Abstract
Cell surfaces in the duodenal mucosa have been studied in maturing tissue of the chick from incubation until hatching. Changes in the distribution of mitoses in this tissue give an indication of its rate of maturation. This rate is paralleled in developmental changes in microvilli and junctional complexes. Concentration of mitotic figures towards the base of villous folds is gradual from day 9 to day 16, then rapid to day 19, after which the mature pattern is acquired. By day 11, microvilli appear in a regular pattern which does not alter through hatching. Their height remains the same to day 16 when it increases gradually to day 19, then very sharply. The angle formed between the microvilli and the cell surface increases gradually to day 16, giving evidence of advancing internal structure. Changes in cell adhesion also occur at day 16. Thereafter, following trypsin treatment cells are held together in patches by the tight junctions of the terminal bar, although the desmosomes are separated. The timing of these morphological changes is compared with that of alkaline phosphatase accumulation in this tissue as reported by Moog (13). Increase in the surface area of the microvilli parallels the increase in the activity of the enzyme.
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Selected References
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- BROWN A. L., Jr Microvilli of the human jejunal epithelial cell. J Cell Biol. 1962 Mar;12:623–627. doi: 10.1083/jcb.12.3.623. [DOI] [PMC free article] [PubMed] [Google Scholar]
- CLARK S. L., Jr The localization of alkaline phosphatase in tissues of mice, using the electron microscope. Am J Anat. 1961 Jul;109:57–83. doi: 10.1002/aja.1001090106. [DOI] [PubMed] [Google Scholar]
- COULOMBRE A. J., COULOMBRE J. L. Intestinal development. I. Morphogenesis of the villi and musculature. J Embryol Exp Morphol. 1958 Sep;6(3):403–411. [PubMed] [Google Scholar]
- DALTON A. J. Electron micrography of epithelial cells of the gastro-intestinal tract and pancreas. Am J Anat. 1951 Jul;89(1):109–133. doi: 10.1002/aja.1000890105. [DOI] [PubMed] [Google Scholar]
- FARQUHAR M. G., PALADE G. E. Junctional complexes in various epithelia. J Cell Biol. 1963 May;17:375–412. doi: 10.1083/jcb.17.2.375. [DOI] [PMC free article] [PubMed] [Google Scholar]
- GRANGER B., BAKER R. F. Electron microscope investigation of the striated border of intestinal epithelium. Anat Rec. 1950 Aug;107(4):423–441. doi: 10.1002/ar.1091070409. [DOI] [PubMed] [Google Scholar]
- LUFT J. H. Improvements in epoxy resin embedding methods. J Biophys Biochem Cytol. 1961 Feb;9:409–414. doi: 10.1083/jcb.9.2.409. [DOI] [PMC free article] [PubMed] [Google Scholar]
- MILLINGTON P. F., FINEAN J. B. Electron microscope studies of the structure of the microvilli on principal epithelial cells of rat jejunum after treatment in hypo- and hypertonic saline. J Cell Biol. 1962 Jul;14:125–139. doi: 10.1083/jcb.14.1.125. [DOI] [PMC free article] [PubMed] [Google Scholar]
- MOE H. The ultrastructure of Brunner's glands of the cat. J Ultrastruct Res. 1960 Oct;4:58–72. doi: 10.1016/s0022-5320(60)80006-8. [DOI] [PubMed] [Google Scholar]
- MOOG F. The functional differentiation of the small intestine. IX. The influence of thyroid function on cellular differentiation and accumulation of alkaline phosphatase in the duodenum of the chick embryo. Gen Comp Endocrinol. 1961 Dec;1:416–432. doi: 10.1016/0016-6480(61)90006-5. [DOI] [PubMed] [Google Scholar]
- MOOG F., WENGER E. L. The occurrence of a neutral mucopolysaccharide at sites of high alkaline phosphatase activity. Am J Anat. 1952 May;90(3):339–377. doi: 10.1002/aja.1000900303. [DOI] [PubMed] [Google Scholar]
- NILSSON O. Ultrastructure of mouse uterine surface epithelium under different estrogenic influences. 2. Early effect of estrogen administered to spayed animals. J Ultrastruct Res. 1958 Nov;2(1):73–95. doi: 10.1016/s0022-5320(58)90048-0. [DOI] [PubMed] [Google Scholar]
- OVERTON J. Desmosome development in normal and reassociating cells in the early chick blastoderm. Dev Biol. 1962 Jun;4:532–548. doi: 10.1016/0012-1606(62)90056-8. [DOI] [PubMed] [Google Scholar]
- PALAY S. L., KARLIN L. J. An electron microscopic study of the intestinal villus. I. The fasting animal. J Biophys Biochem Cytol. 1959 May 25;5(3):363–372. doi: 10.1083/jcb.5.3.363. [DOI] [PMC free article] [PubMed] [Google Scholar]
- PARKS H. F. Morphological study of the extrusion of secretory materials by the parotid glands of mouse and rat. J Ultrastruct Res. 1962 Jun;6:449–465. doi: 10.1016/s0022-5320(62)80002-1. [DOI] [PubMed] [Google Scholar]
- SHELDON H., ZETTERQVIST H., BRANDES D. Histochemical reactions for electron microscopy: acid phosphatase. Exp Cell Res. 1955 Dec;9(3):592–596. doi: 10.1016/0014-4827(55)90092-6. [DOI] [PubMed] [Google Scholar]
- VIAL J. D., ORREGO H. Electron microscope observations on the fine structure of parietal cells. J Biophys Biochem Cytol. 1960 Apr;7:367–372. doi: 10.1083/jcb.7.2.367. [DOI] [PMC free article] [PubMed] [Google Scholar]