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解析视网膜神经节细胞层中的血管周围巨噬细胞和小胶质细胞。

Deciphering perivascular macrophages and microglia in the retinal ganglion cell layers.

作者信息

Jeon Jehwi, Park Yong Soo, Kim Sang-Hoon, Kong Eunji, Kim Jay, Yang Jee Myung, Lee Joo Yong, Kim You-Me, Kim In-Beom, Kim Pilhan

机构信息

Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea.

KI for Health Science and Technology (KIHST), Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea.

出版信息

Front Cell Dev Biol. 2024 Mar 26;12:1368021. doi: 10.3389/fcell.2024.1368021. eCollection 2024.

Abstract

The classically defined two retinal microglia layers are distributed in inner and outer plexiform layers. Although there are some reports that retinal microglia are also superficially located around the ganglion cell layer (GCL) in contact with the vitreous, there has been a lack of detailed descriptions and not fully understood yet. We visualized the microglial layers by using CX3CR1-GFP (C57BL6) transgenic mice with both healthy and disease conditions including NaIO3-induced retinal degeneration models and IRBP-induced auto-immune uveitis models. We found the GCL microglia has two subsets; peripheral (pph) microglia located on the retinal parenchyma and BAM (CNS Border Associated Macrophage) which have a special stretched phenotype only located on the surface of large retinal veins. First, in the pph microglia subset, but not in BAM, Galectin-3 and LYVE1 are focally expressed. However, LYVE1 is specifically expressed in the amoeboid or transition forms, except the typical dendritic morphology in the pph microglia. Second, BAM is tightly attached to the surface of the retinal veins and has similar morphology patterns in both the healthy and disease conditions. CD86 BAM has a longer process which vertically passes the proximal retinal veins. Our data helps decipher the basic anatomy and pathophysiology of the retinal microglia in the GCL. Our data helps decipher the basic anatomy and pathophysiology of the retinal microglia in the GCL.

摘要

传统定义的两层视网膜小胶质细胞分布在内、外丛状层。尽管有一些报道称视网膜小胶质细胞也位于神经节细胞层(GCL)表面并与玻璃体接触,但目前缺乏详细描述且尚未完全了解。我们使用CX3CR1-GFP(C57BL6)转基因小鼠,在包括碘酸钠诱导的视网膜变性模型和视网膜视黄醛结合蛋白诱导的自身免疫性葡萄膜炎模型等健康和疾病状态下,对小胶质细胞层进行了可视化观察。我们发现GCL小胶质细胞有两个亚群:位于视网膜实质的外周(pph)小胶质细胞和仅位于视网膜大静脉表面、具有特殊伸展表型的边界相关巨噬细胞(BAM)。首先,在pph小胶质细胞亚群中,而不是在BAM中,半乳糖凝集素-3和淋巴管内皮透明质酸受体1(LYVE1)呈局灶性表达。然而,LYVE1在pph小胶质细胞的变形虫样或过渡形态中特异性表达,而非典型树突形态。其次,BAM紧密附着于视网膜静脉表面,在健康和疾病状态下具有相似的形态模式。CD86+BAM有一个较长的突起,垂直穿过视网膜近端静脉。我们的数据有助于解读GCL中视网膜小胶质细胞的基本解剖结构和病理生理学。我们的数据有助于解读GCL中视网膜小胶质细胞的基本解剖结构和病理生理学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f42/11002095/c21afe4e561a/fcell-12-1368021-g001.jpg

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