CD8 + T Lymphocytes Regulate the Arteriogenic Response to Ischemia by Infiltrating the Site of Collateral Vessel Development and Recruiting CD4 + Mononuclear Cells Through the Expression of Interleukin-16
Author(s) -
Eugenio Stabile,
Timothy Kinnaird,
Andrea Sala,
Sue Kim Hanson,
Craig Watkins,
Umberto Campia,
Matie Shou,
Stephan Zbinden,
Shmuel Fuchs,
Hardy Kornfeld,
Stephen E. Epstein,
Mary Susan Burnett
Publication year - 2005
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.105.576702
Subject(s) - medicine , cd8 , arteriogenesis , fibrosis , femoral artery , ischemia , infiltration (hvac) , perfusion , t lymphocyte , immunology , immune system , physics , thermodynamics
Previous studies have demonstrated that macrophages and CD4+ T lymphocytes play pivotal roles in collateral development. Indirect evidence suggests that CD8+ T cells also play a role. Thus, after acute cerebral ischemia, CD8+ T cells infiltrate the perivascular space and secrete interleukin-16 (IL-16), a potent chemoattractant for monocytes and CD4+ T cells. We tested whether CD8+ T lymphocytes contribute to collateral vessel development and whether the lack of circulating CD8+ T cells prevents IL-16 expression, impairs CD4+ mononuclear cell recruitment, and reduces collateral vessel growth after femoral artery ligation in CD8(-/-) mice.
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