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[3] K. Gousset, E. Schiff, C. Langevin, Z. Marijanovic, A. Caputo, D. T. Browman, N. Chenouard, F. de Chaumont, A. Martino, J. Enninga, J. C. Olivo-Marin, D. Mannel and C. Zurzolo, “Prions Hijack Tunnelling Nanotubes for In-tercellular Spread,” Nature Cell Biology, Vol. 11, No. 3, 2009, pp. 328-336. doi:10.1038/ncb1841

has been cited by the following article:

• TITLE: Microscopic observation of the intercellular transport of CdTe quantum dot aggregates through tunneling-nanotubes

  AUTHORS: Lan Mi, Rongling Xiong, Yu Zhang, Weidong Yang, Ji-Yao Chen, Pei-Nan Wang

  KEYWORDS: Quantum dot, Tunneling-nanotubes, Active transport, Fluorescence, Microtubule, Filament

  JOURNAL NAME: Journal of Biomaterials and Nanobiotechnology, Vol.2 No.2, February 28, 2011

  ABSTRACT: Various inorganic nanoparticles are being considered for applications in life science as fluorescent labels and for such therapeutic applications as drug delivery or targeted cell destruction. It is of importance to understand their intercellular transport behaviors and mechanisms. Here, the intercellular transport of internalized CdTe quantum dot (QD) aggregates through tunneling-nanotubes (TNTs) between human hepatocellular carcinoma cells was studied by time-resolved confocal fluorescence microscopy. TNTs are known to connect eukaryotic cells to provide important pathways for intercellular communications. The formation, shrinkage, elongation and rupture of TNTs were clearly observed by microscopy. We found TNTs contained only F-actin or both microtubules and F-actin. Two transport modes for QD aggregates through the TNTs were observed: the microtubule-based bidirectional motion and the ac-tin-dependent unidirectional motion. The mean square displacement analyses revealed that the intercellular transportations of QDs along TNTs were mediated by active processes. The bidirectional intercellular transport of QDs within lysosomes through the TNT was also observed.