Proteomic and transcriptomic analysis of lung tissue in OVA-challenged mice

被引:8
作者
Lee, Yongjin [1 ]
Hwang, Yun-Ho [1 ]
Kim, Kwang-Jin [1 ]
Park, Ae-Kyung [1 ]
Paik, Man-Jeong [1 ]
Kim, Seong Hwan [2 ]
Lee, Su Ui [3 ]
Yee, Sung-Tae [1 ]
Son, Young-Jin [1 ]
机构
[1] Sunchon Natl Univ, Dept Pharm, 255 Jungangno, Sunchon 57922, Jeonnam, South Korea
[2] Korea Res Inst Chem Technol, Div Drug Discovery Res, Pharmacol Res Ctr, Lab Translat Therapeut, Daejeon 34114, South Korea
[3] Korea Res Inst Biosci & Biotechnol, Nat Med Res Ctr, Cheongju 56212, Chungcheongbuk, South Korea
基金
新加坡国家研究基金会;
关键词
Asthma; Ovalbumin (OVA); Environmental respiratory disease; Proteomics; RNA-seq; AIRWAY INFLAMMATION; PHOSPHOLIPASE A(2); IFN-GAMMA; ASTHMA; CELLS; TH2; OVEREXPRESSION; PROLIFERATION; TRANSLOCATION; CHITINASES;
D O I
10.1007/s12272-017-0972-4
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Asthma is a long term inflammatory disease of the airway of lungs characterized by variable airflow obstruction and bronchospasm. Asthma is caused by a complex combination of environmental and genetic interactions. In this study, we conducted proteomic analysis of samples derived from control and OVA challenged mice for environmental respiratory disease by using 2-D gel electrophoresis. In addition, we explored the genes associated with the environmental substances that cause respiratory disease and conducted RNA-seq by next-generation sequencing. Proteomic analysis revealed 7 up-regulated (keratin KB40, CRP, HSP27, chaperonin containing TCP-1, TCP-10, keratin, and albumin) and 3 down-regulated proteins (PLC-alpha, PLA2, and precursor ApoA-1). The expression diversity of many genes was found in the lung tissue of OVA challenged moue by RNA-seq. 146 genes were identified as significantly differentially expressed by OVA treatment, and 118 genes of the 146 differentially expressed genes were up-regulated and 28 genes were downregulated. These genes were related to inflammation, mucin production, and airway remodeling. The results presented herein enable diagnosis and the identification of quantitative markers to monitor the progression of environmental respiratory disease using proteomics and genomic approaches.
引用
收藏
页码:87 / 100
页数:14
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