[1]程新潮,曹瑾,杨洁,等.LncRNA NEAT1调控miR-505-3p/VEGFA对碱烧伤大鼠角膜新生血管的影响[J].眼科新进展,2023,43(11):863-868.[doi:10.13389/j.cnki.rao.2023.0173]
 CHENG Xinchao,CAO Jin,YANG Jie,et al.Effect of long non-coding RNA nuclear paraspeckle assembly transcript 1 on corneal neovascularization in alkali-burned rats by regulating the microRNA-505-3p/vascular endothelial growth factor A[J].Recent Advances in Ophthalmology,2023,43(11):863-868.[doi:10.13389/j.cnki.rao.2023.0173]
点击复制

LncRNA NEAT1调控miR-505-3p/VEGFA对碱烧伤大鼠角膜新生血管的影响/HTML
分享到:

《眼科新进展》[ISSN:1003-5141/CN:41-1105/R]

卷:
43卷
期数:
2023年11期
页码:
863-868
栏目:
实验研究
出版日期:
2023-11-05

文章信息/Info

Title:
Effect of long non-coding RNA nuclear paraspeckle assembly transcript 1 on corneal neovascularization in alkali-burned rats by regulating the microRNA-505-3p/vascular endothelial growth factor A
作者:
程新潮曹瑾杨洁吕旭东
437100 湖北省咸宁市,咸宁市中心医院眼科
Author(s):
CHENG XinchaoCAO JinYANG JieL? Xudong
Department of Ophthalmology,Xianning Central Hospital,Xianning 437100,Hubei Province,China
关键词:
碱烧伤角膜新生血管长链非编码RNA核旁斑组装转录本1微小RNA-505-3p血管内皮生长因子A
Keywords:
alkali burn corneal neovascularization long non-coding RNA nuclear paraspeckle assembly transcript 1 microRNA-505-3p vascular endothelial growth factor A
分类号:
R772.2
DOI:
10.13389/j.cnki.rao.2023.0173
文献标志码:
A
摘要:
目的 探讨长链非编码RNA(LncRNA)核旁斑组装转录本1(NEAT1)调控微小RNA-505-3p(miR-505-3p)/血管内皮生长因子A(VEGFA)轴对碱烧伤大鼠角膜新生血管生成的影响及其作用机制。
方法 144只SD大鼠随机分为对照组、模型组、sh-NC组、sh-NEAT1组、sh-NEAT1+antagomir-NC组和sh-NEAT1+miR-505-3p antagomir组,每组24只。除对照组外,其余组大鼠均建立碱烧伤模型。观察大鼠角膜新生血管情况,并计算角膜新生血管面积;实时荧光定量PCR(qRT-PCR)检测大鼠角膜中LncRNA NEAT1、miR-505-3p、VEGFA mRNA表达;苏木素-伊红(HE)染色观察大鼠角膜病理形态学改变;免疫组织化学染色、Western blot检测大鼠角膜中VEGFA、CD31蛋白表达;双荧光素酶报告基因实验验证miR-505-3p与LncRNA NEAT1、VEGFA的靶向关系。
结果 与对照组比较,模型组大鼠角膜新生血管面积增加,LncRNA NEAT1、VEGFA mRNA相对表达水平以及VEGFA、CD31蛋白表达水平均升高,miR-505-3p相对表达水平降低(均为P<0.05),角膜组织存在炎症细胞浸润、上皮细胞缺损等病理学损伤;与sh-NC组比较,sh-NEAT1组大鼠角膜新生血管面积减少,LncRNA NEAT1、VEGFA mRNA相对表达水平以及VEGFA、CD31蛋白表达水平均降低,miR-505-3p相对表达水平升高(均为P<0.05),角膜组织病理学损伤有所改善;与sh-NEAT1+antagomir-NC组比较,sh-NEAT1+miR-505-3p antagomir组大鼠角膜新生血管面积增加,VEGFA mRNA相对表达水平以及VEGFA、CD31蛋白表达水平均升高,miR-505-3p相对表达水平降低(均为P<0.05),角膜组织病理学损伤加重。经验证,大鼠角膜上皮细胞中miR-505-3p与LncRNA NEAT1、VEGFA均存在靶向关系。
结论 干扰LncRNA NEAT1可能通过靶向上调miR-505-3p并下调VEGFA表达抑制碱烧伤大鼠角膜新生血管生成。
Abstract:
Objective To investigate the effect of long non-coding RNA (LncRNA) nuclear paraspeckle assembly transcript 1 (NEAT1) on corneal neovascularization in alkali-burned rats by regulating the microRNA-505-3p (miR-505-3p)/vascular endothelial growth factor A (VEGFA) axis.
Methods A total of 144 SD rats were randomly divided into the control group, model group, sh-NC group, sh-NEAT1 group, sh-NEAT1+antagomir-NC group, and sh-NEAT1+miR-505-3p antagomir group, with 24 rats in each group. Except for the control group, alkali-burn rat models were established in the rest groups. Corneal neovascularization was observed, and its area was measured. The mRNA levels of LncRNA NEAT1, miR-505-3p and VEGFA in the rat cornea were detected by quantitative real-time polymerase chain reaction. The pathomorphological changes in the rat cornea were observed by hematoxylin-eosin staining. The expression levels of VEGFA and CD31 proteins in the rat cornea were measured by immunohistochemical staining and Western blot. The targeting relationship between miR-505-3p and LncRNA NEAT1, VEGFA was verified by the dual luciferase reporter gene assay.
Results Compared with the control group, the corneal neovascularization area and the relative expression levels of LncRNA NEAT1 and VEGFA mRNAs as well as VEGFA and CD31 proteins in the model group increased, while the relative expression level of miR-505-3p decreased (all P<0.05), and pathological damages such as inflammatory cell infiltration and epithelial cell defects existed in corneal tissues. Compared with the sh-NC group, the corneal neovascularization area and the relative expression levels of LncRNA NEAT1 and VEGFA mRNAs as well as VEGFA and CD31 proteins in the sh-NEAT1 group decreased, while the relative expression level of miR-505-3p increased (all P<0.05), and the corneal histopathological damages improved. Compared with the sh-NEAT1+antagomir-NC group, the corneal neovascularization area and the relative expression levels of VEGFA mRNA, VEGFA protein and CD31 protein in the sh-NEAT1+miR-505-3p antagomir group increased, while the relative expression level of miR-505-3p decreased (all P<0.05), and the corneal histopathological damages were aggravated. It was verified that there was a targeting relationship between miR-505-3p and LncRNA NEAT1, miR-505-3p and VEGFA in rat corneal epithelial cells.
Conclusion Interfering with LncRNA NEAT1 may inhibit corneal neovascularization in alkali-burned rats by up-regulating the miR-505-3p expression and down-regulating the VEGFA expression.

