An 18-kDa Translocator Protein (TSPO) Polymorphism Explains Differences in Binding Affinity of the PET Radioligand PBR28

Author:

Owen David R12,Yeo Astrid J3,Gunn Roger N245,Song Kijoung3,Wadsworth Graham2,Lewis Andrew1,Rhodes Chris1,Pulford David J3,Bennacef Idriss2,Parker Christine A24,StJean Pamela L3,Cardon Lon R3,Mooser Vincent E3,Matthews Paul M24,Rabiner Eugenii A24,Rubio Justin P3

Affiliation:

1. Division of Experimental Medicine, Department of Medicine, Imperial College London, Hammersmith Hospital, London, UK

2. Clinical Imaging Centre, GlaxoSmithKline Research and Development, Hammersmith Hospital, London, UK

3. Genetics, GlaxoSmithKline Research and Development, Stevenage, UK and King of Prussia, PA and Research Triangle Park, North Carolina, USA

4. Centre for Neuroscience, Department of Medicine, Imperial College London, Hammersmith Hospital, London, UK

5. Department of Engineering Science, University of Oxford, Oxford, UK

Abstract

[11C]PBR28 binds the 18-kDa Translocator Protein (TSPO) and is used in positron emission tomography (PET) to detect microglial activation. However, quantitative interpretations of signal are confounded by large interindividual variability in binding affinity, which displays a trimodal distribution compatible with a codominant genetic trait. Here, we tested directly for an underlying genetic mechanism to explain this. Binding affinity of PBR28 was measured in platelets isolated from 41 human subjects and tested for association with polymorphisms in TSPO and genes encoding other proteins in the TSPO complex. Complete agreement was observed between the TSPO Ala147Thr genotype and PBR28 binding affinity phenotype (P value = 3.1 times10−13). The TSPO Ala147Thr polymorphism predicts PBR28 binding affinity in human platelets. As all second-generation TSPO PET radioligands tested hitherto display a trimodal distribution in binding affinity analogous to PBR28, testing for this polymorphism may allow quantitative interpretation of TSPO PET studies with these radioligands.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Clinical Neurology,Neurology

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