Synthesis and distribution of cytoskeletal elements in endothelial cells as a function of cell growth and organization
- 4 February 1982
- journal article
- research article
- Published by Wiley in Journal of Cellular Physiology
- Vol. 110 (2) , 129-141
- https://doi.org/10.1002/jcp.1041100205
Abstract
Confluent cultures of adult bovine aortic endothelial (ABAE), correal endothelial (BCE), and fetal bovine heart endothelial (FBHE) cells form a monolayer of highly flattened, closely apposed, and nonoverlapping cells. In ABAE and BCE cultures, this is associated with a 50‐fold decrease in the rate of DNA synthesis and correlates with a 14‐fold decrease in protein synthesis. In contrast, in confluent FBHE cultures only partial decreases in the rates of DNA synthesis (6‐fold) and protein synthesis (3‐fold) are observed. FBHE cells therefore fulfill the morphological, but not the biochemical, criteria for confluent cultured endothelial cell monolayers. The appearance of the cytoskeletal elements actin, tubulin, and vimentin in sparse and confluent cultures of endothelial cells has been analyzed by two‐dimensional gel electrophoresis and immunofluorescence. Sparse versus confluent ABAE, FBHE, and BCE cultures showed no changes in their relative rates of synthesis or cellular content of tubulin. Actin behaved similarly to tubulin in FBHE and BCE cultures, while in ABAE cultures a small increase (3‐fold) in its relative rate of synthesis was observed in confluent versus sparse cultures. BCE cultures showed no change in the rate of synthesis of vimentin, but the cellular content of vimentin was markedly increased when cultures reached confluence. When the distribution of vimentin in both sparse and confluent BCE cultures was analyzed by immunofluorescence, in both cases it appeared distributed throughout the cytoplasm as thin fibers and bundles of fibers. In confluent ABAE cultures, both the relative amount and biosynthetic rate of vimentin increased by 15‐fold. This increase in the intracellular accumulation of vimentin correlated with its immunofluorescent distribution within the cells. While in sparse cultures, vimentin appeared to be distributed as thin fibers, in confluent cultures thick curl‐like fibrous bundles could be seen distributed throughout the cytoplasm and organized in a perinuclear ring. In contrast, in FBHE cultures no significant changes in the distribution and organization of rate of synthesis of vimentin were observed.This publication has 24 references indexed in Scilit:
- Distribution of flourescently labeled α-actinin in living and fixed fibroblastsThe Journal of cell biology, 1980
- Vascular endothelial cells maintained in the absence of fibroblast growth factor undergo structural and functional alterations that are incompatible with their in vivo differentiated properties.The Journal of cell biology, 1979
- Identification with cellular microtubules of one of the co-assembling microtubule-associated proteinsCell, 1979
- Intermediate-sized filaments of human endothelial cells.The Journal of cell biology, 1979
- High resolution two-dimensional electrophoresis of basic as well as acidic proteinsCell, 1977
- Control of proliferation of bovine vascular endothelial cellsJournal of Cellular Physiology, 1977
- Rings of intermediate (100 A) filament bundles in the perinuclear region of vascular endothelial cells. Their mobilization by colcemid and mitosis.The Journal of cell biology, 1976
- Intracellular Protein Degradation in Mammalian and Bacterial Cells: Part 2Annual Review of Biochemistry, 1976
- IN VITRO BEHAVIOR OF GUINEA PIG ARTERIAL AND VENOUS ENDOTHELIAL CELLS *Development, Growth & Differentiation, 1975
- Intracellular Protein Degradation in Mammalian and Bacterial CellsAnnual Review of Biochemistry, 1974