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CSF2在视网膜变性过程中作为炎症调节因子的作用。

Roles of CSF2 as a modulator of inflammation during retinal degeneration.

作者信息

Saita Kosuke, Moriuchi Yuta, Iwagawa Toshiro, Aihara Makoto, Takai Yoshihiro, Uchida Kanji, Watanabe Sumiko

机构信息

Department of Retinal Biology and Pathology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan; Department of Molecular and Developmental Biology, Institute of Medical Science, University of Tokyo, Tokyo, Japan; Department of Anesthesiology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.

Department of Retinal Biology and Pathology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan; Department of Molecular and Developmental Biology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.

出版信息

Cytokine. 2022 Oct;158:155996. doi: 10.1016/j.cyto.2022.155996. Epub 2022 Aug 18.

Abstract

Colony-stimulating factor 2 (CSF2) is a potent cytokine that stimulates myeloid cells, such as dendritic cells and macrophages. We have been analyzing the roles of microglia in retinal degeneration through the modulation of inflammation in the eye, and examined the roles of CSF2 in this process. Both subunits of the CSF2 receptor are expressed in microglia, but no evidence suggesting the involvement of CSF2 in inflammation in the degenerating eye has been reported. We found that Csf2 transcripts were induced in the early phase of in vitro mouse adult retina culture, used as degeneration models, suggesting that CSF2 induction is one of the earliest events occurring in the pathology of retinal degeneration. The administration of CSF2 into the retina after systemic NaIO treatment increased the number of microglia. To examine the roles of CSF2 in retinal inflammation, we overexpressed CSF2 in retinal explants. Induction of CSF2 activated microglia and Müller glia, and the layer structure of the retina was severely perturbed. CC motif chemokine ligand 2 (Ccl2) and C-X-C motif chemokine ligand 10 (Cxcl10), both of which are expressed in activated microglia, were strongly induced by the expression of CSF2 in the retina. The addition of CSF2 to primary retinal microglia and the microglial cell lines MG5 and BV2 showed statistically significant increase in Ccl2 and Il1b transcripts. Furthermore, CSF2 induced proliferation, migration, and phagocytosis in MG5 and/or BV2. The effects of CSF2 on microglia were mild, suggesting that CSF2 induced strong inflammation in the context of the retinal environment.

摘要

集落刺激因子2(CSF2)是一种强效细胞因子,可刺激髓样细胞,如树突状细胞和巨噬细胞。我们一直在通过调节眼部炎症来分析小胶质细胞在视网膜变性中的作用,并研究了CSF2在此过程中的作用。CSF2受体的两个亚基均在小胶质细胞中表达,但尚无证据表明CSF2参与了变性眼中的炎症。我们发现,在用作变性模型的体外小鼠成年视网膜培养的早期阶段可诱导Csf2转录本,这表明CSF2的诱导是视网膜变性病理过程中最早发生的事件之一。在全身注射碘酸钠后向视网膜中注射CSF2可增加小胶质细胞的数量。为了研究CSF2在视网膜炎症中的作用,我们在视网膜外植体中过表达了CSF2。CSF2的诱导激活了小胶质细胞和穆勒胶质细胞,并且视网膜的层结构受到严重干扰。CC基序趋化因子配体2(Ccl2)和C-X-C基序趋化因子配体10(Cxcl10)均在活化的小胶质细胞中表达,它们在视网膜中因CSF2的表达而被强烈诱导。向原代视网膜小胶质细胞以及小胶质细胞系MG5和BV2中添加CSF2后,Ccl2和Il1b转录本有统计学意义的增加。此外,CSF2诱导了MG5和/或BV2的增殖、迁移和吞噬作用。CSF2对小胶质细胞的作用较轻,这表明CSF2在视网膜环境中诱导了强烈的炎症。

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