Inhibition of autophagy suppresses sertraline-mediated primary ciliogenesis in retinal pigment epithelium cells

Eun Sung Kim, Ji Hyun Shin, So Jung Park, Yoon Kyung Jo, Jae Sung Kim, Il Hwan Kang, Jung Bum Nam, Doo Young Chung, Yoonchul Cho, Eun Joo H. Lee, Jong Wook Chang, Dong Hyung Cho

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

Primary cilia are conserved cellular organelles that regulate diverse signaling pathways. Autophagy is a complex process of cellular degradation and recycling of cytoplasmic proteins and organelles, and plays an important role in cellular homeostasis. Despite its potential importance, the role of autophagy in ciliogenesis is largely unknown. In this study, we identified sertraline as a regulator of autophagy and ciliogenesis. Sertraline, a known antidepressant, induced the growth of cilia and blocked the disassembly of cilia in htRPE cells. Following treatment of sertraline, there was an increase in the number of cells with autophagic puncta and LC3 protein conversion. In addition, both a decrease of ATG5 expression and the treatment of an autophagy inhibitor resulted in the suppression of the sertralineinduced activation of autophagy in htRPE cells. Interestingly, we found that genetic and chemical inhibition of autophagy attenuated the growth of primary cilia in htRPE cells. Taken together, our results suggest that the inhibition of autophagy suppresses sertralineinduced ciliogenesis.

Original languageEnglish
Article numbere0118190
JournalPLoS ONE
Volume10
Issue number2
DOIs
StatePublished - 11 Feb 2015

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