Cytoskeletal reorganizations in human umbilical vein endothelial cells as a result of cytokine exposure
Creators
- 1. Department of Cell Biology, Glaxo Research Institute, Research Triangle Park, NC (United States)
Description
Treatment of HUVECs in culture with several cytokines and phorbol esters caused reorganizations of the actin and microtubule networks, as well as a redistribution of focal contract proteins. However, expression of the cytoskeletal proteins which link cells, via integrins, to the substrate, was not significantly affected. Indirect immunofluorescence microscopy of endothelial cells after treatment with interleukin-1 alpha and beta, gamma-interferon, tumor necrosis factor (TNF), phorbol 12-myristate 13-acetate, and phorbol 12,13-dibutyrate allowed us to observe reductions in the areas of cell-cell contact, redistribution of the stress fiber network, and concomitant changes in focal contacts. Microtubule arrays in TNF-treated cells became bundled. Phorbol esters induced formation of microtubule organizing centers not seen in resting or TNF-treated HUVECs. Talin was distributed along stress fibers and not exclusively in focal contacts. Vitronectin receptor was observed in focal contacts, occasionally at cell-cell contacts, and in vesicular structures close to the lumenal surface, after both types of treatment. Although these morphological changes were easily observed by indirect immunofluorescence, no quantitative differences in specific cytoskeletal proteins were detected by immunoblots and [35S]cysteine metabolic labeling experiments
Additional details
Publishing Information
- Journal Title
- Experimental Cell Research
- Journal Volume
- 196
- Journal Issue
- 1
- Series
- Exp. Cell Res.
- Journal Page Range
- 40-48
- ISSN
- 0014-4827
- CODEN
- ECREA
INIS
- Country of Publication
- United States
- Country of Input or Organization
- United States
- INIS RN
- 23022116
- Subject category
- S61: RADIATION PROTECTION AND DOSIMETRY; S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- ANIMAL CELLS; BIOCHEMICAL REACTION KINETICS; BIOLOGICAL EFFECTS; CELL CULTURES; CYSTEINE; ENDOTHELIUM; FLUORESCENCE; LYMPHOKINES; MAN; METABOLISM; MICROTUBULES; MORPHOLOGICAL CHANGES; PHORBOL ESTERS; PROTEINS; SULFUR 35; TRACER TECHNIQUES; VEINS
- Descriptors DEC
- AMINO ACIDS; ANIMALS; BETA DECAY RADIOISOTOPES; BETA-MINUS DECAY RADIOISOTOPES; BLOOD VESSELS; BODY; CARBOXYLIC ACIDS; CARDIOVASCULAR SYSTEM; CELL CONSTITUENTS; DAYS LIVING RADIOISOTOPES; EMISSION; ESTERS; EVEN-ODD NUCLEI; ISOTOPE APPLICATIONS; ISOTOPES; KINETICS; LIGHT NUCLEI; LUMINESCENCE; MAMMALS; NUCLEI; ORGANIC ACIDS; ORGANIC COMPOUNDS; ORGANIC SULFUR COMPOUNDS; ORGANS; PHOTON EMISSION; PRIMATES; RADIOISOTOPES; REACTION KINETICS; SULFUR ISOTOPES; THIOLS; TISSUES; VERTEBRATES