The role of piR-hsa-1282 in lipopolysaccharide-induced 293T cells injury
LI Yang1,2, WANG Ying1,2, WANG Yan1,2, SHI Xin-yu1,2, CHEN Jin1,2, QIAN Hui1,2
(1. Zhenjiang Key Laboratory of High Techonology Research on Exosomes Foundation and Transformation Application; 2. School of Medicine, Jiangsu University, Zhenjiang Jiangsu 212013, China)
Abstract:Objective: To investigate the role of piRhsa1282 in lipopolysaccharide(LPS)induced 293T cells injury. Methods: A 24 h LPStreated 293T cells was established as the acute injury model. qRTPCR was used for determing the expression level of piRhsa1282.ELISA was applied for detection of IL6 expression.Western Bloting was used to detect the expression of cleavedcaspase 3,cleavedcaspase 9 and IL1β after piRhsa1282 inhibition. Results: With stimulation of LPS for 24 h, cell viability was reduced and the expression levels of cleavedcaspase 3 and IL6 were upregulated.Meanwhile,there was a higher level of piRhsa1282. Compared with the control group,piRhsa1282 inhibition led to the downregulation of cleavedcaspase 3,cleavedcaspase 9 and IL1β. Conclusion: piRhsa1282 could be involved in LPSinduced injury through regulation of apoptosis and inflammatory response.
收稿日期: 2019-03-19
基金资助:
国家自然科学基金资助项目(81871496);江苏大学学生科研项目(17A471)
通讯作者:
钱晖(通讯作者),教授,博士生导师,E-mail:lstmmmLst@163.com
作者简介: 李杨(1992—),女,硕士研究生
引用本文:
李杨1,2, 王颖1,2, 王妍1,2, 施鑫钰1,2, 陈瑾1,2, 钱晖1,2. piR-hsa-1282在脂多糖诱导的293T细胞急性损伤中的作用[J]. 江苏大学学报:医学版, 2019, 29(05): 386-389,393.
LI Yang1,2, WANG Ying1,2, WANG Yan1,2, SHI Xin-yu1,2, CHEN Jin1,2, QIAN Hui1,2. The role of piR-hsa-1282 in lipopolysaccharide-induced 293T cells injury . Journal of Jiangsu University(Medicine Edition), 2019, 29(05): 386-389,393.
1]Aravin A, Gaidatzis D, Pfeffer S, et al. A novel class of small RNAs bind to MILI protein in mouse testes\[J\]. Nature, 2006, 442(7099): 203-207.[2]Unhavaithaya Y, Hao Y, Beyret E, et al. MILI, a PIWIinteracting RNAbinding protein, is required for germ line stem cell selfrenewal and appears to positively regulate translation\[J\]. J Biol Chem, 2009, 284(10): 6507-6519.[3]Cheng J, Guo JM, Xiao BX, et al. piRNA, the new noncoding RNA, is aberrantly expressed in human cancer cells\[J\]. Clin Chim Acta, 2011, 412(17-18): 1621-1625.[4]Lu Y, Li C, Zhang K, et al. Identification of piRNAs in Hela cells by massive parallel sequencing\[J\]. BMB Rep, 2010, 43(9): 635-641.[5]Yin J, Jiang XY, Qi W, et al. piR823 contributes to colorectal tumorigenesis by enhancing the transcriptional activity of HSF1\[J\]. Cancer Sci, 2017, 108(9): 1746-1756.[6]Lee EJ, Banerjee S, Zhou H, et al. Identification of piRNAs in the central nervous system\[J\]. RNA, 2011, 17(6): 1090-1099.[7]Tang X, Xie X, Wang X, et al. The Combination of piR823 and eukaryotic initiation factor 3 B (EIF3B) activates hepatic stellate cells via upregulating TGFβ1 in liver fibrogenesis\[J\]. Med Sci Monit, 2018, 24: 9151-9165.[8]Phay M, Kim HH, Yoo S. Analysis of piRNAlike small noncoding RNAs present in axons of adult sensory neurons\[J\]. Mol Neurobiol, 2018, 55(1): 483-494.[9]Sai Lakshmi S, Agrawal S. piRNABank: a web resource on classified and clustered Piwiinteracting RNAs\[J\]. Nucleic Acids Res, 2008, 36(Database issue): D173-177.[10]Cheng J, Deng H, Xiao B, et al. piR823, a novel noncoding small RNA, demonstrates in vitro and in vivo tumor suppressive activity in human gastric cancer cells\[J\]. Cancer Lett, 2012, 315(1): 12-17.[11]Iliev R, Fedorko M, Machackova T, et al. Expression levels of PIWIinteracting RNA, piR823, are deregulated in tumor tissue, blood serum and urine of patients with renal cell carcinoma\[J\]. Anticancer Res, 2016, 36(12): 6419-6423.[12]Li H, Ruan XZ, Powis SH, et al. EPA and DHA reduce LPSinduced inflammation responses in HK2 cells: evidence for a PPARγdependent mechanism\[J\]. Kidney Int, 2005, 67(3): 867-874.[13]Li D, Luo Y, Gao Y, et al. piR651 promotes tumor formation in nonsmall cell lung carcinoma through the upregulation of cyclin D1 and CDK4\[J\]. Int J Mol Med, 2016, 38(3): 927-936.[14]Cordeiro A, Navarro A, Gaya A, et al. PiwiRNA651 as marker of treatment response and survival in classical Hodgkin lymphoma\[J\]. Oncotarget, 2016, 7(29): 46002-46013.15]Law PT, Qin H, Ching AK, et al. Deep sequencing of small RNA transcriptome reveals novel noncoding RNAs in hepatocellular carcinoma\[J\].J Hepatol,2013,58(6): 1165-1173.[16]Chu H, Hui G, Yuan L, et al. Identification of novel piRNAs in bladder cancer\[J\].Cancer Lett,2015,356(2): 561-567.[17]Vella S, Gallo A, Lo Nigro A, et al. PIWIinteracting RNA (piRNA) signatures in human cardiac progenitor cells\[J\]. Int J Biochem Cell Biol, 2016, 76: 1-11.[18]Lucchinetti E, Feng J, Silva R, et al. Inhibition of LINE1 expression in the heart decreases ischemic damage by activation of Akt/PKB signaling\[J\]. Physiol Genomics, 2006, 25(2): 314-324.[19]Roovers EF, Rosenkranz D, Mahdipour M, et al. Piwi proteins and piRNAs in mammalian oocytes and early embryos\[J\]. Cell Rep, 2015, 10(12): 2069-2082.[20]Ng KW, Anderson C, Marshall EA, et al. Piwiinteracting RNAs in cancer: emerging functions and clinical utility\[J\]. Mol Cancer, 2016, 15: 5.[21]董继泉,何坚,柳维林.芍药苷对大鼠颈椎间盘纤维环细胞炎症模型IL1β、IL6和TNFα表达的影响\[J\].亚太传统医药,2018,14(6):8-12.