Research Paper
Fluid Phase Endocytic Uptake of Artificial Nano-Spheres and Fluorescent Quantum Dots by Sycamore Cultured Cells: Evidence for the Distribution of Solutes to Different Intracellular Compartments
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Volume 1, Issue 4 July/August 2006
Pages 196 - 200
http://dx.doi.org/10.4161/psb.1.4.3142
Authors: Ed Etxeberria, Pedro Gonzalez, Edurne Baroja-Fernández and Javier Pozueta Romero
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- Ed Etxeberria
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Corresponding author: eje@crec.ifas.ufl.edu
University of Florida; Institute of Food and Agricultural Sciences; Citrus Research and Education Center; Department of Horticultural Sciences; Lake Alfred, FL USA
- Pedro Gonzalez
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University of Florida; Institute of Food and Agricultural Sciences; Citrus Research and Education Center; Department of Horticultural Sciences; Lake Alfred, FL USA
- Edurne Baroja-Fernández
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Agrobioteknologia Instituta; Consejo Superior de Investigaciones Cientificas and Nafarroako Unibertsitate Publikoa; Mutiloako etorbidea zembaki gabe; Mutiloabeti, Nafarroa, Spain
- Javier Pozueta Romero
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Agrobioteknologia Instituta; Consejo Superior de Investigaciones Cientificas and Nafarroako Unibertsitate Publikoa; Mutiloako etorbidea zembaki gabe; Mutiloabeti, Nafarroa, Spain
Abstract:
Fluid phase endocytic uptake of external solutes in plant cells was further substantiated using artificial polystyrene nano-spheres (40 nm) and CdSe/ZnS quantum dots (20 nm). Both types of artificial nano particles were taken up by sycamore cultured cells. However, whereas polystyrene nano-spheres were delivered to the central vacuole, CdSe/ZnS nano-dots were sequestered into cytoplasmic vesicular structures. Using dextran Texas Red (m.w. 3,000; d-TR) as additional marker, confocal micrographs confirmed the distinct topographic distribution of CdSe/ZnS quantum dots within the cell. Initially, d-TR and CdSe/ZnS quantum dots co-localized within cytoplasmic vesicles. After 18 h incubation, d-TR was distinctly localized in the vacuole whereas CdSe/ZnS quantum dots remained sequestered in cytoplasmic membranous compartments. The data provide a first evidence for the rapid distribution of solutes taken up by endocytosis to distinct intracellular compartments.
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