Eye Center, Renmin Hospital of Wuhan University, Wuhan, China.
Department of Ophthalmology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Pathol Oncol Res. 2022 Apr 19;28:1610385. doi: 10.3389/pore.2022.1610385. eCollection 2022.
Retinal ischemia reperfusion injury (RIRI) is a conventional pathological process in various retinal vascular diseases. Many studies select only one specific time point to apply drugs and then assess the therapeutic effect of drugs; however, the baselines are not the same at different time points, which may cause variation in the judgement. Therefore, further investigation is needed. Accordingly, this study aimed to investigate the pathological changes of retinal structure, expression of JAK-STAT signaling pathway hallmark proteins, and apoptosis at different time points after retinal ischemia reperfusion injury in rats. Sixty-six male SPF Sprague-Dawley rats were randomly divided into six groups: control group, RIRI 0, 6-, 24-, 72-, and 144-h groups. RIRI models were induced by perfusing equilibrium solution into the right eye anterior chamber to increase intraocular pressure to 110 mmHg for 60 min. Rats were sacrificed at different time points after reperfusion. Then hematoxylin-eosin staining, transmission electron microscope, immunohistochemistry, western blot, and TUNEL were used. Hematoxylin-eosin showed the pathological changes while transmission electron microscope revealed the ultra-structure changes of retina after RIRI. Immunohistochemistry showed that JAK2, STAT3, p-JAK2, p-STAT3, Bax, and Bcl-2 proteins mainly located in ganglion cell layer and inner nuclear layer, the relative expression of former five proteins had significant differences vs. control group ( < 0.05), while Bcl-2 had no significant difference. In western blot, the protein expressing of JAK2, STAT3, p-JAK2, p-STAT3, p-Akt, and Bax had significant differences vs. control group ( < 0.05), while Akt and Bcl-2 had no significant differences. TUNEL staining showed the number of apoptosis positive cells rose initially but declined later, with a peak value at RIRI 24 h group. The dynamic changes of hallmark proteins at different time points after RIRI indicate that JAK-STAT signaling pathway activates rapidly but weakens later and plays a vital role in RIRI, and apoptosis is involved in RIRI with a peak value at 24 h in the process, suggesting a potential therapeutic direction and time window for treating RIRI.
视网膜缺血再灌注损伤(RIRI)是各种视网膜血管疾病中的一种常见病理过程。许多研究仅选择一个特定的时间点应用药物,然后评估药物的治疗效果;然而,不同时间点的基线并不相同,这可能导致判断的变化。因此,需要进一步的研究。因此,本研究旨在探讨大鼠视网膜缺血再灌注损伤后不同时间点视网膜结构的病理变化、JAK-STAT 信号通路标志性蛋白的表达和细胞凋亡。
将 66 只雄性 SPF 级 Sprague-Dawley 大鼠随机分为 6 组:对照组、RIRI0、6、24、72 和 144 h 组。通过向右眼前房灌注平衡溶液将眼内压升高至 110 mmHg 60 min 诱导 RIRI 模型。再灌注后不同时间点处死大鼠。然后进行苏木精-伊红染色、透射电镜、免疫组化、Western blot 和 TUNEL。苏木精-伊红染色观察 RIRI 后视网膜的病理变化,透射电镜观察视网膜的超微结构变化。免疫组化显示 JAK2、STAT3、p-JAK2、p-STAT3、Bax 和 Bcl-2 蛋白主要位于神经节细胞层和内核层,前五种蛋白的相对表达与对照组相比均有显著性差异(<0.05),而 Bcl-2 则无显著性差异。Western blot 显示 JAK2、STAT3、p-JAK2、p-STAT3、p-Akt 和 Bax 蛋白的表达与对照组相比均有显著性差异(<0.05),而 Akt 和 Bcl-2 则无显著性差异。TUNEL 染色显示凋亡阳性细胞数量先增加后减少,24 h 组达到峰值。RIRI 后不同时间点标志性蛋白的动态变化表明,JAK-STAT 信号通路迅速激活,但随后减弱,在 RIRI 中发挥重要作用,凋亡参与 RIRI 过程,24 h 时达到峰值,提示 RIRI 可能的治疗方向和时间窗。