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PAMAM nanoparticles promote acute lung injury by inducing autophagic cell death through the Akt-TSC2-mTOR signaling pathway

  • Chenggang Li
  • , Haolin Liu
  • , Yang Sun
  • , Hongliang Wang
  • , Feng Guo
  • , Shuan Rao
  • , Jiejie Deng
  • , Yanli Zhang
  • , Yufa Miao
  • , Chenying Guo
  • , Jie Meng
  • , Xiping Chen
  • , Limin Li
  • , Dangsheng Li
  • , Haiyan Xu
  • , Heng Wang
  • , Bo Li
  • , Chengyu Jiang
  • Institute of Basic Medical Sciences
  • National Institute for the Control of Pharmaceutical and Biological Products
  • Chinese Academy of Medical Sciences
  • CAS - Shanghai Institute of Nutrition and Health

Research output: Contribution to journalArticlepeer-review

247 Scopus citations

Abstract

Nanotechnology is an important and emerging industry with a projected annual market of around one trillion US dollars by 2011-2015. Concerns about the toxicity of nanomaterials in humans, however, have recently been raised. Although studies of nanoparticle toxicity have focused on lung disease the molecular link between nanoparticle exposure and lung injury remained unclear. In this report, we show that cationic Starburst polyamidoamine dendrimer (PAMAM), a class of nanomaterials that are being widely developed for clinical applications can induce acute lung injury in vivo. PAMAM triggers autophagic cell death by deregulating the Akt-TSC2-mTOR signaling pathway. The autophagy inhibitor 3-methyladenine rescued PAMAM dendrimer-induced cell death and ameliorated acute lung injury caused by PAMAM in mice. Our data provide a molecular explanation for nanoparticle-induced lung injury, and suggest potential remedies to address the growing concerns of nanotechnology safety.

Original languageEnglish
Pages (from-to)37-45
Number of pages9
JournalJournal of Molecular Cell Biology
Volume1
Issue number1
DOIs
StatePublished - 2009
Externally publishedYes

Keywords

  • Acute lung injury
  • Akt
  • Autophagy
  • Nanoparticles
  • PAMAM
  • TSC2
  • mTOR

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