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Referenced in 5 patents
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Research Article Free access | 10.1172/JCI115297

Binding domains of stimulatory and inhibitory thyrotropin (TSH) receptor autoantibodies determined with chimeric TSH-lutropin/chorionic gonadotropin receptors.

Y Nagayama, H L Wadsworth, D Russo, G D Chazenbalk, and B Rapoport

Thyroid Molecular Biology Unit, Veterans Administration Medical Center, San Francisco, California 94121.

Find articles by Nagayama, Y. in: PubMed | Google Scholar

Thyroid Molecular Biology Unit, Veterans Administration Medical Center, San Francisco, California 94121.

Find articles by Wadsworth, H. in: PubMed | Google Scholar

Thyroid Molecular Biology Unit, Veterans Administration Medical Center, San Francisco, California 94121.

Find articles by Russo, D. in: PubMed | Google Scholar

Thyroid Molecular Biology Unit, Veterans Administration Medical Center, San Francisco, California 94121.

Find articles by Chazenbalk, G. in: PubMed | Google Scholar

Thyroid Molecular Biology Unit, Veterans Administration Medical Center, San Francisco, California 94121.

Find articles by Rapoport, B. in: PubMed | Google Scholar

Published July 1, 1991 - More info

Published in Volume 88, Issue 1 on July 1, 1991
J Clin Invest. 1991;88(1):336–340. https://doi.org/10.1172/JCI115297.
© 1991 The American Society for Clinical Investigation
Published July 1, 1991 - Version history
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Abstract

We examined the relative effects of thyrotropin (TSH) and TSH receptor autoantibodies in the sera of patients with autoimmune thyroid disease on three TSH-lutropin/chorionic gonadotropin (LH/CG) receptor extracellular domain chimeras. Each chimera binds TSH with high affinity. Only the chimera with TSH receptor extracellular domains ABC (amino acids 1-260) had a functional (cAMP) response to thyroid stimulatory IgG. The chimeras with TSH receptor domains CD (amino acids 171-360) and DE (amino acids 261-418) were unresponsive. The lack of response of the chimera with TSH receptor domains DE was anticipated because it fails to transduce a signal with TSH stimulation, unlike the other two chimeras. A different spectrum of responses occurred when the TSH-LH/CG chimeras were examined in terms of autoantibody competition for TSH binding. IgG with TSH binding-inhibitory activity when tested with the wild-type TSH receptor also inhibited TSH binding to the chimera with TSH receptor domains DE. Dramatically, however, these IgG did not inhibit TSH binding to the chimera with TSH receptor domains CD, and had weak or absent activity with the chimera with TSH receptor domains ABC. Chimeras with TSH receptor domains ABC and DE were equally effective in affinity-purifying IgG with thyroid-stimulatory and TSH binding-inhibitory activities. Nonstimulatory IgG with TSH binding-inhibitory activity inhibited the action of stimulatory IgG on the wild-type TSH receptor, but not with the chimera containing TSH receptor domains ABC. In summary, TSH receptor autoantibodies and TSH bind to regions in both domains ABC and DE of the TSH receptor extracellular region. Stimulatory and inhibitory TSH receptor autoantibodies, as well as TSH, appear to bind to different sites in domains ABC, but similar sites in domains DE, of the receptor. Alternatively, TSH and the different TSH receptor antibodies bind with differing affinities to the same site in the ABC region.

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Referenced in 5 patents
7 readers on Mendeley
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