Hou Chao, Wu Qianni, Ouyang Chen, Huang Ting
State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, Guangdong 510030, P.R. China.
Int J Mol Med. 2016 Sep;38(3):713-20. doi: 10.3892/ijmm.2016.2688. Epub 2016 Jul 22.
In order to explore the potential effects of interleukin (IL)-35 on IL-10, transforming growth factor-β (TGF-β), interferon-γ (INF)-γ, IL-12 and IL-17, a pcDNA3.1‑IL-35 plasmid was injected into the vitreous cavity of BALB/c mice. Enzyme-linked immunosorbent assay, western blot analysis and quantitative PCR analysis were performed to confirm the successful expression of IL-35. Slit-lamp biomicroscopy, hematoxylin and eosin staining and immunofluorescence were employed to detect the status of eyes, and western blot analysis was performed to examine the expression of corneal graft rejection-related cytokines. There were no abnormalities in the eyes pre-mydriasis or post-mydriasis and no injuries to the cornea or retina following the injection of IL-35-expressing plasmid. An immunofluorescence assay detected the positive expression of IL-35 in corneal epithelial cells from IL-35‑injected mice and negative staining in the control group. Further study revealed that IL-35 enhanced the expression of IL-10 and TGF-β which reached their highest levels at 1 and 2 weeks after injection, respectively (p<0.01). Moreover, the expression of INF-γ and IL-12 was decreased significantly at 2 weeks after the injection of IL-35-expressing plasmid (p<0.05), and the expression of IL-17 was suppressed notably at 4 weeks after the injection (p<0.05). The intravitreal injection of IL-35-expressing plasmid in mice downregulates the expression of pro-inflammatory cytokines and upregulates the expression of anti-inflammatory cytokines. Thus, IL-35 may further be assessed as a potential target for the treatment of corneal graft rejection.
为了探究白细胞介素(IL)-35对IL-10、转化生长因子-β(TGF-β)、干扰素-γ(INF-γ)、IL-12和IL-17的潜在影响,将pcDNA3.1-IL-35质粒注入BALB/c小鼠的玻璃体腔。采用酶联免疫吸附测定、蛋白质印迹分析和定量PCR分析来确认IL-35的成功表达。使用裂隙灯生物显微镜检查、苏木精-伊红染色和免疫荧光检测眼睛状况,并通过蛋白质印迹分析检测角膜移植排斥相关细胞因子的表达。注射表达IL-35的质粒后,散瞳前和散瞳后眼睛均无异常,角膜或视网膜也未受到损伤。免疫荧光测定检测到注射IL-35小鼠的角膜上皮细胞中IL-35呈阳性表达,而对照组为阴性染色。进一步研究表明,IL-35增强了IL-10和TGF-β的表达,它们分别在注射后1周和2周达到最高水平(p<0.01)。此外,注射表达IL-35的质粒后2周,INF-γ和IL-12的表达显著降低(p<0.05),注射后4周IL-17的表达明显受到抑制(p<0.05)。向小鼠玻璃体腔内注射表达IL-35的质粒可下调促炎细胞因子的表达并上调抗炎细胞因子的表达。因此,IL-35可能进一步被评估为治疗角膜移植排斥的潜在靶点。