Institute for Anatomy and Cell Biology, Ludwig Maximilian University of Munich, Schillerstr. 42, 80336 Munich, Germany.
Traffic. 2011 Mar;12(3):301-12. doi: 10.1111/j.1600-0854.2010.01147.x. Epub 2011 Jan 7.
Dictyostelium discoideum cells are professional phagocytes that provide an easily accessible system to gain insights into the mechanisms and the regulatory machinery controlling phagocytosis. Here, we describe a novel function for nuclear Dbf2-related (NDR) family kinases in phagocytosis of D. discoideum. Deletion of one of the four NDR kinases of D. discoideum, NdrA, resulted in impaired cell growth caused by reduced phagocytosis rates. Detailed analysis of NdrA-null cells revealed that the formation of phagocytic cups was delayed. Microscopic investigations showed that NdrA localizes to centrosomes, and NdrA was also identified in isolated centrosome preparations. The localization of NdrA is regulated during the cell cycle. In prophase, NdrA disappears from the centrosome and forms a cloud-like structure around the spindle, which is totally absent during later stages until completion of mitosis. Our results suggest that a signal which originates from the NdrA kinase at the centrosome affects the efficiency of phagocytosis. We assume that in NdrA-null cells the defects in phagocytosis may be caused by an impairment of vesicle trafficking, which is involved in providing new membrane at the sites of particle uptake.
粘菌细胞是专业的吞噬细胞,为我们深入了解控制吞噬作用的机制和调节机制提供了一个易于接近的系统。在这里,我们描述了核 Dbf2 相关(NDR)家族激酶在粘菌吞噬作用中的新功能。粘菌的四个 NDR 激酶之一 NdrA 的缺失导致吞噬率降低,从而导致细胞生长受损。对 NdrA 缺失细胞的详细分析表明,吞噬杯的形成被延迟。显微镜研究表明,NdrA 定位于中心体,并且在分离的中心体制剂中也鉴定出 NdrA。NdrA 的定位在细胞周期中受到调节。在前期,NdrA 从中心体消失,并在纺锤体周围形成云状结构,在后期直到有丝分裂完成时完全不存在。我们的结果表明,源自中心体的 NdrA 激酶的信号影响吞噬作用的效率。我们假设在 NdrA 缺失细胞中,吞噬作用的缺陷可能是由于囊泡运输的损伤引起的,这与在颗粒摄取部位提供新膜有关。