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Characterization of human corneal stem cells by synchrotron infrared micro-spectroscopy.

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Characterization of human corneal stem cells by synchrotron infrared micro-spectroscopy. / Bentley, Adam J.; Nakamura, Takahiro; Hammiche, Azzedine et al.
In: Molecular Vision, Vol. 13, 22.02.2007, p. 237-242.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Bentley, AJ, Nakamura, T, Hammiche, A, Pollock, HM, Martin, FL, Kinoshita, S & Fullwood, NJ 2007, 'Characterization of human corneal stem cells by synchrotron infrared micro-spectroscopy.', Molecular Vision, vol. 13, pp. 237-242. <http://www.molvis.org/molvis/v13/a27/>

APA

Bentley, A. J., Nakamura, T., Hammiche, A., Pollock, H. M., Martin, F. L., Kinoshita, S., & Fullwood, N. J. (2007). Characterization of human corneal stem cells by synchrotron infrared micro-spectroscopy. Molecular Vision, 13, 237-242. http://www.molvis.org/molvis/v13/a27/

Vancouver

Bentley AJ, Nakamura T, Hammiche A, Pollock HM, Martin FL, Kinoshita S et al. Characterization of human corneal stem cells by synchrotron infrared micro-spectroscopy. Molecular Vision. 2007 Feb 22;13:237-242.

Author

Bentley, Adam J. ; Nakamura, Takahiro ; Hammiche, Azzedine et al. / Characterization of human corneal stem cells by synchrotron infrared micro-spectroscopy. In: Molecular Vision. 2007 ; Vol. 13. pp. 237-242.

Bibtex

@article{94da7cdcd46841bf9c0ade53c2d64228,
title = "Characterization of human corneal stem cells by synchrotron infrared micro-spectroscopy.",
abstract = "Purpose: The purpose of this study was to use high resolution synchrotron radiation-based Fourier Transform Infrared (FTIR) micro-spectroscopy coupled with multivariate analysis to investigate the characteristics of adult stem cell (SC) and transit amplifying (TA) cell populations of the human corneal epithelium. Methods: Spectra of individual SC and TA cells in situ from cryosections of human cornea were collected using a synchrotron micro-spectroscopy facility at Daresbury laboratory, UK. Multivariate analysis and Mann Whitney U tests were used to analyse the spectral data from the SC and TA cell populations. Results: There were marked differences between the median spectra of the two cell populations. This correlated with their level of differentiation and functional specialization. Multivariate (principal component) analysis revealed that the cell populations could be segregated into distinct clusters, with only slight overlap between the two cell types. Significant (p<0.05) spectral differences were found in the spectral regions associated with nucleic acid, protein and lipids. Conclusions: Synchrotron FTIR micro-spectroscopy together with principal component analysis is able to discriminate between SC and TA cell populations. Our results also suggest a small sub-population of corneal epithelial cells in the SC niche have TA cell-like characteristics. Many of the spectral differences between the SC and TA cell populations relate to differences in nucleic acid conformation.",
author = "Bentley, {Adam J.} and Takahiro Nakamura and Azzedine Hammiche and Pollock, {Hubert M.} and Martin, {Francis L.} and Shigeru Kinoshita and Fullwood, {Nigel J.}",
year = "2007",
month = feb,
day = "22",
language = "English",
volume = "13",
pages = "237--242",
journal = "Molecular Vision",
issn = "1090-0535",
publisher = "Molecular Vision",

}

RIS

TY - JOUR

T1 - Characterization of human corneal stem cells by synchrotron infrared micro-spectroscopy.

AU - Bentley, Adam J.

AU - Nakamura, Takahiro

AU - Hammiche, Azzedine

AU - Pollock, Hubert M.

AU - Martin, Francis L.

AU - Kinoshita, Shigeru

AU - Fullwood, Nigel J.

PY - 2007/2/22

Y1 - 2007/2/22

N2 - Purpose: The purpose of this study was to use high resolution synchrotron radiation-based Fourier Transform Infrared (FTIR) micro-spectroscopy coupled with multivariate analysis to investigate the characteristics of adult stem cell (SC) and transit amplifying (TA) cell populations of the human corneal epithelium. Methods: Spectra of individual SC and TA cells in situ from cryosections of human cornea were collected using a synchrotron micro-spectroscopy facility at Daresbury laboratory, UK. Multivariate analysis and Mann Whitney U tests were used to analyse the spectral data from the SC and TA cell populations. Results: There were marked differences between the median spectra of the two cell populations. This correlated with their level of differentiation and functional specialization. Multivariate (principal component) analysis revealed that the cell populations could be segregated into distinct clusters, with only slight overlap between the two cell types. Significant (p<0.05) spectral differences were found in the spectral regions associated with nucleic acid, protein and lipids. Conclusions: Synchrotron FTIR micro-spectroscopy together with principal component analysis is able to discriminate between SC and TA cell populations. Our results also suggest a small sub-population of corneal epithelial cells in the SC niche have TA cell-like characteristics. Many of the spectral differences between the SC and TA cell populations relate to differences in nucleic acid conformation.

AB - Purpose: The purpose of this study was to use high resolution synchrotron radiation-based Fourier Transform Infrared (FTIR) micro-spectroscopy coupled with multivariate analysis to investigate the characteristics of adult stem cell (SC) and transit amplifying (TA) cell populations of the human corneal epithelium. Methods: Spectra of individual SC and TA cells in situ from cryosections of human cornea were collected using a synchrotron micro-spectroscopy facility at Daresbury laboratory, UK. Multivariate analysis and Mann Whitney U tests were used to analyse the spectral data from the SC and TA cell populations. Results: There were marked differences between the median spectra of the two cell populations. This correlated with their level of differentiation and functional specialization. Multivariate (principal component) analysis revealed that the cell populations could be segregated into distinct clusters, with only slight overlap between the two cell types. Significant (p<0.05) spectral differences were found in the spectral regions associated with nucleic acid, protein and lipids. Conclusions: Synchrotron FTIR micro-spectroscopy together with principal component analysis is able to discriminate between SC and TA cell populations. Our results also suggest a small sub-population of corneal epithelial cells in the SC niche have TA cell-like characteristics. Many of the spectral differences between the SC and TA cell populations relate to differences in nucleic acid conformation.

M3 - Journal article

VL - 13

SP - 237

EP - 242

JO - Molecular Vision

JF - Molecular Vision

SN - 1090-0535

ER -