Department of Psychiatry, University of California, San Diego, La Jolla, CA 92093-0804, USA.
Brain Behav Immun. 2013 Jan;27(1):101-8. doi: 10.1016/j.bbi.2012.10.003. Epub 2012 Oct 6.
Elevated blood pressure (BP) and infiltration of the vasculature by monocytes contribute to vascular pathology; but, monocyte migratory characteristics based on differing inflammatory potential under adrenergic activation remains unclear. We compared nonclassical (CD14(+)CD16(++); HLA-DR(+)), intermediate (CD14(++)CD16(+); HLA-DR(++)), and classical (CD14(++)CD16(-); HLA-DR(+/-)) monocyte trafficking and their LPS-stimulated TNF production in response to a physical stressor (20-min treadmill exercise at 65-70% VO(2peak)) in participants with high prehypertension (PHT), mild PHT or normal BP (NBP). To determine adrenergic receptor (AR) sensitivity, pre-exercise cells were also treated with isoproterenol (Iso). When cells were stimulated with LPS, the CD16 molecules were downregulated, and monocyte subsets were differentiated based on HLA-DR expression. Monocyte subpopulations (as % of total monocytes) and intracellular TNF production were evaluated by flow cytometry. TNF production in all subsets decreased post-exercise and with ex-vivo incubation with Iso, irrespective of BP (p<0.001), with nonclassical and intermediate monocytes being a major source of TNF production. Overall, % nonclassical monocytes increased, % intermediate did not change, whereas % classical decreased post-exercise (p<0.001). However, % increase in nonclassical monocytes under exercise-induced adrenergic activation was blunted in high PHT individuals (p<0.05), but not in individuals with mild PHT and NBP. These findings extend our previous reports by showing that the mobilization of proinflammatory monocytes under physical stress is attenuated with even mild BP elevation. This may be indicative of monocytic AR desensitization and/or greater adhesion of "proinflammatory" monocytes to the vascular endothelium in hypertension with potential clinical implications of vascular pathology.
血压升高(BP)和单核细胞浸润血管导致血管病理学;但是,在肾上腺素激活下,根据不同的炎症潜能,单核细胞迁移特性仍不清楚。我们比较了非经典(CD14(+)CD16(++); HLA-DR(+))、中间(CD14(++)CD16(+); HLA-DR(++))和经典(CD14(++)CD16(-); HLA-DR(+/-))单核细胞的迁移及其对物理应激源(65-70% VO(2peak) 下 20 分钟跑步机运动)的 LPS 刺激 TNF 产生的反应,在高血压前期(PHT)、轻度 PHT 或正常血压(NBP)患者中。为了确定肾上腺素能受体(AR)敏感性,运动前细胞也用异丙肾上腺素(Iso)处理。当用 LPS 刺激细胞时,CD16 分子下调,单核细胞亚群根据 HLA-DR 表达进行分化。通过流式细胞术评估单核细胞亚群(占总单核细胞的百分比)和细胞内 TNF 产生。所有亚群的 TNF 产生在运动后和与 Iso 的体外孵育后减少,与血压无关(p<0.001),非经典和中间单核细胞是 TNF 产生的主要来源。总体而言,运动后非经典单核细胞的百分比增加,中间单核细胞的百分比不变,而经典单核细胞的百分比减少(p<0.001)。然而,高 PHT 个体在运动引起的肾上腺素能激活下,非经典单核细胞的百分比增加受到抑制(p<0.05),但在轻度 PHT 和 NBP 个体中则没有。这些发现通过表明在体力应激下促炎单核细胞的动员被即使轻度血压升高所减弱,扩展了我们以前的报告。这可能表明单核细胞 AR 脱敏和/或高血压中“促炎”单核细胞与血管内皮的粘附增加,具有潜在的血管病理学临床意义。