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Fas stimulation of T lymphocytes promotes rapid intercellular exchange of death signals via membrane nanotubes 被引量:4
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作者 Peter D Arkwright Francesca Luchetti +8 位作者 Julien Tour Charlotte Roberts Rahna Ayub Ana P Morales Jose J Rodriguez andrew gilmore Barbara Canonico Stefano Papa Mauro Degli Esposti 《Cell Research》 SCIE CAS CSCD 2010年第1期72-88,共17页
The Fas/CD95 surface receptor mediates rapid death of various cell types, including autoreactive T cells with the potential for triggering autoimmunity. Here, we present novel aspects of Fas signalling that define a ... The Fas/CD95 surface receptor mediates rapid death of various cell types, including autoreactive T cells with the potential for triggering autoimmunity. Here, we present novel aspects of Fas signalling that define a 'social' dimension to receptor-induced apoptosis. Fas stimulation rapidly induces extensive membrane nanotube formation between neighbouring T cells. This is critically dependent on Rho GTPases but not on caspase activation. Bidirectional transfer of membrane and cytosolic elements including active caspases can be observed to occur via these nanotubes. Nanotube formation and intercellular exchanges of death signals are defective in T lymphocytes from patients with autoimmune iymphoproliferative syndrome harbouring mutations in the Fas receptor. We conclude that nanotuhemediated exchanges constitute a novel form of intercellular communication that augments the propagation of death signalling between neighbouring T cells. 展开更多
关键词 FAS intercellular communication membrane nanotubes T cells
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