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Tunneling nanotube-mediated intercellular vesicle and protein transfer in the stroma-provided imatinib resistance in chronic myeloid leukemia cells

Authors :
Wioleta Dudka
Katja Srpan
Daniel M. Davis
Monika Zaręba-Kozioł
Jakub Wlodarczyk
Agata Klejman
Yannick Schwab
Agata Kominek
Katarzyna Piwocka
Paolo Ronchi
Dominik Cysewski
Laura Turos
Piotr Chroscicki
Marta D. Kolba
Source :
Cell Death and Disease, Vol 10, Iss 11, Pp 1-16 (2019), Cell Death & Disease
Publication Year :
2019
Publisher :
Nature Publishing Group, 2019.

Abstract

Intercellular communication within the bone marrow niche significantly promotes leukemogenesis and provides protection of leukemic cells from therapy. Secreted factors, intercellular transfer of mitochondria and the receptor–ligand interactions have been shown as mediators of this protection. Here we report that tunneling nanotubes (TNTs)—long, thin membranous structures, which have been identified as a novel mode of intercellular cross-talk—are formed in the presence of stroma and mediate transfer of cellular vesicles from stroma to leukemic cells. Importantly, transmission of vesicles via TNTs from stromal cells increases resistance of leukemic cells to the tyrosine kinase inhibitor, imatinib. Using correlative light-electron microscopy and electron tomography we show that stromal TNTs contain vesicles, provide membrane continuity with the cell bodies and can be open-ended. Moreover, trans-SILAC studies to reveal the non-autonomous proteome showed that specific sets of proteins are transferred together with cellular vesicles from stromal to leukemic cells, with a potential role in survival and adaptation. Altogether, our findings provide evidence for the biological role of the TNT-mediated vesicle exchange between stromal and leukemic cells, implicating the direct vesicle and protein transfer in the stroma-provided protection of leukemic cells.

Details

Language :
English
ISSN :
20414889
Volume :
10
Issue :
11
Database :
OpenAIRE
Journal :
Cell Death and Disease
Accession number :
edsair.doi.dedup.....8f6beec026ab8b339b88264f24475adb
Full Text :
https://doi.org/10.1038/s41419-019-2045-8