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Proinflammatory Cytokine Expression Contributes to Brain Injury Provoked By Chronic Monocyte Activation

Overview of attention for article published in Molecular Medicine, April 2001
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Title
Proinflammatory Cytokine Expression Contributes to Brain Injury Provoked By Chronic Monocyte Activation
Published in
Molecular Medicine, April 2001
DOI 10.1007/bf03401841
Pubmed ID
Authors

Anna-Leena Sirén, Richard McCarron, Lan Wang, Patricia Garcia-Pinto, Christl Ruetzler, David Martin, John M. Hallenbeck

Abstract

We have proposed that an increased interaction between monocyte/macrophages and blood vessel endothelium predisposes subjects to strokes. The effect of chronic monocyte activation on the development of cerebral infarcts was thus studied in rats after provocation of a modified local Swartzman reaction, in brain vasculature. Two weeks after an IV bolus of bacillus Calmette-Guérin (BCG), we studied spontaneous superoxide production, integrin expression, endothelial adhesion of monocytes and the neurological symptoms, brain histology, and cytokine immunoreactivity after a provocative dose of LPS (30-300 microg/rat i.c.v.). Monocyte migration into the brain was stimulated by BCG priming. The incidence of paralysis and death in response to LPS was markedly increased in BCG-primed rats. Histological evaluation of the brains of neurologically impaired and moribund animals revealed intravascular thrombosis and pale and hemorrhagic infarcts. Infiltrates of leukocytes expressing immunoreactive IL-1:, IL-6, and TNF-alpha were found around blood vessels, cerebral ventricles, and meninges, and were accompanied by a profound microglial expression of IL1P, endothelial expression of IL-6, and expression of TNF-alpha and TNF-R 1 in glia and neurons of cortex and hippocampus. Treatment (2 x 100 microg/10 ,I, i.c.v.) with recombinant human (rh-)TNF 55kDa receptor completely prevented, and treatment with rh-IL- I receptor antagonist significantly decreased the incidence of paralysis and death in response to BCG + LPS. The improvement of neurological symptoms was accompanied by reduced histological damage and supppression of IL-1P/ expression in the brain tissue. The data demonstrate that chronic monocyte activation predisposes subjects to thrombosis and hemorrhage via an exaggerated release of proinflammatory cytokines.

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The data shown below were compiled from readership statistics for 22 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Germany 1 5%
Unknown 21 95%

Demographic breakdown

Readers by professional status Count As %
Student > Master 5 23%
Student > Ph. D. Student 4 18%
Student > Doctoral Student 2 9%
Student > Bachelor 2 9%
Professor 2 9%
Other 3 14%
Unknown 4 18%
Readers by discipline Count As %
Medicine and Dentistry 7 32%
Agricultural and Biological Sciences 3 14%
Neuroscience 3 14%
Engineering 1 5%
Unknown 8 36%