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Basic Stereology

Published online by Cambridge University Press:  14 March 2018

John M. Basgen*
Affiliation:
University of Minnesota

Extract

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Many us who use microscopes are interested in the internal structure or components of three-dimensional objects. Often we must section these objects to observe these internal components. For many years, microtomes have been used to make physical sections, but in recent years confocal microscopes, MR imaging, CT scanners, and even standard optical microscopes have been used to obtain “optical” sections. Two-dimensional images of these different types of sections can be used to extract three-dimensional quantitative information about the objects and their internal components, The sectioning process reduces the observed dimensions of the object and components. With apologies to Rene Magritte, the structure portrayed in Figure 1 is not a three-dimensional glomerulus but a two-dimensional profile of a glomerulus. In most cases, interest is on the structure of the three-dimensional object and not the structure in the two-dimensional image. Thus, care must be taken when obtaining and interpreting data from two-dimensional images.

Type
Research Article
Copyright
Copyright © Microscopy Society of America 2003

References

1. Elias, H. (1971) Three-dimensional structure identified from single sections. Science 171:993-100.Google Scholar
2. Gaunt, PN and Gaunt, WA. (1978) Three dimensional reconstruction in biology. University Park Press, Baltimore.Google Scholar
3. Elias, H. (1962) Stereologia 1:1.Google Scholar
4. Weibei, ER. (1979) Stereological Methods: Practical Methods for Biological Morphornetry Academic Press, New York p. 1.Google Scholar
5. Howard, CV and Reed, MG. (1998), Unbiased StereologyThree-Dimensional Measurement in Microscopy, Bios Scientific Pub., New York pp. 5568.Google Scholar
6. Howard, CV and Reed, MG. (1998), Unbiased Stereology Three-Dimensional Measurement in Microscopy, Bios Scientific Pub., NY pp. 107108.Google Scholar
7. Baddeley, AJ, HJG, Gundersen and Cruz-Orive, LM. (1986) Estimation of surface area from vertical sections. Journal of Microscopy 142:259-276.Google Scholar
8. Howard, CV and Reed, MG. (1998), Unbiased Stereology Three-Dimensional Measurement in Microscopy, Bios Scientific Pub., NY pp. 125128.Google Scholar
9. Gokhale, AM. (1993) Utility of the horizontal slice for stereological characterization of linear features. Journal of Microscopy 170:3-8.Google Scholar
10. Sterio, DC. (1984) The unbiased estimation of number and sizes of arbitrary particles using the disector. Jouma! of Microscopy 134:127-136.Google Scholar
11. Braendgaard, H, Evans, SM, Howard, CV and Gundersen, HJG. (1990) The total number of neurons In the human neocortex unbiasedly estimated using optical disectors. Journal of Microscopy 157:285-304.CrossRefGoogle Scholar
12. Gundersen, HJG and Jensen, EB. (1987) The efficiency of sampling in stereology and its prediction. Journal of Microscopy 147:229-263.Google Scholar
13. Russ, JC. (1995) The Image Processing Handbook, 2nd Edition, CRC Press, Boca Raton.Google Scholar
14. Basgen, JM, Rich, SS, Mauer, SM and Steffes, MW. (1988) On measuring volume density of the glomerular mesangium. Nephron 50:182-186.Google Scholar
15. Gundersen, HJG and ∅sterby, R, (1980) Optimizing sampling efficiency of stereological studies in biology: or “do more less well!'. Journal of Microscopy 121:65-73.CrossRefGoogle Scholar