Department of Molecular Immunology, Institute of Basic Medical Sciences, Beijing, P. R. China ; Department of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, P. R. China.
PLoS One. 2013 Sep 18;8(9):e74497. doi: 10.1371/journal.pone.0074497. eCollection 2013.
Chronic psychological stress has been shown to adversely impact immune system functions and compromise host defenses against various infections. However, the underlying mechanisms remain elusive. Recent studies have demonstrated that myeloid-derived suppressor cells (MDSCs) play an important role in regulating immunity. It is of interest to explore whether or not chronic psychological stress plays immunosuppressive functions partially by inducing MDSCs accumulation. In this work, we report that chronic psychological stress led to the accumulation of CD11b+Gr1+ cells in the bone marrow of BALB/c mice. Repeated β-agonist infusion showed no such effect. However, β-adrenergic blockade, but not glucocorticoids blockade, partially reversed the accumulation of CD11b+Gr1+ cells under the condition of chronic psychological stress, suggesting catecholamines collaborate with other factors to induce the accumulation. Further exploration indicates that cyclooxygenase 2 (COX-2)-prostaglandin E2 (PGE2) loop might act downstream to induce the accumulation. A majority of the accumulated CD11b+Gr1+ cells were Ly6G+Ly6C(low) immature neutrophils, which inhibited cytokine release of macrophages as well as T cell responsiveness. Moreover, the accumulated CD11b+Gr1+ cells under the condition of chronic psychological stress expressed multiple inhibitory molecules. Taken together, our data demonstrate for the first time that chronic psychological stress induces MDSCs accumulation in mice, which can contribute to immunosuppression.
慢性心理应激已被证明会对免疫系统功能产生不利影响,并损害宿主对各种感染的防御能力。然而,其潜在机制仍不清楚。最近的研究表明,髓系来源的抑制细胞(MDSCs)在调节免疫中发挥重要作用。值得探讨的是,慢性心理应激是否通过诱导 MDSCs 积累来发挥免疫抑制作用。在这项工作中,我们报告慢性心理应激导致 BALB/c 小鼠骨髓中 CD11b+Gr1+细胞的积累。重复β-激动剂输注没有这种作用。然而,β-肾上腺素能阻断,但不是糖皮质激素阻断,部分逆转了慢性心理应激条件下 CD11b+Gr1+细胞的积累,表明儿茶酚胺与其他因素协同诱导其积累。进一步的探索表明,环加氧酶 2(COX-2)-前列腺素 E2(PGE2)循环可能在下游起作用诱导其积累。大多数积累的 CD11b+Gr1+细胞是 Ly6G+Ly6C(低)幼稚中性粒细胞,其抑制巨噬细胞细胞因子释放和 T 细胞反应性。此外,慢性心理应激条件下积累的 CD11b+Gr1+细胞表达多种抑制性分子。总之,我们的数据首次表明,慢性心理应激可诱导小鼠 MDSCs 积累,从而导致免疫抑制。