Cell Motility and Metastatic Potential Studies Based on Quantum Dot Imaging of Phagokinetic Tracks

A wide variety of eukaryotic cells are shown to engulf colloidal semiconductor nanocrystals, or quantum dots, when they migrate. Here we show that the uptake of the nanocrystals is directly correlated with the cell motility, by comparing in detail the motions of both cancerous and healthy human breast cancer cells, as well as several other cell types. The nanocrystals are more photochemically robust than organic dyes (which fade quickly) and do not perturb the cells. The ability to examine these behaviors in live cells over extended time periods, and to quantify changes in response to various molecular manipulations, provides a powerful tool for studying the processes of cell motility and migration – behaviors that are responsible for metastases of primary cancers.

[1]  D. Balding,et al.  HLA Sequence Polymorphism and the Origin of Humans , 2006 .

[2]  Steven R. Cordero,et al.  Photo-activated luminescence of CdSe quantum dot monolayers , 2000 .

[3]  Louis E. Brus,et al.  The Quantum Mechanics of Larger Semiconductor Clusters ("Quantum Dots") , 1990 .

[4]  R. R. Bürk A factor from a transformed cell line that affects cell migration. , 1973, Proceedings of the National Academy of Sciences of the United States of America.

[5]  M. Dahan,et al.  Time-gated biological imaging by use of colloidal quantum dots. , 2001, Optics letters.

[6]  A. Alivisatos Semiconductor Clusters, Nanocrystals, and Quantum Dots , 1996, Science.

[7]  S. Nie,et al.  Quantum dot bioconjugates for ultrasensitive nonisotopic detection. , 1998, Science.

[8]  T. Vicsek,et al.  Proliferative and migratory responses of astrocytes to in vitro injury , 2000, Journal of neuroscience research.

[9]  V. Quaranta,et al.  Migration of breast epithelial cells on Laminin-5: differential role of integrins in normal and transformed cell types , 1998, Breast Cancer Research and Treatment.

[10]  S. Pathak,et al.  Hydroxylated quantum dots as luminescent probes for in situ hybridization. , 2001, Journal of the American Chemical Society.

[11]  G. Albrecht-Buehler,et al.  The phagokinetic tracks of 3T3 cells , 1977, Cell.

[12]  D. English,et al.  Enhancement of the migration of metastatic human breast cancer cells by phosphatidic acid. , 2000, Biochemical and biophysical research communications.

[13]  S. Boyden THE CHEMOTACTIC EFFECT OF MIXTURES OF ANTIBODY AND ANTIGEN ON POLYMORPHONUCLEAR LEUCOCYTES , 1962, The Journal of experimental medicine.

[14]  G. Albrecht-Buehler,et al.  Phagokinetic tracks of 3T3 cells: Parallels between the orientation of track segments and of cellular structures which contain actin or tubulin , 1977, Cell.

[15]  A W Partin,et al.  Fourier analysis of cell motility: correlation of motility with metastatic potential. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[16]  T. Rajah,et al.  The motile behavior of human breast cancer cells characterized by time-lapse videomicroscopy , 1998, In Vitro Cellular & Developmental Biology - Animal.

[17]  C. Colton,et al.  Chemotaxis by a CNS macrophage, the microglia , 1990, Journal of neuroscience research.