|
|
|
|
|
The potential role and significance of longchain non-coding RNA in sepsis induced cardiomyopathy |
Zhang Ling, Zhang Hai-dan, Zhao Jing, Xiao Dan-yang, Li Pei-wu |
Department of Emergency Medicine, the Second Hospital of Lanzhou University, Lanzhou 730000, China |
|
|
Abstract Sepsis should be defined as life-threatening organ dysfunction caused by a dysregulated host response to infection. The mortality rate is still high, and the increasing mortality caused by sepsis induced cardiomyopathy (SIC) is a great challenge for emergency and critical care medicine. The “inflammatory waterfalls” are closely related to the “genetic storms” in sepsis. Long chain non-coding RNAs (lncRNAs) have important effects on sepsis and SIC by regulating the inflammatory reactions and immune regulation processes. This article reviews the inflammatory regulation mechanism of lncRNAs in SIC recently.
|
|
Corresponding Authors:
Li Pei-wu, E-mail: wuzi360@126.com
|
|
|
|
[1]Singer M, Deutschman CS, Seymour CW, et al. The third international consensus definitions for sepsis and septic shock (Sepsis-3)[J]. JAMA, 2016, 315(8):801-810.[2]Grandel U, Fink L, Blum A, et al. Endotoxin-induced myocardial tumor necrosis factor-alpha synthesis depresses contractility of isolated rat hearts: evidence for a role of sphingosine and cyclooxygenase-2-derived thromboxane production[J]. Circulation,〖JP〗 2000, 102(22):2758-2764.[3]Zou X, Xu J, Yao S, et al. Endoplasmic reticulum stress-mediated autophagy protects against lipopolysaccharide-induced apoptosis in HL-1 cardiomyocytes[J]. Exp Physiol, 2014, 99(10):1348-1358.[4]Perner A, Cecconi M, Cronhjort M, et al. Expert statement for the management of hypovolemia in sepsis[J]. Intensive Care Med, 2018, 44(6):791-798.[5]Zanotti-Cavazzoni SL, Hollenberg SM. Cardiac dysfunction in severe sepsis and septic shock[J]. Curr Opin Crit Care, 2009, 15(5):392-397.[6]Celes MR, Prado CM, Rossi MA. Sepsis: going to the heart of the matter[J]. Pathobiology, 2013, 80(2):70-86.[7]Court O, Kumar A, Parrillo JE, et al. Clinical review: Myocardial depression in sepsis and septic shock[J]. Crit Care, 2002, 6(6):500-508.[8]Flierl MA, Rittirsch D, Huber-Lang MS, et al. Molecular events in the cardiomyopathy of sepsis[J]. Mol Med, 2008, 14(5-6):327-336.[9]Scarabelli T, Stephanou A, Rayment N, et al. Apoptosis of endothelial cells precedes myocyte cell apoptosis in ischemia/reperfusion injury[J]. Circulation, 2001, 104(3):253-256.[10]Lush CW, Kvietys PR. Microvascular dysfunction in sepsis[J]. Microcirculation, 2000, 7(2):83-101.[11]Salmon AH, Satchell SC. Endothelial glycocalyx dysfunction in disease: albuminuria and increased microvascular permeability[J]. J Pathol, 2012, 226(4):562-574.[12]Heward JA, Lindsay MA. Long non-coding RNAs in the regulation of the immune response[J]. Trends Immunol, 2014, 35(9):408-419.[13]Hackermuller J, Reiche K, Otto C, et al. Cell cycle, oncogenic and tumor suppressor pathways regulate numerous long and macro non-protein-coding RNAs[J]. Genome Biol, 2014, 15(3):R48.[14]Kung JT, Colognori D, Lee JT. Long noncoding RNAs: past, present, and future[J]. Genetics, 2013, 193(3):651-669.