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视网膜裂孔猪模型中视网膜下羊膜移植。

Subretinal Amniotic Membrane Transplantation in a Porcine Model of Retinal Hole.

机构信息

Department of Ophthalmology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

Faculty of Health and Medical Sciences, Institute of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.

出版信息

Invest Ophthalmol Vis Sci. 2024 Nov 4;65(13):52. doi: 10.1167/iovs.65.13.52.

Abstract

PURPOSE

To investigate the histopathological changes following subretinal amniotic membrane transplantation in an in vivo porcine model of retinal holes.

METHODS

Left eyes of 12 Danish Landrace pigs were vitrectomized under full anesthesia. A subretinal bleb was created before excising a retinal hole (1154-2934 µm) using a 23-gauge vitrector. The pigs underwent transplantation of human freeze-dried amniotic membrane into the subretinal space, with no tamponade applied. Optical coherence tomography and color fundus photography were performed just after surgery and at 2 and 4 weeks post-surgery. At the end of follow-up, the eyes were enucleated for hematoxylin and eosin staining and fluorescence immunohistochemistry, using antibodies against retinal glial cells and inner retinal neurons.

RESULTS

The amniotic membrane sheets facilitated hole closure by gliosis and centripetal migration of the edges of the hole. Immunohistochemical examination showed that the cells within the closed hole expressed anti-glial fibrillary acidic protein (GFAP) and anti-S100B, but not anti-glutamine synthetase (GS), suggesting that astrocytes were the predominant glial cells involved in hole closure. Gliosis was observed between the amniotic membrane sheet and the overlying photoreceptors of the surrounding retina. Morphological restoration of the retinal layers within the closed retinal hole was not observed.

CONCLUSIONS

The amniotic membrane acted as a stimulator for retinal hole closure by inducing glial cell proliferation and providing a scaffold for the centripetal migration of the edges of the hole. No morphological restoration was observed.

摘要

目的

在猪视网膜裂孔模型中研究视网膜下羊膜移植后的组织病理学变化。

方法

12 只丹麦长白猪在全麻下接受玻璃体切除术。使用 23 号玻璃体切割器切除视网膜裂孔(1154-2934µm)之前,先在视网膜下形成一个视网膜下隆起。猪接受人冻干羊膜移植到视网膜下腔,未进行填塞。术后即刻、术后 2 周和 4 周进行光学相干断层扫描和眼底彩色照相检查。随访结束时,眼球行苏木精-伊红染色和荧光免疫组织化学检查,使用针对视网膜神经胶质细胞和内层神经元的抗体。

结果

羊膜片通过胶质增生和孔缘向心性迁移促进孔闭合。免疫组织化学检查显示,闭合孔内的细胞表达抗神经胶质纤维酸性蛋白(GFAP)和抗 S100B,但不表达抗谷氨酰胺合成酶(GS),提示参与孔闭合的主要胶质细胞是星形胶质细胞。羊膜片和周围视网膜的光感受器之间观察到胶质增生。未观察到闭合视网膜裂孔内视网膜层的形态恢复。

结论

羊膜作为视网膜裂孔闭合的刺激物,通过诱导神经胶质细胞增殖并为孔缘向心性迁移提供支架来发挥作用。未观察到形态学恢复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/454e/11601133/4bcf212a7ba6/iovs-65-13-52-f001.jpg

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