Department of Ophthalmology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Faculty of Health and Medical Sciences, Institute of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
Invest Ophthalmol Vis Sci. 2024 Aug 1;65(10):35. doi: 10.1167/iovs.65.10.35.
To investigate retinal wound healing, we created a new porcine model of retinal hole and identified the cells involved in hole closure.
Sixteen landrace pigs underwent vitrectomy, and a subretinal bleb was created before cutting a retinal hole using a 23G vitrector. No tamponade was used. Before surgery and one, two, and four weeks after surgery, the eyes were examined by optical coherence tomography and color fundus photos. At the end of follow-up, the eyes were enucleated for histology. Tissue sections of 5 µm were prepared for hematoxylin-eosin staining and immunohistochemical analysis with antibodies to retinal glial and epithelial cells.
Retinal holes below 1380 µm in diameter closed spontaneously within four weeks, whereas larger holes remained open. Hole closure was mediated by central movement of the edges of the hole and in most cases the formation of a gliotic plug. Fluorescence microscopy revealed that the plug consisted of cells positive for glial fibrillary acidic protein, indicating the presence of macroglial cell types. Specifically, the plug was positive for S100 calcium-binding protein B, mainly representing astrocytes, while it was negative for anti-glutamine syntethase, representing Müller glia. These findings suggest that astrocytes are the predominating cell type in the plug. Minimal glial reaction was seen in the retinal holes that did not close.
We present a new porcine model for investigating large retinal holes. The retinal holes closed by approximation of hole edges, and the remnant retinal defect was closed with an astroglial plug.
为了研究视网膜伤口愈合,我们创建了一个新的猪视网膜裂孔模型,并确定了参与裂孔闭合的细胞。
16 头长白猪接受玻璃体切除术,在使用 23G 玻璃体切割器切割视网膜裂孔之前,先在视网膜下形成一个气泡。未使用任何填塞物。在手术前和手术后 1、2、4 周,通过光学相干断层扫描和眼底彩色照相检查眼睛。在随访结束时,眼球被眼球摘出进行组织学检查。制备 5µm 的组织切片,用于视网膜神经胶质细胞和上皮细胞的苏木精-伊红染色和免疫组织化学分析。
直径小于 1380µm 的视网膜裂孔在四周内可自发闭合,而较大的裂孔仍保持开放。裂孔的闭合是通过裂孔边缘的中央移动和在大多数情况下形成胶质塞来介导的。荧光显微镜显示,塞子由胶质纤维酸性蛋白阳性的细胞组成,表明存在大胶质细胞类型。具体而言,塞子对 S100 钙结合蛋白 B 呈阳性,主要代表星形胶质细胞,而对抗谷氨酰胺合成酶呈阴性,代表 Müller 胶质细胞。这些发现表明星形胶质细胞是塞子中的主要细胞类型。未闭合的视网膜裂孔中仅有轻微的胶质反应。
我们提出了一种新的用于研究大的视网膜裂孔的猪模型。视网膜裂孔通过裂孔边缘的接近而闭合,残余的视网膜缺损通过星形胶质细胞塞闭合。