Enhanced expression of HNF4 alpha during intestinal epithelial differentiation is involved in the activation of ER stress

Tuncer S., Sade-Memisoglu A., Keskus A. G., Sheraj I., GÜNER G., AKYOL A., ...Daha Fazla

FEBS JOURNAL, cilt.287, sa.12, ss.2504-2523, 2020 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 287 Sayı: 12
  • Basım Tarihi: 2020
  • Doi Numarası: 10.1111/febs.15152
  • Dergi Adı: FEBS JOURNAL
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, Agricultural & Environmental Science Database, Aquatic Science & Fisheries Abstracts (ASFA), BIOSIS, CAB Abstracts, EMBASE, Food Science & Technology Abstracts, MEDLINE, Veterinary Science Database
  • Sayfa Sayıları: ss.2504-2523
  • Anahtar Kelimeler: ATF6, autophagy, colon, differentiation, ER stress, HNF4 alpha, XBP1, UNFOLDED PROTEIN RESPONSE, NUCLEAR FACTOR 4-ALPHA, GENE-EXPRESSION, CELL-DEATH, AUTOPHAGY, HOMEOSTASIS, LIVER, XBP1, METHYLATION, MECHANISM
  • Orta Doğu Teknik Üniversitesi Adresli: Evet

Özet

Intestinal epithelial cells are derived from stem cells at the crypts that undergo differentiation into transit-amplifying cells, which in turn form terminally differentiated enterocytes as these cells reach the villus. Extensive alterations in both transcriptional and translational programs occur during differentiation, which can induce the activation of cellular stress responses such as ER stress-related unfolded protein response (UPR) and autophagy, particularly in the cells that are already committed to becoming absorptive cells. Using an epithelial cell model of enterocyte differentiation, we report a mechanistic study connecting enterocyte differentiation to UPR and autophagy. We report that differentiated colon epithelial cells showed increased cytosolic Ca2+ levels and activation of all three pathways of UPR: inositol-requiring enzyme 1 (IRE1), protein kinase RNA-like ER kinase, and activating transcription factor 6 (ATF6) compared to the undifferentiated cells. Enhanced UPR in the differentiated cells was accompanied by the induction of autophagy as evidenced by increased ratio of light chain 3 II/I, upregulation of Beclin-1, and downregulation of p62. We show for the first time that mechanistically, the upregulation of hepatocyte nuclear factor 4 alpha (HNF4 alpha) during differentiation led to increased promoter binding and transcriptional upregulation of two major proteins of UPR: X-box binding protein-1 and ATF6, implicating HNF4 alpha as a key regulator of UPR response during differentiation. Integrating wet-lab with in silico analyses, the present study links differentiation to cellular stress responses, and highlights the importance of transcription factor signaling and cross-talk between the cellular events in the regulation of intestinal cell differentiation.