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Published in: Journal of Neuro-Oncology 1/2007

01-10-2007 | Clinical-Patient Study

The lack of expression of the peripheral benzodiazepine receptor characterises microglial response in anaplastic astrocytomas

Authors: Shigetoshi Takaya, Kazuo Hashikawa, Federico E. Turkheimer, Nicholas Mottram, Manuel Deprez, Koichi Ishizu, Hidekazu Kawashima, Haruhiko Akiyama, Hidenao Fukuyama, Richard B. Banati, Federico Roncaroli

Published in: Journal of Neuro-Oncology | Issue 1/2007

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Abstract

The peripheral benzodiazepine receptor (PBR) is a 18 kDa molecule mainly involved in cholesterol transport through the mitochondrial membrane. In microglia, PBR is expressed from the earliest stages of activation and appears to exert a pro-inflammatory function. This molecule is commonly up-regulated in inflammatory, degenerative, infective and ischaemic lesions of the central nervous system but it has never been reported in glioma-infiltrating microglia. We examined two anaplastic astrocytomas showing minimal contrast-enhancement and therefore little damage of the blood brain barrier to minimise the presence of blood borne macrophages within tumour tissue. The two lesions were studied in vivo using positron emission tomography (PET) with the specific PBR ligand [11C](R)-PK11195 and the corresponding tumour tissue was investigated with an anti-PBR antibody. Glioma-infiltrating microglia were characterised for molecules involved in antigen presentation and cytotoxic activity. As comparison, PBR was investigated in three brains with multiple sclerosis (MS) and three with Parkinson’s disease (PD). The expression profile of four anaplastic astrocytomas was also exploited and results were compared to the profile of eleven samples of normal temporal lobe and nine cases of PD. PET studies showed that [11C](R)-PK11195 binding was markedly lower in tumours than in the contralateral grey matter. Pathological investigation revealed that glioma-infiltrating microglia failed to express PBR and cytotoxic molecules although some cells still expressed antigen presenting molecules. PBR and cytotoxic molecules were highly represented in MS and PD. Evaluation of microarray datasets confirmed these differences. Our results demonstrated PBR suppression in glioma-infiltrating microglia and suggested that PBR may have a relevant role in modulating the anti-tumour inflammatory response in astrocytic tumours.
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Metadata
Title
The lack of expression of the peripheral benzodiazepine receptor characterises microglial response in anaplastic astrocytomas
Authors
Shigetoshi Takaya
Kazuo Hashikawa
Federico E. Turkheimer
Nicholas Mottram
Manuel Deprez
Koichi Ishizu
Hidekazu Kawashima
Haruhiko Akiyama
Hidenao Fukuyama
Richard B. Banati
Federico Roncaroli
Publication date
01-10-2007
Publisher
Springer US
Published in
Journal of Neuro-Oncology / Issue 1/2007
Print ISSN: 0167-594X
Electronic ISSN: 1573-7373
DOI
https://doi.org/10.1007/s11060-007-9396-1

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