Abstract |
The present study was designed to determine the subcellular localization of histidyl-tRNA synthetase (Jo-1) in human laryngeal epithelial carcinoma cell line (HEp-2 cells). Indirect immunofluorescence using commercial HEp-2 cells with human serum and human-affinity-purified anti-Jo-1 antibodies was performed using confocal microscopy. Anti- histidyl-tRNA-synthetase-positive sera showed distinct nuclear and cytoplasmic granular staining in HEp-2 cells. Affinity purified anti-Jo-1 produced an identical pattern to the whole serum, whereas the serum fraction that did not bind to the affinity column was negative by immunofluorescence on HEp-2 cells. Two commercial human anti-Jo-1-positive control sera and seven anti-Jo-1-positive sera from patients with myositis reproduced the nuclear and cytoplasmic granular pattern. We conclude that Jo-1 is present in cytoplasm and in intact nuclei from HEp-2 cells. The presence of tRNA synthetases in intact nuclei suggests that they have an unsuspected function in the nucleus.
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Authors | D Vázquez-Abad, J H Carson, N Rothfield |
Journal | Cell and tissue research
(Cell Tissue Res)
Vol. 286
Issue 3
Pg. 487-91
(Dec 1996)
ISSN: 0302-766X [Print] Germany |
PMID | 8929351
(Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
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Topics |
- Cell Nucleus
(metabolism)
- Cytoplasm
(metabolism)
- HeLa Cells
- Histidine-tRNA Ligase
(metabolism)
- Humans
- Laryngeal Neoplasms
(pathology)
- Myositis
(blood, immunology)
- Tumor Cells, Cultured
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