参考文献/References:

[1] NICHOLAS M P,MYSORE N.Corneal neovascularization[J].Exp Eye Res,2021,202:108363.
[2] CURSIEFEN C,HOS D.Cutting edge:novel treatment options targeting corneal neovascularization to improve high-risk corneal graft survival[J].Cornea,2021,40(12):1512-1518.
[3] HU X,XING H,WANG X,DU L,HUANG Y,HAO Y,et al.Knockdown of LncRNA SNHG1 suppresses corneal angiogenesis by the regulation of miR-195-5p/VEGF-A[J].J Ophthalmol,2021,2021:6646512.
[4] QIAN J,YU J,ZHU X,LIANG S.MiR-335 promotes corneal neovascularization by targeting EGFR[J].BMC Ophthalmol,2022,22(1):267.
[5] BAI Y H,LV Y,WANG W Q,SUN G L,ZHANG H H.LncRNA NEAT1 promotes inflammatory response and induces corneal neovascularization[J].J Mol Endocrinol,2018,61(4):231-239.
[6] LIU S,GAO J,CHEN J.Knockdown of LncRNA TUG1 suppresses corneal angiogenesis through regulating miR-505-3p/VEGFA[J].Microvasc Res,2021,138:104233.
[7] 石琛,肖启国,王智,刘翀,张亚兰,刘明之.米诺环素对碱烧伤大鼠角膜新生血管生成的影响及其作用机制[J].眼科新进展,2021,41(2):136-139.
SHI C,XIAO Q G,WANG Z,LIU C,ZHANG Y L,LIU M Z.Effect of minocycline on corneal neovascularization after alkali burns and its mechanisms[J].Rec Adv Ophthalmol,2021,41(2):136-139.
[8] 赵凌军,杨潇远,王新茹,李季.LncRNA-MIAT靶向miR-150-5p对病理性血管化角膜及VEGF、MMP-9的影响[J].眼科新进展,2022,42(1):20-24.
ZHAO L J,YANG X Y,WANG X R,LI J.Effect of LncRNA-MIAT targeting miR-150-5p on pathological vascularized cornea,vascular endothelial growth factor,and matrix metalloproteinase-9[J].Rec Adv Ophthalmol,2022,42(1):20-24.
[9] CHEN M,BAO L,ZHAO M,CAO J,ZHENG H.Progress in research on the role of FGF in the formation and treatment of corneal neovascularization[J].Front Pharmacol,2020,11:111.
[10] SHEN T,WU Y,CAI W,JIN H,YU D,YANG Q,et al.LncRNA Meg3 knockdown reduces corneal neovascularization and VEGF-induced vascular endothelial angiogenesis via SDF-1/CXCR4 and Smad2/3 pathway[J].Exp Eye Res,2022,222:109166.
[11] SUN B,DING Y,JIN X,XU S,ZHANG H.Long non-coding RNA H19 promotes corneal neovascularization by targeting microRNA-29c[J].Biosci Rep,2019,39(5):BSR20182394.
[12] MENG Y,HAO Z,ZHANG H,BAI P,GUO W,TIAN X,et al.LncRNA NEAT1/miR-495-3p regulates angiogenesis in burn sepsis through the TGF-β1 and SMAD signaling pathways[J].Immun Inflamm Dis,2023,11(1):e758.
[13] GUO J,YUAN Q,FANG Y,LIAO J,ZHANG Z.Long non-coding RNA NEAT1 promotes angiogenesis in hepatoma carcinoma via the miR-125a-5p/VEGF pathway[J].Open Life Sci,2022,17(1):1229-1239.
[14] LYU N,ZHAO Y,XIANG J,FAN X,HUANG C,SUN X,et al.Inhibiting corneal neovascularization by sustainably releasing anti-VEGF and anti-inflammation drugs from silica-thermogel nanohybrids[J].Mater Sci Eng C Mater Biol Appl,2021,128:112274.
[15] YA AR M,AKMAK H,DNDAR S,RENAY BOYACO GˇLU S,AL KAN M,ERGIN K.The role of microRNAs in corneal neovascularization and its relation to VEGF[J].Cutan Ocul Toxicol,2020,39(4):341-347.
[16] ELENK M,YILDIRIM H,TEKTEMUR A,BALBABA M,ERDA Gˇ M.Effect of topical motesanib in experimental corneal neovascularization model[J].Int Ophthalmol,2023,43(8):2989-2997.
[17] XU Z,ZHANG D,ZHANG Z,LUO W,SHI R,YAO J,et al.MicroRNA-505,suppressed by oncogenic long non-coding RNA LINC01448,acts as a novel suppressor of glycolysis and tumor progression through inhibiting HK2 expression in pancreatic cancer[J].Front Cell Dev Biol,2020,8:625056.
[18] XIE X,WEN Q,YANG X,CHEN W,LIU Y,LIU W,et al.H3K27ac-activated lncRNA KTN1-AS1 aggravates tumor progression by miR-505-3p/ZNF326 axis in ovarian cancer[J].Ann Transl Med,2022,10(10):599.

