Genome-wide transcriptome analysis to further understand neutrophil activation and lncRNA transcript profiles in Kawasaki disease View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2019-01-23

AUTHORS

Tai-Ming Ko, Jeng-Sheng Chang, Shih-Ping Chen, Yi-Min Liu, Chia-Jung Chang, Fuu-Jen Tsai, Yi-Ching Lee, Chien-Hsiun Chen, Yuan-Tsong Chen, Jer-Yuarn Wu

ABSTRACT

Kawasaki disease (KD) is the most common cause of acquired cardiac disease in children in developed countries. However, little is known regarding the role of transcriptomic targets of KD in the disease progression and development of complications, especially coronary artery aneurysms (CAA). The aim of our study was to identify transcripts affected by KD and their potential role in the disease. We enrolled 37 KD patients and collected blood samples along a comprehensive time-course. mRNA profiling demonstrated an abundance of CD177 transcript in acute KD, and in the intravenous immunoglobulin (IVIG)-resistant group compared to in the IVIG-sensitive group. lncRNA profiling identified XLOC_006277 as the most highly expressed molecule. XLOC_006277 expression in patients at acute stage was 3.3-fold higher relative to patients with convalescent KD. Moreover, XLOC_006277 abundance increased significantly in patients with CAA. XLOC_006277 knockdown suppressed MMP-8 and MMP-9 expression, both associated with heart lesions. Our result suggested that the increase of CD177pos neutrophils was associated with KD. Moreover, this study provided global long non-coding RNA transcripts in the blood of patients with KD, IVIG-resistant KD, or CAA. Notably, XLOC_006277 abundance was associated with CAA, which might contribute to further understanding of CAA pathogenesis in KD. More... »

PAGES

328

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/s41598-018-36520-y

DOI

http://dx.doi.org/10.1038/s41598-018-36520-y

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1111618787

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/30674924


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