M
Matthew R. G. Russell
Researcher at Francis Crick Institute
Publications - 26
Citations - 1231
Matthew R. G. Russell is an academic researcher from Francis Crick Institute. The author has contributed to research in topics: Endosome & ESCRT. The author has an hindex of 14, co-authored 22 publications receiving 959 citations. Previous affiliations of Matthew R. G. Russell include University of Colorado Boulder & University of Cambridge.
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Journal ArticleDOI
Depletion of TSG101 forms a mammalian "Class E" compartment: a multicisternal early endosome with multiple sorting defects.
TL;DR: Depletion of tumour susceptibility gene 101 impairs the selection of epidermal growth factor receptor away from recycling receptors within the limiting membrane of the early endosome, resulting in inhibition of cargo recycling and profound structural rearrangement of theEarly Endosome.
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Subcellular antibiotic visualization reveals a dynamic drug reservoir in infected macrophages
Daniel J. Greenwood,Mariana Silva dos Santos,Song Huang,Matthew R. G. Russell,Lucy M. Collinson,James I. MacRae,Andrew West,Haibo Jiang,Maximiliano G. Gutierrez +8 more
TL;DR: Bedaquiline accumulated primarily in host cell lipid droplets, but heterogeneously in mycobacteria within a variety of intracellular compartments, which constituted a transferable reservoir that enhanced antibacterial efficacy.
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Molecular mechanisms of late endosome morphology, identity and sorting
TL;DR: Current evidence supports a model of maturation in which the lipids, cargo proteins and Rab population at the endosome determine its competence to perform the functions of late endosomes, including the sorting of cargoes into lumenal vesicles and fusion with lysosomes.
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3D correlative light and electron microscopy of cultured cells using serial blockface scanning electron microscopy
Matthew R. G. Russell,Thomas R. Lerner,Jemima J. Burden,David O. Nkwe,Annegret Pelchen-Matthews,Marie-Charlotte Domart,Joanne Durgan,Anne Weston,Martin L. Jones,Christopher J. Peddie,Raffaella Carzaniga,Oliver Florey,Mark Marsh,Maximiliano G. Gutierrez,Lucy M. Collinson +14 more
TL;DR: The workflow revealed new insight into the replicative niche of Mycobacterium tuberculosis in primary human lymphatic endothelial cells, HIV-1 in human monocyte-derived macrophages, and the composition of the entotic vacuole.
Journal ArticleDOI
Mycobacterium tuberculosis replicates within necrotic human macrophages.
Thomas R. Lerner,Sophie Borel,Daniel J. Greenwood,Urska Repnik,Matthew R. G. Russell,Susanne Herbst,Martin L. Jones,Lucy M. Collinson,Gareth Griffiths,Maximiliano G. Gutierrez +9 more
TL;DR: After infection, a population of macrophages became necrotic, providing a niche for M. tuberculosis replication before escaping into the extracellular milieu, and it is discovered that IFN-&ggr; enhanced bacterial replication in macrophage colony-stimulating factor–differentiated Macrophages more than in granulocyte–macrophage Colony-stimulation factor– differentiated macrophaging.