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Inflammation

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Protein Kinase C Theta Inhibition Attenuates Lipopolysaccharide-Induced Acute Lung Injury through Notch Signaling Pathway via Suppressing Th17 Cell Response in Mice

  • Mengqin Li
  • Yan Zhao
  • Jing He
  • Wang Deng
  • Li Cheng
  • Zhi Jiang
  • Daoxin WangEmail author
Original Article
  • 33 Downloads

Abstract

Acute lung injury (ALI)/acute respiratory distress syndrome is characterized by increased pulmonary inflammation, where T helper 17 (Th17) cells play an important regulatory role. Notch signaling critically regulates Th17 differentiation and is known to be linked with proximal T cell by protein kinase C theta (PKCθ). We hypothesized that PKCθ inhibition could attenuate ALI by suppressing Th17 response via the Notch signaling pathway. Male C57BL/6 mice were treated with phosphate-buffered saline (PBS), lipopolysaccharide (LPS), LPS and N-[N-(3,5-difluorophenacetyl)-l-alanyl]-S-phenylglycine t-butyl ester (DAPT, a Notch signaling inhibitor), or LPS and PKCθ inhibitor (PI), and the bronchoalveolar lavage fluid (BALF), blood, and lung tissues were harvested at 48 h after the LPS challenge. CD4+ T cells were treated with DAPT or PI and harvested after 72 h. PKCθ inhibition markedly attenuated pathological changes and decreased the wet to dry weight ratio of the mouse lungs. The total cell and neutrophil counts, tumor necrosis factor-α (TNF- α) in BALF, myeloperoxidase activity in lung tissue, and the leukocyte count in whole blood were markedly reduced by PKCθ inhibition. The concentration of interleukin (IL)-17 and IL-22 in BALF, and the percentage of CD4+IL-17A+ T cells in the lungs were significantly downregulated by PKCθ inhibition. A similar trend was observed for the expression of retinoic acid-related orphan receptor gamma t and IL-23 receptor after PKCθ inhibition accompanied with inactivation of the Notch signaling pathway in vivo and in vitro. Collectively, these data demonstrated that PKCθ inhibition protects against LPS-induced ALI by suppressing the differentiation and pathogenicity of Th17, at least partially, through a Notch-dependent mechanism.

KEY WORDS

Acute lung injury PKCθ Th17 Notch IL-23R RORγt 

Notes

Authors’ Contribution

Mengqin Li performed the experiments and wrote the manuscript. Yan Z, Jing He, Wang Deng, Li Cheng, and Zhi Jiang analyzed the data. Daoxin Wang designed the study and revised the manuscript. All the authors read and approved the final manuscript.

Funding

This study was funded by the National Natural Science Foundation of China (Project number 81670071).

Compliance with Ethical Standards

All animal experiments were performed in accordance with the ethical guidelines of the National Institutes of Health on Animal Care, and the study protocol was approved by the Ethics Committee of the Second Affiliated Hospital of Chongqing Medical University.

Conflict of Interest

The authors declare that they have no conflict of interest.

Ethical Approval

All applicable international, national, and/or institutional guidelines for the care and use of animals were followed. All procedures performed in studies involving animals were in accordance with the ethical standards of the institution or practice at which the studies were conducted.

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Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2019

Authors and Affiliations

  1. 1.Department of Respiratory and critical care medicineThe Second Affiliated Hospital of Chongqing Medical UniversityChongqingChina
  2. 2.Physical Examination CenterThe Second Affiliated Hospital of Chongqing Medical UniversityChongqingChina
  3. 3.Department of EmergencyThe Affiliated Hospital of North Sichuan Medical CollegeChongqingChina

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