Membrane Traffic and Cell Division Unit, Institut Pasteur, Université Paris Cité, CNRS UMR3691, Paris F-75015, France.
Virology department, Virus and Immunity Lab, Institut Pasteur, Université Paris Cité, Paris F-75015, France.
Proc Natl Acad Sci U S A. 2024 Nov 26;121(48):e2407835121. doi: 10.1073/pnas.2407835121. Epub 2024 Nov 18.
Many enveloped viruses bud from the plasma membrane that is tightly associated with a dense and thick actin cortex. This actin network represents a significant challenge for membrane deformation and scission, and how it is remodeled during the late steps of the viral cycle is largely unknown. Using superresolution microscopy, we show that HIV-1 buds in areas of the plasma membrane with low cortical F-actin levels. We find that the cellular oxidoreductase MICAL1 locally depolymerizes actin at budding sites to promote HIV-1 budding and release. Upon MICAL1 depletion, F-actin abnormally remains at viral budding sites, incompletely budded viruses accumulate at the plasma membrane and viral release is impaired. Remarkably, normal viral release can be restored in MICAL1-depleted cells by inhibiting Arp2/3-dependent branched actin networks. Mechanistically, we find that MICAL1 directly disassembles branched-actin networks and controls the timely recruitment of the Endosomal Sorting Complexes Required for Transport scission machinery during viral budding. In addition, the MICAL1 activator Rab35 is recruited at budding sites, functions in the same pathway as MICAL1, and is also required for viral release. This work reveals a role for oxidoreduction in triggering local actin depolymerization to control HIV-1 budding, a mechanism that may be widely used by other viruses. The debranching activity of MICAL1 could be involved beyond viral budding in various other cellular functions requiring local plasma membrane deformation.
许多包膜病毒从与密集而厚的肌动蛋白皮层紧密相关的质膜出芽。这个肌动蛋白网络是膜变形和分裂的重大挑战,其在病毒周期后期如何重塑在很大程度上尚不清楚。使用超分辨率显微镜,我们表明 HIV-1 在质膜中皮质 F-肌动蛋白水平低的区域出芽。我们发现细胞氧化还原酶 MICAL1 在出芽部位局部解聚肌动蛋白以促进 HIV-1 出芽和释放。在 MICAL1 耗竭后,F-肌动蛋白异常地保留在病毒出芽部位,不完全出芽的病毒在质膜上积累,病毒释放受损。值得注意的是,通过抑制 Arp2/3 依赖性分支肌动蛋白网络,可以在 MICAL1 耗竭的细胞中恢复正常的病毒释放。在机制上,我们发现 MICAL1 直接解聚分支肌动蛋白网络,并控制内体分选复合物所需的运输分裂机制在病毒出芽过程中的及时募集。此外,MICAL1 的激活子 Rab35 被募集到出芽部位,与 MICAL1 发挥相同的作用,并且也需要病毒释放。这项工作揭示了氧化还原在触发局部肌动蛋白解聚以控制 HIV-1 出芽中的作用,这一机制可能被其他病毒广泛使用。MICAL1 的去分支活性可能不仅涉及病毒出芽,还涉及各种其他需要局部质膜变形的细胞功能。