丝状体
细胞生物学
细胞内
细胞
细胞膜
生物物理学
细胞外
生物
材料科学
肌动蛋白
生物化学
作者
Stefanie Sowinski,Clare Jolly,Otto Berninghausen,Marco A. Purbhoo,Anne Chauveau,Karsten Köhler,Stéphane Oddos,Philipp Eissmann,Frances M. Brodsky,Colin R. Hopkins,Björn Önfelt,Quentin J. Sattentau,Daniel M. Davis
摘要
Transmission of HIV-1 via intercellular connections has been estimated as 100-1000 times more efficient than a cell-free process, perhaps in part explaining persistent viral spread in the presence of neutralizing antibodies. Such effective intercellular transfer of HIV-1 could occur through virological synapses or target-cell filopodia connected to infected cells. Here we report that membrane nanotubes, formed when T cells make contact and subsequently part, provide a new route for HIV-1 transmission. Membrane nanotubes are known to connect various cell types, including neuronal and immune cells, and allow calcium-mediated signals to spread between connected myeloid cells. However, T-cell nanotubes are distinct from open-ended membranous tethers between other cell types, as a dynamic junction persists within T-cell nanotubes or at their contact with cell bodies. We also report that an extracellular matrix scaffold allows T-cell nanotubes to adopt variably shaped contours. HIV-1 transfers to uninfected T cells through nanotubes in a receptor-dependent manner. These data lead us to propose that HIV-1 can spread using nanotubular connections formed by short-term intercellular unions in which T cells specialize.
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