Amar Nawel, Labbé Antoine, Hamard Pascale, Dupas Bénédicte, Baudouin Christophe
Department of Ophthalmology III, Quinze-Vingts National Ophthalmology Hospital, Paris, France.
Ophthalmology. 2008 Jul;115(7):1154-1161.e4. doi: 10.1016/j.ophtha.2007.10.024. Epub 2007 Dec 21.
To characterize and understand, at the cellular level, the aqueous humor pathways after filtering surgery, using in vivo confocal microscopy and impression cytology (IC).
Observational case series.
Thirty-two blebs of 29 patients after trabeculectomy were retrospectively evaluated.
In vivo confocal microscopy and immunofluorescence staining of IC samples taken on and around the bleb area were performed. Impression cytology samples were examined under confocal microscopy after goblet cell and inflammatory cell immunostaining with anti-MUC5AC and antivimentin antibodies, respectively. Eyes were classified into 3 groups: (1) functioning blebs (11 eyes), (2) nonfunctioning blebs (10 eyes), and (3) functioning blebs after mitomycin C application (12 eyes). Impression cytology specimens and in vivo confocal microscopy images were analyzed and compared in a masked manner.
Conjunctival epithelium changes of each type of bleb were analyzed using both impression cytology specimens and in vivo confocal microscopy and correlated to clinical outcomes.
In all IC specimens, numerous MUC5AC-positive cells were observed outside the edges of the blebs. Few MUC5AC-positive cells were observed at the surface of nonfunctioning blebs. Numerous goblet cells with immunostaining that was weak or limited to the membrane were clearly visible morphologically at the surface of functioning blebs (with and without adjunctive mitomycin C). Using in vivo confocal microscopy, all functioning blebs showed numerous intraepithelial optically empty microcysts, whereas nonfunctioning blebs had none or only a few. All blebs contained dendritiform inflammatory cells, especially after mitomycin C application.
Impression cytology and in vivo confocal microscopy provide a new approach to filtering blebs. Microcysts observed at the surface of functioning blebs seemed to correspond to goblet cells, mostly containing aqueous humor instead of highly hydrophilic gel-forming mucins. Although this hypothesis requires further confirmation, the transcellular pathway of the aqueous humor could be hypothesized to occur at the level of goblet cells toward the ocular surface.
运用活体共聚焦显微镜和印迹细胞学(IC)技术,在细胞水平上表征和了解滤过性手术后的房水引流途径。
观察性病例系列。
回顾性评估了29例小梁切除术后患者的32个滤过泡。
对取自滤过泡区域及其周围的IC样本进行活体共聚焦显微镜检查和免疫荧光染色。分别用抗MUC5AC和抗波形蛋白抗体对杯状细胞和炎性细胞进行免疫染色后,在共聚焦显微镜下检查印迹细胞学样本。将眼睛分为3组:(1)功能性滤过泡(11只眼),(2)非功能性滤过泡(10只眼),(3)丝裂霉素C应用后的功能性滤过泡(12只眼)。以盲法分析和比较印迹细胞学标本和活体共聚焦显微镜图像。
使用印迹细胞学标本和活体共聚焦显微镜分析每种类型滤过泡的结膜上皮变化,并与临床结果相关联。
在所有IC标本中,在滤过泡边缘外观察到大量MUC5AC阳性细胞。在非功能性滤过泡表面观察到很少的MUC5AC阳性细胞。在功能性滤过泡(使用和未使用辅助丝裂霉素C)表面,形态上可见大量免疫染色弱或仅限于细胞膜的杯状细胞。使用活体共聚焦显微镜,所有功能性滤过泡均显示大量上皮内光学空泡微囊肿,而非功能性滤过泡没有或只有少数。所有滤过泡均含有树突状炎性细胞,尤其是在应用丝裂霉素C后。
印迹细胞学和活体共聚焦显微镜为滤过泡研究提供了一种新方法。在功能性滤过泡表面观察到的微囊肿似乎对应于杯状细胞,其中大部分含有房水而非高度亲水性的凝胶形成粘蛋白。尽管这一假设需要进一步证实,但可以推测房水的跨细胞途径可能发生在杯状细胞朝向眼表的水平。