## Abstract Previous studies showed that nerve growth factor (NGF) decreases the proliferation of neuroectodermal tumor (NET) cells (C‐1300 and Neuro2A murine neuroblastoma, PC12 rat pheochromocytoma) within 5–7 days in a dose‐dependent manner. This effect is regulated by the concentration of serum
Chromatin and cell surface receptors mediate melanoma cell growth response to nerve growth factor
✍ Scribed by Ewa M. Rakowicz-Szulczynska; Usha Reddy; Andrzej Vorbrodt; Dorothee Herlyn; Hilary Koprowski
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 873 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0899-1987
No coin nor oath required. For personal study only.
✦ Synopsis
Growth response to nerve growth factor (NGF) was tested in the primary melanoma cell line WM 164, which expressed a low level of NGF cell-surface receptor, and in WM 164 cells transfected with cDNA for the cell-surface receptor (TrWM 164 cells), which expressed a higher level of the cell-surface receptor. Neither cell line expressed the chromatin receptor for NGF or internalized NGF. Both cell lines were stimulated to growth by NGF. After 10 d of exposure to NGF, a 230,000 Mr chromatin protein (receptor) was induced in both cell lines; as a result, NGF bound to the chromatin, and ribosomal RNA synthesis and cell proliferation were inhibited. We suggest that the cell-surface and chromatin receptors each mediate a different function of NGF.
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