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The types II and III transforming growth factor-beta receptors form homo-oligomers.
Open accessAbstract
Affinity-labeling experiments have detected hetero-oligomers of the types I, II, and III transforming growth factor beta (TGF-beta) receptors which mediate intracellular signaling by TGF-beta, but the oligomeric state of the individual receptor types remains unknown. Here we use two types of experiments to show that a major portion of the receptor types II and III forms homo-oligomers both in the absence and presence of TGF-beta. Both experiments used COS-7 cells co-transfected with combinations of these receptors carrying different epitope tags at their extracellular termini. In immunoprecipitation experiments, radiolabeled TGF-beta was bound and cross-linked to cells co-expressing two differently tagged type II receptors. Sequential immunoprecipitations using anti-epitope monoclonal antibodies showed that type II TGF-beta receptors form homo-oligomers. In cells co-expressing epitope-tagged types II and III receptors, a low level of co-precipitation of the ligand-labeled receptors was observed, indicating that some hetero-oligomers of the types II and III receptors exist in the presence of ligand. Antibody-mediated cross-linking studies based on double-labeling immunofluorescence explored co-patching of the receptors at the cell surface on live cells. In cells co-expressing two differently tagged type II receptors or two differently tagged type III receptors, forcing one receptor into micropatches by IgG induced co-patching of the receptor carrying the other tag, labeled by noncross-linking monovalent Fab'. These studies showed that homo-oligomers of the types II and III receptors exist on the cell surface in the absence or presence of TGF-beta 1 or -beta 2. In cells co-expressing types II and III receptors, the amount of heterocomplexes at the cell surface was too low to be detected in the immunofluorescence co-patching experiments, confirming that hetero-oligomers of the types II and III receptors are minor and probably transient species.
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Andres, J. L., Stanley, K., Cheifetz, S., & Massagué, J. (1989) · The Journal of cell biology · doi:10.1083/jcb.109.6.3137 · Cited by 354
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Metadata
- Authors
- Henis, Y. I., Moustakas, A., Lin, H. Y., & Lodish, H. F.
- Venue
- The Journal of cell biology
- Publisher
- Rockefeller University Press
- Published
- 1994-07-01
- Volume
- 126
- Issue
- 1
- Pages
- 139-154
- ISSN
- 0021-9525 (ISSN-L)
- 1540-8140
- OpenAlex
- W2020328367
- Cited by
- 205
- References
- 1
- FWCI
- 6.86
- Type
- journal article
- Language
- en
- Open access
- green
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- Henis, Y. I., Moustakas, A., Lin, H. Y., & Lodish, H. F. (1994). The types II and III transforming growth factor-beta receptors form homo-oligomers. The Journal of cell biology. https://doi.org/10.1083/jcb.126.1.139
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