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Protein corona of airborne nanoscale PM2.5 induces aberrant proliferation of human lung fibroblasts based on a 3D organotypic culture

  • Yan Li
  • , Pengcheng Wang
  • , Chuanlin Hu
  • , Kun Wang
  • , Qing Chang
  • , Lieju Liu
  • , Zhenggang Han
  • , Yang Shao
  • , Ying Zhai
  • , Zhengyu Zuo
  • , Michael Mak
  • , Zhiyong Gong
  • , Yang Wu
  • Wuhan Polytechnic University
  • Yale University
  • Wuhan University of Technology
  • New York University
  • Hong Kong University of Science and Technology

Research output: Contribution to journalArticlepeer-review

25 Scopus citations

Abstract

Exposure to PM2.5 has become one of the most important factors affecting public health in the world. Both clinical and research studies have suggested that PM2.5 inhalation is associated with impaired lung function. In this study, material characterization identified the existence of nanoscale particulate matter (NPM) in airborne PM2.5 samples. When coming into contact with protein-rich fluids, the NPM becomes covered by a protein layer that forms a "protein corona". Based on a 3D organotypic cell culture, the protein corona was shown to mitigate NPM cytotoxicity and further stimulate the proliferation of human lung fibroblasts (HLFs). ROS-activated alpha-smooth muscle actin (α-SMA) is considered to be one of the proliferation pathways. In this research, 3D cell cultures exhibited more tissue-like properties compared with the growth in 2D models. Animal models have been widely used in toxicological research. However, species differences make it impossible to directly translate discoveries from animals to humans. In this research, the 3D HLF model could partly simulate the biological responses of NPM-protein corona-induced aberrant HLF proliferation in the human lung. Our 3D cellular results provide auxiliary support for an animal model in research on PM2.5-induced impaired lung function, particularly in lung fibrosis.

Original languageEnglish
Article number1939
JournalScientific Reports
Volume8
Issue number1
DOIs
StatePublished - Jan 31 2018

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