ArticleCell and tissue research1979
Development of the structural components of the brush border in absorptive cells of the chick intestine.
Article in Cell and tissue research, 1979. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.
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Who cites it
17 citing papers in PubMed.
- Intra-amniotic administration of l-glutamine promotes intestinal maturation and enteroendocrine stimulation in chick embryos.Scientific reports · 2022Article
- Intestinal brush border assembly during the peri-hatch period and its contribution to surface area expansion.Poultry science · 2021Article
- A novel function for the MAP kinase SMA-5 in intestinal tube stability.Molecular biology of the cell · 2016Article
- Dynamic assembly of surface structures in living cells.Proceedings of the National Academy of Sciences of the United States of America · 2003Article
- Why are two different cross-linkers necessary for actin bundle formation in vivo and what does each cross-link contribute?The Journal of cell biology · 1998Article
- F actin bundles in Drosophila bristles. I. Two filament cross-links are involved in bundling.The Journal of cell biology · 1995Article
- Functional differences between L- and T-plastin isoforms.The Journal of cell biology · 1994Article
- Demonstration of sucrase immunoreactivity of the brush border induced by duodenal mesenchyme in chick stomach endoderm.Roux's archives of developmental biology : the official organ of the EDBO · 1992Article
- Changes in keratin expression during fetal and postnatal development of intestinal epithelial cells.The Biochemical journal · 1992Article
- Assembly of the intestinal brush border: appearance and redistribution of microvillar core proteins in developing chick enterocytes.The Journal of cell biology · 1987Article
- Movement of the actin filament bundle in Mytilus sperm: a new mechanism is proposed.The Journal of cell biology · 1987Article
- Differentiation of the segmented tubular nephron and excretory duct during lamprey metamorphosis.Anatomy and embryology · 1984Article
- The changes in structural organization of actin in the sea urchin egg cortex in response to hydrostatic pressure.The Journal of cell biology · 1983Article
- Structural organization of actin in the sea urchin egg cortex: microvillar elongation in the absence of actin filament bundle formation.The Journal of cell biology · 1982Article
- Establishment of regional differences in brush border enzymatic activities during the development of fetal mouse small intestine.Cell and tissue research · 1981Article
- Rapid synthesis of photoreceptor membrane and assembly of new microvilli in a crab at dusk.Cell and tissue research · 1980Article
- The role of actin bundling proteins in the assembly of filopodia in epithelial cells.Cell adhesion & migrationReview
Corrections and comments
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The spatial and temporal relationships between cytoplasmic filaments and the morphogenesis of the intestinal brush border were examined by transmission electron microscopy of normally developing tissue and of tissue exposed to a variety of experimental conditions in organ culture. Distinct stages in the development of the brush border were identified: (1) Irregular projections of the apical plasma membrane that contain a network of microfilaments are converted to uniform projections filled with a core bundle of straight microfilaments (7-11d of incubation). (2) Rootlets form by an elongation or aggregation of filaments (11-15d). (3) The terminal web forms first as a network of short filaments just below the apical plasma membrane, then secondarily stratifies into two layers (19d of incubation to 3d posthatching). (4) Core filaments elongate as microvilli achieve their maturity (21d of incubation to 5d posthatching). Microvillus formation was not perturbed by culturing 9d tissue in high concentrations of Ca++ or Mg++, either with or without the ionophore, A23187. Rootlet formation was stimulated by high Mg++, with or without A23187, and, for reasons unknown, by ethanol. Terminal web formation was not stimulated by Mg++ or Ca++, but the integrity of the terminal web was lost when 21d embryonic tissue was cultured with EGTA or cytochalasin B. After stratification, the terminal web could not be disrupted by EGTA, but instead was aggregated to the center of the apical end of the cell.
Indexed as
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.