,发现交感中枢下丘脑室旁核(PVN)中的小胶质细胞是高血压挑战的早期响应者。血管分析表明,与其他脑区相比,下丘脑室旁核具有毛细血管密度高、血管直径细和血管拓扑结构复杂的特点。因此,当血压升高后血流动力学紊乱时,血管中释放的 ATP 很容易渗透到 PVN 中。从机理上讲,ATP 与小胶质细胞 P2Y12 受体的连接是导致小胶质细胞炎症激活和最终交感神经溢出的原因。总之,这些发现确定了一种独特的血管模式,它使 PVN 前交感神经元容易受到高血压相关的小胶质细胞介导的炎症损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Microglia in the hypothalamic paraventricular nucleus sense hemodynamic disturbance and promote sympathetic excitation in hypertension

Microglia in the hypothalamic paraventricular nucleus sense hemodynamic disturbance and promote sympathetic excitation in hypertension

Hypertension is usually accompanied by elevated sympathetic tonicity, but how sympathetic hyperactivity is triggered is not clear. Recent advances revealed that microglia-centered neuroinflammation contributes to sympathetic excitation in hypertension. In this study, we performed a temporospatial analysis of microglia at both morphological and transcriptomic levels and found that microglia in the hypothalamic paraventricular nucleus (PVN), a sympathetic center, were early responders to hypertensive challenges. Vasculature analyses revealed that the PVN was characterized by high capillary density, thin vessel diameter, and complex vascular topology relative to other brain regions. As such, the PVN was susceptible to the penetration of ATP released from the vasculature in response to hemodynamic disturbance after blood pressure increase. Mechanistically, ATP ligation to microglial P2Y12 receptor was responsible for microglial inflammatory activation and the eventual sympathetic overflow. Together, these findings identified a distinct vasculature pattern rendering vulnerability of PVN pre-sympathetic neurons to hypertension-associated microglia-mediated inflammatory insults.

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来源期刊
Immunity
Immunity 医学-免疫学
CiteScore
49.40
自引率
2.20%
发文量
205
审稿时长
6 months
期刊介绍: Immunity is a publication that focuses on publishing significant advancements in research related to immunology. We encourage the submission of studies that offer groundbreaking immunological discoveries, whether at the molecular, cellular, or whole organism level. Topics of interest encompass a wide range, such as cancer, infectious diseases, neuroimmunology, autoimmune diseases, allergies, mucosal immunity, metabolic diseases, and homeostasis.
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