Impaired progression of cerebral aneurysms in interleukin-1beta-deficient mice

Stroke. 2006 Mar;37(3):900-5. doi: 10.1161/01.STR.0000204028.39783.d9. Epub 2006 Jan 26.

Abstract

Background and purpose: Subarachnoid hemorrhage caused by cerebral aneurysm rupture remains a life-threatening emergency despite advances in treatment. However, the mechanisms underlying aneurysm initiation, progression, and rupture remain unclear. We developed a method to induce experimental cerebral aneurysms in rats, monkeys, and mice. Interleukin-1beta (IL-1beta) is a key inflammatory mediator, and it is thought to be a promising target for the treatment of inflammatory diseases. In the present study, we examined the role of IL-1beta in cerebral aneurysm development.

Methods: Cerebral aneurysms were experimentally induced in 5-week-old male C57BL/6 mice, IL-1beta gene-deficient (IL-1beta-/-) mice, and age-matched control B10 mice (wild-type). Their cerebral arteries were dissected and examined histologically and immunohistochemically.

Results: IL-1beta was expressed in vascular media in mice at an early stage of aneurysmal models' cerebral arteries. No differences were seen in the rate of aneurysm development between IL-1beta-/- and wild-type mice, but the percentage of advanced aneurysm change was significantly larger in wild-type animals. Furthermore, in IL-1beta-/- mice, increased caspase-1 expression was seen compared with wild-type animals. Additionally, the number of apoptotic cells assessed by single-stranded DNA immunoreactivity and TUNEL was significantly reduced in IL-1beta-/- mice compared with wild-type animals.

Conclusions: IL-1beta is important for the progression of cerebral aneurysms in a mouse model. Disruption of the IL-1beta gene results in the reduced incidence of mature experimental cerebral aneurysms.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aneurysm / pathology
  • Animals
  • Apoptosis
  • Caspase 1 / biosynthesis
  • Cerebrovascular Disorders / genetics
  • Cerebrovascular Disorders / pathology
  • DNA, Single-Stranded / metabolism
  • Disease Models, Animal
  • Disease Progression
  • Immunohistochemistry
  • In Situ Nick-End Labeling
  • Inflammation
  • Interleukin-1 / genetics*
  • Interleukin-1 / metabolism
  • Interleukin-1 / physiology*
  • Intracranial Aneurysm / genetics
  • Intracranial Aneurysm / pathology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Models, Statistical
  • RNA / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Time Factors

Substances

  • DNA, Single-Stranded
  • Interleukin-1
  • RNA
  • Caspase 1