Krysko D V, Denecker G, Festjens N, Gabriels S, Parthoens E, D'Herde K, Vandenabeele P
Department of Human Anatomy, Embryology, Histology and Medical Physics, Ghent University, Ghent 9000, Belgium.
Cell Death Differ. 2006 Dec;13(12):2011-22. doi: 10.1038/sj.cdd.4401900. Epub 2006 Apr 21.
The present study characterized two different internalization mechanisms used by macrophages to engulf apoptotic and necrotic cells. Our in vitro phagocytosis assay used a mouse macrophage cell line, and murine L929sAhFas cells that are induced to die in a necrotic way by TNFR1 and heat shock or in an apoptotic way by Fas stimulation. Scanning electron microscopy (SEM) revealed that apoptotic bodies were taken up by macrophages with formation of tight fitting phagosomes, similar to the 'zipper'-like mechanism of phagocytosis, whereas necrotic cells were internalized by a macropinocytotic mechanism involving formation of multiple ruffles directed towards necrotic debris. Two macropinocytosis markers (Lucifer Yellow (LY) and horseradish peroxidase (HRP)) were excluded from the phagosomes containing apoptotic bodies, but they were present inside the macropinosomes containing necrotic material. Wortmannin (phosphatidylinositol 3'-kinase (PI3K) inhibitor) reduced the uptake of apoptotic cells, but the engulfment of necrotic cells remained unaffected. Our data demonstrate that apoptotic and necrotic cells are internalized differently by macrophages.
本研究对巨噬细胞用于吞噬凋亡细胞和坏死细胞的两种不同内化机制进行了表征。我们的体外吞噬试验使用了小鼠巨噬细胞系,以及通过TNFR1和热休克以坏死方式诱导死亡或通过Fas刺激以凋亡方式诱导死亡的小鼠L929sAhFas细胞。扫描电子显微镜(SEM)显示,凋亡小体被巨噬细胞摄取,形成紧密贴合的吞噬体,类似于吞噬作用的“拉链”样机制,而坏死细胞则通过一种巨胞饮机制内化,该机制涉及形成多个指向坏死碎片的褶皱。两种巨胞饮标志物(荧光黄(LY)和辣根过氧化物酶(HRP))被排除在含有凋亡小体的吞噬体之外,但它们存在于含有坏死物质的巨胞饮体内部。渥曼青霉素(磷脂酰肌醇3'-激酶(PI3K)抑制剂)减少了凋亡细胞的摄取,但坏死细胞的吞噬不受影响。我们的数据表明,巨噬细胞对凋亡细胞和坏死细胞的内化方式不同。