白细胞介素-10 在通过运动减轻老龄小鼠内质网应激中的作用。

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM American journal of physiology. Endocrinology and metabolism Pub Date : 2024-09-01 Epub Date: 2024-07-31 DOI:10.1152/ajpendo.00204.2024
Bruno Brieda Marafon, Ana Paula Pinto, Ivo Vieira de Sousa Neto, Caroline Mantovani da Luz, José Rodrigo Pauli, Dennys Esper Cintra, Eduardo Rochete Ropelle, Fernando Moreira Simabuco, Leandro Pereira de Moura, Ellen Cristini de Freitas, Donato Americo Rivas, Adelino Sanchez Ramos da Silva
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引用次数: 0

摘要

尽管未折叠蛋白反应(UPR)对细胞保护至关重要,但其长期激活可能会诱发细胞凋亡,损害细胞寿命。衰老过程会增加骨骼肌的内质网(ER)应激。然而,综合运动能否防止骨骼肌中由年龄引起的内质网应激仍是未知数。有证据表明,ER应激可能会抵消白细胞介素-10(IL-10)的积极作用,从而增加炎症,而在细胞中施用IL-10可抑制ER应激和细胞凋亡。本研究验证了衰老和联合运动对小鼠股四头肌的体能、ER应激指标和炎症的影响。此外,我们还验证了IL-10对ER应激指标的影响。我们将C57BL/6小鼠分为年轻组(Y,6月龄)、老年静坐组(OS,静坐,24月龄)和老年训练组(OT,接受短期联合运动,24月龄)。为了明确IL-10在UPR通路中的作用,使用了缺乏IL-10的基因敲除小鼠。OS组小鼠的体能表现较差,ER应激相关蛋白(如CHOP和p-eIF2α/eIF2α)较高。与OS相比,运动方案增加了OT的肌肉力量和IL-10蛋白水平,同时导致CHOP蛋白水平下调。此外,缺乏IL-10的小鼠增加了BiP、CHOP和p-eIF2α/eIF2α蛋白水平,表明这种细胞因子能调节骨骼肌的ER应激反应。生物信息学分析表明,耐力和阻力训练会下调老年人侧阔肌中DDIT3和XBP1基因的表达,这进一步证实了我们的研究结果。因此,联合运动是一种潜在的治疗干预措施,可促进老年骨骼肌中ER应激标记物的调整。
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The role of interleukin-10 in mitigating endoplasmic reticulum stress in aged mice through exercise.

Although unfolded protein response (UPR) is essential for cellular protection, its prolonged activation may induce apoptosis, compromising cellular longevity. The aging process increases the endoplasmic reticulum (ER) stress in skeletal muscle. However, whether combined exercise can prevent age-induced ER stress in skeletal muscle remains unknown. Evidence suggests that ER stress may increase inflammation by counteracting the positive effects of interleukin-10 (IL-10), whereas its administration in cells inhibits ER stress and apoptosis. This study verified the effects of aging and combined exercise on physical performance, ER stress markers, and inflammation in the quadriceps of mice. Moreover, we verified the effects of IL-10 on ER stress markers. C57BL/6 mice were distributed into young (Y, 6 mo old), old sedentary (OS, sedentary, 24 mo old), and old trained group (OT, submitted to short-term combined exercise, 24 mo old). To clarify the role of IL-10 in UPR pathways, knockout mice lacking IL-10 were used. The OS mice presented worse physical performance and higher ER stress-related proteins, such as C/EBP homologous protein (CHOP) and phospho-eukaryotic translation initiation factor 2 alpha (p-eIF2α/eIF2α). The exercise protocol increased muscle strength and IL-10 protein levels in OT while inducing the downregulation of CHOP protein levels compared with OS. Furthermore, mice lacking IL-10 increased BiP, CHOP, and p-eIF2α/eIF2α protein levels, indicating this cytokine can regulate the ER stress response in skeletal muscle. Bioinformatics analysis showed that endurance and resistance training downregulated DNA damage inducible transcript 3 (DDIT3) and XBP1 gene expression in the vastus lateralis of older people, reinforcing our findings. Thus, combined exercise is a potential therapeutic intervention for promoting adjustments in ER stress markers in aged skeletal muscle.NEW & NOTEWORTHY Aging elevates endoplasmic reticulum (ER) stress in skeletal muscle, potentially heightening inflammation by opposing interleukin-10 (IL-10) effects. This study found that short-term combined exercise boosted strength and IL-10 protein levels while reducing CHOP protein levels in older mice. In addition, IL-10-deficient mice exhibited increased ER stress markers, highlighting IL-10's role in regulating ER stress in skeletal muscle. Consequently, combined exercise emerges as a therapeutic intervention to elevate IL-10 and adjust ER stress markers in aging.

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来源期刊
CiteScore
9.80
自引率
0.00%
发文量
98
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Endocrinology and Metabolism publishes original, mechanistic studies on the physiology of endocrine and metabolic systems. Physiological, cellular, and molecular studies in whole animals or humans will be considered. Specific themes include, but are not limited to, mechanisms of hormone and growth factor action; hormonal and nutritional regulation of metabolism, inflammation, microbiome and energy balance; integrative organ cross talk; paracrine and autocrine control of endocrine cells; function and activation of hormone receptors; endocrine or metabolic control of channels, transporters, and membrane function; temporal analysis of hormone secretion and metabolism; and mathematical/kinetic modeling of metabolism. Novel molecular, immunological, or biophysical studies of hormone action are also welcome.
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