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Autoantibody of NRIP, a novel AChR‐interacting protein, plays a detrimental role in myasthenia gravis

BACKGROUND: Nuclear receptor interaction protein (NRIP) co‐localizes with acetylcholine receptor (AChR) at the neuromuscular junction (NMJ), and NRIP deficiency causes aberrant NMJ architecture. However, the normal physiological and pathophysiological roles of NRIP in NMJ are still unclear. METHODS:...

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Autores principales: Tsai, Li‐Kai, Chen, I‐Hsin, Chao, Chi‐Chao, Hsueh, Hsueh‐Wen, Chen, Hsin‐Hsiung, Huang, Yun‐Hsin, Weng, Rong‐Wei, Lai, Tzu‐Yun, Tsai, Yi‐Chieh, Tsao, Yeou‐Ping, Chen, Show‐Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8200423/
https://www.ncbi.nlm.nih.gov/pubmed/33773096
http://dx.doi.org/10.1002/jcsm.12697
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author Tsai, Li‐Kai
Chen, I‐Hsin
Chao, Chi‐Chao
Hsueh, Hsueh‐Wen
Chen, Hsin‐Hsiung
Huang, Yun‐Hsin
Weng, Rong‐Wei
Lai, Tzu‐Yun
Tsai, Yi‐Chieh
Tsao, Yeou‐Ping
Chen, Show‐Li
author_facet Tsai, Li‐Kai
Chen, I‐Hsin
Chao, Chi‐Chao
Hsueh, Hsueh‐Wen
Chen, Hsin‐Hsiung
Huang, Yun‐Hsin
Weng, Rong‐Wei
Lai, Tzu‐Yun
Tsai, Yi‐Chieh
Tsao, Yeou‐Ping
Chen, Show‐Li
author_sort Tsai, Li‐Kai
collection PubMed
description BACKGROUND: Nuclear receptor interaction protein (NRIP) co‐localizes with acetylcholine receptor (AChR) at the neuromuscular junction (NMJ), and NRIP deficiency causes aberrant NMJ architecture. However, the normal physiological and pathophysiological roles of NRIP in NMJ are still unclear. METHODS: We investigated the co‐localization and interaction of NRIP with AChR‐associated proteins using immunofluorescence and immunoprecipitation assay, respectively. The binding affinity of AChR‐associated proteins was analysed in muscle‐restricted NRIP knockout mice and NRIP knockout muscle cells (C2C12). We further collected the sera from 43 patients with myasthenia gravis (MG), an NMJ disorder. The existence and features of anti‐NRIP autoantibody in sera were studied using Western blot and epitope mapping. RESULTS: NRIP co‐localized with AChR, rapsyn and α‐actinin 2 (ACTN2) in gastrocnemius muscles of mice; and α‐bungarotoxin (BTX) pull‐down assay revealed NRIP with rapsyn and ACTN2 in complexes from muscle tissues and cells. NRIP directly binds with α subunit of AChR (AChRα) in vitro and in vivo to affect the binding affinity of AChR with rapsyn and rapsyn with ACTN2. In 43 patients with MG (age, 58.4 ± 14.5 years; female, 55.8%), we detected six of them (14.0%) having anti‐NRIP autoantibody. The presence of anti‐NRIP autoantibody correlated with a more severe type of MG when AChR autoantibody existed (P = 0.011). The higher the titre of anti‐NRIP autoantibody, the more severe MG severity (P = 0.032). The main immunogenic region is likely on the IQ motif of NRIP. We also showed the IgG subclass of anti‐NRIP autoantibody mainly to be IgG1. CONCLUSIONS: NRIP is a novel AChRα binding protein and involves structural NMJ formation, which acts as a scaffold to stabilize AChR–rapsyn–ACTN2 complexes. Anti‐NRIP autoantibody is a novel autoantibody in MG and plays a detrimental role in MG with the coexistence of anti‐AChR autoantibody.
