Journal
STEM CELLS
Volume 26, Issue 1, Pages 108-118Publisher
WILEY-BLACKWELL
DOI: 10.1634/stemcells.2007-0196
Keywords
crypts; Fourier transform infrared microspectroscopy; intestinal; principal component analysis; symmetric phosphate synchrotron
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Funding
- BBSRC [BB/D010055/1] Funding Source: UKRI
- Biotechnology and Biological Sciences Research Council [BB/D010055/1] Funding Source: Medline
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Complex biomolecules absorb in the mid-infrared (lambda = 2-20 mu m), giving vibrational spectra associated with structure and function. We used Fourier transform infrared (FTIR) microspectroscopy to fingerprint locations along the length of human small and large intestinal crypts. Paraffin-embedded slices of normal human gut were sectioned (10 mu m thick) and mounted to facilitate infrared (IR) spectral analyses. IR spectra were collected using globar (15 mu m x 15 mu m aperture) FTIR microspectroscopy in reflection mode, synchrotron (<= 10 mu m x 10 mu m aperture) FTIR microspectroscopy in transmission mode or near-field photothermal microspectroscopy. Dependent on the location of crypt interrogation, clear differences in spectral characteristics were noted. Epithelial-cell IR spectra were subjected to principal component analysis to determine whether wavenumber-absorbance relationships expressed as single points in hyperspace might on the basis of multivariate distance reveal biophysical differences along the length of gut crypts. Following spectroscopic analysis, plotted clusters and their loadings plots pointed toward symmetric (v(s)) PO(2)(-) (1,080 cm(-1)) vibrations as a discriminating factor for the putative stem cell region; this proved to be a more robust marker than other phenotypic markers, such as beta-catenin or CD133. This pattern was subsequently confirmed by image mapping and points to a novel approach of nondestructively identifying a tissue's stem cell location. v(s)PO(2)(-), probably associated with DNA conformational alterations, might facilitate a means of identifying stem cells, which may have utility in other tissues where the location of stem cells is unclear.
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