Activated microglia do not increase 18 kDa translocator protein (TSPO) expression in the multiple sclerosis brain. Issue 10 (19th June 2021)

• Record Type: Journal Article
• Authors: Nutma, Erik; Gebro, Emeline; Marzin, Manuel C.; van der Valk, Paul; Matthews, Paul M.; Owen, David R.; Amor, Sandra
• Is Part Of: Glia. Volume 69:Issue 10(2021)
• Page Start: 2447
• Page End: 2458
• Publication Date: 2021-06-19
• Subjects: CD68 -- HLA‐DR -- IBA‐1 -- microglia -- multiple sclerosis -- P2ry12 -- TSPO; Neuroglia -- Periodicals; Neurology -- Periodicals; 611.0188
• DOI: 10.1002/glia.24052
• Languages: English
• ISSNs: 0894-1491

Abstract

Abstract: To monitor innate immune responses in the CNS, the 18 kDa Translocator protein (TSPO) is a frequently used target for PET imaging. The frequent assumption that increased TSPO expression in the human CNS reflects pro‐inflammatory activation of microglia has been extrapolated from rodent studies. However, TSPO expression does not increase in activated human microglia in vitro. Studies of multiple sclerosis (MS) lesions reveal that TSPO is not restricted to pro‐inflammatory microglia/macrophages, but also present in homeostatic or reparative microglia. Here, we investigated quantitative relationships between TSPO expression and microglia/macrophage phenotypes in white matter and lesions of brains with MS pathology. In white matter from brains with no disease pathology, normal appearing white matter (NAWM), active MS lesions and chronic active lesion rims, over 95% of TSPO+ cells are microglia/macrophages. Homeostatic microglial markers in NAWM and control tissue are lost/reduced in active lesions and chronic active lesion rims, reflecting cell activation. Nevertheless, pixel analysis of TSPO+ cells ( n = 12, 225) revealed that TSPO expression per cell is no higher in active lesions and chronic active lesion rims (where myeloid cells are activated) relative to NAWM and control. This data suggests that whilst almost all the TSPO signal in active lesions, chronic active lesion rims, NAWM and control is associated with microglia/macrophages, their TSPO expression predominantly reflects cell density and not activation phenotype. This finding has implications for the interpretation of TSPO PET signal in MS and other CNS diseases, and further demonstrates the limitation of extrapolating TSPO biology from rodents to humans. MAIN POINTS: Increased TSPO in the MS brain is due to an increase in microglia/macrophage cell density rather than activation of these cells. TSPO expression per microglia is similar in control and MS brain regardless of their activation state or morphology.