[15]Spizzo R, Almeida MI, Colombatti A, et al. Long non-coding RNAs and cancer: a new frontier of translational research [J]. Oncogene, 2012, 31(43):4577-4587.[16]Congrains A, Kamide K, Oguro R, et al. Genetic variants at the 9p21 locus contribute to atherosclerosis through modulation of ANRIL and CDKN2A/B[J]. Atherosclerosis, 2012, 220(2):449-455.[17]Johnson R. Long non-coding RNAs in Huntington′s disease neurodegeneration[J]. Neurobiol Dis, 2012, 46(2):245-254.[18]Carpenter S, Aiello D, Atianand MK, et al. A long noncoding RNA mediates both activation and repression of immune response genes[J]. Science, 2013, 341(6147):789-792.[19]Rapicavoli NA, Qu K, Zhang J, et al. A mammalian pseudogene lncRNA at the interface of inflammation and anti-inflammatory therapeutics[J].Elife, 2013, 2:e00 762.[20]Li Z, Chao TC, Chang KY, et al. The long noncoding RNA THRIL regulates TNFalpha expression through its interaction with hnRNPL[J]. Proc Natl Acad Sci U S A, 2014, 111(3):1002-1007.[21]Xiao W, Mindrinos MN, Seok J, et al. A genomic storm in critically injured humans[J]. J Exp Med, 2011, 208(13):2581-2590.[22]Hawiger J. Heartfelt sepsis: microvascular injury due to genomic storm[J]. Kardiol Pol, 2018, 76(8):1203-1216.[23]Pellegrina D, Severino P, Barbeiro HV, et al. insights into the function of long noncoding RNAs in sepsis revealed by gene co-expression network analysis[J].Noncoding RNA, 2017, 3(1):E5.[24]Ho J, Chan H, Wong SH, et al. The involvement of regulatory non-coding RNAs in sepsis: a systematic review[J]. Crit Care, 2016, 20(1):383.[25]Mao AP, Shen J, Zuo Z. Expression and regulation of long noncoding RNAs in TLR4 signaling in mouse macrophages[J]. BMC Genomics, 2015, 16:45.[26]Zhou J, Chaudhry H, Zhong Y, et al. Dysregulation in microRNA expression in peripheral blood mononuclear cells of sepsis patients is associated with immunopathology[J]. Cytokine, 2015, 71(1):89-100.[27]Wang W, Lou C, Gao J, et al. LncRNA SNHG16 reverses the effects of miR-15a/16 on LPS-induced inflammatory pathway[J]. Biomed Pharmacother, 2018, 106:1661-1667.[28]Wu H, Liu J, Li W, et al. LncRNA-HOTAIR promotes TNF-alpha production in cardiomyocytes of LPS-induced sepsis mice by activating NF-kappaB pathway[J]. Biochem Biophys Res Commun, 2016, 471(1):240-246.[29]Xue WL, Bai X, Zhang L. rhTNFR:Fc increases Nrf2 expression via miR-27a mediation to protect myocardium against sepsis injury[J]. Biochem Biophys Res Commun, 2015, 464(3):855-861.[30]Wang H, Bei Y, Shen S, et al. miR-21-3p controls sepsis-associated cardiac dysfunction via regulating SORBS2[J]. J Mol Cell Cardiol, 2016, 94:43-53.[31]Wu Y, Huang C, Meng X, et al. Long Noncoding RNA MALAT1: Insights into its Biogenesis and Implications in Human Disease[J]. Curr Pharm Des, 2015, 21(34):5017-5028.[32]Guo F, Li Y, Liu Y, et al. Inhibition of metastasis-associated lung adenocarcinoma transcript 1 in CaSki human cervical cancer cells suppresses cell proliferation and invasion[J]. Acta Biochim Biophys Sin (Shanghai), 2010, 42(3):224-229.