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性和身体活动对肌肉疼痛局部免疫反应的影响。

The impact of sex and physical activity on the local immune response to muscle pain.

机构信息

Department of Physical Therapy & Rehabilitation Sciences, University of Iowa, Iowa City, IA, USA.

Iowa Institute of Human Genetics, University of Iowa, Iowa City, IA, USA.

出版信息

Brain Behav Immun. 2023 Jul;111:4-20. doi: 10.1016/j.bbi.2023.03.020. Epub 2023 Mar 25.

Abstract

Induction of muscle pain triggers a local immune response to produce pain and this mechanism may be sex and activity level dependent. The purpose of this study was to measure the immune system response in the muscle following induction of pain in sedentary and physically active mice. Muscle pain was produced via an activity-induced pain model using acidic saline combined with fatiguing muscle contractions. Prior to induction of muscle pain, mice (C57/BL6) were sedentary or physically active (24hr access to running wheel) for 8 weeks. The ipsilateral gastrocnemius was harvested 24hr after induction of muscle pain for RNA sequencing or flow cytometry. RNA sequencing revealed activation of several immune pathways in both sexes after induction of muscle pain, and these pathways were attenuated in physically active females. Uniquely in females, the antigen processing and presentation pathway with MHC II signaling was activated after induction of muscle pain; activation of this pathway was blocked by physical activity. Blockade of MHC II attenuated development of muscle hyperalgesia exclusively in females. Induction of muscle pain increased the number of macrophages and T-cells in the muscle in both sexes, measured by flow cytometry. In both sexes, the phenotype of macrophages shifted toward a pro-inflammatory state after induction of muscle pain in sedentary mice (M1 + M1/2) but toward an anti-inflammatory state in physically active mice (M2 + M0). Thus, induction of muscle pain activates the immune system with sex-specific differences in the transcriptome while physical activity attenuates immune response in females and alters macrophage phenotype in both sexes.

摘要

肌肉疼痛的诱导会引发局部免疫反应,产生疼痛,而这种机制可能依赖于性别和活动水平。本研究的目的是测量在久坐和活跃的小鼠中,疼痛诱导后肌肉中的免疫系统反应。通过使用酸性盐水和疲劳性肌肉收缩相结合的活动诱导性疼痛模型来产生肌肉疼痛。在诱导肌肉疼痛之前,将小鼠(C57/BL6)分为久坐组或活跃组(24 小时可使用跑步轮)8 周。在诱导肌肉疼痛后 24 小时收获同侧比目鱼肌,用于 RNA 测序或流式细胞术。RNA 测序显示,在两种性别中,诱导肌肉疼痛后都会激活几种免疫途径,而这些途径在活跃的雌性中被减弱。在雌性中,独特的是,抗原加工和呈递途径与 MHC II 信号被激活;而体力活动则阻断了该途径的激活。MHC II 的阻断仅在雌性中减弱了肌肉痛觉过敏的发展。通过流式细胞术测量,诱导肌肉疼痛会增加两性肌肉中的巨噬细胞和 T 细胞数量。在两种性别中,在久坐小鼠的肌肉疼痛诱导后,巨噬细胞的表型向促炎状态转变(M1+M1/2),而在活跃的小鼠中则向抗炎状态转变(M2+M0)。因此,诱导肌肉疼痛会激活免疫系统,转录组存在性别特异性差异,而体力活动则会减弱雌性的免疫反应,并改变两性的巨噬细胞表型。

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