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Neuroscience
Um ensaio simples baseada em célula imunofluorescência para detectar anticorpos contra o Receptor...
Um ensaio simples baseada em célula imunofluorescência para detectar anticorpos contra o Receptor...
JoVE Journal
Neuroscience
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JoVE Journal Neuroscience
A Simple Cell-based Immunofluorescence Assay to Detect Autoantibody Against the N-Methyl-D-Aspartate (NMDA) Receptor in Blood

Um ensaio simples baseada em célula imunofluorescência para detectar anticorpos contra o Receptor N-metil-D-aspartato (NMDA) no sangue

Full Text
10,329 Views
07:20 min
January 9, 2018

DOI: 10.3791/56676-v

Chia-Hsiang Chen1,2, Yu-Syuan Chang1

1Department of Psychiatry,Chang Gung Memorial Hospital-Linkou, 2Department and Graduate Institute of Biomedical Sciences,Chang Gung University

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Please note that some of the translations on this page are AI generated. Click here for the English version.

Overview

This study investigates the detection of autoantibodies against the NMDA receptor in patients suspected of autoimmune encephalitis using a cell-based assay. Human embryonic kidney cells (HEK293) expressing the NR1 subunit tagged with green fluorescent protein (GFP) serve as the model system. This simple and reliable method provides a potential screening tool for clinical settings.

Key Study Components

Area of Science

  • Neuroscience
  • Immunology
  • Cell biology

Background

  • Autoimmune encephalitis can present with acute neuro-psychiatric symptoms.
  • Detection of autoantibodies is crucial for differential diagnosis.
  • Existing methods may be complicated or lack sensitivity.
  • This study introduces a straightforward assay for screening autoantibodies.

Purpose of Study

  • To develop a reliable method for screening NMDA receptor autoantibodies.
  • To assist in the diagnosis of autoimmune encephalitis.
  • To evaluate the feasibility of this approach in clinical practice.

Methods Used

  • This study employs a cell culture platform using HEK293 cells.
  • HEK293 cells are transfected with the NR1-GFP plasmid to express the NMDA receptor.
  • The assay involves several incubation and washing steps, along with fluorescence microscopy for detection.
  • Important steps include preparing gelatin-coated culture plates and using primary and secondary antibodies for detection.
  • The entire procedure can be completed in approximately four hours.

Main Results

  • Detection of NR1-GFP expression in HEK293 cells, showing around 30% expression.
  • Positive detection of autoantibodies indicated by colocalization of NR1-GFP and anti-NMDA antibody signals.
  • Confirmation of specific binding of antibodies to NR1-GFP highlighted significant results.
  • The method demonstrates potential utility with clear positive and negative control assays.

Conclusions

  • This study provides a method to effectively screen for NMDA receptor autoantibodies.
  • The efficiency of the technique opens avenues for further research in psychiatric conditions.
  • This approach could facilitate better understanding and diagnosis of acute mental health emergencies.

Frequently Asked Questions

What are the advantages of using HEK293 cells for this assay?
HEK293 cells are easy to culture and transfect, allowing for robust expression of the NR1 subunit and efficient detection of autoantibodies against NMDA receptors.
How is the primary antibody used in the assay?
The primary antibody, diluted in PBST, is incubated with the HEK293 cells to bind any existing autoantibodies in the plasma samples being tested.
What outcomes are measured in this assay?
The assay measures the presence of autoantibodies based on the colocalization of the fluorescence signals from NR1-GFP and the secondary antibody conjugated with Alexa Fluor 594.
Can this method be adapted for other receptors?
Yes, the method can potentially be adapted for other receptor assays by substituting the plasmid to express different receptor subunits once optimized.
What are the limitations of this screening method?
While it is a quick screening tool, it may require further confirmation through methods like western blot analysis to validate the presence of autoantibodies.

Ectopically manifestámos NR1 subunidade do receptor NMDA marcado com proteína verde fluorescente em células embrionárias humanas (HEK293) como antígeno para detectar anticorpos contra o receptor NMDA no sangue de pacientes suspeitado com encefalite auto-imune. Este método simples pode ser adequado para fins em situações clínicas de triagem.

O objetivo geral deste ensaio é detectar autoanticorpos contra o receptor NMDA no sangue de pacientes com suspeita de encefalite autoimune. A medida ajuda a responder às questões-chave no diagnóstico diferencial de pacientes com sintomas neuropsiquiátricos agudos. A principal vantagem dessa técnica é que ela é uma medida de triagem simples e confiável.

Comece este procedimento preparando placas de cultura revestidas com gelatina. Alíquota de 200 microlitros de uma solução de gelatina a 2% para cada poço de uma placa de cultura de 48 poços e incube a placa a 37 graus Celsius por pelo menos 30 minutos. Após 30 minutos, aspire a solução de gelatina dos poços.

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