Microglia in Gemistocytic Astrocytomas

Background: Gemistocytic astrocytomas behave more aggressively than other diffusely growing astrocytic tumours. They are characterised by a high mutation rate of the p53 gene and cytological as well as immunological abnormalities including frequent perivascular mononuclear infiltrates. Microglia are...

Full description

Bibliographic Details
Main Authors: F Geranmayeh, BW Scheithauer, MB Graeber
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2005-03-01
Series:Iranian Journal of Public Health
Subjects:
Online Access:https://ijph.tums.ac.ir/index.php/ijph/article/view/2979
_version_ 1818947630782218240
author F Geranmayeh
BW Scheithauer
MB Graeber
author_facet F Geranmayeh
BW Scheithauer
MB Graeber
author_sort F Geranmayeh
collection DOAJ
description Background: Gemistocytic astrocytomas behave more aggressively than other diffusely growing astrocytic tumours. They are characterised by a high mutation rate of the p53 gene and cytological as well as immunological abnormalities including frequent perivascular mononuclear infiltrates. Microglia are resident brain macrophage precursor cells that form a network of immune competent cells within the normal central nervous system. They are of increasing interest in the context of glioma growth. Material and Methods: We selected 23 tumour samples from among 201 samples obtained from patients with gemistocytic astrocytomas operated on at the Mayo Clinic between 1985 and 1998. These tumours have been previously analysed for p53 mutations, p53 protein and proliferative activity (Neurosurgery 48:187-194, 2001). Immunolabelling for three established microglial markers, CR3/43, Ki-M1P and iba1 was carried out on adjacent tissue sections. In addition radioactive in-situ hybridization was carried out. Results: A high number of microglial cells were detected in gemistocytic astrocytomas. More microglia were present when the fraction of gemistocytes was high (correlation coefficient= 0.740, P< .0000542). Varying numbers of gemistocytic tumour cells expressed MHC class II molecules. Importantly, the more class II immunoreactive gemistocytes were present, the fewer class II positive microglial cells could be detected (correlation coefficient= -0.623, P
first_indexed 2024-12-20T08:33:58Z
format Article
id doaj.art-3d797c43f1ce49588d5465c453ad14dd
institution Directory Open Access Journal
issn 2251-6085
2251-6093
language English
last_indexed 2024-12-20T08:33:58Z
publishDate 2005-03-01
publisher Tehran University of Medical Sciences
record_format Article
series Iranian Journal of Public Health
spelling doaj.art-3d797c43f1ce49588d5465c453ad14dd2022-12-21T19:46:36ZengTehran University of Medical SciencesIranian Journal of Public Health2251-60852251-60932005-03-0134Supple 1Microglia in Gemistocytic Astrocytomas F Geranmayeh0 BW Scheithauer1 MB Graeber2 Background: Gemistocytic astrocytomas behave more aggressively than other diffusely growing astrocytic tumours. They are characterised by a high mutation rate of the p53 gene and cytological as well as immunological abnormalities including frequent perivascular mononuclear infiltrates. Microglia are resident brain macrophage precursor cells that form a network of immune competent cells within the normal central nervous system. They are of increasing interest in the context of glioma growth. Material and Methods: We selected 23 tumour samples from among 201 samples obtained from patients with gemistocytic astrocytomas operated on at the Mayo Clinic between 1985 and 1998. These tumours have been previously analysed for p53 mutations, p53 protein and proliferative activity (Neurosurgery 48:187-194, 2001). Immunolabelling for three established microglial markers, CR3/43, Ki-M1P and iba1 was carried out on adjacent tissue sections. In addition radioactive in-situ hybridization was carried out. Results: A high number of microglial cells were detected in gemistocytic astrocytomas. More microglia were present when the fraction of gemistocytes was high (correlation coefficient= 0.740, P< .0000542). Varying numbers of gemistocytic tumour cells expressed MHC class II molecules. Importantly, the more class II immunoreactive gemistocytes were present, the fewer class II positive microglial cells could be detected (correlation coefficient= -0.623, Phttps://ijph.tums.ac.ir/index.php/ijph/article/view/2979MicrogliaGemistocytic astrocytomas
spellingShingle F Geranmayeh
BW Scheithauer
MB Graeber
Microglia in Gemistocytic Astrocytomas
Iranian Journal of Public Health
Microglia
Gemistocytic astrocytomas
title Microglia in Gemistocytic Astrocytomas
title_full Microglia in Gemistocytic Astrocytomas
title_fullStr Microglia in Gemistocytic Astrocytomas
title_full_unstemmed Microglia in Gemistocytic Astrocytomas
title_short Microglia in Gemistocytic Astrocytomas
title_sort microglia in gemistocytic astrocytomas
topic Microglia
Gemistocytic astrocytomas
url https://ijph.tums.ac.ir/index.php/ijph/article/view/2979
work_keys_str_mv AT fgeranmayeh microgliaingemistocyticastrocytomas
AT bwscheithauer microgliaingemistocyticastrocytomas
AT mbgraeber microgliaingemistocyticastrocytomas