Metabotropic glutamate receptor 3 (mGlu3; mGluR3; GRM3) in schizophrenia: Antibody characterisation and a semi-quantitative western blot study

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• 作者：Aintzane Garcí ; a-Bea^a ; Mary A. Walker^a ; Thomas M. Hyde^b ; ^c ; ^d ; Joel E. Kleinman^b ; Paul J. Harrison^a ; ^e ; ¹ ; Tracy A. Lane^a ; ¹ ; ^{tracy.lane@psych.ox.ac.uk" class="auth_mail" title="E-mail the corresponding author}
• 关键词：Group II metabotropic glutamate receptor ; Methods ; Human brain ; Psychosis ; Antibody validation
• 刊名：Schizophrenia Research
• 出版年：2016
• 出版时间：November 2016
• 年：2016
• 卷：177
• 期：1-3
• 页码：18-27
• 全文大小：698 K

文摘

Metabotropic glutamate receptor 3 (mGlu3, mGluR3), encoded by GRM3, is a risk gene for schizophrenia and a therapeutic target. It is unclear whether expression of the receptor is altered in the disorder or related to GRM3 risk genotype. Antibodies used to date to assess mGlu3 in schizophrenia have not been well validated.

Objective

To characterise six commercially available anti-mGlu3 antibodies for use in human brain, and then conduct a semi-quantitative study of mGlu3 immunoreactivity in schizophrenia.

Methods

Antibodies tested using Grm3^−/− and Grm2^−/−/3^−/− mice and transfected HEK293T/17 cells. Western blotting on membrane protein isolated from superior temporal cortex of 70 patients with schizophrenia and 87 healthy comparison subjects, genotyped for GRM3 SNP rs10234440.

Results

One (out of six) anti-mGlu3 antibodies was fully validated, a C-terminal antibody which detected monomeric (~ 100 kDa) and dimeric (~ 200 kDa) mGlu3. A second, N-terminal, antibody detected the 200 kDa band but also produced non-specific bands. Using the C-terminal antibody for western blotting in human brain, mGlu3 immunoreactivity was found to decline with age, and was affected by pH and post mortem interval. There were no differences in monomeric or dimeric mGlu3 immunoreactivity in schizophrenia or in relation to GRM3 genotype. The antibody was not suitable for immunohistochemistry.

Interpretation

These data highlight the value of knockout mouse tissue for antibody validation, and the need for careful antibody characterisation. The schizophrenia data show that involvement of GRM3 in the disorder and its genetic risk architecture is not reflected in total membrane mGlu3 immunoreactivity in superior temporal cortex.