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Expression profiling of microRNAs in lipopolysaccharide-induced acute lung injury after hypothermia treatment.
Lee, Woonjeong; Kim, Insoo; Shin, Soyoung; Park, Kicheol; Yang, Keumjin; Eun, Jung Woo; Sul, Haejoung; Jeong, Sikyoung.
Affiliation
  • Lee W; 1Department of Emergency Medicine, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
  • Kim I; 1Department of Emergency Medicine, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
  • Shin S; 2Department of Laboratory Medicine, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
  • Park K; 3Clinical Research Institute, Daejeon St. Mary's Hospital, The Catholic University of Korea, Seoul, Republic of Korea.
  • Yang K; 3Clinical Research Institute, Daejeon St. Mary's Hospital, The Catholic University of Korea, Seoul, Republic of Korea.
  • Eun JW; 4Department of Pathology, Functional RNomics Research Center, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
  • Sul H; 5Department of Pathology, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
  • Jeong S; 1Department of Emergency Medicine, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Mol Cell Toxicol ; 12(3): 243-253, 2016.
Article in En | MEDLINE | ID: mdl-32226458
ABSTRACT
We investigated the expression profiles of miRNAs in acute lung injury (ALI) rats after hypothermia treatment. ALI rats were induced with lipopolysaccharide (LPS) and maintained with hypothermia (HT) or normothermia (NT) for 6 hours. HT attenuated inflammatory cell infiltration in the lung and improved biochemical indicators of multi-organ dysfunction. Nineteen miRNAs were significantly differentially expressed in the HT group compared with the NT group. miR-142, miR-98, miR-541, miR-503, miR-653, miR- 223, miR-323 and miR-196b exhibited opposite patterns of expression between the two groups. These dysregulated miRNAs were mainly involved in the immune and inflammatory response on functional annotation analyses. This study shows that HT has lung protective effects and influences expression profiles of miRNAs in ALI. And dysregulated miRNAs after HT modulate the immune and inflammation in ALI. These results suggest that dysregulated miRNAs play a role in the mechanism of the lung protective effects of HT in ALI.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Mol Cell Toxicol Year: 2016 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Mol Cell Toxicol Year: 2016 Document type: Article