Sheedlo H J, Turner J E
Department of Anatomy and Cell Biology, North Texas Eye Research Institute, University of North Texas Health Science Center, Fort Worth 76107, USA.
J Anat. 1998 Aug;193 ( Pt 2)(Pt 2):223-32. doi: 10.1046/j.1469-7580.1998.19320223.x.
In a previous study, an antigen consisting of proteins secreted by retinal pigment epithelial (RPE) cells was injected into a sheep and the specificity of the resulting antiserum was shown by Western blotting and its effects on retinal development were determined in vitro and in vivo. In the present study, the distribution of these secreted proteins was determined by light microscopy immunocytochemistry in cultured neonatal rat RPE cells and retinas of normal and Royal College of Surgeons (RCS) dystrophic rats and cerebrum of normal adult rats. Immunolabelling for these RPE-secreted proteins was detected in cytoplasmic vesicles surrounding nuclei and within processes of cultured normal and transformed rat RPE. In retinas of late postnatal and adult rats, dense immunostaining was found in the cytoplasm of RPE cells and ganglion cell bodies. In addition to RPE and ganglion cells, scattered photoreceptors within the thin outer nuclear layer and small structures within the debris zone were also densely immunoreactive in retinas of 2-mo-old RCS dystrophic rats. The numbers of immunostained ganglion cells appeared to decrease in retinas of older RCS rats, although the immunoreactivity within the RPE appeared to increase in density. No other neuron within the retina, i.e. bipolar, amacrine or horizontal, was immunoreactive for RPE-secreted proteins. In the cerebral cortex of adult rats, immunoreactivity for RPE-secreted proteins was primarily detected within large perikarya of pyramidal neurons and smaller granule neurons. In conclusion, we report an immunocytochemical analysis of an antiserum raised against secreted proteins of rat RPE. This antiserum recognised proteins within secretory-like vesicles of cultured neonatal normal and transformed rat RPE and showed a specificity for RPE and ganglion cells in normal rat retinas, that appeared to be developmentally regulated, and neuron perikarya in adult rat cerebrum.
在先前的一项研究中,将一种由视网膜色素上皮(RPE)细胞分泌的蛋白质组成的抗原注射到一只绵羊体内,通过蛋白质印迹法显示了所得抗血清的特异性,并在体外和体内确定了其对视网膜发育的影响。在本研究中,通过光学显微镜免疫细胞化学方法,确定了这些分泌蛋白在培养的新生大鼠RPE细胞、正常大鼠和皇家外科学院(RCS)营养不良大鼠的视网膜以及正常成年大鼠大脑中的分布。在培养的正常和转化大鼠RPE的核周细胞质囊泡和突起内检测到了针对这些RPE分泌蛋白的免疫标记。在出生后晚期和成年大鼠的视网膜中,RPE细胞的细胞质和神经节细胞体中发现了密集的免疫染色。除了RPE细胞和神经节细胞外,在2月龄RCS营养不良大鼠的视网膜中,薄的外核层内的散在光感受器和碎片区内的小结构也呈强免疫反应性。在年龄较大的RCS大鼠的视网膜中,免疫染色的神经节细胞数量似乎减少,尽管RPE内的免疫反应性密度似乎增加。视网膜内的其他神经元,即双极神经元、无长突神经元或水平神经元,对RPE分泌蛋白无免疫反应性。在成年大鼠的大脑皮层中,主要在锥体细胞和较小颗粒细胞的大胞体中检测到了对RPE分泌蛋白的免疫反应性。总之,我们报告了对一种针对大鼠RPE分泌蛋白产生的抗血清的免疫细胞化学分析。这种抗血清识别培养的新生正常和转化大鼠RPE的分泌样囊泡内的蛋白质,并显示出对正常大鼠视网膜中RPE细胞和神经节细胞具有特异性,这种特异性似乎受发育调节,以及对成年大鼠大脑中的神经元胞体也具有特异性。