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Caspase-1对氧诱导视网膜病变中小胶质细胞参与视网膜新生血管生成的促进作用及其机制 被引量:4
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作者 胡至察 王雨生 +1 位作者 徐文芹 张自峰 《国际眼科杂志》 CAS 北大核心 2018年第4期615-620,共6页
目的:探讨Caspase-1对小鼠氧诱导视网膜病变(oxygen-induced retinopathy,OIR)中小胶质细胞参与视网膜新生血管生成的作用及其机制。方法:随机将12只7日龄(P7)C57BL/6J小鼠分为正常组、OIR组和OIR+VX-765组,正常组在正常氧环境中饲养,... 目的:探讨Caspase-1对小鼠氧诱导视网膜病变(oxygen-induced retinopathy,OIR)中小胶质细胞参与视网膜新生血管生成的作用及其机制。方法:随机将12只7日龄(P7)C57BL/6J小鼠分为正常组、OIR组和OIR+VX-765组,正常组在正常氧环境中饲养,其余两组构建OIR模型;P12~P16,OIR+VX-765组和OIR组分别每天腹腔注射Caspase-1抑制剂VX-765(4mg/kg)和等量0.4%聚乙二醇(VX-765溶剂);于P17制作视网膜铺片行Lectin染色,比较三组间视网膜无血管区和新生血管区面积的大小;采用免疫荧光染色法观察视网膜组织中Caspase-1的表达和活化小胶质细胞的分布。培养小胶质细胞BV-2细胞分为对照组、缺氧组及抑制剂组,抑制剂组和缺氧组分别经VX-765和0.4%聚乙二醇预处理3h后,缺氧条件下培养24h;对照组常规培养相同时间。通过Western blot检测Caspase-1、p20(Caspase-1活化形式)、IL-1β和VEGF的蛋白表达变化;用各组BV-2细胞培养上清液作为条件培养基,刺激培养血管内皮细胞RF/6A,进行管腔形成和细胞迁移实验,并比较各组间的差异。结果:P17正常组小鼠视网膜血管化完全,未见明显无血管区及视网膜新生血管;OIR组视网膜无血管区和新生血管面积百分比分别为16.58%±1.14%、4.00%±0.41%;OIR+VX-765组两者明显减少,分别为12.23%±1.02%和2.16%±0.52%(P<0.01)。免疫荧光染色结果显示,Caspase-1在正常小鼠视网膜组织中表达较弱,在OIR小鼠中主要在神经节细胞层和内丛状层有明显的阳性表达,并与活化的小胶质细胞有明确的共定位。Western blot检测结果显示,缺氧处理的培养小胶质细胞BV-2中Caspase-1、p20、IL-1β和VEGF蛋白表达明显提高,而Caspase-1抑制剂则可明显下调p20、IL-1β和VEGF的蛋白表达水平(P<0.05)。管腔形成和细胞迁移实验结果显示,RF/6A细胞经缺氧组BV-2培养上清液处理后,管腔形成长度和细胞迁移数目分别为271±12和347±34个,而加入抑制剂后,二者明显减少,分别为171±22和212±27个(P<0.05)。结论:在小鼠OIR中,Caspase-1能够调节小胶质细胞促进视网膜新生血管的生成,其作用机制可能与Caspase-1活化小胶质细胞中其下游炎性效应分子IL-1β。 展开更多
关键词 CASPASE-1 小胶质细胞 视网膜新生血管 氧诱导视网膜病变 早产儿视网膜病变
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Infrared autofluorescence, short-wave autofluorescence and spectral-domain optical coherence tomography of optic disk melanocytomas 被引量:3
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作者 Peng Zhang Yan-Nian Hui +4 位作者 wen-qin xu Zi-Feng Zhang Hai-Yan Wang Dong-Jie Sun Yu-Sheng Wang 《International Journal of Ophthalmology(English edition)》 SCIE CAS 2016年第5期713-716,共4页
AIM: To investigate the findings of infrared fundus autofluorescence(IR-AF) and spectral-domain optical coherence tomography(SD-OCT) in eyes with optic disc melanocytoma(ODM).· METHODS: IR-AF findings and... AIM: To investigate the findings of infrared fundus autofluorescence(IR-AF) and spectral-domain optical coherence tomography(SD-OCT) in eyes with optic disc melanocytoma(ODM).· METHODS: IR-AF findings and those of other ophthalmologic imaging examinations, including short-wave autofluorescence(SW-AF), fluorescein angiography(FA), fundus color photography, and SD-OCT of 8 eyes of 8 consecutive cases with ODM were assessed.·RESULTS: The ODMs in all cases(100%) presented similar IR-AF, SW-AF, and FA findings. On IR-AF images, ODMs showed outstanding hyper-AF with well-defined outline. On SW-AF images, the area of ODMs presented as hypo-AF. FA images revealed the leaking retinal telangiectasia on the surface of the ODMs. On SDOCT images in 8 cases(100%), the ODMs were sloped with highly reflective surface, which were disorganized retina and optic nerve layers. In 7 cases(87.5%), peripapillary choroids were involved. The melanocytomas of 8 cases(100%) presented as optically empty spaces. Vitreous seeds were found in one case(12.5%).· CONCLUSION: IR-AF imaging may provide a new modality to evaluate the pathologic features of ODMs,and together with SW-AF imaging, offers a new tool to study biological characteristics associated with ODMs.SD-OCT is a valuable tool in delimitating the tumor extension and providing morphological information about the adjacent retinal tissue. 展开更多
关键词 MELANOCYTOMA ANGIOGRAPHY AUTOFLUORESCENCE optical coherence tomography
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Effect of integrin α5β1 inhibition on SDF-l/CXCR4-mediated choroidal neovascularization 被引量:2
