Comprehensive Analysis of lncRNA and mRNA Expression Profile of Macrophage RAW264.7 Stimulated by Antimicrobial Peptide BSN-37

Author:

Qin Ting1,Liu Mingcheng12,Lv Yanhe1,Zheng Airong3,Wang Lei1,Wu Yundi4,Kasianenko Oksana2,Wei Xiaobing1,Teng Zhanwei1,Xia Xiaojing1ORCID,Hu Jianhe1

Affiliation:

1. College of Animal Science and Veterinary Medicine, Henan Institute of Science and Technology, Xinxiang, China

2. Faculty of Veterinary Medicine, Sumy National Agrarian University, Sumy, Ukraine

3. Forage and Feed Station of Henan Province, Zhengzhou, China

4. State Key Laboratory of Marine Resource Utilization in South China Sea, Hainan University, Haikou, China

Abstract

Background: BSN-37, a novel antimicrobial peptide (AMP) containing 37 amino acid residues isolated from the bovine spleen, has not only antibacterial activity but also immunomodulatory activity. Recent evidence shows that long non-coding RNAs (lncRNAs) play an important role in regulating the activation and function of immune cells. The purpose of this experiment was to investigate the lncRNA and mRNA expression profile of mouse macrophages RAW264.7 stimulated by bovine antimicrobial peptide BSN-37. Methods: The whole gene expression microarray was used to detect the differentially expressed lncRNA and mRNA between antimicrobial peptide BSN-37 activated RAW264.7 cells and normal RAW264.7 cells. KEGG pathway analysis and GO function annotation analysis of differentially expressed lncRNAs and mRNA were carried out. Eight kinds of lncRNAs and nine kinds of mRNA with large differences were selected for qRT-PCR verification, respectively. Results: In the current study, we found that 1294 lncRNAs and 260 mRNAs were differentially expressed between antibacterial peptide BSN-37 treatment and control groups. Among them, Bcl2l12, Rab44, C1s, Cd101 and other genes were associated with immune responses and were all significantly up-regulated. Mest and Prkcz are related to cell growth, and other genes are related to glucose metabolism and lipid metabolism. In addition, some immune-related terms were also found in the GO and KEGG analyses. At the same time, real-time quantitative PCR was used to verify selected lncRNA and mRNA with differential expression. The results of qRT-PCR verification were consistent with the sequencing results, indicating that our data were reliable. Conclusion: This study provides the lncRNA and mRNA expression profiles of RAW264.7 macrophages stimulated by antimicrobial peptide BSN-37 and helps to provide a reference value for subsequent studies on lncRNA regulation of antimicrobial peptide BSN-37 immune function.

Funder

National Natural Science Foundation of China

Excellent Youth Science Foundation of Henan Province

Program for Innovative Talents (in Science and Technology) in University of Henan Province

Youth Backbone Teacher Project of Colleges and Universities of Henan Province

key scientific research projects of Colleges and Universities of Henan Province

Publisher

Bentham Science Publishers Ltd.

Subject

Biochemistry,General Medicine,Structural Biology

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