Concentration, distribution, and influence of aging on the 18 kDa translocator protein in human brain: Implications for brain imaging studies. Issue 5 (May 2020)

• Record Type: Journal Article
• Authors: Tong, Junchao; Williams, Belinda; Rusjan, Pablo M.; Mizrahi, Romina; Lacapère, Jean-Jacques; McCluskey, Tina; Furukawa, Yoshiaki; Guttman, Mark; Ang, Lee-Cyn; Boileau, Isabelle; Meyer, Jeffrey H; Kish, Stephen J
• Is Part Of: Journal of cerebral blood flow & metabolism. Volume 40:Issue 5(2020)
• Page Start: 1061
• Page End: 1076
• Publication Date: 2020-05
• Subjects: Translocator protein TSPO -- postmortem human brain -- aging -- multiple system atrophy -- positron emission tomography; Cerebral circulation -- Periodicals; Brain -- Metabolism -- Periodicals; Brain -- Blood-vessels -- Periodicals; Cerebrovascular disease -- Periodicals; 612.824
• DOI: 10.1177/0271678X19858003
• Languages: English
• ISSNs: 0271-678X

Abstract

Positron emission tomography (PET) imaging of the translocator protein (TSPO) is widely used as a biomarker of microglial activation. However, TSPO protein concentration in human brain has not been optimally quantified nor has its regional distribution been compared to TSPO binding. We determined TSPO protein concentration, change with age, and regional distribution by quantitative immunoblotting in autopsied human brain. Brain TSPO protein concentration (>0.1 ng/µg protein) was higher than those reported by in vitro binding assays by at least 2 to 70 fold. TSPO protein distributed widely in both gray and white matter regions, with distribution in major gray matter areas ranked generally similar to that of PET binding in second-generation radiotracer studies. TSPO protein concentration in frontal cortex was high at birth, declined precipitously during the first three months, and increased modestly during adulthood/senescence (10%/decade; vs. 30% for comparison astrocytic marker GFAP). As expected, TSPO protein levels were significantly increased (+114%) in degenerating putamen in multiple system atrophy, providing further circumstantial support for TSPO as a gliosis marker. Overall, findings show some similarities between TSPO protein and PET binding characteristics in the human brain but also suggest that part of the TSPO protein pool might be less available for radioligand binding.