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Formyl peptide receptor 1 up-regulation and formyl peptide receptor 2/3 down-regulation of blood immune cells along with defective lipoxin A4/resolvin D1 production in obstructive sleep apnea patients

  • Yung Che Chen
  • , Mao Chang Su
  • , Chien Hung Chin
  • , I. Chun Lin
  • , Po Yuan Hsu
  • , Chia Wei Liou
  • , Kuo Tung Huang
  • , Ting Ya Wang
  • , Yong Yong Lin
  • , Yi Xin Zheng
  • , Chang Chun Hsiao*
  • , Meng Chih Lin
  • *此作品的通信作者
  • Chang Gung University
  • Chang Gung University of Science and Technology

研究成果: 期刊稿件文章同行評審

12 引文 斯高帕斯(Scopus)

摘要

Background This study aims to investigate the role of FPR 1/2/3 expressions in patients with obstructive sleep apnea (OSA). Method We made cross-sectional comparisons of FPR1/2/3 expressions of blood neutrophil, M1/ M2a monocyte, and natural killer (NK) cell between 16 healthy subjects (HS), 16 primary snoring (PS) subjects, 46 treatment-naive OSA patients, and 18 severe OSA patients under long-term continuous positive airway pressure treatment (severe OSA on CPAP). Results FPR1 expressions on neutrophil were increased in treatment-naive OSA and severe OSA on CPAP groups versus either HS or PS. FPR2 expressions on neutrophil were decreased in treatment-naive OSA versus HS, and returned to normal in severe OSA on CPAP group. FPR1/FPR2 expression ratio on neutrophil was increased in treatment-naive OSA versus either HS or PS. Serum lipoxin A4, resolvin D1 levels, and FPR3 expressions of M1, M2a and NK cells were all decreased in treatment-naive OSA versus HS. OSA patients with hypertension had decreased FPR2 expressions on neutrophil and FPR3 expressions of NK cell. FPR1 expression, FPR1/FPR2 expression ratio on neutrophil, and FPR3 expression of M1 cell were all reversed after > 6-month CPAP treatment in 9 selected patients. In vitro intermittent hypoxia with re-oxygenation treatment in THP-1 cells resulted in increased FPR1/FPR2 expression ratio of M1 cells, and increased FPR1/FPR3 expression ratio of M2a cells. Conclusions FPR1 over-expression and insufficiency of FPR2 and FPR3 in association with defective lipoxin A4 and resolving D1 production were associated with disease severity of OSA and its adverse consequences.

原文英語
文章編號e0216607
期刊PLoS ONE
14
發行號5
DOIs
出版狀態已出版 - 05 2019

文獻附註

Publisher Copyright:
© 2019 Chen et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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