Pei Gang, Repnik Urska, Griffiths Gareth, Gutierrez Maximiliano Gabriel
Research Group Phagosome Biology, Helmholtz Centre for Infection Research, Inhoffenstrasse 7, 38124 Braunschweig, Germany.
J Cell Sci. 2014 May 1;127(Pt 9):2071-82. doi: 10.1242/jcs.144923. Epub 2014 Feb 25.
Interferon-γ (IFN-γ) has been shown to regulate phagosome trafficking and function in macrophages, but the molecular mechanisms involved are poorly understood. Here, we identify Rab20 as part of the machinery by which IFN-γ controls phagosome maturation. We found that IFN-γ stimulates the association of Rab20 with early phagosomes in macrophages. By using imaging of single phagosomes in live cells, we found that Rab20 induces an early delay in phagosome maturation and extends the time for which Rab5a and phosphatidylinositol 3-phosphate (PI3P) remain associated with phagosomes. Moreover, Rab20 depletion in macrophages abrogates the delay in phagosome maturation induced by IFN-γ. Finally, we demonstrate that Rab20 interacts with the Rab5a guanine nucleotide exchange factor Rabex-5 (also known as RABGEF1) and that Rab20 knockdown impairs the IFN-γ-dependent recruitment of Rabex-5 and Rab5a into phagosomes. Taken together, here, we uncover Rab20 as a key player in the Rab cascade by which IFN-γ induces a delay in phagosome maturation in macrophages.
γ干扰素(IFN-γ)已被证明可调节巨噬细胞中吞噬体的运输和功能,但其中涉及的分子机制仍知之甚少。在此,我们确定Rab20是IFN-γ控制吞噬体成熟的机制的一部分。我们发现IFN-γ刺激Rab20与巨噬细胞中的早期吞噬体结合。通过对活细胞中单个吞噬体进行成像,我们发现Rab20会导致吞噬体成熟早期延迟,并延长Rab5a和磷脂酰肌醇3-磷酸(PI3P)与吞噬体结合的时间。此外,巨噬细胞中Rab20的缺失消除了IFN-γ诱导的吞噬体成熟延迟。最后,我们证明Rab20与Rab5a鸟嘌呤核苷酸交换因子Rabex-5(也称为RABGEF1)相互作用,并且Rab20的敲低会损害IFN-γ依赖性的Rabex-5和Rab5a募集到吞噬体中。综上所述,我们在此揭示Rab20是Rab级联反应中的关键因子,通过该级联反应IFN-γ诱导巨噬细胞中吞噬体成熟延迟。