Department of Chemistry, The University of Chicago, Chicago, IL 60637.
Grossman Institute of Neuroscience, Quantitative Biology and Human Behavior, The University of Chicago, Chicago, IL 60637.
Proc Natl Acad Sci U S A. 2021 Oct 12;118(41). doi: 10.1073/pnas.2113174118.
Lysosomes adopt dynamic, tubular states that regulate antigen presentation, phagosome resolution, and autophagy. Tubular lysosomes are studied either by inducing autophagy or by activating immune cells, both of which lead to cell states where lysosomal gene expression differs from the resting state. Therefore, it has been challenging to pinpoint the biochemical properties lysosomes acquire upon tubulation that could drive their functionality. Here we describe a DNA-based assembly that tubulates lysosomes in macrophages without activating them. Proteolytic activity maps at single-lysosome resolution revealed that tubular lysosomes were less degradative and showed proximal to distal luminal pH and Ca gradients. Such gradients had been predicted but never previously observed. We identify a role for tubular lysosomes in promoting phagocytosis and activating MMP9. The ability to tubulate lysosomes without starving or activating immune cells may help reveal new roles for tubular lysosomes.
溶酶体呈现动态管状状态,调节抗原呈递、吞噬体分解和自噬。管状溶酶体可以通过诱导自噬或激活免疫细胞来研究,这两种方法都会导致溶酶体基因表达与静息状态不同的细胞状态。因此,确定管状化后溶酶体获得的能够驱动其功能的生化特性一直具有挑战性。在这里,我们描述了一种基于 DNA 的组装方法,可以在不激活巨噬细胞的情况下将溶酶体管状化。蛋白酶活性的单溶酶体分辨率图谱显示,管状溶酶体的降解能力较弱,并且在近侧到远侧腔室 pH 和 Ca 梯度。这些梯度已经被预测,但以前从未观察到。我们确定了管状溶酶体在促进吞噬作用和激活 MMP9 中的作用。无需饥饿或激活免疫细胞即可管状化溶酶体的能力可能有助于揭示管状溶酶体的新作用。