Embryogenic stem cell-derived intestinal crypt fission directs de novo crypt genesis

Abstract

Intestinal epithelial replenishment is fueled by continuously dividing intestinal stem cells (ISCs) resident at the crypt niche. However, the cell type(s) enabling replenishment upon damage and subsequent loss of whole crypts remain largely unclear. Using Set domain-containing protein 4 (Setd4), we identify a small population with reserve stem cell characteristics in the mouse intestine. Upon irradiation-induced injury, Setd4-expressing (Setd4⁺) cells survive radiation exposure and then activate to produce Sca-1-expressing cell types to restore the epithelial wall and regenerate crypts de novo via crypt fission. Setd4⁺ cells are confirmed to originate from the early fetal period, subsequently contributing to the development of embryonic gut and the establishment of postnatal crypts. Setd4⁺ cells are therefore represented as both originators and key regenerators of the intestine.

Keywords: CP: Developmental biology; CP: Stem cell research; Setd4; crypt fission; crypt genesis; embryonic gut development; homeostasis; intestinal stem cells; postnatal gut development; regeneration; reserve stem cells.