Lung natural killer cells play a major counter-regulatory role in pulmonary vascular hyperpermeability after myocardial infarction

Xiaoxiang Yan, Ahmed E. Hegab, Jin Endo, Atsushi Anzai, Tomohiro Matsuhashi, Yoshinori Katsumata, Kentaro Ito, Tsunehisa Yamamoto, Tomoko Betsuyaku, Ken Shinmura, Weifeng Shen, Eric Vivier, Keiichi Fukuda, Motoaki Sano

研究成果: Article査読

16 被引用数 (Scopus)

抄録

RATIONALE:: Natural killer (NK) cells are lymphocytes of the innate immune system that play specialized and niche-specific roles in distinct organs. OBJECTIVE:: We investigated the possible function of NK cells in the pathogenesis of congestive heart failure after myocardial infarction. METHODS AND RESULTS:: Depletion of NK cells from mice had little effect on cytokine expression (tumor necrosis factor-α, interleukin [IL]-6, and IL-1β), neutrophil and macrophage infiltration into infarcted myocardium, or left ventricular remodeling after myocardial infarction. However, these mice exhibited severe respiratory distress associated with protein-rich, high-permeability alveolar edema accompanied by neutrophil infiltration. In addition, there were 20-fold more NK cells in the mouse lungs than in heart, and these cells were accumulated around the vasculature. CD107a-positive and interferon-γ-positive cell populations were unchanged, whereas IL-10-positive populations increased. Adoptive transfer of NK cells from wild-type mice, but not from IL-10 knockout mice, into the NK cell-depleted mice rescued the respiratory phenotype. IL-1β-mediated dextran leakage from a lung endothelial cell monolayer was also blocked by coculture with NK cells from wild-type mice but not from IL-10 knockout mice. CONCLUSIONS:: This study is the first to identify a critical role for lung NK cells in protecting lung from the development of cardiogenic pulmonary edema after myocardial infarction.

本文言語English
ページ(範囲)637-649
ページ数13
ジャーナルCirculation research
114
4
DOI
出版ステータスPublished - 2014 2 14

ASJC Scopus subject areas

  • 生理学
  • 循環器および心血管医学

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