Transforming growth factor (TGF) cross-talk with the unfolded protein response is critical for hepatic stellate cell activation

Zhikui Liu, Chao Li, Ningling Kang, Harmeet Malhi, Vijay H. Shah, Jessica L. Maiers

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

Transforming growth factor (TGF) potently activates hepatic stellate cells (HSCs), which promotes production and secretion of extracellular matrix (ECM) proteins and hepatic fibrogenesis. Increased ECM synthesis and secretion in response to TGF is associated with endoplasmic reticulum (ER) stress and the unfolded protein response (UPR). TGF and UPR signaling pathways are tightly intertwined during HSC activation, but the regulatory mechanism that connects these two pathways is poorly understood. Here, we found that TGF treatment of immortalized HSCs (i.e. LX-2 cells) induces phosphorylation of the UPR sensor inositol-requiring enzyme 1 (IRE1) in a SMAD2/3-procollagen I– dependent manner. We further show that IRE1 mediates HSC activation downstream of TGF and that its role depends on activation of a signaling cascade involving apoptosis signaling kinase 1 (ASK1) and c-Jun N-terminal kinase (JNK). ASK1–JNK signaling promoted phosphorylation of the UPR-associated transcription factor CCAAT/enhancer binding protein (C/EBP), which is crucial for TGF- or IRE1-mediated LX-2 activation. Pharmacological inhibition of C/EBP expression with the antiviral drug adefovir dipivoxil attenuated TGF-mediated activation of LX-2 or primary rat HSCs in vitro and hepatic fibrogenesis in vivo. Finally, we identified a critical relationship between C/EBP and the transcriptional regulator p300 during HSC activation. p300 knockdown disrupted TGF- or UPR-induced HSC activation, and pharmacological inhibition of the C/EBP–p300 complex decreased TGF-induced HSC activation. These results indicate that TGF-induced IRE1 signaling is critical for HSC activation through a C/EBP-p300 – dependent mechanism and suggest C/EBP as a druggable target for managing fibrosis.

Original languageEnglish (US)
Pages (from-to)3137-3151
Number of pages15
JournalJournal of Biological Chemistry
Volume294
Issue number9
DOIs
StatePublished - Jan 1 2019
Externally publishedYes

Bibliographical note

Funding Information:
This work was supported by NIDDK, National Institutes of Health, Grants K01 DK112915, RO1 DK111378, R01 DK59615, and P30DK084567; NCI, National Institutes of Health, Grant R01 CA160069; and a research fellowship from the China Scholarship Council. The authors declare that they have no con-flicts of interest with the contents of this article. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

Publisher Copyright:
© 2019 Liu et al. Published under exclusive license by The American Society for Biochemistry and Molecular Biology, Inc.

PubMed: MeSH publication types

  • Journal Article
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

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