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一种 18kDa 移位蛋白(TSPO)多态性解释了 PET 放射性配体 PBR28 结合亲和力的差异。

An 18-kDa translocator protein (TSPO) polymorphism explains differences in binding affinity of the PET radioligand PBR28.

机构信息

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

出版信息

J Cereb Blood Flow Metab. 2012 Jan;32(1):1-5. doi: 10.1038/jcbfm.2011.147. Epub 2011 Oct 19.

Abstract

[(11)C]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 × 10(-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.

摘要

[(11)C]PBR28 与 18kDa 转位蛋白(TSPO)结合,用于正电子发射断层扫描(PET)以检测小胶质细胞的激活。然而,由于结合亲和力的个体间差异很大,信号的定量解释受到干扰,这种差异呈三峰分布,与显性遗传特征相容。在这里,我们直接测试了潜在的遗传机制来解释这一点。从 41 个人类受试者分离的血小板中测量了 PBR28 的结合亲和力,并测试了其与 TSPO 多态性和编码 TSPO 复合物中其他蛋白质的基因之间的关联。在 TSPO Ala147Thr 基因型和 PBR28 结合亲和力表型之间观察到完全一致(P 值=3.1×10(-13))。TSPO Ala147Thr 多态性预测了人类血小板中 PBR28 的结合亲和力。由于迄今为止测试的所有第二代 TSPO PET 放射性配体在结合亲和力上均呈三峰分布,类似于 PBR28,因此测试这种多态性可能允许对这些放射性配体进行 TSPO PET 研究的定量解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4571/3323305/a6f8dfd199d0/jcbfm2011147f1.jpg

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