Transcriptome analysis of six tissues obtained post-mortem from sepsis patients

IF 5.3 2区 医学 Q1 Biochemistry, Genetics and Molecular Biology Journal of Cellular and Molecular Medicine Pub Date : 2023-09-20 DOI:10.1111/jcmm.17938
Fabiano Pinheiro da Silva, André Nicolau Aquime Gonçalves, Amaro Nunes Duarte-Neto, Thomaz Lüscher Dias, Hermes Vieira Barbeiro, Cristiane Naffah Souza Breda, Leandro Carvalho Dantas Breda, Niels Olsen Saraiva Câmara, Helder I. Nakaya
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Abstract

Septic shock is a life-threatening clinical condition characterized by a robust immune inflammatory response to disseminated infection. Little is known about its impact on the transcriptome of distinct human tissues. To address this, we performed RNA sequencing of samples from the prefrontal cortex, hippocampus, heart, lung, kidney and colon of seven individuals who succumbed to sepsis and seven uninfected controls. We identified that the lungs and colon were the most affected organs. While gene activation dominated, strong inhibitory signals were also detected, particularly in the lungs. We found that septic shock is an extremely heterogeneous disease, not only when different individuals are investigated, but also when comparing different tissues of the same patient. However, several pathways, such as respiratory electron transport and other metabolic functions, revealed distinctive alterations, providing evidence that tissue specificity is a hallmark of sepsis. Strikingly, we found evident signals of accelerated ageing in our sepsis population.

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败血症患者死后获得的六个组织的转录组分析。
败血症休克是一种危及生命的临床疾病,其特征是对播散性感染有强烈的免疫炎症反应。人们对其对不同人类组织转录组的影响知之甚少。为了解决这一问题,我们对七名死于败血症的患者和七名未感染的对照组的前额叶皮层、海马体、心脏、肺、肾脏和结肠样本进行了RNA测序。我们发现肺部和结肠是受影响最严重的器官。虽然基因激活占主导地位,但也检测到强烈的抑制信号,尤其是在肺部。我们发现,感染性休克是一种极其异质的疾病,不仅在调查不同的个体时,而且在比较同一患者的不同组织时也是如此。然而,几种途径,如呼吸电子传输和其他代谢功能,揭示了独特的变化,提供了组织特异性是败血症标志的证据。引人注目的是,我们在败血症人群中发现了明显的加速衰老的信号。
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来源期刊
CiteScore
10.00
自引率
1.90%
发文量
496
审稿时长
28 weeks
期刊介绍: Bridging physiology and cellular medicine, and molecular biology and molecular therapeutics, Journal of Cellular and Molecular Medicine publishes basic research that furthers our understanding of the cellular and molecular mechanisms of disease and translational studies that convert this knowledge into therapeutic approaches.
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