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作者 Yang Lyu wen-qin xu +3 位作者 Li-Juan Sun Xiao-Yan Pan Jian Zhang Yu-Sheng Wang 《International Journal of Ophthalmology(English edition)》 SCIE CAS 2018年第5期726-735,共10页
AIM:To investigate the roles of integrins in choroidal neovascularization(CNV) and their associations with the stromal cell-derived factor-1(SDF-1)/CXCR4 axis.METHODS:CNV lesions were induced in mice using laser... AIM:To investigate the roles of integrins in choroidal neovascularization(CNV) and their associations with the stromal cell-derived factor-1(SDF-1)/CXCR4 axis.METHODS:CNV lesions were induced in mice using laser photocoagulation.After CNV induction,all animals were randomly assigned to:control,SDF-1,SDF-1+age-related macular degeneration(AMD) 3100(CXCR4 inhibitor),and SDF-1+ATN161(integrin α5β1 inhibitor) groups;their effects on CNV progression were observed using hematoxylin eosin(HE) staining,fundus fluorescein angiography(FFA) grading and optical coherence tomography(OCT),and their effects on CXCR4/integrin α5 expression were evaluated using Western blot and double immunofluorescence staining.Hypoxia-exposed endothelial cells(ECs) were used to simulate CNV in vitro,they were treated with SDF-1,combined with CXCR4 siRNA/AMD3100 or ATN161,and expression of integrin α5,cell migration and tube formation were analyzed.RESULTS:Integrin subunit α5 increased at 3^ rd and 7^ th day and decreased at 14 ^th day in CNV mice,with no significant change of β1-integrin.CXCR4 expression in CNV mice had persistent increase within 14 d after induction.SDF-1 treatment significantly promoted the CNV progression during 3-14 d.The mean CNV length in AMD3100 andATN161 group at day 7 was 270.13 and 264.23 μm in HE images,significantly lower than the mean length in SDF-1(345.70 μm) group.AMD3100 and ATN161 also significantly reduced thickness and leakage of CNV induced by SDF-1.Mean integrin α5 positive area in SDF-1 group reached 2.31×104 μm^2,significantly higher than control(1.25×104 μm^2),which decreased to 1.78×104 μm^2 after AMD3100 treatment.About 61.36% of ECs in CNV lesions expressed α5 in SDF-1 group,which significantly decreased to 43.12% after AMD3100 treatment.In vitro,integrin α5 peaked by 6 folds after 6 h of hypoxia exposure and CXCR4 gradually increased by up to 2.3 folds after 24 h of hypoxia.Approximately 25.12% of ECs expressed integrin α5 after SDF-1 stimulation,which decreased to 7.2%-9.5% after si-CXCR4 or AMD3100 treatment.ATN161 exerted an inhibitory effect comparable to that of si-CXCR4 on EC migration and tube formation in the presence of SDF-1.CONCLUSION:SDF-1/CXCR4 signaling induces integrin α5β1 expression in ECs to promote CNV. 展开更多
关键词 choroidal neovascularization endothelial cells stromal cell-derived factor-1 CXCR4 integrin α5β1 HYPOXIA
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The role of Toll-like receptors in retinal ischemic diseases 被引量:2
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作者 wen-qin xu Yu-Sheng Wang 《International Journal of Ophthalmology(English edition)》 SCIE CAS 2016年第9期1343-1351,共9页
