Edwards Malia M, McLeod D Scott, Bhutto Imran A, Grebe Rhonda, Duffy Maeve, Lutty Gerard A
Department of Ophthalmology, Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States.
Invest Ophthalmol Vis Sci. 2017 Mar 1;58(3):1352-1367. doi: 10.1167/iovs.16-21229.
Müller cells create the external limiting membrane (ELM) by forming junctions with photoreceptor cells. This study evaluated the relationship between focal photoreceptors and RPE loss in geographic atrophy (GA) and Müller cell extension into the subretinal space.
Human donor eyes with no retinal disease or geographic atrophy (GA) were fixed and the eye cups imaged. The retinal posterior pole was stained for glial fibrillary acidic protein (GFAP; astrocytes and activated Müller cells) and vimentin (Müller cells) while the submacular choroids were labeled with Ulex Europaeus Agglutinin lectin (blood vessels). Choroids and retinas were imaged using a Zeiss 710 confocal microscope. Additional eyes were cryopreserved or processed for transmission electron microscopy (TEM) to better visualize the Müller cells.
Vimentin staining of aged control retinas (n = 4) revealed a panretinal cobblestone-like ELM. While this pattern was also observed in the GA retinas (n = 7), each also had a distinct area in which vimentin+ and vimentin+/GFAP+ processes created a subretinal membrane. Subretinal glial membranes closely matched areas of RPE atrophy in the gross photos. Choroidal vascular loss was also evident in these atrophic areas. Smaller glial projections were noted, which correlated with drusen in gross photos. The presence of glia in the subretinal space was confirmed by TEM and cross cross-section immunohistochemistry.
In eyes with GA, subretinal Müller cell membranes present in areas of RPE atrophy may be a Müller cell attempt to replace the ELM. These membranes could interfere with treatments such as stem cell therapy.
Müller细胞通过与光感受器细胞形成连接来构建外界限制膜(ELM)。本研究评估了地图样萎缩(GA)中局灶性光感受器和视网膜色素上皮(RPE)丢失与Müller细胞延伸至视网膜下间隙之间的关系。
对无视网膜疾病或地图样萎缩(GA)的人类供体眼进行固定并对眼杯进行成像。视网膜后极部用胶质纤维酸性蛋白(GFAP;星形胶质细胞和活化的Müller细胞)和波形蛋白(Müller细胞)染色,而黄斑下脉络膜用荆豆凝集素(血管)标记。使用蔡司710共聚焦显微镜对脉络膜和视网膜进行成像。另外的眼睛进行冷冻保存或用于透射电子显微镜(TEM)检查,以更好地观察Müller细胞。
老年对照视网膜(n = 4)的波形蛋白染色显示全视网膜呈鹅卵石样ELM。虽然在GA视网膜(n = 7)中也观察到这种模式,但每个GA视网膜都有一个独特的区域,其中波形蛋白阳性和波形蛋白/GFAP双阳性的突起形成了视网膜下膜。视网膜下胶质膜与大体照片中RPE萎缩区域紧密匹配。这些萎缩区域的脉络膜血管丢失也很明显。注意到较小的胶质突起,这与大体照片中的玻璃膜疣相关。通过TEM和横断面免疫组织化学证实了视网膜下间隙中存在胶质细胞。
在患有GA的眼中,RPE萎缩区域存在的视网膜下Müller细胞膜可能是Müller细胞试图替代ELM。这些膜可能会干扰诸如干细胞治疗等疗法。