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范志刚

作品数:30 被引量:206H指数:7
供职机构:中山大学中山眼科中心更多>>
发文基金:国家自然科学基金国家教育部博士点基金广东省科技计划工业攻关项目更多>>
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30 条 记 录,以下是 1-10
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早期高危角膜移植中的RORγt+Foxp3+T辅助细胞
杨斯婧范志刚欧阳晨杨丽君梁美欣黄挺葛坚
猴表皮干细胞横向分化为角膜上皮细胞的研究被引量:7
2006年
表皮干细胞可以作为角膜上皮细胞的替代物,在自体眼表修复及组织工程生物角膜的构建中将产生不可估量的作用.将体外分离培养的2~4代猴表皮干细胞和人角膜缘基质组织及角膜上皮细胞进行共培养Crranswell法),于共培养前后使用流式细胞仪、RT—PCR和免疫组织化学技术对其分化情况进行检测和鉴定.并于第2,4,6,8和10天进行免疫组织化学染色观察表皮干细胞转分化的比率.实验采用条件培养基诱导法作为对照.表皮干细胞在共培养前表达表皮干细胞标志,K15和整合素β1阳性,K3/K12阴性;共培养后转为表达K3/K12,从基因水平和蛋白质水平表现出角膜上皮细胞的特征,但是条件培养基诱导法阳性率较低.可见,表皮干细胞具有可塑性,在角膜缘基质组织及角膜上皮细胞的调控下,可以横向分化为类角膜上皮细胞,有可能重建角膜上皮,进行自体生物角膜的构建.
高楠王智崇黄冰葛坚陈系古卢蓉张可飞范志刚卢丽彭展崔光辉
关键词:表皮干细胞角膜上皮细胞
中国年轻早期原发性开角型青光眼患者焦虑和抑郁的评估
赵珍妮郭聪聪刘佳凡陈登辉孙楠楠张嘉敏张妙张丹丹范志刚
应用全基因组测序技术研究真性小眼球家系
赵珍妮刘佳凡李中文郭聪聪李剑龙张嘉敏张丹丹范志刚
Protection of retinal ganglion cells against glaucomatous neuropathy by neurotrophin-producing,genetically modified neural progenitor cells in a rat model被引量:8
2002年
OBJECTIVE: To investigate in vivo survival of retinal ganglion cells (RGCs) after partial blockage of optic nerve (ON) axoplasmic flow by sub-retinal space or vitreous cavity injection of brain-derived neural factor (BDNF) produced by genetically modified neural progenitor cells (NPCs). METHODS: Adult Sprague-Dawley (SD) rat RGCs were labeled with granular blue (GB) applied to their main targets in the brain. Seven days later, the left ON was intra-obitally crushed with a 40 g power forceps to partially block ON axoplasmic flow. Animals were randomized to three groups. The left eye of each rat received a sham injection, NPCs injection or an injection of genetically modified neural progenitors producing BDNF (BDNF-NPCs). Seven, 15 and 30 days after ON crush, retinas were examined under a fluorescence microscope. By calculating and comparing the average RGCs densities and RGC apoptosis density, RGC survival was estimated and the neuro-protective effect of transplanted cells was evaluated. RESULTS: Seven, 15 and 30 days after crush, in the intra-vitreous injection group, mean RGC densities had decreased to 1885 +/- 68, 1562 +/- 20, 1380 +/- 7 and 1837 +/- 46, 1561 +/- 58, 1370 +/- 16, respectively with sham injection or neural progenitors injection. However, RGCs density in the groups treated with intra-vitreous injection of BDNF-NPC was 2101 +/- 15, 1809 +/- 19 and 1625 +/- 34. Similar results were found in groups after sub-retinal injection. Higher densities were observed in groups treated with BDNF-NPCs. There were statistically significant differences among groups through nonparametric tests followed by the Mann-Whitely test. RGC apoptosis density in BDNF-NPC at each follow-up time was less than in other groups. CONCLUSIONS: A continuous supply of neurotrophic factors by the injection of genetically modified neural progenitors presents a highly effective approach to counteract optic neuropathy and RGC degeneration after partial ON axoplasmic flow blockage.
