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Published on: November 16, 2011
Function of the type V transforming growth factor beta receptor in transforming growth factor beta-induced growth
1Department of Biochemistry and Molecular Biology, St. Louis University School of Medicine, St. Louis, Missouri 63104, USA.
Abstract:
The type V transforming growth factor beta (TGF-beta) is a 400-kDa nonproteoglycan membrane protein that co-expresses with the type I, type II, and type III TGF-beta receptors in most cell types. The type V TGF-beta receptor exhibits a Ser/Thr-specific protein kinase activity with distinct substrate specificity (Liu, Q., Huang, S. S., and Huang, J. (1994) J. Biol. Chem. 269, 9221-9226). In mink lung epithelial cells, the type V TGF-beta receptor was found to form heterocomplexes with the type I TGF-beta receptor by immunoprecipitation with antiserum to the type V TGF-beta receptor after 125I-TGF-beta affinity labeling or Trans35S-label metabolic labeling of the cells. The kinase activity of the type V TGF-beta receptor was stimulated after treatment of mink lung epithelial cells with TGF-beta. TGF-beta stimulation resulted in the growth inhibition of wild-type mink lung epithelial cells and to a lesser extent of the type I and type II TGF-beta receptor-defective mutants, although higher concentrations of TGF-beta were required for the growth inhibition of these mutants. TGF-beta was unable to induce growth inhibition in human colorectal carcinoma cells lacking the type V TGF-beta receptor but expressing the type I and type II TGF-beta receptors. These results suggest that the type V TGF-beta receptor can mediate the TGF-beta-induced growth inhibitory response in the absence of the type I or type II TGF-beta receptor. These results also support the hypothesis that loss of the type V TGF-beta receptor may contribute to the malignancy of certain carcinoma cells.
Insights
Type V transforming growth factor beta (TGF-beta) receptor mediates TGF-beta growth inhibition, even without type I or II receptors. Loss of this receptor may link to carcinoma cell malignancy.
Area of Science:
- Cell Biology
- Molecular Biology
- Oncology
Background:
- Type V transforming growth factor beta (TGF-beta) is a membrane protein co-expressed with TGF-beta receptors.
- Type V TGF-beta receptor possesses Ser/Thr-specific protein kinase activity.
Purpose of the Study:
- To investigate the role of the type V TGF-beta receptor in TGF-beta signaling and cellular response.
- To determine if type V TGF-beta receptor can mediate TGF-beta-induced growth inhibition independently of type I or II receptors.
Main Methods:
- Immunoprecipitation and metabolic labeling in mink lung epithelial cells.
- Affinity labeling with 125I-TGF-beta.
- Cell growth inhibition assays with TGF-beta stimulation.
Main Results:
- Type V TGF-beta receptor forms heterocomplexes with type I TGF-beta receptor.
- Kinase activity of type V TGF-beta receptor is stimulated by TGF-beta.
- TGF-beta induced growth inhibition in wild-type cells and mutants, with higher concentrations needed for mutants.
- Human colorectal carcinoma cells lacking type V TGF-beta receptor did not show TGF-beta-induced growth inhibition.
Conclusions:
- Type V TGF-beta receptor can mediate TGF-beta-induced growth inhibition independently of type I or II TGF-beta receptors.
- Loss of type V TGF-beta receptor function may contribute to the development of certain carcinoma malignancies.
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