Department of Nephrology and Hypertension, Friedrich-Alexander University, Erlangen-Nürnberg, Germany.
Hypertension. 2010 Mar;55(3):755-61. doi: 10.1161/HYPERTENSIONAHA.109.143339. Epub 2010 Feb 8.
We showed recently that mononuclear phagocyte system (MPS) cells provide a buffering mechanism for salt-sensitive hypertension by driving interstitial lymphangiogenesis, modulating interstitial Na(+) clearance, and increasing endothelial NO synthase protein expression in response to very high dietary salt via a tonicity-responsive enhancer binding protein/vascular endothelial growth factor C regulatory mechanism. We now tested whether isotonic saline and deoxycorticosterone acetate (DOCA)-salt treatment leads to a similar regulatory response in Sprague-Dawley rats. Male rats were fed a low-salt diet and received tap water (low-salt diet LSD), 1.0% saline (high-salt diet HSD), or DOCA+1.0% saline (DOCA-HSD). To test the regulatory role of interstitial MPS cells, we further depleted MPS cells with clodronate liposomes. HSD and DOCA-HSD led to Na(+) accumulation in the skin, MPS-driven tonicity-responsive enhancer binding protein/vascular endothelial growth factor C-mediated hyperplasia of interstitial lymph capillaries, and increased endothelial NO synthase protein expression in skin interstitium. Clodronate liposome MPS cell depletion blocked MPS infiltration in the skin interstitium, resulting in unchanged tonicity-responsive enhance binding protein/vascular endothelial growth factor C levels and absent hyperplasia of the lymph capillary network. Moreover, no increased skin endothelial NO synthase protein expression occurred in either clodronate liposome-treated HSD or DOCA-salt rats. Thus, absence of the MPS-cell regulatory response converted a salt-resistant blood-pressure state to a salt-sensitive state in HSD rats. Furthermore, salt-sensitive hypertension in DOCA-salt rats was aggravated. We conclude that MPS cells act as onsite controllers of interstitial volume and blood pressure homeostasis, providing a local regulatory salt-sensitive tonicity-responsive enhancer binding protein/vascular endothelial growth factor C-mediated mechanism in the skin to maintain normal blood pressure in states of interstitial Na(+) and Cl(-) accumulation. Failure of this physiological extrarenal regulatory mechanism leads to a salt-sensitive blood pressure response.
我们最近表明,单核吞噬细胞系统 (MPS) 细胞通过驱动间质淋巴管生成、调节间质钠离子清除以及增加内皮型一氧化氮合酶蛋白表达,为盐敏感性高血压提供了缓冲机制,以响应非常高的饮食盐通过渗透压反应增强子结合蛋白/血管内皮生长因子 C 调节机制。我们现在测试了等渗盐水和脱氧皮质酮醋酸盐 (DOCA)-盐处理是否会在 Sprague-Dawley 大鼠中导致类似的调节反应。雄性大鼠喂食低盐饮食并接受自来水(低盐饮食 LSD)、1.0%盐水(高盐饮食 HSD)或 DOCA+1.0%盐水(DOCA-HSD)。为了测试间质 MPS 细胞的调节作用,我们进一步用氯膦酸盐脂质体耗尽 MPS 细胞。HSD 和 DOCA-HSD 导致皮肤中的 Na+积累,MPS 驱动的渗透压反应增强子结合蛋白/血管内皮生长因子 C 介导的间质淋巴毛细血管增生,以及皮肤间质中内皮型一氧化氮合酶蛋白表达增加。氯膦酸盐脂质体 MPS 细胞耗竭阻止了 MPS 细胞在皮肤间质中的浸润,导致渗透压反应增强子结合蛋白/血管内皮生长因子 C 水平不变,淋巴毛细血管网络增生消失。此外,氯膦酸盐脂质体处理的 HSD 或 DOCA-盐大鼠的皮肤内皮型一氧化氮合酶蛋白表达均未增加。因此,MPS 细胞调节反应的缺失将 HSD 大鼠的盐抵抗血压状态转变为盐敏感状态。此外,DOCA-盐大鼠的盐敏感性高血压加重。我们得出结论,MPS 细胞作为间质体积和血压稳态的原位控制器,在皮肤中提供局部调节的盐敏感性渗透压反应增强子结合蛋白/血管内皮生长因子 C 介导的机制,以在间质 Na+和 Cl-积累的情况下维持正常血压。这种生理肾外调节机制的失败导致盐敏感性血压反应。