Affiliation:
1. Children’s Hospital of Soochow University, No. 92 Zhongnan Street, Wuzhong District, Suzhou, Jiangsu 215000, China
2. Department of Pediatrics, The Second Affiliated Hospital of Nantong University, Nantong First People’s Hospital, No. 6, North Haierxiang Road, Nantong 226001, China
Abstract
The aim of the study was to explore the serum expression of long noncoding RNA (lncRNA) growth arrest-specific transcript 5 (GAS5) in Mycoplasma pneumoniae pneumonia (MPP) and its effect on lipid-associated membrane proteins (LAMPs)-induced apoptosis and inflammation. Totally, 56 children with MPP (MPP group) and 56 healthy children (NC group) were enrolled. lncRNA GAS5 expression was measured by quantitative real-time polymerase chain reaction (qRT-PCR). Serum levels of tumor necrosis factor α (TNF-α) and interleukin-6 (IL-6) were detected using ELISA, and the high mobility family protein B1 (HMGBl) was detected by qRT-PCR. The methylated binding protein 2 (MECP2) was inhibited by gene silencing, and the expression of MECP2, TNF-α, IL-6, HMGBl, p-p65, and p-IκBα was measured. lncRNA GAS5 and TNF-α, IL-6, and HMGBl in the peripheral blood of the MPP group were positively correlated
. The expression of TNF-α, IL-6, HMGBl, and lncRNA GAS5 showed a positive correlation with that of LAMPs. The GAS5-siRNA group showed an increased cell survival rate compared with the scrambled-RNAi group
while showing decreased apoptosis and cell death rates
. In addition, the expression of IL-6, TNF-α, HMGBl, p-p65, and p-IκBα was significantly reduced
. lncRNA GAS5 is highly expressed in the serum of children with MPP and inhibits LAMPs-induced apoptosis and alveolar macrophage inflammation.
Subject
Radiology, Nuclear Medicine and imaging