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Diagnostic Potential of Plasma Extracellular Vesicle miR-483-3p and Let-7d-3p for Sepsis

Guanguan Qiu, Jiajie Fan, Guoping Zheng, Jiangping He, Fangping Lin, Menghua Ge, Lan-Fang Huang, Jiangmei Wang, Jie Xia, Ruoqiong Huang, Qiang Shu, Jianguo Xu

2022Frontiers in Molecular Biosciences18 citationsDOIOpen Access PDF

Abstract

Background: microRNAs (miRNAs) from circulating extracellular vesicles (EVs) have been reported as disease biomarkers. This study aimed to identify the diagnostic value of plasma EV-miRNAs in sepsis. Methods: EVs were separated from the plasma of sepsis patients at admission and healthy controls. The expression of EV-miRNAs was evaluated by microarray and qRT-PCR. Results: A preliminary miRNA microarray of plasma EVs from a discovery cohort of 3 sepsis patients at admission and three healthy controls identified 11 miRNAs with over 2-fold upregulation in sepsis group. Based on this finding, EV samples from a validation cohort of 37 sepsis patients at admission and 25 healthy controls were evaluated for the expression of the 6 miRNAs relating injury and inflammation via qRT-PCR. Elevated expression of miR-483-3p and let-7d-3p was validated in sepsis patients and corroborated in a mouse model of sepsis. miR-483-3p and let-7d-3p levels positively correlated with the disease severity. Additionally, a combination of miR-483-3p and let-7d-3p had diagnostic value for sepsis. Furthermore, bioinformatic analysis and experimental validation showed that miR-483-3p and let-7d-3p target pathways regulating immune response and endothelial function. Conclusion: The present study reveals the potential role of plasma EV-miRNAs in the pathogenesis of sepsis and the utility of combining miR-483-3p and let-7d-3p as biomarkers for early sepsis diagnosis.

Topics & Concepts

SepsismicroRNAPathogenesisExtracellular vesicleDownregulation and upregulationMicroarrayMedicineInflammationCohortImmunologyInternal medicineBiologyMicrovesiclesGene expressionGeneGeneticsExtracellular vesicles in diseaseMicroRNA in disease regulationImmune cells in cancer
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