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A Novel Method to Determine the Engulfment of Apoptotic Cells by Macrophages using pHrodo Succinimidyl Ester

机译:用pHrodo琥珀酰亚胺酯测定巨噬细胞吞噬凋亡细胞的新方法

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摘要

Apoptotic cell phagocytosis has recently raised considerable interest, particularly due to its intricate molecular mechanisms and negative immunologic impact of incompetent clearance of apoptotic cells. There is a need for simple and reliable methods to clearly determine the internalization of apoptotic cells. Labeling with pHrodo succinimidyl ester (SE), a pH-sensitive fluorescent dye, makes engulfed apoptotic cells detectable due to the increased post-phagocytic light emission. This is a valuable tool for phagocytosis studies via FACS. We designed an ex vivo assay, using apoptotic pHrodo-labeled lymphocytes as prey and anti-CD11b-labeled tissue macrophages. To demonstrate its validity of detecting internalized apoptotic lymphocytes, we used MFGE8-/- macrophages, known to have impaired phagocytic ability. Uptake of apoptotic lymphocytes was accelerated and enhanced in splenic macrophages after stimulation with recombinant MFGE8, while peritoneal macrophages were able to compensate for the delayed uptake. This novel assay is a quick and reliable method to evaluate the internalization of apoptotic cells.
机译:凋亡细胞吞噬作用最近引起了人们的极大兴趣,特别是由于其复杂的分子机制和凋亡细胞清除不当所产生的负面免疫学影响。需要简单可靠的方法来清楚地确定凋亡细胞的内在化。对pH敏感的荧光染料pHrodo琥珀酰亚胺酯(SE)进行标记,由于吞噬后的发光增加,吞噬的凋亡细胞可被检测到。这是通过FACS进行吞噬作用研究的有价值的工具。我们设计了一种离体测定,使用凋亡的pHrodo标记的淋巴细胞作为猎物和抗CD11b标记的组织巨噬细胞。为了证明其检测内在凋亡淋巴细胞的有效性,我们使用了已知具有吞噬能力受损的MFGE8 -/-巨噬细胞。重组MFGE8刺激后,脾巨噬细胞中凋亡淋巴细胞的摄取被加速并增强,而腹膜巨噬细胞能够补偿延迟的摄取。这种新颖的测定方法是一种快速而可靠的方法,可以评估凋亡细胞的内在化。

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