Department of Evolutionary Immunology, Institute of Zoology and Biomedical Research, Faculty of Biology, Jagiellonian University, Krakow, Poland.
Doctoral School of Exact and Natural Sciences, Jagiellonian University, Krakow, Poland.
Front Immunol. 2024 Mar 7;15:1330995. doi: 10.3389/fimmu.2024.1330995. eCollection 2024.
Stress may pose a serious challenge to immune homeostasis. Stress however also may prepare the immune system for challenges such as wounding or infection, which are likely to happen during a fight or flight stress response.
In common carp ( L.) we studied the stress-induced redistribution of neutrophils into circulation, and the expression of genes encoding CXC chemokines known to be involved in the regulation of neutrophil retention (CXCL12) and redistribution (CXCL8), and their receptors (CXCR4 and CXCR1-2, respectively) in blood leukocytes and in the fish hematopoietic organ - the head kidney. The potential involvement of CXC receptors and stress hormone receptors in stress-induced neutrophil redistribution was determined by an study with selective CXCR inhibitors and antagonists of the receptors involved in stress regulation: glucocorticoid/mineralocorticoid receptors (GRs/MRs), adrenergic receptors (ADRs) and the melanocortin 2 receptor (MC2R).
The stress-induced increase of blood neutrophils was accompanied by a neutrophil decrease in the hematopoietic organs. This increase was cortisol-induced and GR-dependent. Moreover, stress upregulated the expression of genes encoding CXCL12 and CXCL8 chemokines, their receptors, and the receptor for granulocytes colony-stimulation factor (GCSFR) and matrix metalloproteinase 9 (MMP9). Blocking of the CXCR4 and CXCR1 and 2 receptors with selective inhibitors inhibited the stress-induced neutrophil redistribution and affected the expression of genes encoding CXC chemokines and CXCRs as well as GCSFR and MMP9.
Our data demonstrate that acute stress leads to the mobilization of the immune system, characterized by neutrophilia. CXC chemokines and CXC receptors are involved in this stress-induced redistribution of neutrophils from the hematopoietic tissue into the peripheral blood. This phenomenon is directly regulated by interactions between cortisol and the GR/MR. Considering the pivotal importance of neutrophilic granulocytes in the first line of defense, this knowledge is important for aquaculture, but will also contribute to the mechanisms involved in the stress-induced perturbation in neutrophil redistribution as often observed in clinical practice.
压力可能对免疫稳态构成严重挑战。然而,压力也可能使免疫系统为诸如创伤或感染等挑战做好准备,这些挑战很可能在战斗或逃跑应激反应期间发生。
在鲤鱼(L.)中,我们研究了应激诱导的中性粒细胞向循环中的重新分布,以及编码已知参与中性粒细胞保留(CXCL12)和重新分布(CXCL8)调节的 CXC 趋化因子的基因的表达,以及它们的受体(分别为 CXCR4 和 CXCR1-2)在血液白细胞和鱼类造血器官-头肾中。通过使用选择性 CXCR 抑制剂以及参与应激调节的受体(皮质醇/盐皮质激素受体(GRs/MRs)、肾上腺素能受体(ADRs)和黑素皮质素 2 受体(MC2R)的拮抗剂,研究了 CXC 受体和应激激素受体在应激诱导的中性粒细胞重新分布中的潜在作用。
应激诱导的血液中性粒细胞增加伴随着造血器官中性粒细胞减少。这种增加是皮质醇诱导的,并且依赖于 GR。此外,应激上调了编码 CXCL12 和 CXCL8 趋化因子、其受体以及粒细胞集落刺激因子受体(GCSFR)和基质金属蛋白酶 9(MMP9)的基因的表达。用选择性抑制剂阻断 CXCR4 和 CXCR1 和 2 受体抑制了应激诱导的中性粒细胞重新分布,并影响了编码 CXC 趋化因子和 CXCR 以及 GCSFR 和 MMP9 的基因的表达。
我们的数据表明,急性应激会导致免疫系统动员,其特征是嗜中性粒细胞增多。CXC 趋化因子和 CXC 受体参与了这种从造血组织到外周血的应激诱导的中性粒细胞重新分布。这种现象直接受皮质醇与 GR/MR 之间相互作用的调节。考虑到嗜中性粒细胞在第一道防线中的重要性,这一知识对水产养殖很重要,但也将有助于解释在临床实践中经常观察到的应激诱导的中性粒细胞重新分布紊乱的机制。