相似文献/References:

[1]王军花 高桂平.Avastin不同给药途径对兔角膜新生血管及超微结构的影响[J].眼科新进展,2012,32(5):000.
[2]程文武 江萍 席祖莲 张汉武 訾世莉 聂军 董彩虹.蛹虫草提取物抑制大鼠角膜新生血管的实验研究[J].眼科新进展,2012,32(5):000.
[3]赵伟 周瑾 郭梦翔 项道满.地塞米松对碱烧伤后大鼠角膜核转录因子-κB活化的影响[J].眼科新进展,2013,33(7):000.
[4]付馨余 邹文进 黄明汉 赵静博.多西环素对碱烧伤大鼠角膜组织中NF-κB和bcl-2表达的影响[J].眼科新进展,2013,33(4):000.
[5]闵捷 胡丹 孙丽娟 雷润佳 王鹤霏 蔡莉.紫外光核黄素胶原交联对兔角膜碱烧伤作用的实验研究[J].眼科新进展,2013,33(5):000.
[6]叶芬 吴艳 施宇华 黄振平. 羊膜匀浆提取液对大鼠碱烧伤后角膜瘢痕形成的抑制作用[J].眼科新进展,2014,34(3):222.
[7]罗杰,胡琦,史学良,等.As2O3 对兔角膜碱烧伤后IL-1β及VCAM-1表达的影响[J].眼科新进展,2014,34(5):414.[doi:10.13389/j.cnki.rao.2014.0114]
 LUO Jie,HU Qi.SHI Xue-Liang,Ll Dan-Dan,et al.Effects of As2O3 on IL-1β and VCAM-1 expression following corneal alkali burns in rabbits[J].Recent Advances in Ophthalmology,2014,34(11):414.[doi:10.13389/j.cnki.rao.2014.0114]
[8]付馨余,邹文进,喻谦,等.多西环素对碱烧伤大鼠角膜组织中IL-1和TNF-α表达的影响[J].眼科新进展,2014,34(10):915.[doi:10.13389/j.cnki.rao.2014.0253]
[9]付敏,喻谦,付馨余,等. 大鼠角膜碱烧伤后角膜及房水中缺氧诱导因子-1α的表达[J].眼科新进展,2015,35(6):532.[doi:10.13389/j.cnki.rao.2015.0144]
 FU Min,YU Qian,FU Xin-Yu,et al. Expression of HIF-1 in cornea and aqueous humor after corneal alkali burns in rats[J].Recent Advances in Ophthalmology,2015,35(11):532.[doi:10.13389/j.cnki.rao.2015.0144]
[10]徐硕,张红.角膜新生血管药物治疗的最新进展[J].眼科新进展,2015,35(10):989.[doi:10.13389/j.cnki.rao.2015.0271]
 XU Shuo,ZHANG Hong.Recent advances in drug therapy of corneal neovascularization[J].Recent Advances in Ophthalmology,2015,35(11):989.[doi:10.13389/j.cnki.rao.2015.0271]
[11]邹文进 刘祖国 刘曼丽 付馨余 赵静博 王松 黄海.多西环素与地塞米松抑制碱烧伤大鼠角膜新生血管的对比研究[J].眼科新进展,2013,33(8):000.
[12]郝瑞霖,杨炜,张奕霞,等.乙酰半胱氨酸对角膜新生血管形成过程中瘦素和PEDF表达的调节[J].眼科新进展,2014,34(8):718.[doi:10.13389/j.cnki.rao.2014.0196]
 HAO Rui-Lin,YANG Wei,ZHANG Yi-Xia,et al.Regulative effects of acetylcysteine on leptin and PEDF in corneal neovascularization[J].Recent Advances in Ophthalmology,2014,34(11):718.[doi:10.13389/j.cnki.rao.2014.0196]
