Single- and two-photon imaging of human micrometastases and disseminated tumour cells with conjugates of nanobodies and quantum dots.
Fernanda Ramos-GomesJulia BodeAlyona SukhanovaSvetlana V BozrovaMara SaccomanoMiso MitkovskiJulia Eva KruegerAnja K WegeWalter StuehmerPavel S SamokhvalovDaniel BatyPatrick ChamesIgor R NabievFrauke AlvesPublished in: Scientific reports (2018)
Early detection of malignant tumours and, especially, micrometastases and disseminated tumour cells is still a challenge. In order to implement highly sensitive diagnostic tools we demonstrate the use of nanoprobes engineered from nanobodies (single-domain antibodies, sdAbs) and fluorescent quantum dots (QDs) for single- and two-photon detection and imaging of human micrometastases and disseminated tumour cells in ex vivo biological samples of breast and pancreatic metastatic tumour mouse models expressing human epidermal growth factor receptor 2 (HER2) or carcinoembryonic antigen (CEA). By staining thin (5-10 µm) paraffin and thick (50 µm) agarose tissue sections, we detected HER2- and CEA-positive human tumour cells infiltrating the surrounding tissues or metastasizing to different organs, including the brain, testis, lung, liver, and lymph nodes. Compared to conventional fluorescently labelled antibodies the sdAb-HER2-QD and sdAb-CEA-QD nanoprobes are superior in detecting micrometastases in tissue sections by lower photobleaching and higher brightness of fluorescence signals ensuring much better discrimination of positive signals versus background. Very high two-photon absorption cross-sections of QDs and small size of the nanoprobes ensure efficient imaging of thick tissue sections unattainable with conventional fluorescent probes. The nanobody-QD probes will help to improve early cancer diagnosis and prognosis of progression by assessing metastasis.
Keyphrases
- quantum dots
- induced apoptosis
- endothelial cells
- living cells
- cell cycle arrest
- epidermal growth factor receptor
- fluorescence imaging
- high resolution
- induced pluripotent stem cells
- squamous cell carcinoma
- pluripotent stem cells
- endoplasmic reticulum stress
- small cell lung cancer
- small molecule
- single molecule
- early stage
- fluorescent probe
- simultaneous determination
- brain injury
- cell proliferation
- tyrosine kinase
- subarachnoid hemorrhage
- multiple sclerosis
- resting state
- functional connectivity
- germ cell
- tandem mass spectrometry