小鼠视网膜髓系细胞的多色流式细胞术研究。

Wei Xiao, Rami A Shahror, Carol A Morris, Ruth B Caldwell, Abdelrahman Y Fouda
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摘要

髓系细胞,特别是小胶质细胞和巨噬细胞,在视网膜疾病中被激活,并可根据其炎症表型改善或恶化视网膜病变的结果。然而,评估小鼠视网膜损伤后骨髓细胞的反应仍然具有挑战性,因为组织尺寸小,并且很难区分小胶质细胞和浸润性巨噬细胞。在这篇协议论文中,我们描述了一种基于流式细胞术的方案来评估视网膜小胶质细胞/巨噬细胞及其损伤后的炎症表型。该方案适用于纳入其他研究人员感兴趣的其他标记。本协议描述了一种基于流式细胞术的方法来分析视网膜病变小鼠模型中的骨髓细胞反应。该方案可以区分小胶质细胞和单核细胞来源的巨噬细胞。它可以被修改为包含感兴趣的标记。我们展示了三种不同视网膜病变模型的代表性结果,即缺血再灌注损伤、内毒素诱导的葡萄膜炎和氧诱导的视网膜病变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Multi-color Flow Cytometry Protocol to Characterize Myeloid Cells in Mouse Retina Research.

Myeloid cells, specifically microglia and macrophages, are activated in retinal diseases and can improve or worsen retinopathy outcomes based on their inflammatory phenotype. However, assessing the myeloid cell response after retinal injury in mice remains challenging due to the small tissue size and the challenges of distinguishing microglia from infiltrating macrophages. In this protocol paper, we describe a flow cytometry-based protocol to assess retinal microglia/macrophage and their inflammatory phenotype after injury. The protocol is amenable to the incorporation of other markers of interest to other researchers. Key features This protocol describes a flow cytometry-based method to analyze the myeloid cell response in retinopathy mouse models. The protocol can distinguish between microglia- and monocyte-derived macrophages. It can be modified to incorporate markers of interest. We show representative results from three different retinopathy models, namely ischemia-reperfusion injury, endotoxin-induced uveitis, and oxygen-induced retinopathy.

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