Wenhao JIANG, Hong YI, Rui PENG, et al. LncRNA Gm4419 regulates inflammatory cytokines expression via NF-κB signaling pathway in mesangial cells under high glucose condition[J]. Journal of Third Military Medical University, 2018, 40(7): 577-583.
DOI:
Wenhao JIANG, Hong YI, Rui PENG, et al. LncRNA Gm4419 regulates inflammatory cytokines expression via NF-κB signaling pathway in mesangial cells under high glucose condition[J]. Journal of Third Military Medical University, 2018, 40(7): 577-583. DOI: 10.16016/j.1000-5404.201711099.
LncRNA Gm4419 regulates inflammatory cytokines expression via NF-κB signaling pathway in mesangial cells under high glucose condition
摘要
目的
2
探讨长链非编码RNA Gm4419通过核转录因子-kappa B (nuclear factor-kappa B
To investigate the mechanism of long non-coding RNA (lncRNA) Gm4419 regulating the expression of inflammatory cytokines in glomerular mesangial cells under high glucose condition
via
mediating nuclear factor-kappa B (NF-κB) signaling pathway.
Methods
2
The subcellular distribution of Gm4419 and expression of NF-κB subunits p50 and p65 were detected by RT-qPCR in mouse glomerular mesangial cells (MCs) under high or low glucose condition. Moreover
RT-qPCR and immunofluorescence assay were used to measure the expression of MCP-1 and TNF-α when Gm4419 was up-or down-regulated. Additionally
bioinformatics analysis was carried out to predict the relationship between Gm4419 and NF-κB. Western blot assay was used to determine the expression of p50 and p65 in the nucleus of MCs
and the effect of specific p50 inhibitor on the expression of MCP-1 was studied in MCs with Gm4419 over-expression.
Results
2
The expression of Gm4419 was significantly higher in MCs under high glucose condition than those under low condition (
P
<
0.05)
and Gm4419 mainly located in the cytoplasm. The expression levels of MCP-1 and TNF-α were significantly increased in the low glucose group when Gm4419 was over-expressed (
P
<
0.01)
while the levels were decreased in high glucose group when Gm4419 was silenced (
P
<
0.01). Moreover
the binding sites of Gm4419 and p
50 and p65 were predicted
and over-expression of Gm4419 resulted in the increases in p50 and p65 expression levels and enhancement in NF-κB activity (
P
<
0.01). However
silencing Gm4419 induced opposite effects (
P
<
0.01). Additionally
specific p50 inhibitor could block the up-reguation of MCP-1 induced by Gm4419 over-expression.
Conclusion
2
Gm4419 may play an important role in the enhanced expression of inflammatory cytokines in mesangial cells under high glucose condition
and its mechanism may be related to the NF-κB signaling pathway.
关键词
Keywords
references
ATKINS R C, ZIMMET P. Diabetic kidney disease: act now or pay later[J]. Kidney Blood Press Res, 2010, 33(1): 48-51. DOI: 10.1159/000285849.
KOLSET S O, REINHOLT F P, JENSSSEN T. Diabetic nephropathy and extracellular matrix[J]. J Histochem Cytochem, 2012, 60(12):976-986. DOI: 10.1369/ 0022155412465073.
MASON R M, WAHAB N A. Extracellular matrix metabolism in diabetic nephropathy[J]. J Am Soc Nephrol, 2003, 14(5): 1358-1373. DOI:10.1097/01.asn.0000065640.77499.d7.
NAVARRO-GONZÁLEZ J F, MORA-FERNÁNDEZ C, MUROS DE FUENTES M, et al . Inflammatory molecules and pathways in the pathogenesis of diabetic nephropathy[J ] . Nat Rev Nephrol, 2011, 7(6):327-340. DOI: 10.1038/nrneph.2011.51.
YI H, PENG R, SUN Y, et al . Effect of lncRNA-Gm4419 on proliferation and fibrosis in high glucose-inducedglomerulus mesangial cells[J ] . J Third Mil Med Univ, 2017, 39(3): 216-222. DOI: 10.16016 /j.1000-5404.201608102.
SUN Y M, SU Y, LI J, et al . Recent advances in understanding the biochemical and molecular mechanism of diabetic nephropathy[J ] . Biochem Biophys Res Commun, 2013, 433(4):359-361. DOI: 10.1016/j.bbrc.2013.02.120.
