Application of Computer-assisted Morphometry to the Analysis of Prenatal Development of Human Lung

• Published in: Anatomia, histologia, embryologia histologia, embryologia, 1997-06, Vol.26 (2), p.135-139
• Main Authors: Kayser, K., Jacinto, S. D., Böhm, G., Fritz, P., Kunze, W. P., Nehrlich, A., Gabius, H. J.
• Format: Article
• Language: English
• Subjects: Cell Differentiation - physiology; Cell Division - physiology; Cell Nucleus - ultrastructure; Embryonic and Fetal Development - physiology; Entropy; Female; Fetus - cytology; Fetus - physiology; Humans; Image Processing, Computer-Assisted - methods; Lung - cytology; Lung - embryology; Lung - physiology; Male; S Phase
• ISSN: 0340-2096; 1439-0264
• DOI: 10.1111/j.1439-0264.1997.tb00113.x

Summary Morphometry is well‐established in tumour pathology. To evaluate its potential usefulness for description of developmental processes, histological slides from paraffin‐embedded specimens of 67 human fetal lungs were Feulgen‐stained, and morphometric characteristics of nuclei of epithelial pulmonary cells were analysed with an automated image analysis system. The measured cytometric features comprised of integrated optical density (IOD), S‐phase‐related IOD fraction, IOD entropy and nuclear area. Histometric features of the specimens were based upon the minimum spanning tree (MST) and included distances between neighboring epithelial cells, between epithelial cells and neighboring lymphocytes, and assessment of MST entropy. Notably, certain parameters revealed a non‐uniform level during prenatal development. S‐phase‐related IOD fraction increased from 5% to 8% between 14 and 16 weeks of gestation, then declined to 6% until birth. The IOD entropy steadily increased during development, whereas the extent of nuclear area remained constant. In accordance with an increase of the S‐phase‐related fraction the MST entropy displayed a singular peak between 14 and 16 weeks of gestation, which is probably associated with development of glandular structures in the lung. Correlation of expression of binding sites for markers, presumably involved in functional aspects of development, with such alterations, is shown for binding capacities of biotinylated fucoidan and the S‐phase‐related fraction. This may be helpful to infer immunoor ligando histochemically defined tissue sites with potential physiological significance in morphometrically distinguished periods of development.