Neutrophil depletion diminishes monocyte infiltration and improves functional outcome after experimental intracerebral hemorrhage

Acta Neurochir Suppl. 2011:111:173-8. doi: 10.1007/978-3-7091-0693-8_29.

Abstract

Inflammation contributes to secondary injury and neuronal loss after intracerebral hemorrhage, but the role of individual immune populations in these processes is unclear. In a mouse model, the injection of autologous blood into the striatum was associated with an intense inflammatory cell infiltrate composed of neutrophils, monocytes, and dendritic cells. Selective depletion of neutrophils resulted in decreased infiltration of monocytes and improved functional outcomes at day 3 post-hemorrhage. These findings indicate that neutrophil infiltration into the site of hemorrhage contributes to brain injury either by direct cellular damage or the recruitment of monocytes.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Antibodies, Monoclonal / adverse effects
  • Antigens, Ly / immunology
  • CD11b Antigen / metabolism
  • CD11c Antigen / metabolism
  • Cerebral Hemorrhage* / complications
  • Cerebral Hemorrhage* / pathology
  • Cerebral Hemorrhage* / therapy
  • Dendritic Cells / immunology
  • Disease Models, Animal
  • Functional Laterality / physiology
  • Inflammation / etiology*
  • Lymphocyte Count
  • Male
  • Mice
  • Mice, Inbred C3H
  • Monocytes / physiology*
  • Neutrophil Infiltration / physiology*
  • Neutrophils / immunology

Substances

  • Antibodies, Monoclonal
  • Antigens, Ly
  • CD11b Antigen
  • CD11c Antigen
  • Ly6G antigen, mouse