Toll-like receptors(TLRs) are commonly referred to a series of evolutionary conserved receptors which recognize and respond to various microbes and endogenous ligands.Growing evidence has demonstrated that the expre... Toll-like receptors(TLRs) are commonly referred to a series of evolutionary conserved receptors which recognize and respond to various microbes and endogenous ligands.Growing evidence has demonstrated that the expression of TLRs in the retina is regulated during retinal ischemic diseases,including ischemia-reperfusion injury,glaucoma,diabetic retinopathy(DR) and retinopathy of prematurity(ROP).TLRs can be expressed in multiple cells in the retina,such as glial cells,retinal pigment epithelium(RPE),as well as photoreceptor cells and endothelium cells.Activation of TLRs in retina could initiate a complex signal transduction cascade,induce the production of inflammatory cytokines and regulate the level of costimulatory molecules,which play prominent roles in the pathogenesis of retinal ischemic diseases.In this review,we summarized current studies about the relationship between TLRs and ischemic retinopathy.A greater understanding of the effect of TLRs on ischemic injuries may contribute to the development of specific TLR targeted therapeutic strategies in these conditions. 展开更多
关键词 Toll-like receptors RETINOPATHY retinal ischemic diseases retinal regeneration
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A modified laser-induced choroidal neovascularization animal model with intravitreal oxidized low-density lipoprotein 被引量:2
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作者 Tong Wu Kuan-Rong Dang +6 位作者 Ya-Fen Wang Bao-Zhen Lyu wen-qin xu Guo-Rui Dou Jian Zhou Yan-Nian Hui Hong-Jun Du 《International Journal of Ophthalmology(English edition)》 SCIE CAS 2020年第8期1187-1194,共8页
AIM: To investigate whether intravitreal injection of oxidized low-density lipoprotein(OxLDL) can promote laserinduced choroidal neovascularization(CNV) formation in mice and the mechanism involved, thereby to develop... AIM: To investigate whether intravitreal injection of oxidized low-density lipoprotein(OxLDL) can promote laserinduced choroidal neovascularization(CNV) formation in mice and the mechanism involved, thereby to develop a better animal model.METHODS: C57BL6/J mice were randomized into three groups. Immediately after CNV induction with 532 nm laser photocoagulation, 1.0 μL of OxLDL [100 μg/m L in phosphate-buffered saline(PBS)] was intravitreally injected, whereas PBS and the same volume low-density lipoprotein(LDL;100 μg/m L in PBS) were injected into the vitreous as controls. Angiogenic and inflammatory cytokines were measured by quantitative real-time polymerase chain reaction(q RT-PCR) and Western blotting(WB) after 5 d, and CNV severity was analyzed by choroid flat mount and immunofluorescence staining after 1wk. In vitro, retinal pigment epithelial(RPE) cell line(ARPE19) were treated with OxLDL(LDL as control) for 8 h. Angiogenic and inflammatory cytokine levels were measured. A specific inhibitor of lectin-like oxidized low-density lipoprotein receptor 1(LOX1) was used to evaluate the role of LOX1 in this process.RESULTS: At 7 d after intravitreal injection of 1 μL(100 μg/mL) OxLDL, T15-labeled OxLDL was mainly deposited around the CNV area, and the F4/80-labeled macrophages, the CD31-labeled vascular endothelial cells number and CNV area were increased. Meanwhile, WB and qR T-PCR results showed that vascular endothelial growth factor(VEGF), CC chemokine receptor 2(CCR2), interleukin-6(IL-6), IL-1β, and matrix metalloproteinase 9(MMP9) expressions were increased, which was supported by in vitro experiments in RPE cells. LOX1 inhibitors significantly reduced expressions of inflammatory factors IL-1β and VEGF. CONCLUSION: A modified laser-induced CNV animal model is established with intravitreal injection of 1 μL(100 μg/mL) of OxLDL at 7 d, which at least partially through LOX1. This animal model can be used as a simple model for studying the role of OxLDL in age-related macular degeneration. 展开更多
关键词 age-related macular degeneration choroidal neovascularization oxidized low-density lipoprotein animal model
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