4.7 Article

Organophosphorus flame retardant TDCPP-induced cytotoxicity and associated mechanisms in normal human skin keratinocytes

Journal

SCIENCE OF THE TOTAL ENVIRONMENT
Volume 726, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.scitotenv.2020.138526

Keywords

TDCPP; Human skin keratinocytes; Cell cycle arrest; Apoptosis; Gene expression

Funding

  1. National Key Research and Development Program of China [2018YFC1800504]
  2. National Natural Science Foundation of China [21906134, 41967026]
  3. Basic Research Program of Yunan Province [2019FB014]
  4. Yunnan Thousand Youth Talent Program [YNQR-QNRC-2018-049]
  5. Yunnan Agricultural Joint Foundation Projects [2018FG001-048]
  6. Research Foundation of Southwest Forestry University [111819]
  7. Key Disciplines (Ecology) Project of Yunnan Education Department
  8. Yunnan Innovative Research Team [YNQRCXTD-2018-006]
  9. Open Fund of Guangdong Key Laboratory of Environmental Catalysis and Health Risk Control [GKECHRC-10]

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Tris(1,3-dichloro-2-propyl) phosphate (TDCPP), a widely used organophosphorus flame retardant, has been frequently detected in the environment including indoor dust. Long-term exposure to TDCPP-containing dust may adversely affect human skin, however, little is known about its potential cytotoxicity. In this study, human skin keratinocytes (HaCaT) were employed to study TDCPP-induced cytotoxicity and associated mechanisms. The effects of TDCPP on cell morphology, viability, apoptosis, and cycle, and the mRNA levels of apoptosis (Bcl-2, Bax and Caspase-3) and cell cycle (cyclin D1, CDK2, CDK4 and CDK6) regulatory genes were investigated. The results showed that TDCPP caused a concentration-dependent decrease in cell viability after exposing to TDCPP >= 100 mu g/mL for 48 h, with a median lethal concentration of 163 mu g/mL (LC50). In addition, TDCPP induced cell apoptosis and arrested cell cycle in the G0/G1 phase at 16 and 160 mu g/mL by enhancing Bax and Caspase-3 expression besides inhibiting cyclin D1, CDK2, CDK6 and Bcl-2 expression. Our results showed that TDCPP-induced toxicity in HaCaT cells was probably through cell apoptosis and cell cycle arrest. This study provides information on the toxicity of TDCPP to human skin cells, which may help to reduce its toxicity to human skin.

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