[33]Gutschner T, Hammerle M, Diederichs S. MALAT1-a paradigm for long noncoding RNA function in cancer[J]. J Mol Med (Berl), 2013, 91(7):791-801.[34]Zhao G, Su Z, Song D, et al. The long noncoding RNA MALAT1 regulates the lipopolysaccharide-induced inflammatory response through its interaction with NF-kappaB[J]. FEBS Lett, 2016, 590(17):2884-2895.[35]周佾龙,杨韶华,张弛,等.长链非编码基因MALAT1对LPS诱导的脓毒症大鼠免疫反应的调节作用及机制[J].四川大学学报(医学版), 2018, 49(6):865-870,875.[36]Zhuang YT, Xu DY, Wang GY, et al. IL-6 induced lncRNA MALAT1 enhances TNF-alpha expression in LPS-induced septic cardiomyocytes via activation of SAA3[J]. Eur Rev Med Pharmacol Sci, 2017, 21(2):302-309.[37]Yu Z, Rayile A, Zhang X, et al. Ulinastatin protects against lipopolysaccharide-induced cardiac microvascular endothelial cell dysfunction via downregulation of lncRNA MALAT1 and EZH2 in sepsis[J]. Int J Mol Med, 2017, 39(5):1269-1276.[38]Chen H, Wang X, Yan X, et al. LncRNA MALAT1 regulates sepsis-induced cardiac inflammation and dysfunction via interaction with miR-125b and p38 MAPK/NFkappaB[J].Int Immunopharmacol, 2018, 55:69-76.[39]Rinn JL, Kertesz M, Wang JK, et al. Functional demarcation of active and silent chromatin domains in human HOX loci by noncoding RNAs[J]. Cell, 2007, 129(7):1311-1323.[40]Shen J, Zhang J, Jiang X, et al. LncRNA HOX transcript antisense RNA accelerated kidney injury induced by urine-derived sepsis through the miR-22/high mobility group box 1 pathway[J]. Life Sci, 2018, 210:185-191.[41]Paraskevopoulou MD, Georgakilas G, Kostoulas N, et al. DIANA-LncBase: experimentally verified and computationally predicted microRNA targets on long non-coding RNAs[J]. Nucleic Acids Res, 2013, 41(Database issue):D239-245.[42]Carrion K, Dyo J, Patel V, et al. The long non-coding HOTAIR is modulated by cyclic stretch and WNT/beta-CATENIN in human aortic valve cells and is a novel repressor of calcification genes[J].PloS One, 2014, 9(5):e96 577.[43]Zhou X, Ye F, Yin C, et al. The Interaction Between MiR-141 and lncRNA-H19 in Regulating Cell Proliferation and Migration in Gastric Cancer[J]. Cell Physiol Biochem, 2015, 36(4):1440-1452.[44]Li H, Yu B, Li J, et al. Overexpression of lncRNA H19 enhancescarcinogenesis and metastasis of gastric cancer[J]. Oncotarget, 2014, 5(8):2318-2329.[45]Zhu N, Feng X, He C, et al. Defective macrophage function in aquaporin-3 deficiency[J]. FASEB J, 2011, 25(12):4233-4239.[46]Fang Y, Hu J, Wang Z, et al. LncRNA H19 functions as an quaporin 1 competitive endogenous RNA to regulate microRNA-874 expression in LPS sepsis[J]. Biomed Pharmacother, 2018, 105:1183-1191.[47]Morchikh M, Cribier A, Raffel R, et al. HEXIM1 and NEAT1 Long Non-coding RNA Form a Multi-subunit Complex that Regulates DNA-Mediated Innate Immune Response[J]. Mol Cell, 2017, 67(3):387-399.[48]Huang S, Qian K, Zhu Y, et al. Diagnostic Value of the lncRNA NEAT1 in peripheral blood mononuclear cells of patients with sepsis[J]. Dis Markers, 2017, 2017:7 962 836.[49]Huang Q, Huang C, Luo Y, et al. Circulating lncRNA NEAT1 correlates with increased risk, elevated severity and unfavorable prognosis in sepsis patients[J]. Am J Emerg Med, 2018, 36(9):1659-1663. |
|
|
|