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Skin tight: macrophage-specific COX-2 induction links salt handling in kidney and skin

机译:皮肤紧致:巨噬细胞特异性COX-2诱导作用与肾脏和皮肤中的盐处理有关

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The relationship between dietary salt intake and the associated risk of hypertension and cardiovascular disease is an important public health concern. In this issue of the JCI , a study by Zhang and associates shows that consumption of a high-sodium diet induces expression of cyclooxygenase-2 (COX-2) in macrophages, resulting in enhanced levels of prostaglandin E_(2) (PGE_(2)), autocrine activation of the macrophage E-prostanoid 4 (EP4) receptor, and subsequent triggering of parallel pathways in the kidney and in skin that help dispose of excess sodium. The authors found that blockade or genetic elimination of the COX-2/PGE_(2)/EP4 receptor pathway in hematopoietic cells causes salt-sensitive hypertension in mice. These studies illuminate an unexpected central role for the macrophage in coordinating homeostatic responses to dietary salt intake and suggest a complex pathophysiology for hypertension associated with NSAID use.
机译:饮食中盐的摄入量与高血压和心血管疾病的相关风险之间的关系是重要的公共卫生问题。在本期JCI中,Zhang及其同事进行的一项研究表明,食用高钠饮食会诱导巨噬细胞中环氧合酶2(COX-2)的表达,从而导致前列腺素E_(2)(PGE_(2 )),巨噬细胞E-前列腺素4(EP4)受体的自分泌激活,以及随后触发的肾脏和皮肤平行途径的触发,这有助于处理过量的钠。作者发现,造血细胞中COX-2 / PGE_(2)/ EP4受体途径的阻断或遗传消除会引起小鼠对盐敏感的高血压。这些研究阐明了巨噬细胞在协调对饮食盐摄入的稳态反应中的出乎意料的中心作用,并暗示了与NSAID使用相关的高血压的复杂病理生理。

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