王宁利曾明兵阮奕文吴河坪陈静嫦范志刚郑湖玲
关键词:RATS
Primary angle closure glaucoma in Chinese and Western populations被引量:35
2002年
OBJECTIVE: To review the major progress in primary angle closure glaucoma (PACG). METHODS: Contents of this article were selected from the original papers or reviews related to primary angle closure glaucoma published in Chinese and foreign journals. A total of 76 articles were selected from several hundred original articles or reviews. The content of selected articles is in accordance with our purpose and the authors are authorized scientists in the study of glaucoma. RESULTS: Primary angle closure glaucoma is the most common type of glaucoma in the Sino-Mongoloid population. PACG in Chinese can be classified into three types depending on the mechanism of angle closure: 1. Multimechanism: 54.8% of Chinese PACG is caused by co-existing factors. The pattern of angle closure appears to mainly be creeping closure. After iridectomy, almost 40% of the cases still manifest a positive response to the darkroom provocative test and progressive synechial closure or recurrent angle closure may occur. Several mechanisms are involved in this form of PACG such as pupillary blocking component, iris crowding component and anterior positioned ciliary body. These factors can coexist in the follow patterns: pupillary blocking and iris crowding coexist; pupillary blocking and anterior positioned ciliary body coexist or three of them co-exist. 2. Pupillary block: (38.1% of Chinese PACG) is caused by iris bombe due to pupillary block with acute or subacute attack. It responds well to iridectomy or laser iridotomy. 3. Non-pupillary blocking: (7.8% of Chinese PACG). They usually have a deeper anterior chamber, and tend to be younger (below 40 years of age). Angle closure in this form of PACG is caused by: iris crowding mechanism or/and anteriorly positioned ciliary body against iris root to angle. It is critical to distinguish multi-mechanism PACG from other types. The initial treatment for this type of PACG is also iridectomy, but after the pupillary block component is eliminated by iridectomy, the residual non-pupillary blocking compo
王宁利吴河坪范志刚
小鼠视神经再生研究动物模型的建立被引量:2
2006年
目的 总结制作小鼠视神经完全截断性动物模型作为视神经再生研究的经验和体会。方法 将雄性Bcl-2高表达转基因小鼠(Bcl-2 transgenic mice)和受GFAP启动子控制表达疱疹病毒-胸苷激酶转基因雌性小鼠(GFAP-TK)交配产生的4只8~12周成年小鼠(20~30g),Bcl-2/GFAP-TK双转基因小鼠作为实验组,同周龄4只Bcl-2转基因小鼠作为对照组。其中Bcl-2/GFAP-TK双转基因小鼠皮下植入缓释泵,连续7d释放更昔洛韦(GCV)100mg·kg^-1·d“^-1选择性地去除视神经损伤后激活的星形胶质细胞。更昔洛韦缓释泵植入术后2d在两组动物中制作右侧单眼标准完全性视神经钳夹损伤模型,视神经钳夹10d后获取组织标本。采用免疫荧光染色特异性检测再生轴突纤维并进行定量分析;结合罗丹明的霍乱毒索B亚单位(CTB-R)或增强表达绿色荧光蛋白的复制缺陷型腺相关病毒(AAV-EGFP)用作顺行性标记物以显示再生轴突是否到达大脑靶器官。结果 在Bcl-2/GFAP-TK双转基因小鼠中存在免疫荧光阳性的再生视神经轴突,再生轴突计数为71.99±24.04,并可见生长锥(growth cone)样结构,但是再生轴突纤维未能延伸达到大脑靶器官。在对照组Bcl-2转基因小鼠中未见明显再生迹象。结论 小鼠视神经完全截断性动物模型可用于视神经病变的再生研究。
范志刚Chen Dong-feng葛坚
关键词:星形胶质细胞视神经再生青光眼转基因小鼠
包裹脑源性神经营养因子壳聚糖/海藻酸钠微囊的制备及体外释药研究被引量:1
2011年
目的研制包裹脑源性神经营养因子(brain derived neurotrophic factor,BDNF)的壳聚糖/海藻酸钠微囊,并测定其体外药物释放动力学。方法采用改良超声雾化法,将含BDNF的壳聚糖溶液加入超声雾化仪中雾化喷入海藻酸钠溶液中制成包裹BDNF的壳聚糖/海藻酸钠微囊混悬液。采用高效液相色谱法(high performance liquidchromatography,HPLC)测定BDNF的标准曲线,并测定微囊中BDNF的体外每日释放量。结果微囊形态为圆形透明颗粒状,粒径在3~5μm之间。用SPSS统计软件进行分析微囊中BDNF的体外每日释放量,显示药物累积释放量与时间之间是直线关系,基本符合药物零级释放动力学。结论本法所制微囊工艺稳定,在体外具有缓释作用。
吴河坪王宁利曾明兵陈静嫦范志刚
关键词:脑源性神经营养因子海藻酸钠微囊释药
7.青光眼视神经损伤机制与视神经保护
本主要介绍了青光眼视神经损伤机制与视神经保护,首先对青光眼进行了概述,青光眼是由于眼内压升高或者视神经血流灌注压降低等多种因素所引起的视神经损害.目前,青光眼最主要的致盲原因是视神经病变引起的视野损害,而视野损害的病理基...
葛坚范志刚郭彦钟兴武
关键词:青光眼视神经
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包裹脑源性神经营养因子壳聚糖/海藻酸钠微囊对大鼠视神经损伤保护作用被引量:2
2011年
目的观察包裹脑源性神经营养因子(brain derived neurotrophic factor,BDNF)的壳聚糖/海藻酸钠微囊对大鼠视神经损伤的保护作用。方法在视神经损伤模型的大鼠玻璃体腔内注入包裹BDNF的壳聚糖/海藻酸钠微囊。第一组中对视神经作单次损伤,第二组中两次损伤视神经。通过视网膜神经节细胞(retinal ganglion cells,RGCs)密度计数,评价包裹BDNF的壳聚糖/海藻酸钠微囊对RGCs的保护作用。结果 BDNF微囊注入组和游离BD-NF注射组,在注入后14天和28天组与空白PBS及壳聚糖/海藻酸钠微囊组比较RGC密度差异均有统计学意义(P<0.01),BDNF微囊注入组和游离BDNF注射组的RGCs的密度高于空白对照组。单次损伤视神经的BDNF微囊注入组与游离BDNF注射组的两组间RGC密度差异无统计学意义(P>0.05)。而两次损伤视神经的BDNF微囊注入组与游离BDNF单次注射组的两组间RGC密度差异有统计学意义(P<0.01),BDNF微囊注入组的RGCs的密度高于游离BDNF单次注射组。BDNF微囊注入组与BDNF两次注射组的两组间RGC差异无统计学意义(P>0.05)。结论对于受到反复损伤的RGCs,BDNF微囊释放的BDNF在注入后对损伤下的RGCs起到了明显的保护作用,优于单次注入BDNF。而对只受到单次损伤的RGCs,BDNF微囊释放的BDNF与单次注入BDNF效果相同。
吴河坪王宁利曾明兵陈静嫦范志刚
关键词:视神经损伤视网膜神经节细胞脑源性神经营养因子
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