Downregulation of cyclin D1-CDK4 protein in human embryonic lung fibroblasts (HELF) induced by silica is mediated through the ERK and JNK pathway

Fuhai Shen, Xueyun Fan, Bingci Liu, Xiaowei Jia, Ai Gao, Hongju Du, Meng Ye, Baorong You, Chuanshu Huang, Xianglin Shi

Research output: Contribution to journalArticlepeer-review

9 Scopus citations


Silica is a factor in the induction of acute injury and chronic pulmonary fibrosis. In 1996, silica was also listed as a human carcinogen by the International Agency for Research on Cancer (IARC). However, the molecular mechanisms involved in its pathologic effects are not well understood. We found that exposure of human embryonic lung fibroblasts (HELF) to crystalline silica for 2 h decreased cyclin D1 and cyclin-dependent kinase 4 (CDK4) expression levels. Extracellular signal-regulated protein kinase (ERKs), c-Jun NH2-terminal amino kinase (JNKs), and p38 kinase, as well as their downstream transcription factor, AP-1, had different effects on the regulation of expression levels of cyclin D1 and CDK4 alterations induced by silica. Silica activates multiple signal transduction pathways involved in coordinating cellular responses to stress. We established the requirements for ERK and JNK, members of the mitogen-activated protein kinase (MAPK) family, in mediating G1 phase arrest of HELF induced by silica. Silica treatment activated ERK in a dose-dependent manner. AG126 (a chemical inhibitor of the ERK signaling pathway) and the dominant negative mutant of ERK2 (a molecular inhibitor of ERK2) prevented decreases in cyclin D1 and CDK4 expression levels. A chemical inhibitor of JNK, SP600125, prevented the decreased expression of both cyclin D1 and CDK4, whereas SB203580, a chemical inhibitor of p38, did not. Interestingly, curcumin prevented the decrease in DK4 expression, but not in cyclin D1. These results demonstrate that ERKs and JNKs are responsible for the decrease of cyclin D1 and CDK4 expression levels in HELF induced by silica. Activator protein-1 (AP-1) was responsible for the decrease of CDK4 expression level, but not that of cyclin D1. The findings help to explain the mechanisms of diseases induced by silica.

Original languageEnglish
Pages (from-to)1284-1292
Number of pages9
JournalCell Biology International
Issue number10
StatePublished - Oct 2008

Bibliographical note

Funding Information:
This work was supported by grants of the National Natural Science Foundation of China (30371206, 30440420593), the 973 National Key Basic Research and Development Program (2002 CB 512905), and also supported in part by Philip Morris USA Inc. and Philip Morris International.


  • AP-1
  • CDK4
  • MAPK
  • Silica
  • cyclin D1

ASJC Scopus subject areas

  • Cell Biology


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