PICHLER R, AFKARIAN M, DIETER B P, et al . Immunity and inflammation in diabetic kidney disease: translating mechanisms to biomarkers and treatment targets[J ] . Am J Physiol Renal Physiol, 2017, 312(4): F716-F731. DOI: 10.1152/ajprenal.00314.2016.
HALLER H, BERTRAM A, NADROWITZ F, et al . Monocyte chemoattractant protein-1 and the kidney[J ] . Curr Opin Nephrol Hypertens, 2016, 25(1):42-49. DOI: 10.1097/MNH.0000000000000186.
DURAN-SALGADO M B, RUBIO-GUERRA A F. Diabetic nephropathy and inflammation[J]. World J Diabetes, 2014, 5(3): 393-398. DOI: 10.4239/wjd.v5.i3.393.
SUN Y, PENG R, PENG H, et al . miR-451 suppresses the NF-kappaB-mediated proinflammatory molecules expression through inhibiting LMP7 in diabetic nephropathy[J ] . Mol Cell Endocrinol, 2016, 433:75-86. DOI: 10.1016/j.mce.2016.06.004.
ZHANG E B, KONG R, YIN D D, et al . Long noncoding RNA ANRIL indicates a poor prognosis of gastric cancer and promotes tumor growth by epigenetically silencing of miR-99a/miR-449a[J ] . Oncotarget, 2014, 5(8): 2276-2292.DOI: 10.18632/oncotarget.1902.
YOU J, ZHANG Y, LIU B, et al . MicroRNA-449a inhibits cell growth in lung cancer and regulates long noncoding RNA nuclear enriched abundant transcript 1[J ] . Indian J Cancer, 2014, 51(Suppl 3): e77-e81. DOI: 10.4103/0019-509X.154055.
EMMRICH S, STRELTSOV A, SCHMIDT F, et al .LincRNAs MONC and MIR100HG act as oncogenes in acute megakaryoblastic leukemia[J ] . Mol Cancer, 2014, 13: 171. DOI: 10.1186/1476-4598-13-171.
HU M, WANG R, LI X, et al . LncRNA MALAT1 is dysregulated in diabetic nephropathy and involved in high glucose-induced podocyte injury via its interplay with β-catenin[J ] . J Cell Mol Med, 2017, 21(11):2732-2747. DOI: 10.1111/jcmm.13189..
LONG J, BADAL S S, YE Z, et al . Long noncoding RNA Tug1 regulates mitochondrial bioenergetics in diabetic nephropathy[J ] . J Clin Invest, 2016, 126(11): 4205-4218. DOI: 10.1172/JCI87927.
LI X, ZHOU J, HUANG K. Inhibition of the lncRNA mirt1 attenuates acute myocardial infarction by suppressing NF-κB activation[J]. Cell Physiol Biochem, 2017, 42(3):1153-1164. DOI: 10.1159/000478870.
SUN D, YU Z, FANG X, et al . LncRNA GAS5 inhibits microglial M2 polarization and exacerbates demyelination[J ] . EMBO Rep, 2017, 18(10):1801-1816. DOI: 10.15252/embr.201643668.
TSAI M C, MANOR O, WAN Y, et al . Long noncoding RNA as modular scaffold of histone modification complexes[J ] . Science, 2010, 329(5992):689-693. DOI: 10.1126/science.1192002.
MARTIANOV I, RAMADASS A, SERRA BARROS A, et al . Repression of the human dihydrofolate reductase gene by a non-coding interfering transcript[J ] .Nature, 2007, 445(7128):666-670. DOI: 10.1038/nature 05519.
BAKER R G, HAYDEN M S, GHOSH S. NF-κB, inflammation, and metabolic disease[J]. Cell Metab, 2011, 13(1): 11-22. DOI: 10.1016/j.cmet.2010.12.008.
WANG S, YANG Z, XIONG F, et al . Betulinic acid ameliorates exp erimental diabetic-induced renal inflammation and fibrosis via inhibiting the activation of NF-κB signaling pathway[J ] . Mol Cell Endocrinol, 2016, 434:135-143. DOI: 10.1016/j.mce.2016.06.019..
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