正常角膜内抗原呈递细胞的分层。

Jared E Knickelbein, Simon C Watkins, Paul G McMenamin, Robert L Hendricks
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引用次数: 87

摘要

专业抗原呈递细胞(APC)的组成和位置在不同的粘膜表面是不同的。长期以来,角膜被认为是一种缺乏apc的免疫特权组织,现在已知它拥有骨髓来源细胞的异质网络。在这里,我们利用表达CD11c启动子(pCD11c)增强绿色荧光蛋白(EGFP)的转基因小鼠,结合免疫组织化学染色,在非炎症小鼠角膜中展示了apc的有趣分层。pCD11c(+)树突状细胞(dc)位于基底上皮,似乎嵌入基底膜。大多数dc至少在一些树突上表达MHC II类,树突长度可达50µm,向上皮顶端表面切向20µm。直流电密度从角膜周围到中央逐渐降低。在dc下方和基底膜基质侧附近存在pCD11c(-) CD11b(+)巨噬细胞,它们表达低水平的MHC II类。最后,MHC II类(-)pCD11c(-) CD11b(+)细胞在基质的其余部分形成一个网络。这种高度可复制的骨髓源性细胞分层表明,暴露在角膜表面的APC功能向基质深处的先天免疫屏障功能发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Stratification of Antigen-presenting Cells within the Normal Cornea.

Stratification of Antigen-presenting Cells within the Normal Cornea.

Stratification of Antigen-presenting Cells within the Normal Cornea.

Stratification of Antigen-presenting Cells within the Normal Cornea.

The composition and location of professional antigen presenting cells (APC) varies in different mucosal surfaces. The cornea, long considered an immune-privileged tissue devoid of APCs, is now known to host a heterogeneous network of bone marrow-derived cells. Here, we utilized transgenic mice that express enhanced green fluorescent protein (EGFP) from the CD11c promoter (pCD11c) in conjunction with immunohistochemical staining to demonstrate an interesting stratification of APCs within non-inflamed murine corneas. pCD11c(+) dendritic cells (DCs) reside in the basal epithelium, seemingly embedded in the basement membrane. Most DCs express MHC class II on at least some dendrites, which extend up to 50 µm in length and traverse up 20 µm tangentially towards the apical surface of the epithelium. The DC density diminishes from peripheral to central cornea. Beneath the DCs and adjacent to the stromal side of the basement membrane reside pCD11c(-) CD11b(+) putative macrophages that express low levels of MHC class II. Finally, MHC class II(-)pCD11c(-) CD11b(+) cells form a network throughout the remainder of the stroma. This highly reproducible stratification of bone marrow-derived cells is suggestive of a progression from an APC function at the exposed corneal surface to an innate immune barrier function deeper in the stroma.

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