| Autor: |
Parker I; Department of Neurobiology and Behavior, University of California, Irvine, CA, USA.; Department of Physiology and Biophysics, University of California, Irvine, CA, USA., Evans KT; Department of Physiology and Biophysics, University of California, Irvine, CA, USA., Ellefsen K; Department of Neurobiology and Behavior, University of California, Irvine, CA, USA., Lawson DA; Department of Physiology and Biophysics, University of California, Irvine, CA, USA., Smith IF; Department of Neurobiology and Behavior, University of California, Irvine, CA, USA. ismith@uci.edu. |
| Abstrakt: |
Membrane nanotubes are cytosolic protrusions with diameters <1 µm that extend between cells separated by tens of µm. They mediate several forms of intercellular communication and are upregulated in diverse diseases. Difficulties in visualizing and studying nanotubes within intact tissues have, however, prompted skepticism regarding their in vivo relevance, and most studies have been confined to cell culture systems. Here, we introduce lattice-light sheet imaging of MDA-MB-231 human breast cancer cells genetically engineered to brightly express membrane-targeted GFP as a promising approach to visualize membrane nanotubes in vitro and in situ. We demonstrate that cultured cells form multiple nanotubes that mediate intercellular communication of Ca 2+ signals and actively traffic GFP-tagged membrane vesicles along their length. Furthermore, we directly visualize nanotubes in situ, interconnecting breast cancer cells in live acute brain slices from an experimental mouse model of breast cancer brain metastasis. This amenable experimental system should facilitate the transition of the study of intercellular communication by membrane nanotubes from cell culture to the whole animal. |
