线粒体呼吸链缺陷与老年男性HIV患者骨骼肌再生反应受损和纤维化有关。

IF 6 Q2 GERIATRICS & GERONTOLOGY
Matthew Hunt, Amy E Vincent, Megan M McNiff, Gareth Ettridge, Caroline Sabin, Alan Winston, Brendan Ai Payne
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引用次数: 0

摘要

尽管进行了抑制性抗逆转录病毒治疗(ART),一些老年艾滋病毒感染者仍表现出不利的衰老表型,其潜在机制仍不完全清楚。我们招募了30名年龄≥50岁的HIV男性和15名匹配良好的非HIV男性,并对骨骼肌活检和血浆生物标志物测量进行了组织学分析,并结合临床和功能评估。与未感染艾滋病毒的男性相比,感染艾滋病毒的男性表现出更高的虚弱、虚弱前期、肌肉减少和肌肉减少前期的频率。在评估骨骼肌时,感染HIV的男性线粒体复合体I和IV蛋白丰度降低,肌纤维再生减少,纤维化增加,血浆tnf - α和MCP-4水平升高。Spearman相关分析表明,炎症和线粒体呼吸链缺陷可能导致骨骼肌损伤反应,并通过纤维化而不是再生来解决。因此,这些发现为老年艾滋病毒感染者的不良衰老表型(包括虚弱和肌肉减少症)提供了合理的解释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mitochondrial respiratory chain deficiency is associated with an impaired skeletal muscle regenerative response and fibrosis in older men with HIV.

Despite suppressive anti-retroviral therapy (ART), some older people with HIV show adverse ageing phenotypes, and the underlying mechanisms remain incompletely understood. We recruited 30 men with HIV aged ≥ 50 years and 15 well-matched men without HIV and performed histological analyses on skeletal muscle biopsies and plasma biomarker measurement, in combination with clinical and functional assessments. Men with HIV showed higher frequencies of frailty, pre-frailty, sarcopenia, and pre-sarcopenia when compared to men without HIV. When assessing skeletal muscle, men with HIV had decreased mitochondrial complex I and IV protein abundance and myofibre regeneration, whilst fibrosis was increased, and plasma TNFα and MCP-4 levels were elevated. Spearman correlation analyses suggested that inflammation and mitochondrial respiratory chain deficiency may result in a damage response in skeletal muscle with resolution by fibrosis rather than regeneration. These findings thus provide plausible rationales for adverse ageing phenotypes in older men with HIV, including frailty and sarcopenia.

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