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Cited by 205

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

The types II and III transforming growth factor-beta receptors form homo-oligomers.

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Henis, Y I, Moustakas, A, Lin, H Y, Lodish, H F·1994·The Journal of cell biology

Abstract

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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Metadata

Authors
Henis, Y. I., Moustakas, A., Lin, H. Y., & Lodish, H. F.
Venue
The Journal of cell biology
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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CoChat. (2026). Citation check: The types II and III transforming growth factor-beta receptors form homo-oligomers. https://app.cochat.ai/papers/10.1083/jcb.126.1.139
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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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