血管周围巨噬细胞将物理创伤信号转化为快速血管反应。

Zaza Gelashvili, Zhouyang Shen, Yanan Ma, Mark Jelcic, Philipp Niethammer
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引用次数: 0

摘要

白细胞在几秒到几分钟内发现远处的伤口,这对有效的病原体防御、组织愈合和再生至关重要。血管必须同样迅速地发现远处的伤口,以启动局部白细胞外溢,但这种即时血管反应背后的机制尚不清楚。利用活斑马鱼幼虫的高速成像,我们研究了血管如何实现快速伤口检测。我们监测了两个标志性的血管反应:血管扩张和血清渗出。我们的实验——包括遗传、药理学和渗透干扰,以及化学发生性白细胞消耗——揭示了血管周围巨噬细胞中的cppla 2核形状感知途径在损伤后几秒钟内将快速(~ 50 μm/s)渗透伤口信号转化为血管通透性的5-脂氧合酶(Alox5a)衍生的脂质。这些发现表明,血管周围巨噬细胞作为物理化学继电器,桥接渗透伤口信号和血管反应。通过揭示这种新型的沟通方式,我们为免疫和血管对损伤反应的协调提供了新的见解。
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Perivascular Macrophages Convert Physical Wound Signals Into Rapid Vascular Responses.

Leukocytes detect distant wounds within seconds to minutes, which is essential for effective pathogen defense, tissue healing, and regeneration. Blood vessels must detect distant wounds just as rapidly to initiate local leukocyte extravasation, but the mechanism behind this immediate vascular response remains unclear. Using high-speed imaging of live zebrafish larvae, we investigated how blood vessels achieve rapid wound detection. We monitored two hallmark vascular responses: vessel dilation and serum exudation. Our experiments-including genetic, pharmacologic, and osmotic perturbations, along with chemogenetic leukocyte depletion-revealed that the cPla2 nuclear shape sensing pathway in perivascular macrophages converts a fast (~50 μm/s) osmotic wound signal into a vessel-permeabilizing, 5-lipoxygenase (Alox5a) derived lipid within seconds of injury. These findings demonstrate that perivascular macrophages act as physicochemical relays, bridging osmotic wound signals and vascular responses. By uncovering this novel type of communication, we provide new insights into the coordination of immune and vascular responses to injury.

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