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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1 July 1994
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July 01 1994
The types II and III transforming growth factor-beta receptors form homo-oligomers.
Y I Henis,
Y I Henis
Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142.
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A Moustakas,
A Moustakas
Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142.
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H Y Lin,
H Y Lin
Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142.
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H F Lodish
H F Lodish
Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142.
Search for other works by this author on:
Y I Henis
Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142.
A Moustakas
Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142.
H Y Lin
Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142.
H F Lodish
Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142.
Online ISSN: 1540-8140
Print ISSN: 0021-9525
J Cell Biol (1994) 126 (1): 139–154.
Citation
Y I Henis, A Moustakas, H Y Lin, H F Lodish; The types II and III transforming growth factor-beta receptors form homo-oligomers.. J Cell Biol 1 July 1994; 126 (1): 139–154. doi: https://doi.org/10.1083/jcb.126.1.139
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