An imaging dataset of cervical cells using scanning near-field optical microscopy coupled to an infrared free electron laser

Using a scanning near-field optical microscope coupled to an infrared free electron laser (SNOM-IR-FEL) in low-resolution transmission mode, we collected chemical data from whole cervical cells obtained from 5 pre-menopausal, non-pregnant women of reproductive age, and cytologically classified as no...

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Published inScientific data Vol. 4; no. 1; p. 170084
Main Authors Halliwell, Diane E., Morais, Camilo L.M., Lima, Kássio M.G., Trevisan, Júlio, Siggel-King, Michele R.F., Craig, Tim, Ingham, James, Martin, David S., Heys, Kelly, Kyrgiou, Maria, Mitra, Anita, Paraskevaidis, Evangelos, Theophilou, Georgios, Martin-Hirsch, Pierre L., Cricenti, Antonio, Luce, Marco, Weightman, Peter, Martin, Francis L.
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 11.07.2017
Nature Publishing Group
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Online AccessGet full text
ISSN2052-4463
2052-4463
DOI10.1038/sdata.2017.84

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Summary:Using a scanning near-field optical microscope coupled to an infrared free electron laser (SNOM-IR-FEL) in low-resolution transmission mode, we collected chemical data from whole cervical cells obtained from 5 pre-menopausal, non-pregnant women of reproductive age, and cytologically classified as normal or with different grades of cervical cell dyskaryosis. Imaging data are complemented by demography. All samples were collected before any treatment. Spectra were also collected using attenuated total reflection, Fourier-transform (ATR-FTIR) spectroscopy, to investigate the differences between the two techniques. Results of this pilot study suggests SNOM-IR-FEL may be able to distinguish cervical abnormalities based upon changes in the chemical profiles for each grade of dyskaryosis at designated wavelengths associated with DNA, Amide I/II, and lipids. The novel data sets are the first collected using SNOM-IR-FEL in transmission mode at the ALICE facility (UK), and obtained using whole cells as opposed to tissue sections, thus providing an ‘intact’ chemical profile. These data sets are suited to complementing future work on image analysis, and/or applying the newly developed algorithm to other datasets collected using the SNOM-IR-FEL approach. Design Type(s) replicate design • disease state design • observation design Measurement Type(s) isolated subcellular component • reflectance spectrum Technology Type(s) scanning near-field optical microscopy • attenuated total reflectance Fourier transform infrared spectroscopy Factor Type(s) cell phenotype • biomolecule target Sample Characteristic(s) Homo sapiens • cervical epithelium Machine-accessible metadata file describing the reported data (ISA-Tab format)
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D.E.H. and G.T. prepared the samples and slides for the SNOM-IR-FEL experiment. C.L.M.M. and K.M.G.L. developed the mathematical and computational analyses for both the SNOM-IR-FEL and ATR-FTIR data. J.T. reviewed the original raw data and provided early guidance on potential approaches for analysis. M.R.F.S.-K., T.C., J.I., D.S.M., M.L., A.C. and P.W. performed the SNOM-IR-FEL experiment and were also second commissioners along with D.E.H. and K.H. at the ALICE facility. D.S.M. performed the AFM measurements. D.E.H. prepared the samples for ATR-FTIR spectral acquisition and collected the patient spectra. M.K. and A.M. recruited patients and collected clinical information for the study. M.K., E.P. and P.L.M.-H. contributed to the clinical evaluation of the results. All authors critically reviewed the paper. F.L.M. conceived and directed the project and wrote the manuscript with the help of D.E.H.
ISSN:2052-4463
2052-4463
DOI:10.1038/sdata.2017.84