Abstract
AbstractThe intestine is critical for not only processing and resorbing nutrients but also protecting the organism from the environment. These functions are mainly carried out by the epithelium, which is constantly being self-renewed. Many genes and pathways can influence intestinal epithelial cell proliferation. Among them is mTORC1, whose activation increases cell proliferation. Here, we report the first intestinal epithelial cell-specific knockout (ΔIEC) of an amino acid transporter capable of activating mTORC1. We show that the transporter, SLC7A5, is highly expressed in mouse intestinal crypt andSlc7a5ΔIECreduces mTORC1 signaling. Surprisingly,Slc7a5ΔIECmice have increased cell proliferation but reduced secretory cells, particularly mature Paneth cells. scRNA-seq and electron microscopic analyses revealed dedifferentiation of Paneth cells inSlc7a5ΔIECmice, leading to markedly reduced secretory granules with little effect on Paneth cell number. We further show thatSlc7a5ΔIECmice are prone to experimental colitis. Thus, SLC7A5 regulates secretory cell differentiation to affect stem cell niche and/or inflammatory response to regulate cell proliferation.
Publisher
Cold Spring Harbor Laboratory
Cited by
1 articles.
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