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Neuroscience
Un análisis de la inmunofluorescencia celular Simple para detectar autoanticuerpos contra el Rece...
Un análisis de la inmunofluorescencia celular Simple para detectar autoanticuerpos contra el Rece...
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

Un análisis de la inmunofluorescencia celular Simple para detectar autoanticuerpos contra el Receptor N-metil-D-Aspartato (NMDA) en sangre

Full Text
10,335 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.

Hemos expresado ectopically subunidad NR1 del receptor NMDA etiquetada con proteína verde fluorescente en células embrionarias humanas (HEK293) como antígeno para detectar autoanticuerpos contra el receptor de NMDA en la sangre de pacientes con encefalitis autoinmune. Este sencillo método puede ser adecuado para la detección de propósitos en contextos clínicos.

El objetivo general de este ensayo es detectar autoanticuerpos contra el receptor NMDA en la sangre de pacientes con sospecha de encefalitis autoinmune. La medida ayuda a responder a las preguntas clave en el diagnóstico diferencial de pacientes con síntomas neuropsiquiátricos agudos. La principal ventaja de esta técnica es que se trata de una medida de cribado sencilla y fiable.

Comience este procedimiento preparando placas de cultivo recubiertas de gelatina. Alícuota 200 microlitros de una solución de gelatina al 2% en cada pocillo de una placa de cultivo de 48 pocillos e incubar la placa a 37 grados centígrados durante al menos 30 minutos. Después de 30 minutos, aspire la solución de gelatina de los pocillos.

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Neurociencia número 131 autoanticuerpo de Anti-NMDA receptor la subunidad NR1 proteína verde fluorescente encefalitis autoinmune análisis de la inmunofluorescencia celular diagnóstico diferencial síntomas neuropsiquiátricos

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