Use of 3-D-computer graphics for imaging of distribution of hepatic metabolites
In conjunction with the investigation of intercellular compartmentation of liver metabolism and as a logical further step, following the introduction of a new sample isolation procedure for microchemical analysis of functional liver cell heterogeneity, the possible benefit of computer-assisted three-dimensional imaging procedures for the reconstruction of hepatic metabolite distribution was investigated. In this intent, we elected to access a central computer facility by means of a small microcomputer system which, nevertheless, permitted to take full advantage of a large capacity main-frame computer and a high quality graphics plotter, at comparatively low overal costs. Commercially available software (SAS/GRAPH) was tailored to the specific requirements of this application. The threedimensional imaging process recombines microchemical data (metabolite or enzyme values) with those of the size and location of samples within a particular cross-sectional area of a liver unit and provides an integrated view of metabolite distributions. The three-dimensional images were then used to define general distribution characteristics, as well as, differences in metabolite distribution along sinusoids of portal and septal origin. Glucose increased, whereas glucose-6-P decreased along sinusoids from the beginning to the end and values of both metabolites were found to be higher along ‘portal/central’ than along ‘septal/central’ sinusoids. Co-distribution of glucose-6-phosphatase with its substrate (glucose-6-P) was indicated by histochemical and microchemical results and is anticipated to be of considerable regulatory importance, since it further enhances the differences among hepatocytes at different locations along sinusoids with respect to their ability to produce glucose. In view of the results obtained, the new procedure which takes advantage of electronic acquisition, manipulation and graphical representation of data, is considered a valuable new tool and important part of a methodological approach that combines staining histochemistry, microdissection of minute tissue samples from frozen-dried cryosections and microchemical assays of high analytical sensitivity.
KeywordsOveral Microcomputer System Regulatory Importance Quality Graphic Microchemical Analysis
Unable to display preview. Download preview PDF.
- Harder KL, Desmarais RN (1972) Interpolation using surface splines. J Aircraft 9:189–191Google Scholar
- Matsumoto T, Kawakami M (1982) The unit-concept of hepatic parenchyma. A re-examination based on angioarchitectural studies. Acta Pathol Jpn 32 (Suppl 2):285–314Google Scholar
- Meinguet J (1979) Multivariate interpolation at arbitrary points made simple. J Appl Math Phys 30:292–304Google Scholar
- Nordlie RC (1974) Metabolic regulation by multifunctional glucose-6-phosphatase. Curr Top Cell Regul 8:33–117Google Scholar
- Teutsch HF (1981) Chemomorphology of liver parenchyma. Prog Histochem Cytochem 14:1–92Google Scholar
- Teutsch HF (1984) Sex-specific regionality of liver metabolism during starvation; with special reference to the heterogeneity of the lobular periphery. Histochemistry 81:87–92Google Scholar
- Teutsch HF (1985) Quantitative histochemical assessment of regional differences in hepatic glucose uptake and release. Histochemistry 82:159–164Google Scholar
- Teutsch HF (1986) A new isolation procedure for microchemical analysis of functional liver cell heterogeneity. J Histochem Cytochem 34:263–267Google Scholar