TY - JOUR
T1 - Enteroendocrine cells switch hormone expression along the crypt-to-villus BMP signalling gradient
AU - Beumer, Joep
AU - Artegiani, Benedetta
AU - Post, Yorick
AU - Reimann, Frank
AU - Gribble, Fiona
AU - Nguyen, Thuc Nghi
AU - Zeng, Hongkui
AU - Van den Born, Maaike
AU - Van Es, Johan H.
AU - Clevers, Hans
N1 - Funding Information:
We thank S. van der Elst, R. van der Linden and Y. Bar-Ephraim for their help with FACS experiments. B.A. is supported by NWO/VENI 863.15.015.
Publisher Copyright:
© 2018, The Author(s).
PY - 2018/8/1
Y1 - 2018/8/1
N2 - Enteroendocrine cells (EECs) control a wide range of physiological processes linked to metabolism1. We show that EEC hormones are differentially expressed between crypts (for example, Glp1) and villi (for example, secretin). As demonstrated by single-cell mRNA sequencing using murine Lgr5+ cell-derived organoids, BMP4 signals alter the hormone expression profiles of individual EECs to resemble those found in the villus. Accordingly, BMP4 induces hormone switching of EECs migrating up the crypt–villus axis in vivo. Our findings imply that EEC lineages in the small intestine exhibit a more flexible hormone repertoire than previously proposed. We also describe a protocol to generate human EECs in organoids and demonstrate a similar regulation of hormone expression by BMP signalling. These findings establish alternative strategies to target EECs with therapeutically relevant hormone production through BMP modulation.
AB - Enteroendocrine cells (EECs) control a wide range of physiological processes linked to metabolism1. We show that EEC hormones are differentially expressed between crypts (for example, Glp1) and villi (for example, secretin). As demonstrated by single-cell mRNA sequencing using murine Lgr5+ cell-derived organoids, BMP4 signals alter the hormone expression profiles of individual EECs to resemble those found in the villus. Accordingly, BMP4 induces hormone switching of EECs migrating up the crypt–villus axis in vivo. Our findings imply that EEC lineages in the small intestine exhibit a more flexible hormone repertoire than previously proposed. We also describe a protocol to generate human EECs in organoids and demonstrate a similar regulation of hormone expression by BMP signalling. These findings establish alternative strategies to target EECs with therapeutically relevant hormone production through BMP modulation.
UR - http://www.scopus.com/inward/record.url?scp=85050562735&partnerID=8YFLogxK
U2 - 10.1038/s41556-018-0143-y
DO - 10.1038/s41556-018-0143-y
M3 - Comment/Letter to the editor
C2 - 30038251
AN - SCOPUS:85050562735
SN - 1465-7392
VL - 20
SP - 909
EP - 916
JO - Nature Cell Biology
JF - Nature Cell Biology
IS - 8
ER -