Tissue and species differences in the application of quantum dots as probes for biomolecular targets in the inner ear and kidney.
Quantum dots (QDs) are useful biological probes because of the increased photostability and quantum efficiency they offer over organic fluorophores. However, toxicity concerns arise because the QD core is composed of cadmium and selenium, metals known to be unsafe for humans and animals. We investigated the feasibility of quantum dots as biological labels for imaging studies of inner ear and kidney, tissues that share a polarized epithelial arrangement and drug susceptibility. We found that methods for labeling the actin cytoskeleton of monolayers of cultured amphibian kidney cells (Xenopus A6) with 565 nm QD conjugates were not feasible with large Xenopus inner ear organs. We then compared the uptake of 565 nm cationic peptide-targeted and nontargeted QDs in live kidney cell lines (amphibian, A6 and XLK-WG; human, HEK-293). Results showed that targeted QDs are internalized by all three kidney cell lines, and that nontargeted CdSe nanocrystals are sequestered only by human kidney cells. CellTracker Red CMTPX confirmed the membrane integrity and viability of HEK-293 cells that internalized QDs. Our results demonstrate species and tissue differences in QD uptake and labeling, and underscore the need for long-term studies of QD toxicity and fate in cells.
PubMed ID: 17181024
Grant support: DC003292 NIDCD NIH HHS , P50GM068762 NIGMS NIH HHS , S06GM008136 NIGMS NIH HHS , R01 DC003292-06 NIDCD NIH HHS , R01 DC003292-07 NIDCD NIH HHS , S06 GM008136-310029 NIGMS NIH HHS , S06 GM008136-320029 NIGMS NIH HHS , S06 GM008136-330029 NIGMS NIH HHS , R01 DC003292 NIDCD NIH HHS , S06 GM008136 NIGMS NIH HHS
Genes referenced: krt5.5