Schlötzer-Schrehardt Ursula, Zenkel Matthias, Nüsing Rolf M
Department of Ophthalmology, University of Erlangen-Nürnberg, Schwabachanlage 6, D-91054 Erlangen, Germany.
Invest Ophthalmol Vis Sci. 2002 May;43(5):1475-87.
To determine the expression and precise cellular and subcellular localization of the EP prostanoid receptor subtypes EP(1) through EP(4) and the FP receptor in normal human ocular tissues on the protein and mRNA levels.
Expression of EP and FP receptor proteins was examined by immunohistochemistry on the light microscopic level, using subtype-specific antibodies on frozen and paraffin-embedded tissue sections of 10 normal human donor eyes. The subcellular distribution of the receptor proteins was studied by electron microscopic immunogold labeling. mRNA expression in various ocular tissues was analyzed by reverse transcription-polymerase chain reaction, using subtype-specific primers.
The highest expression of the EP(1) receptor protein was found in the epithelia of the cornea, conjunctiva, lens, and the ciliary body; trabecular cells; iris vessels; and retinal ganglion cells. EP(2) receptor labeling was most prominent in the corneal epithelium and choriocapillaries. EP(3) and EP(4) receptor labeling was primarily observed in the corneal endothelium and keratocytes, trabecular cells, ciliary epithelium, and conjunctival and iridal stroma cells, and EP(3) was found, in addition, in retinal Müller cells. The highest expression of FP receptor protein was found in the corneal epithelium, ciliary epithelium, the circular portion of ciliary muscle, and iris stromal and smooth muscle cells. Immunoelectron microscopy showed a subcellular distribution of all prostanoid receptors along plasma membranes and the nuclear envelope. EP and FP receptor mRNA expression largely paralleled the proteins' expression patterns.
The findings demonstrate a wide distribution but differential expression of FP and EP prostanoid receptor subtypes in human ocular tissues. EP(1) through EP(4) receptor subtype expression in human outflow pathways could be significant for future pharmacologic management strategies for the glaucomas.
在蛋白质和mRNA水平上,确定前列腺素E受体亚型EP(1)至EP(4)以及FP受体在正常人眼组织中的表达情况及其精确的细胞和亚细胞定位。
采用免疫组织化学方法,在光学显微镜水平上,使用亚型特异性抗体,对10例正常人类供体眼的冷冻和石蜡包埋组织切片进行EP和FP受体蛋白表达检测。通过电子显微镜免疫金标记研究受体蛋白的亚细胞分布。使用亚型特异性引物,通过逆转录-聚合酶链反应分析各种眼组织中的mRNA表达。
EP(1)受体蛋白在角膜、结膜、晶状体和睫状体的上皮细胞、小梁细胞、虹膜血管和视网膜神经节细胞中表达最高。EP(2)受体标记在角膜上皮和脉络膜毛细血管中最为突出。EP(3)和EP(4)受体标记主要见于角膜内皮细胞和角膜细胞、小梁细胞、睫状体上皮细胞以及结膜和虹膜基质细胞,此外,在视网膜Müller细胞中也发现了EP(3)。FP受体蛋白在角膜上皮细胞、睫状体上皮细胞、睫状肌环形部分以及虹膜基质和平滑肌细胞中表达最高。免疫电子显微镜显示,所有前列腺素受体沿质膜和核膜呈亚细胞分布。EP和FP受体mRNA表达在很大程度上与蛋白表达模式平行。
研究结果表明,FP和前列腺素E受体亚型在人眼组织中分布广泛但表达存在差异。EP(1)至EP(4)受体亚型在人房水流出途径中的表达可能对未来青光眼的药物治疗策略具有重要意义。