[13]修立恒,刘洪涛,曾小平. iNOS对兔角膜碱烧伤后新生血管形成的影响[J].眼科新进展,2014,34(9):830.[doi:10.13389/j.cnki.rao.2014.0229]
[14]王军梅,孙艳,周明明,等.兔角膜碱烧伤后角膜基质注射脐带间充质干细胞的疗效[J].眼科新进展,2016,36(7):622.[doi:10.13389/j.cnki.rao.2016.0165]
 WANG Jun-Mei,SUN Yan,ZHOU Ming-Ming,et al.Effects of corneal stromal injection of umbilical cord mesenchymal stem cells after rabbit corneal alkali burn[J].Recent Advances in Ophthalmology,2016,36(11):622.[doi:10.13389/j.cnki.rao.2016.0165]
[15]吴艳,叶芬,黄振平.不同浓度KH902对兔碱烧伤后角膜新生血管的抑制作用[J].眼科新进展,2016,36(8):720.[doi:10.13389/j.cnki.rao.2016.0191]
 WU Yan,YE Fen,HUANG Zhen-Ping.Inhibitive effects of different concentrations of KH902 eye drops on corneal neovascularization after rabbit corneal alkali burn[J].Recent Advances in Ophthalmology,2016,36(11):720.[doi:10.13389/j.cnki.rao.2016.0191]
[16]王群,姜严明,赵杰,等.血管内皮生长因子靶向抗体对大鼠角膜碱烧伤后新生血管抑制作用的研究[J].眼科新进展,2017,37(11):1010.[doi:10.13389/j.cnki.rao.2017.0256]
 WANG Qun,JIANG Yan-Ming,ZHAO Jie,et al.Inhibitory effects of anti-vascular endothelial growth factor (VEGF) antibody MIL60 on alkali-induced corneal angiogenesis in rats[J].Recent Advances in Ophthalmology,2017,37(11):1010.[doi:10.13389/j.cnki.rao.2017.0256]
[17]张慧,单伟.阿柏西普对碱烧伤大鼠角膜新生血管的抑制作用[J].眼科新进展,2020,40(2):120.[doi:10.13389/j.cnki.rao.2020.0029]
 ZHANG Hui,SHAN Wei.Inhibitory effect of Aflibercept on corneal neovascularization in rats with alkali burns[J].Recent Advances in Ophthalmology,2020,40(11):120.[doi:10.13389/j.cnki.rao.2020.0029]
[18]石琛,肖启国,王智,等.米诺环素对碱烧伤大鼠角膜新生血管生成的影响及其作用机制[J].眼科新进展,2021,41(2):136.[doi:10.13389/j.cnki.rao.2021.0028]
 SHI Chen,XIAO Qiguo,WANG Zhi,et al.Effect of minocycline on corneal neovascularization after alkali burns and its mechanisms[J].Recent Advances in Ophthalmology,2021,41(11):136.[doi:10.13389/j.cnki.rao.2021.0028]

备注/Memo

备注/Memo:
湖北省卫生健康委员会面上项目(编号:WJ2019M097);2021年度咸宁市中心医院院级科研项目(编号:2021XYB017)
更新日期/Last Update: 2023-11-05