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Glycine Receptor Autoantibodies Impair Receptor Function and Induce Motor Dysfunction.
- Source :
- Annals of Neurology; Sep2020, Vol. 88 Issue 3, p544-561, 18p
- Publication Year :
- 2020
-
Abstract
- <bold>Objective: </bold>Impairment of glycinergic neurotransmission leads to complex movement and behavioral disorders. Patients harboring glycine receptor autoantibodies suffer from stiff-person syndrome or its severe variant progressive encephalomyelitis with rigidity and myoclonus. Enhanced receptor internalization was proposed as the common molecular mechanism upon autoantibody binding. Although functional impairment of glycine receptors following autoantibody binding has recently been investigated, it is still incompletely understood.<bold>Methods: </bold>A cell-based assay was used for positive sample evaluation. Glycine receptor function was assessed by electrophysiological recordings and radioligand binding assays. The in vivo passive transfer of patient autoantibodies was done using the zebrafish animal model.<bold>Results: </bold>Glycine receptor function as assessed by glycine dose-response curves showed significantly decreased glycine potency in the presence of patient sera. Upon binding of autoantibodies from 2 patients, a decreased fraction of desensitized receptors was observed, whereas closing of the ion channel remained fast. The glycine receptor N-terminal residues 29 A to 62 G were mapped as a common epitope of glycine receptor autoantibodies. An in vivo transfer into the zebrafish animal model generated a phenotype with disturbed escape behavior accompanied by a reduced number of glycine receptor clusters in the spinal cord of affected animals.<bold>Interpretation: </bold>Autoantibodies against the extracellular domain mediate alterations of glycine receptor physiology. Moreover, our in vivo data demonstrate that the autoantibodies are a direct cause of the disease, because the transfer of human glycine receptor autoantibodies to zebrafish larvae generated impaired escape behavior in the animal model compatible with abnormal startle response in stiff-person syndrome or progressive encephalitis with rigidity and myoclonus patients. ANN NEUROL 2020;88:544-561. [ABSTRACT FROM AUTHOR]
- Subjects :
- GLYCINE receptors
MYOCLONUS
AUTOANTIBODIES
N-terminal residues
ANIMAL behavior
RADIOLIGAND assay
ENCEPHALITIS
RESEARCH
ANIMAL experimentation
RESEARCH methodology
CELL receptors
EVALUATION research
MEDICAL cooperation
COMPARATIVE studies
MUSCLE rigidity
FISHES
RESEARCH funding
STIFF-person syndrome
ANTIGENS
Subjects
Details
- Language :
- English
- ISSN :
- 03645134
- Volume :
- 88
- Issue :
- 3
- Database :
- Complementary Index
- Journal :
- Annals of Neurology
- Publication Type :
- Academic Journal
- Accession number :
- 145278612
- Full Text :
- https://doi.org/10.1002/ana.25832