The multifaceted role of vitreous hyalocytes: Orchestrating inflammation, angiomodulation and erythrophagocytosis in proliferative diabetic retinopathy.

IF 9.3 1区 医学 Q1 IMMUNOLOGY Journal of Neuroinflammation Pub Date : 2024-11-14 DOI:10.1186/s12974-024-03291-5
Stefaniya K Boneva, Julian Wolf, Malte Jung, Gabriele Prinz, Toco Y P Chui, Jacqueline Jauch, Anne Drougard, J Andrew Pospisilik, Anja Schlecht, Felicitas Bucher, Richard B Rosen, Hansjürgen Agostini, Günther Schlunck, Clemens A K Lange
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Abstract

Background: Despite great advances in proliferative diabetic retinopathy (PDR) therapy over the last decades, one third of treated patients continue to lose vision. While resident vitreous macrophages called hyalocytes have been implicated in the pathophysiology of vitreoretinal proliferative disease previously, little is known about their exact role in PDR. In this study, we address molecular and cellular alterations in the vitreous of PDR patients as a means towards assessing the potential contribution of hyalocytes to disease pathogenesis.

Results: A total of 55 patients were included in this study encompassing RNA-Sequencing analysis of hyalocytes isolated from the vitreous of PDR and control patients, multiplex immunoassay and ELISA analyses of vitreous samples from PDR and control patients, as well as isolation and immunohistochemical staining of cultured porcine hyalocytes. Transcriptional analysis revealed an enhanced inflammatory response of hyalocytes contributing to the cytokine pool within the vitreous of PDR patients by expressing interleukin-6, among others. Further, increased angiopoietin-2 expression indicated that hyalocytes from PDR patients undergo a proangiogenic shift and may thus mediate the formation of retinal neovascularizations, the hallmark of PDR. Finally, RNA-Sequencing revealed an upregulation of factors known from hemoglobin catabolism in hyalocytes from PDR patients. By immunohistochemistry, cultured porcine hyalocytes exposed to red blood cells were shown to engulf and phagocytose these, which reveals hyalocytes' potential to dispose of erythrocytes. Thus, our data suggest a potential role for vitreous macrophages in erythrophagocytosis and, thereby, clearance of vitreous hemorrhage, a severe complication of PDR.

Conclusion: Our results strongly indicate a critical role for vitreous hyalocytes in key pathophysiological processes of proliferative diabetic retinopathy: inflammation, angiomodulation and erythrophagocytosis. Immunomodulation of hyalocytes may thus prove an essential novel therapeutic approach in diabetic vitreoretinal disease.

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玻璃体透明细胞的多重作用:在增殖性糖尿病视网膜病变中协调炎症、血管调节和红细胞吞噬。
背景:尽管过去几十年来增殖性糖尿病视网膜病变(PDR)治疗取得了巨大进步,但三分之一接受治疗的患者视力仍在下降。虽然被称为透明细胞的玻璃体巨噬细胞与玻璃体视网膜增殖性疾病的病理生理学有关,但人们对其在 PDR 中的确切作用知之甚少。在本研究中,我们探讨了 PDR 患者玻璃体内的分子和细胞变化,以此评估透明细胞对疾病发病机制的潜在作用:本研究共纳入55名患者,包括对从PDR患者和对照组患者玻璃体中分离出的透明细胞进行RNA测序分析,对PDR患者和对照组患者的玻璃体样本进行多重免疫测定和ELISA分析,以及对培养的猪透明细胞进行分离和免疫组织化学染色。转录分析表明,PDR 患者玻璃体内的透明细胞通过表达白细胞介素-6 等细胞因子而增强了炎症反应。此外,血管生成素-2表达的增加表明,PDR患者的透明细胞发生了促血管生成的转变,从而可能介导视网膜新生血管的形成,而这正是PDR的特征。最后,RNA 序列测定显示,在 PDR 患者的透明细胞中,已知的血红蛋白分解因子上调。通过免疫组化,暴露于红细胞的猪透明质酸培养细胞可吞噬红细胞,这表明透明质酸细胞具有处理红细胞的潜力。因此,我们的数据表明了玻璃体巨噬细胞在红细胞吞噬中的潜在作用,从而清除了玻璃体出血(PDR的一种严重并发症):我们的研究结果有力地表明了玻璃体透明细胞在增殖性糖尿病视网膜病变的关键病理生理过程中的关键作用:炎症、血管调节和红细胞吞噬。因此,对透明质细胞的免疫调节可能被证明是糖尿病玻璃体视网膜病变的一种重要的新型治疗方法。
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来源期刊
Journal of Neuroinflammation
Journal of Neuroinflammation 医学-神经科学
CiteScore
15.90
自引率
3.20%
发文量
276
审稿时长
1 months
期刊介绍: The Journal of Neuroinflammation is a peer-reviewed, open access publication that emphasizes the interaction between the immune system, particularly the innate immune system, and the nervous system. It covers various aspects, including the involvement of CNS immune mediators like microglia and astrocytes, the cytokines and chemokines they produce, and the influence of peripheral neuro-immune interactions, T cells, monocytes, complement proteins, acute phase proteins, oxidative injury, and related molecular processes. Neuroinflammation is a rapidly expanding field that has significantly enhanced our knowledge of chronic neurological diseases. It attracts researchers from diverse disciplines such as pathology, biochemistry, molecular biology, genetics, clinical medicine, and epidemiology. Substantial contributions to this field have been made through studies involving populations, patients, postmortem tissues, animal models, and in vitro systems. The Journal of Neuroinflammation consolidates research that centers around common pathogenic processes. It serves as a platform for integrative reviews and commentaries in this field.
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