Institute for Experimental Cancer Research in Pediatrics, Goethe-University, Komturstraße 3a, 60528 Frankfurt, Germany.
Faculty of Medicine, Institute of Biochemistry I, Goethe-University, Theodor-Stern-Kai 7, 60590 Frankfurt, Germany.
Int J Mol Sci. 2021 Feb 24;22(5):2230. doi: 10.3390/ijms22052230.
The interaction of macrophages with apoptotic cells is required for efficient resolution of inflammation. While apoptotic cell removal prevents inflammation due to secondary necrosis, it also alters the macrophage phenotype to hinder further inflammatory reactions. The interaction between apoptotic cells and macrophages is often studied by chemical or biological induction of apoptosis, which may introduce artifacts by affecting the macrophages as well and/or triggering unrelated signaling pathways. Here, we set up a pure cell death system in which NIH 3T3 cells expressing dimerizable Caspase-8 were co-cultured with peritoneal macrophages in a transwell system. Phenotype changes in macrophages induced by apoptotic cells were evaluated by RNA sequencing, which revealed an unexpectedly dominant impact on macrophage proliferation. This was confirmed in functional assays with primary peritoneal macrophages and IC-21 macrophages. Moreover, inhibition of apoptosis during Zymosan-induced peritonitis in mice decreased mRNA levels of cell cycle mediators in peritoneal macrophages. Proliferation of macrophages in response to apoptotic cells may be important to increase macrophage numbers in order to allow efficient clearance and resolution of inflammation.
巨噬细胞与凋亡细胞的相互作用是炎症有效消退所必需的。虽然凋亡细胞的清除可防止由于继发性坏死引起的炎症,但它也改变了巨噬细胞的表型,从而阻碍了进一步的炎症反应。凋亡细胞与巨噬细胞之间的相互作用通常通过化学或生物诱导凋亡来研究,这可能会通过影响巨噬细胞本身和/或触发不相关的信号通路而引入假象。在这里,我们建立了一个纯细胞死亡系统,其中表达二聚化 Caspase-8 的 NIH 3T3 细胞与腹膜巨噬细胞在 Transwell 系统中共培养。通过 RNA 测序评估凋亡细胞诱导的巨噬细胞表型变化,结果显示对巨噬细胞增殖具有出乎意料的主导影响。这在用原代腹膜巨噬细胞和 IC-21 巨噬细胞进行的功能测定中得到了证实。此外,在小鼠酵母聚糖诱导的腹膜炎中抑制凋亡会降低腹膜巨噬细胞中细胞周期调节剂的 mRNA 水平。凋亡细胞刺激的巨噬细胞增殖可能对于增加巨噬细胞数量以允许有效清除和消退炎症很重要。