Graduate Program in Immunology, Sackler School of Graduate Biomedical Sciences, Tufts University, 155 Harrison Avenue, Boston, Massachusetts 02111, USA.
Infect Immun. 2010 Dec;78(12):5307-13. doi: 10.1128/IAI.00630-10. Epub 2010 Oct 4.
Borrelia burgdorferi stimulates a strong inflammatory response during infection of a mammalian host. To understand the mechanisms of immune regulation employed by the host to control this inflammatory response, we focused our studies on adrenomedullin, a peptide produced in response to bacterial stimuli that exhibits antimicrobial activity and regulates inflammatory responses by modulating the expression of inflammatory cytokines. Specifically, we investigated the effect of B. burgdorferi on the expression of adrenomedullin as well as the ability of adrenomedullin to dampen host inflammatory responses to the spirochete. The concentration of adrenomedullin in the synovial fluid of untreated Lyme arthritis patients was elevated compared with that in control osteoarthritis patient samples. In addition, coculture with B. burgdorferi significantly increased the expression of adrenomedullin in RAW264.7 macrophages through MyD88-, phosphatidylinositol 3-kinase (PI3-K)-, and p38-dependent signaling cascades. Furthermore, the addition of exogenous adrenomedullin to B. burgdorferi-stimulated RAW264.7 macrophages resulted in a significant decrease in the induction of proinflammatory cytokines. Taken together, these results suggest that B. burgdorferi increases the production of adrenomedullin, which in turn negatively regulates the B. burgdorferi-stimulated inflammatory response.
伯氏疏螺旋体在感染哺乳动物宿主时会引发强烈的炎症反应。为了了解宿主用来控制这种炎症反应的免疫调节机制,我们专注于研究肾上腺髓质素,这是一种对细菌刺激产生的肽,具有抗菌活性,并通过调节炎症细胞因子的表达来调节炎症反应。具体来说,我们研究了伯氏疏螺旋体对肾上腺髓质素表达的影响,以及肾上腺髓质素抑制宿主对螺旋体炎症反应的能力。未经治疗的莱姆关节炎患者的滑液中肾上腺髓质素的浓度与对照骨关节炎患者样本相比升高。此外,通过 MyD88、磷脂酰肌醇 3-激酶 (PI3-K) 和 p38 依赖的信号级联反应,与伯氏疏螺旋体共培养显著增加了 RAW264.7 巨噬细胞中肾上腺髓质素的表达。此外,向伯氏疏螺旋体刺激的 RAW264.7 巨噬细胞中添加外源性肾上腺髓质素会导致促炎细胞因子的诱导显著减少。总之,这些结果表明伯氏疏螺旋体增加了肾上腺髓质素的产生,而肾上腺髓质素反过来又负调控伯氏疏螺旋体刺激的炎症反应。