4.6 Article

Zinc Transporter SLC39A7/ZIP7 Promotes Intestinal Epithelial Self-Renewal by Resolving ER Stress

Journal

PLOS GENETICS
Volume 12, Issue 10, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pgen.1006349

Keywords

-

Funding

  1. Japan Society for the Promotion of Science [25860573, 15K19319, 221S0003, 25293114, 26116709, 23592239]
  2. Takeda Science Foundation
  3. Nestle Nutrition Council Japan
  4. NOVARTIS Foundation for the Promotion of Science
  5. SENSHIN Medical Research Foundation
  6. Nukada memorial foundation
  7. Institute of Medical Science, University of Tokyo
  8. Grants-in-Aid for Scientific Research [23592239, 26116709, 26115007, 15K19319, 25860573, 15K08974, 15K15297, 26293177, 26462324, 25293114] Funding Source: KAKEN

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Zinc transporters play a critical role in spatiotemporal regulation of zinc homeostasis. Although disruption of zinc homeostasis has been implicated in disorders such as intestinal inflammation and aberrant epithelial morphology, it is largely unknown which zinc transporters are responsible for the intestinal epithelial homeostasis. Here, we show that Zrt-Irt-like protein (ZIP) transporter ZIP7, which is highly expressed in the intestinal crypt, is essential for intestinal epithelial proliferation. Mice lacking Zip7 in intestinal epithelium triggered endoplasmic reticulum (ER) stress in proliferative progenitor cells, leading to significant cell death of progenitor cells. Zip7 deficiency led to the loss of Olfm4(+) intestinal stem cells and the degeneration of post-mitotic Paneth cells, indicating a fundamental requirement for Zip7 in homeostatic intestinal regeneration. Taken together, these findings provide evidence for the importance of ZIP7 in maintenance of intestinal epithelial homeostasis through the regulation of ER function in proliferative progenitor cells and maintenance of intestinal stem cells. Therapeutic targeting of ZIP7 could lead to effective treatment of gastrointestinal disorders.

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