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spelling pubmed-82004232021-06-15 Autoantibody of NRIP, a novel AChR‐interacting protein, plays a detrimental role in myasthenia gravis Tsai, Li‐Kai Chen, I‐Hsin Chao, Chi‐Chao Hsueh, Hsueh‐Wen Chen, Hsin‐Hsiung Huang, Yun‐Hsin Weng, Rong‐Wei Lai, Tzu‐Yun Tsai, Yi‐Chieh Tsao, Yeou‐Ping Chen, Show‐Li J Cachexia Sarcopenia Muscle Original Articles BACKGROUND: Nuclear receptor interaction protein (NRIP) co‐localizes with acetylcholine receptor (AChR) at the neuromuscular junction (NMJ), and NRIP deficiency causes aberrant NMJ architecture. However, the normal physiological and pathophysiological roles of NRIP in NMJ are still unclear. METHODS: We investigated the co‐localization and interaction of NRIP with AChR‐associated proteins using immunofluorescence and immunoprecipitation assay, respectively. The binding affinity of AChR‐associated proteins was analysed in muscle‐restricted NRIP knockout mice and NRIP knockout muscle cells (C2C12). We further collected the sera from 43 patients with myasthenia gravis (MG), an NMJ disorder. The existence and features of anti‐NRIP autoantibody in sera were studied using Western blot and epitope mapping. RESULTS: NRIP co‐localized with AChR, rapsyn and α‐actinin 2 (ACTN2) in gastrocnemius muscles of mice; and α‐bungarotoxin (BTX) pull‐down assay revealed NRIP with rapsyn and ACTN2 in complexes from muscle tissues and cells. NRIP directly binds with α subunit of AChR (AChRα) in vitro and in vivo to affect the binding affinity of AChR with rapsyn and rapsyn with ACTN2. In 43 patients with MG (age, 58.4 ± 14.5 years; female, 55.8%), we detected six of them (14.0%) having anti‐NRIP autoantibody. The presence of anti‐NRIP autoantibody correlated with a more severe type of MG when AChR autoantibody existed (P = 0.011). The higher the titre of anti‐NRIP autoantibody, the more severe MG severity (P = 0.032). The main immunogenic region is likely on the IQ motif of NRIP. We also showed the IgG subclass of anti‐NRIP autoantibody mainly to be IgG1. CONCLUSIONS: NRIP is a novel AChRα binding protein and involves structural NMJ formation, which acts as a scaffold to stabilize AChR–rapsyn–ACTN2 complexes. Anti‐NRIP autoantibody is a novel autoantibody in MG and plays a detrimental role in MG with the coexistence of anti‐AChR autoantibody. John Wiley and Sons Inc. 2021-03-26 2021-06 /pmc/articles/PMC8200423/ /pubmed/33773096 http://dx.doi.org/10.1002/jcsm.12697 Text en © 2021 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of Society on Sarcopenia, Cachexia and Wasting Disorders https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Tsai, Li‐Kai
Chen, I‐Hsin
Chao, Chi‐Chao
Hsueh, Hsueh‐Wen
Chen, Hsin‐Hsiung
Huang, Yun‐Hsin
Weng, Rong‐Wei
Lai, Tzu‐Yun
Tsai, Yi‐Chieh
Tsao, Yeou‐Ping
Chen, Show‐Li
Autoantibody of NRIP, a novel AChR‐interacting protein, plays a detrimental role in myasthenia gravis
title Autoantibody of NRIP, a novel AChR‐interacting protein, plays a detrimental role in myasthenia gravis
title_full Autoantibody of NRIP, a novel AChR‐interacting protein, plays a detrimental role in myasthenia gravis
title_fullStr Autoantibody of NRIP, a novel AChR‐interacting protein, plays a detrimental role in myasthenia gravis
title_full_unstemmed Autoantibody of NRIP, a novel AChR‐interacting protein, plays a detrimental role in myasthenia gravis
title_short Autoantibody of NRIP, a novel AChR‐interacting protein, plays a detrimental role in myasthenia gravis
title_sort autoantibody of nrip, a novel achr‐interacting protein, plays a detrimental role in myasthenia gravis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8200423/
https://www.ncbi.nlm.nih.gov/pubmed/33773096
http://dx.doi.org/10.1002/jcsm.12697
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