M. tuberculosisinfection of human iPSDM reveals complex membrane dynamics during xenophagy evasion
Year: 2020
Type: article
Abstract: (Mtb). Activation of xenophagy in macrophages targets Mtb to autophagosomes; however, how Mtb is targeted to autophagosomes in human macrophages at a high spatial and temporal resolution is unknown. Here, we use human induced pluripotent stem cell-derived macrophages (iPSDMs) to study the human macrophage response to Mtb infection and the role of the ESX-1 type VII secretion system. Using RNA-seq, we identify ESX-1-dependent transcriptional responses in iPSDMs after infection with Mtb. This analysis revealed differential inflammatory responses and dysregulated pathways such as eukaryotic initiation factor 2 (eIF2) signalling and protein ubiquitylation. Moreover, live-cell imaging revealed that Mtb infection in human macrophages induces dynamic ESX-1-dependent, LC3B-positive tubulovesicular autophagosomes (LC3-TVS). Through a correlative live-cell and focused ion beam scanning electron microscopy (FIB SEM) approach, we show that upon phagosomal rupture, Mtb induces the formation of LC3-TVS, from which the bacterium is able to escape to reside in the cytosol. Thus, iPSDMs represent a valuable model for studying spatiotemporal dynamics of human macrophage-Mtb interactions, and Mtb is able to evade capture by autophagic compartments.
Source: Journal of Cell Science
DOI: 10.1242/jcs.252973
Institutions: The Francis Crick Institute, Imperial College London
Language: English
Subfield: Infectious Diseases
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Awards: G130052744, REspiratory Science Promoted by International Research Exchanges 3, G2499293911, G2612492280, Single-cell spatiotemporal analysis of Mycobacterium tuberculosis responses to antibiotics within host microenvironments, G3072083260, G366052922, G3727094181, G434337789, G4937468798, G6595762086, G6653160136, G7210654649
OpenAlex ID: W3086811648
