Suppr超能文献

调节性T细胞与外周血单个核细胞的生物能量学与儿童肥胖症相关。

Regulatory T cells and bioenergetics of peripheral blood mononuclear cells linked to pediatric obesity.

作者信息

Rose Shannon, Landes Reid D, Vyas Kanan K, Delhey Leanna, Blossom Sarah

机构信息

Department of Pediatrics, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, AR, USA.

Arkansas Children's Research Institute, Little Rock, AR, USA.

出版信息

Immunometabolism (Cobham). 2024 Apr 25;6(2):e00040. doi: 10.1097/IN9.0000000000000040. eCollection 2024 Apr.

Abstract

BACKGROUND

Obesity-associated inflammation drives the development of insulin resistance and type 2 diabetes. We sought to identify associations of circulating regulatory T cells (Treg) with the degree of obesity (eg, body mass index -score [BMIz]), insulin resistance (homeostatic model of insulin resistance [HOMA-IR]), and glycemic control (HbA1c) in children and adolescents. We further sought to examine associations among bioenergetics of peripheral blood mononuclear cells (PBMCs) and CD4 T cells and BMIz, HOMA-IR, and HbA1c.

METHODS

A total of 65 children and adolescents between the ages 5 and 17 years were studied. HbA1c and fasting levels of plasma glucose and insulin were measured. We quantified circulating Tregs (CD3CD4CD25CD127FoxP3) by flow cytometry, and measured mitochondrial respiration (oxygen consumption rate [OCR]) and glycolysis (extracellular acidification rate [ECAR]) in PBMCs and isolated CD4 T cells by Seahorse extracellular flux analysis.

RESULTS

Tregs (% CD4) are negatively associated with BMIz but positively associated with HOMA-IR. In PBMCs, OCR/ECAR (a ratio of mitochondrial respiration to glycolysis) is positively associated with BMIz but negatively associated with HbA1c.

CONCLUSIONS

In children, Tregs decrease as body mass index increases; however, the metabolic stress and inflammation associated with insulin resistance may induce a compensatory increase in Tregs. The degree of obesity is also associated with a shift away from glycolysis in PBMCs but as HbA1c declines, metabolism shifts back toward glycolysis. Comprehensive metabolic assessment of the immune system is needed to better understand the implications immune cell metabolic alterations in the progression from a healthy insulin-sensitive state toward glucose intolerance in children.

TRIAL REGISTRATION

This observational study was registered at the ClinicalTrials.gov (NCT03960333, https://clinicaltrials.gov/study/NCT03960333?term=NCT03960333&rank=1).

摘要

背景

肥胖相关炎症促使胰岛素抵抗和2型糖尿病的发展。我们试图确定循环调节性T细胞(Treg)与儿童和青少年肥胖程度(如体重指数评分[BMIz])、胰岛素抵抗(胰岛素抵抗稳态模型[HOMA-IR])及血糖控制(糖化血红蛋白[HbA1c])之间的关联。我们还进一步探究外周血单个核细胞(PBMC)和CD4 T细胞的生物能量学与BMIz、HOMA-IR及HbA1c之间的关联。

方法

共研究了65名5至17岁的儿童和青少年。测量了HbA1c以及空腹血糖和胰岛素水平。我们通过流式细胞术对循环Treg(CD3CD4CD25CD127FoxP3)进行定量,并通过海马细胞外流量分析测量PBMC和分离的CD4 T细胞中的线粒体呼吸(氧消耗率[OCR])和糖酵解(细胞外酸化率[ECAR])。

结果

Treg(% CD4)与BMIz呈负相关,但与HOMA-IR呈正相关。在PBMC中,OCR/ECAR(线粒体呼吸与糖酵解的比率)与BMIz呈正相关,但与HbA1c呈负相关。

结论

在儿童中,随着体重指数增加,Treg减少;然而,与胰岛素抵抗相关的代谢应激和炎症可能会诱导Treg代偿性增加。肥胖程度还与PBMC中糖酵解的减少有关,但随着HbA1c下降,代谢会向糖酵解方向转变。需要对免疫系统进行全面的代谢评估,以更好地理解免疫细胞代谢改变在儿童从健康的胰岛素敏感状态向葡萄糖不耐受进展过程中的影响。

试验注册

本观察性研究已在ClinicalTrials.gov注册(NCT03960333,https://clinicaltrials.gov/study/NCT03960333?term=NCT03960333&rank=1)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7d4/11045398/3c1f0d2e5b7f/in9-6-e00040-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验