Baiula Monica, Caligiana Alberto, Bedini Andrea, Zhao Junwei, Santino Federica, Cirillo Martina, Gentilucci Luca, Giacomini Daria, Spampinato Santi
Laboratory of Cellular and Molecular Pharmacology, Department of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy.
Department of Chemistry "G. Ciamician", University of Bologna, Bologna, Italy.
Front Pharmacol. 2021 Jan 29;11:617836. doi: 10.3389/fphar.2020.617836. eCollection 2020.
Age-related macular degeneration (AMD) is a complex multifactorial degenerative disease that leads to irreversible blindness. AMD affects the macula, the central part of the retina responsible for sharp central vision. Retinal pigment epithelium (RPE) is the main cellular type affected in dry AMD. RPE cells form a monolayer between the choroid and the neuroretina and are in close functional relationship with photoreceptors; moreover, RPE cells are part of the blood retina barrier that is disrupted in ocular diseases such as AMD. During ocular inflammation lymphocytes and macrophages are recruited, contact RPE and produce pro-inflammatory cytokines, which play an important role in AMD pathogenesis. The interaction between RPE and immune cells is mediated by leukocyte integrins, heterodimeric transmembrane receptors, and adhesion molecules, including VCAM-1 and ICAM-1. Within this frame, this study aimed to characterize RPE-leukocytes interaction and to investigate any potentially beneficial effects induced by integrin antagonists (DS-70, MN27 and SR714), developed in previous studies. ARPE-19 cells were co-cultured for different incubation times with Jurkat cells and apoptosis and necrosis levels were analyzed by flow cytometry. Moreover, we measured the mRNA levels of the pro-inflammatory cytokine IL-1β and the expression of adhesion molecules VCAM-1 and ICAM-1. We found that RPE-lymphocyte interaction increased apoptosis and necrosis levels in RPE cells and the expression of IL-1β. This interaction was mediated by the binding of αβ and αβ integrins to VCAM-1 and ICAM-1, respectively. The blockade of RPE-lymphocyte interaction with blocking antibodies highlighted the pivotal role played by integrins. Therefore, αβ and αβ integrin antagonists were employed to disrupt RPE-lymphocyte crosstalk. Small molecule integrin antagonists proved to be effective in reducing RPE cell death and expression of IL-1β, demonstrating that integrin antagonists could protect RPE cells from detrimental effects induced by the interaction with immune cells recruited to the retina. Overall, the leukocyte integrin antagonists employed in the present study may represent a novel opportunity to develop new drugs to fight dry AMD.
年龄相关性黄斑变性(AMD)是一种复杂的多因素退行性疾病,可导致不可逆的失明。AMD影响黄斑,即视网膜的中央部分,负责敏锐的中央视觉。视网膜色素上皮(RPE)是干性AMD中受影响的主要细胞类型。RPE细胞在脉络膜和神经视网膜之间形成单层,并与光感受器保持密切的功能关系;此外,RPE细胞是血视网膜屏障的一部分,在诸如AMD等眼部疾病中会被破坏。在眼部炎症期间,淋巴细胞和巨噬细胞被募集,与RPE接触并产生促炎细胞因子,这些细胞因子在AMD发病机制中起重要作用。RPE与免疫细胞之间的相互作用由白细胞整合素、异二聚体跨膜受体和黏附分子介导,包括血管细胞黏附分子-1(VCAM-1)和细胞间黏附分子-1(ICAM-1)。在此框架内,本研究旨在表征RPE与白细胞的相互作用,并研究先前研究中开发的整合素拮抗剂(DS-70、MN27和SR714)诱导的任何潜在有益作用。将ARPE-19细胞与Jurkat细胞共培养不同的孵育时间,并通过流式细胞术分析细胞凋亡和坏死水平。此外,我们测量了促炎细胞因子白细胞介素-1β(IL-1β)的mRNA水平以及黏附分子VCAM-1和ICAM-1的表达。我们发现RPE与淋巴细胞的相互作用增加了RPE细胞的凋亡和坏死水平以及IL-1β的表达。这种相互作用分别由αβ和αβ整合素与VCAM-1和ICAM-1的结合介导。用阻断抗体阻断RPE与淋巴细胞的相互作用突出了整合素所起的关键作用。因此,采用αβ和αβ整合素拮抗剂来破坏RPE与淋巴细胞的串扰。小分子整合素拮抗剂被证明可有效减少RPE细胞死亡和IL-1β的表达,表明整合素拮抗剂可以保护RPE细胞免受与募集到视网膜的免疫细胞相互作用所诱导的有害影响。总体而言,本研究中使用的白细胞整合素拮抗剂可能为开发治疗干性AMD的新药提供新的契机。