Department of Pharmacology and Toxicology College of Medicine, University of Arkansas for Medical Sciences (UAMS), 4301 West Markham Street, Slot 611, BIOMED-1, B306, Little Rock, Office, AR, 72205, USA.
Clinical Pharmacy Department, Cairo University, Cairo, Egypt.
J Neuroinflammation. 2024 Jul 12;21(1):170. doi: 10.1186/s12974-024-03159-8.
Ischemia-induced retinopathy is a hallmark finding of common visual disorders including diabetic retinopathy (DR) and central retinal artery and vein occlusions. Treatments for ischemic retinopathies fail to improve clinical outcomes and the design of new therapies will depend on understanding the underlying disease mechanisms. Histone deacetylases (HDACs) are an enzyme class that removes acetyl groups from histone and non-histone proteins, thereby regulating gene expression and protein function. HDACs have been implicated in retinal neurovascular injury in preclinical studies in which nonspecific HDAC inhibitors mitigated retinal injury. Histone deacetylase 3 (HDAC3) is a class I histone deacetylase isoform that plays a central role in the macrophage inflammatory response. We recently reported that myeloid cells upregulate HDAC3 in a mouse model of retinal ischemia-reperfusion (IR) injury. However, whether this cellular event is an essential contributor to retinal IR injury is unknown. In this study, we explored the role of myeloid HDAC3 in ischemia-induced retinal neurovascular injury by subjecting myeloid-specific HDAC3 knockout (M-HDAC3 KO) and floxed control mice to retinal IR. The M-HDAC3 KO mice were protected from retinal IR injury as shown by the preservation of inner retinal neurons, vascular integrity, and retinal thickness. Electroretinography confirmed that this neurovascular protection translated to improved retinal function. The retinas of M-HDAC3 KO mice also showed less proliferation and infiltration of myeloid cells after injury. Interestingly, myeloid cells lacking HDAC3 more avidly engulfed apoptotic cells in vitro and after retinal IR injury in vivo compared to wild-type myeloid cells, suggesting that HDAC3 hinders the reparative phagocytosis of dead cells, a process known as efferocytosis. Further mechanistic studies indicated that although HDAC3 KO macrophages upregulate the reparative enzyme arginase 1 (A1) that enhances efferocytosis, the inhibitory effect of HDAC3 on efferocytosis is not solely dependent on A1. Finally, treatment of wild-type mice with the HDAC3 inhibitor RGFP966 ameliorated the retinal neurodegeneration and thinning caused by IR injury. Collectively, our data show that HDAC3 deletion enhances macrophage-mediated efferocytosis and protects against retinal IR injury, suggesting that inhibiting myeloid HDAC3 holds promise as a novel therapeutic strategy for preserving retinal integrity after ischemic insult.
缺血性视网膜病变是包括糖尿病视网膜病变(DR)和视网膜中央动脉和静脉阻塞在内的常见视觉障碍的标志性发现。缺血性视网膜病变的治疗未能改善临床结果,新疗法的设计将取决于对潜在疾病机制的理解。组蛋白去乙酰化酶(HDACs)是一类从组蛋白和非组蛋白蛋白中去除乙酰基的酶,从而调节基因表达和蛋白功能。在非特异性 HDAC 抑制剂减轻视网膜损伤的临床前研究中,HDACs 被牵连到视网膜神经血管损伤中。组蛋白去乙酰化酶 3(HDAC3)是一种 I 类组蛋白去乙酰化酶同工型,在巨噬细胞炎症反应中发挥核心作用。我们最近报道,在视网膜缺血再灌注(IR)损伤的小鼠模型中,髓样细胞上调 HDAC3。然而,这种细胞事件是否是视网膜 IR 损伤的一个重要贡献者尚不清楚。在这项研究中,我们通过对髓样细胞特异性 HDAC3 敲除(M-HDAC3 KO)和 floxed 对照小鼠进行视网膜 IR,探讨了髓样细胞 HDAC3 在缺血诱导的视网膜神经血管损伤中的作用。M-HDAC3 KO 小鼠的视网膜 IR 损伤得到保护,表现为内视网膜神经元、血管完整性和视网膜厚度的保留。视网膜电图证实,这种神经血管保护转化为视网膜功能的改善。M-HDAC3 KO 小鼠的视网膜损伤后,髓样细胞的增殖和浸润也减少。有趣的是,与野生型髓样细胞相比,缺乏 HDAC3 的髓样细胞在体外和体内视网膜 IR 损伤后更有效地吞噬凋亡细胞,这表明 HDAC3 阻碍了对死亡细胞的修复性吞噬,这一过程称为吞噬作用。进一步的机制研究表明,尽管 HDAC3 KO 巨噬细胞上调增强吞噬作用的修复性酶精氨酸酶 1(A1),但 HDAC3 对吞噬作用的抑制作用并不完全依赖于 A1。最后,用 HDAC3 抑制剂 RGFP966 治疗野生型小鼠可改善 IR 损伤引起的视网膜神经退行性变和变薄。总之,我们的数据表明,HDAC3 缺失增强了巨噬细胞介导的吞噬作用,并防止了视网膜 IR 损伤,这表明抑制髓样细胞 HDAC3 有望成为缺血性损伤后保持视网膜完整性的一种新的治疗策略。