ER Stress Causes Rapid Loss of Intestinal Epithelial Stemness through Activation of the Unfolded Protein Response

作者:Heijmans Jarom y; de Jeude Jooske F van Lidth; Koo Bon Kyoung; Rosekrans Sanne L; Wielenga Mattheus C B; van de Wetering Marc; Ferrante Marc; Lee Amy S; Onderwater Jos J M; Paton James C; Paton Adrienne W; Mommaas A Mieke; Kodach Liudmila L; Hardwick James C; Hommes Daniel W; Clevers Hans; Muncan Vanesa; van den Brink Gijs R*
来源:Cell Reports, 2013, 3(4): 1128-1139.
DOI:10.1016/j.celrep.2013.02.031

摘要

Stem cells generate rapidly dividing transit-amplifying cells that have lost the capacity for self-renewal but cycle for a number of times until they exit the cell cycle and undergo terminal differentiation. We know very little of the type of signals that trigger the earliest steps of stem cell differentiation and mediate a stem cell to transit-amplifying cell transition. We show that in normal intestinal epithelium, endoplasmic reticulum (ER) stress and activity of the unfolded protein response (UPR) are induced at the transition from stem cell to transit-amplifying cell. Induction of ER stress causes loss of stemness in a Perk-eIF2 alpha-dependent manner. Inhibition of Perk-eIF2 alpha signaling results in stem cell accumulation in organoid culture of primary intestinal epithelium. Our findings show that the UPR plays an important role in the regulation of intestinal epithelial stem cell differentiation.

  • 出版日期2013-4