Yoshida Kazuhiko, Kase Satoru, Nakayama Keiko, Nagahama Hiroyasu, Harada Takayuki, Ikeda Hiromi, Harada Chikako, Imaki Junko, Ohgami Kazuhiro, Shiratori Kenji, Ohno Shigeaki, Nakayama Keiichi I
Department of Ophthalmology, Hokkaido University School of Medicine, N15 W7, Kita-ku, 060-8638 Sapporo, Japan.
Graefes Arch Clin Exp Ophthalmol. 2004 May;242(5):437-41. doi: 10.1007/s00417-004-0861-7. Epub 2004 Mar 17.
To examine the expression of the p27(KIP1), cyclin D1, and proliferating cell nuclear antigen (PCNA) in the retina and retinal pigment epithelium (RPE) after retinal detachment.
Normal eyes and eyes at 2 or 4 days after retinal detachment with the C57B16 mouse were analyzed by immunocytochemistry using anti-p27(KIP1), anti-cyclin D1, and anti-proliferating cell nuclear antigen (PCNA) antibodies as well as anti-glutamate synthetase (GS) antibody.
The p27(KIP1) positive nuclei were distributed in the inner nuclear layer (INL) and the RPE of the normal mice eye. In the INL, p27(KIP1) was detected in the middle sublayer, where the nuclei of glutamate synthetase positive Müller cells were situated. In contrast, cyclin D1 was not detected either in the retina or in the RPE. At 2 and 4 days after the retinal detachment, RPE cells under the detached retina were negative for p27(KIP1) and positive for cyclin D1 and PCNA. In the INL of the detached retina, p27(KIP1) was detected after 2 days, but was not detected after 4 days. In contrast, PCNA was not detected in the INL after 2 days, but was detected after 4 days. Cyclin D1 was detected in the middle sublayer of the INL at both 2 and 4 days after the retinal detachment.
These results suggested that degradation of p27(KIP1) and expression of cyclin D1 was involved in the proliferation of the Müller cells as well as RPE cells after retinal detachment.
研究视网膜脱离后视网膜及视网膜色素上皮(RPE)中p27(KIP1)、细胞周期蛋白D1和增殖细胞核抗原(PCNA)的表达情况。
使用抗p27(KIP1)、抗细胞周期蛋白D1、抗增殖细胞核抗原(PCNA)抗体以及抗谷氨酸合成酶(GS)抗体,通过免疫细胞化学方法分析正常C57B16小鼠眼睛以及视网膜脱离2天或4天后的眼睛。
p27(KIP1)阳性细胞核分布于正常小鼠眼睛的内核层(INL)和RPE中。在INL中,p27(KIP1)在中间亚层被检测到,该亚层是谷氨酸合成酶阳性的穆勒细胞的细胞核所在位置。相比之下,在视网膜或RPE中均未检测到细胞周期蛋白D1。视网膜脱离后2天和4天,脱离视网膜下方的RPE细胞p27(KIP1)呈阴性,细胞周期蛋白D1和PCNA呈阳性。在脱离视网膜的INL中,2天后检测到p27(KIP1),但4天后未检测到。相反,2天后INL中未检测到PCNA,但4天后检测到。视网膜脱离后2天和4天,在INL的中间亚层均检测到细胞周期蛋白D1。
这些结果表明,p27(KIP1)的降解和细胞周期蛋白D1的表达与视网膜脱离后穆勒细胞以及RPE细胞的增殖有关。