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国家重点基础研究发展计划(2013CB967503)

作品数:8 被引量:34H指数:4
相关作者:陈暐陈玲更多>>
相关机构:复旦大学复旦大学上海医学院更多>>
发文基金:国家重点基础研究发展计划国家自然科学基金教育部留学回国人员科研启动基金更多>>
相关领域:医药卫生更多>>

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多巴胺与免疫反应调节的研究进展被引量:10
2018年
神经递质多巴胺(dopamine,DA)是联接神经和免疫的重要分子。白细胞能合成和转运DA,几乎所有的免疫细胞亚群都表达DA受体,DA与其受体结合,通过自分泌/旁分泌方式调节免疫细胞的活化、增殖和细胞因子分泌。在中枢神经系统和外周组织,DA主要通过D_1和D_2受体抑制或加强免疫效应细胞的功能。中枢神经系统退行性疾病表现出免疫功能失调,可能与免疫细胞上DA受体表达水平以及信号传导通路的变化相关。因此,选择性针对免疫细胞的DA受体激动剂或拮抗剂在治疗DA介导的免疫失调性疾病中可能发挥重要作用。本文就DA受体在免疫细胞上的表达、DA作为免疫调节分子的作用以及在免疫功能障碍相关疾病中的研究进展作一综述。
黄洁徐格致
关键词:多巴胺多巴胺受体免疫白细胞炎症
自身免疫性葡萄膜炎与Th1、Th17相关细胞因子的研究进展被引量:7
2014年
人类自身免疫性葡萄膜炎是一组常见的眼部炎症性疾病,不明因素导致的自身免疫紊乱可对眼部组织产生不可逆性损害,因此长期以来,对人类自身免疫性葡萄膜炎的致病原因、发病机制的研究从未停止。以往的研究认为,1型辅助性T细胞群(Th1)是诱发人类自身免疫性葡萄膜炎的关键因素,但近年来发现,Th17是诱导自身免疫性葡萄膜炎病变的主要因素。由于每种Th细胞群都有其特定的细胞因子及转录因子,这些细胞因子通过调节Th1、Th2、Th17的表达及平衡决定着自身免疫性葡萄膜炎的发生和发展。研究Th1及Th17相关细胞因子在病变中的作用是探讨自身免疫性葡萄膜炎发生和发展的重要基础之一。就近年来Th1及Th17主要的相关细胞因子在葡萄膜炎的致病性、调节及治疗作用方面的研究进展进行综述。
陈暐陈玲
关键词:细胞因子
Retinal displacement after closure of idiopathic macular hole
2018年
Objective: To study the foveal displacement during the closure of idiopathic macular holes(MHs).Methods: Thirty-seven idiopathic MH patients treated by pars plana vitrectomy and internal limiting membrane peeling were studied prospectively.Locations of MH center and foveal pit were measured by optic coherence tomography.Retinal displacement was observed using confocal scanning laser ophthalmoscopy.Results: A total of 40 eyes were included in this study and MHs were closed in 37 eyes(92.5%).The confocal scanning laser ophthalmoscopy showed that all of the retinal capillaries in the superior, inferior, nasal and temporal sides of the MHs moved toward the optic nerve head(ONH).The optic coherence tomography results showed that the mean nasal displacements of foveal pits were(102.9±61.2),(109.6±53.1), and(137.0±52.0) μm at 3, 6 and 12 months, respectively.And the mean vertical displacements were(55.9±49.4),(61.4±57.8) and(67.8±54.3) μm, respectively.Post-operative foveal pits were located in the nasal side of the MH centers.The extension of retina and nasal to the MH were in opposite directions: the nasal hole margin moved toward the MH, but the retina located closer to the ONH moved toward the ONH.The fellow eyes of three patients developed into idiopathic MH during the follow-up period and operations were performed for all of the three patients.Conclusion: Our results showed that center of macula does not move when an idiopathic MH develops, but it moves toward ONH during closure of hole; thus, new fovea is in nasal side of original fovea.
