Journal article
Macrophage imbalance (M1 vs. M2) and upregulation of mast cells in wall of ruptured human cerebral aneurysms: preliminary results
Journal of neuroinflammation, Vol.9(1), pp.222-222
09/21/2012
DOI: 10.1186/1742-2094-9-222
PMCID: PMC3488554
PMID: 22999528
Abstract
M1 and M2 cells are two major subsets of human macrophages that exert opposite effects on the inflammatory response. This study aims to investigate the role of macrophage M1/M2 imbalance and mast cells in the progression of human cerebral aneurysms to rupture.
Ten patients with cerebral aneurysms (five ruptured and five unruptured) underwent microsurgical clipping. During the procedure, a segment of the aneurysm dome was resected and immunostained with monoclonal antibodies for M1 cells (anti-HLA DR), M2 cells (anti-CD 163), and mast cells (anti-tryptase clone AA). A segment of the superficial temporal artery (STA) was also removed and immunostained with monoclonal antibodies for M1, M2, and mast cells.
All ten aneurysm tissues stained positive for M1, M2, and mast cells. M1 and M2 cells were present in equal proportions in unruptured aneurysms. This contrasted with a marked predominance of M1 over M2 cells in ruptured aneurysms (p = 0.045). Mast cells were also prominently upregulated in ruptured aneurysms (p = 0.001). Few M1 and M2 cells were present in STA samples.
M1/M2 macrophages and mast cells are found in human cerebral aneurysms; however, M1 and mast cell expression seems to markedly increase in ruptured aneurysms. These findings suggest that macrophage M1/M2 imbalance and upregulation of mast cells may have a role in the progression of cerebral aneurysms to rupture.
Details
- Title: Subtitle
- Macrophage imbalance (M1 vs. M2) and upregulation of mast cells in wall of ruptured human cerebral aneurysms: preliminary results
- Creators
- David Hasan - Department of Neurosurgery, Carver College of Medicine, University of Iowa, Iowa City, IA, USA. david-hasan@uiowa.eduNohra ChalouhiPascal JabbourTomoki Hashimoto
- Resource Type
- Journal article
- Publication Details
- Journal of neuroinflammation, Vol.9(1), pp.222-222
- DOI
- 10.1186/1742-2094-9-222
- PMID
- 22999528
- PMCID
- PMC3488554
- NLM abbreviation
- J Neuroinflammation
- ISSN
- 1742-2094
- eISSN
- 1742-2094
- Publisher
- England
- Grant note
- P01 NS044155 / NINDS NIH HHS R03NS07922 / NINDS NIH HHS R01 NS055876 / NINDS NIH HHS
- Language
- English
- Date published
- 09/21/2012
- Academic Unit
- Roy J. Carver Department of Biomedical Engineering; Neurosurgery; Otolaryngology
- Record Identifier
- 9984040003802771
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