Tumor-cell migration plays an essential role in invasion into surrounding tissues and the formation of metastatic colonies in distant organs. Metastatic human A2058 melanoma and rostransfected NIH3T3 cells produce autocrine motility factors (AMFs) which stimulate their own motility, and the A2058 ce
Microheterogeneity of human interleukin 6 synthesized by transfected NIH/3T3 cells: Comparison with human monocytes, fibroblasts and endothelial cells
✍ Scribed by Xaver Schiel; Stefan Rose-John; Gabi Dufhues; Heidi Schooltink; Volker Gross; Peter C. Heinrich
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 612 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0014-2980
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✦ Synopsis
Abstract
A cDNA containing the entire coding region of human interleukin 6 (IL 6) was stably expressed in murine NIH/3T3 fibroblasts using a bovine papilloma virus‐based expression vector with a metallothionein promoter. Expression of IL 6 in transfected cells was highly inducible by heavy metals like cadmium as measured at mRNA and protein levels. Cadmium‐stimulated transfected NIH/3T3 cells synthesized and exported biologically active IL 6 (1.7 × 10^4^ U/10^6^ cells/24 h). IL 6 from the culture medium of transfected NIH/3T3 cells exhibited at least eight bands on Western blots after sodium dodecyl sulfate‐polyacrylamide gel electrophoresis, indicating that human IL 6 expressed in NIH/3T3 cells shows a complex glycosylation pattern. Using glycosidases and the N‐glycosylation inhibitor tunicamycin it was possible to discriminate between five species carrying N‐linked carbohydrate side chains and two species carrying only O‐linked side chains. In addition, a substantial amount of unglycosylated IL 6 was observed. IL 6 from transfected NIH/3T3 cells differed markedly in its glycosylation pattern from those of stimulated human monocytes, fibroblasts and endothelial cells.
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We have studied the expression of several cell surface antigens in NIH 3T3 cells after neoplastic transformation with activated human ras and myc oncogenes. The binding of monoclonal antibodies (MAbs), specific for mouse differentiation antigens Ly-6.2, Thy-I and 9F3, to normal and transformed cells