Zhong-Cui SunMin WangJia-Wen FanGe-Zhi Xu
Phacoemulsification combined with transpupillary removal of silicone oil and intracapsular intraocular lens implantation被引量:6
2017年
AIM: To estimate the effectiveness of phacoemulsification and foldable intraocular lens(IOL) implantation combined with transpupillary silicone oil removal.METHODS: There were 168 eyes of 168 candidate patients with cataract and silicone oil-filled eyes recruited in our study. All of the patients received the intraocular silicone oil removal surgery by transpupillary drainage and cataract extraction by phacoemulsification. Then the IOL implantation were also performed through corneal incision. RESULTS: The surgery was successfully completed in all eyes. Best corrected visual acuity(BCVA) and postoperative complications were recorded in three months after surgery. There were 143 eyes with BCVA improved, otherwise 25 eyes remained stable at the last follow-up visit. The mean BCVA statistically improved from 20/400±0.02 to 20/100±0.15(P〈0.001) and mean postoperative IOP was 13.85±2.18 mm Hg(P=0.415). No intra-operative complications were reported.CONCLUSION: Phacoemulsification combined with transpupillary removal of silicone oil is a safe and simple effective method. In general, it enables quick recovery of visual acuity with less complication rate.
Yu-Cheng ZhuDong-Qing YuanPing XieXiao-Yi LiuSong-Tao YuanQing-Huai Liu
Long-term follow-up of vitrectomy in patients with pathologic myopic foveoschisis被引量:6
2017年
AIM: To report the long-term surgical outcomes of pathologic myopic foveoschisis(MF) following vitrectomy.METHODS: We performed a retrospective case series analysis of 50 consecutive patients diagnosed with MF who experienced vision loss due to progression of foveoschisis.The 50 patients(67 eyes) were treated in our hospital with vitrectomy with internal limiting membrane(ILM) peeling from December 2004 to September 2010.Best corrected visual acuity(BCVA),refractive error,optical coherence tomography(OCT),and routine examination results were analysed.The changes of BCVA,foveal anatomical features on OCT scan,and complications were the main outcome measures.RESULTS: The mean follow-up duration was 42±17mo(range 24 to 93mo).BCVA improved significantly postoperatively(0.76±0.65 logM AR) compared with preoperative baselines(1.31±0.78 log MAR,P〈0.0001),and in 53 eyes(79%) including 3 lines gain in 44 eyes(66%) at the last follow-up visit.OCT scans showed that central retinal thickness decreased from 580.0±270.0 μm preoperatively(n=67) to 179.7±84.7 μm postoperatively(n=58,P〈0.0001).Total resolution of foveoschisis occurred in 41 eyes(61%).Preoperative BCVA correlated well with postoperative BCVA,whereas other factors such as age,axial length,and refractive error were not correlated.The most common complications were cataract and full-thickness macular hole formation in 14 and 9 cases,respectively.CONCLUSION: Patients with progressive vision loss due to MF who were treated with vitrectomy with ILM peelingshow favourable outcomes.In most eyes,visual acuity and foveal structure remain stable during long-term observation.
