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Rno_circRNA_006061 participates in apoptosis induced by formaldehyde via activating p38/ATF3 pathway

  • Pan Ge
  • , Xue wei Yuan
  • , Xiang Zhang
  • , Zhi hao Liu
  • , Si yu Wang
  • , Yan qi Yang
  • , Qian nan Wang
  • , Li jian Qian
  • , Ya zhao Li
  • , Dang xia Zhou
  • Xi'an Jiaotong University
  • Xi’an Children’s Hospital
  • The First Affiliated Hospital of Xi’an Jiaotong University

科研成果: 期刊稿件文章同行评审

5 引用 (Scopus)

摘要

Formaldehyde, a common indoor air pollutant, is significantly toxic to the respiratory system, whereas its mechanism is unclear. CircRNAs exert critical functions via sponging microRNAs (miRNAs). To evaluate the effect of long-term formaldehyde exposure on rno_circRNA_006061 expression profiles, the downstream targets and signaling pathways associated with rno_circRNA_006061 were predicted and validated using bioinformatics methods and dual-luciferase reporter assay. Previously, our circRNA microarray showed that rno_circRNA_006061 was up-regulated in the formaldehyde-exposed lung tissue. Subsequently, bioinformatics analysis predicted that rno_circRNA_006061 bound to rno-miR-128-3p and co-regulated the p38/ATF3 signaling pathway. Meanwhile, the expressions of rno_circRNA_006061, rno-miR-128-3p and p38 were correlated with the lung histomorphopathological injury assessment. Furthermore, TUNEL and Bax/Bcl-2 ratio results revealed that up-regulated rno_circRNA_00606 induced by formaldehyde stimulated apoptosis in the lung. After the knockdown of rno_circRNA_006061, the expression of rno-miR-128-3p increased and the expression of p38 decreased slightly, which partially restored formaldehyde-induced apoptosis in alveolar epithelial cells. In conclusion, our study hinted that the rno_circRNA_006061 might enhance p38/ATF3 pathway expression via sponging the rno-miR-128-3p, thus significantly promoting apoptosis in lung tissues, which may provide potential new targets for preventing and treating lung injury by formaldehyde inhalation.

源语言英语
文章编号110584
期刊Chemico-Biological Interactions
381
DOI
出版状态已出版 - 25 8月 2023

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