Ting ZhangYing ZhuChun-Hui JiangGe-Zhi Xu
关键词:VITRECTOMY
人脐带间充质干细胞对光诱导视网膜色素上皮细胞损伤的保护作用被引量:4
2019年
目的体外观察脐带间充质干细胞(UCMSCs)对光诱导视网膜色素上皮(RPE)细胞损伤是否具有保护作用。方法培养扩增人UCMSCs,对UCMSCs的免疫表型进行流式检测鉴定。原代分离培养人眼RPE细胞,制备蓝光损伤的RPE细胞模型。利用Transwell小室建立光损伤RPE细胞与UCMSCs的非接触共培养体系。RPE细胞分为正常对照组、模型对照组和UCMSCs共培养组。正常对照组不予处理,模型对照组采用蓝光照射诱导RPE细胞损伤,UCMSCs共培养组为光损伤RPE细胞+UCMSCs共培养。光损伤RPE细胞与UCMSCs共培养后24 h和48 h,采用四甲基偶氮唑盐(MTT)法检测各组RPE细胞增生活力;共培养48 h,收集各组细胞培养上清液,酶联免疫吸附测定(ELISA)法定量检测色素上皮衍生因子(PEDF)、碱性成纤维细胞生长因子(bFGF)质量浓度,并进行RPE细胞吞噬感光细胞外节段膜盘(POS)试验。结果UCMSCs形态呈梭形,细胞表面抗原CD29、CD44、CD90和CD105呈阳性表达,同时细胞表面抗原CD34和CD45呈阴性表达。RPE细胞呈多边形,阳性表达特异性标志物RPE65蛋白。各组共培养后不同时间点RPE细胞增生能力(A值)总体比较,差异均有统计学意义(F组别=132.388,P=0.000;F时间=231.440,P=0.000),其中培养后24 h、48 h,模型对照组和UCMSCs共培养组的细胞A值均较正常对照组明显下降,差异均有统计学意义(均P<0.01);UCMSCs共培养组细胞在相应时间点的细胞A值显著高于模型对照组,差异均有统计学意义(均P<0.01)。RPE细胞POS吞噬试验的量化计算结果显示,3个组RPE细胞平均吞噬POS颗粒数总体比较,差异有统计学意义(F=28.087,P=0.000),其中模型对照组RPE细胞平均吞噬POS颗粒数较正常对照组明显减少,UCMSCs共培养组RPE细胞平均吞噬POS颗粒数较模型对照组明显增加,差异均有统计学意义(均P<0.01)。ELISA法检测结果显示,正常对照组、模型对照组和UCMSCs共培养组RPE细胞上清液中PEDF质量浓度分�
庄宏张荣舒秦蒙章淑杰徐格致
关键词:视网膜脐带间充质干细胞光损伤视网膜色素上皮细胞神经营养作用
Digenic heterozygous mutations in EYS/LRP5 in a Chinese family with retinitis pigmentosa
2017年
Dear Editor,I am Dr.Ji-Hong Wu,from the Department of Ophthalmology,Eye&ENT Hospital of Fudan University,China.I write to present a case report of retinitis pigmentosa(RP)caused by novel digenic heterozygous mutations in a Chinese family.
Feng-Juan GaoSheng-Hai ZhangJun-Yi ChenGe-Zhi XuJi-Hong Wu
关键词:LRPGENE
R102W mutation in the RS1 gene responsible for retinoschisis and recurrent glaucoma被引量:1
2014年
AIM: To identify the mutations in RS1 gene associated with typical phenotype of X-linked juvenile retinoschisis(XLRS) and a rare condition of concomitant glaucoma. ·METHODS: Complete ophthalmic examinations were performed in the proband. The coding regions of the RS1 gene that encode retinoschisin were amplified by polymerase chain reaction and directly sequenced. ·RESULTS: The proband showed a typical phenotype of XLRS with large peripheral retinal schisis in both eyes,involving the macula and combined with foveal cystic change,reducing visual acuity. A typical phenotype of recurrent glaucoma with high intraocular pressure(IOP) and reduced visual field was also demonstrated with the patient. Mutation analysis of RS1 gene revealed R102W(c.304C>T) mutations in the affected male,and his mother was proved to be a carrier with the causative mutation and another synonymous polymorphism(c.576C>CT). ·CONCLUSION: We identified the genetic variations of a Chinese family with typical phenotype of XLRS and glaucoma. The severe XLRS phenotypes associated with R102W mutations reveal that the mutation determines a notable alteration in the function of the retinoschisin protein. Identification of the disease-causing mutation is beneficial for future clinical references.
Xiu-Feng HuangChang-Sen TuDong-Jun XingDe-Kang GanGe-Zhi XuZi-Bing Jin
关键词:GLAUCOMAMUTATION
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