TY - JOUR
T1 - Nutritional control of thyroid morphogenesis through gastrointestinal hormones
AU - Takagishi, Maki
AU - Aleogho, Binta Maria
AU - Okumura, Masako
AU - Ushida, Kaori
AU - Yamada, Yuichiro
AU - Seino, Yusuke
AU - Fujimura, Sayoko
AU - Nakashima, Kaoru
AU - Shindo, Asako
N1 - Publisher Copyright:
© 2022 The Author(s)
PY - 2022/4/11
Y1 - 2022/4/11
N2 - Developing animals absorb nutrients either through the placenta or from ingested food; however, the mechanisms by which embryos use external nutrients for individual organ morphogenesis remain to be elucidated. In this study, we assessed nutrient-dependent thyroid follicle morphogenesis in Xenopus laevis and investigated the role of secreted gastrointestinal (GI) hormones post-feeding. We found that feeding triggers thyroid follicle formation, and the thyroid cells showed transient inactivation of cell proliferation after feeding. In addition, the thyroid cells with multi-lumina were frequently observed in the fed tadpoles. The expression of the particular GI hormone incretin, glucose-dependent insulinotropic polypeptide (GIP), responded to feeding in the intestines of Xenopus tadpoles. Inhibition of dipeptidyl peptidase 4 (Dpp4), a degradative enzyme of incretin, increased the size of the thyroid follicles by facilitating follicular lumina connection, whereas inhibition of the sodium-glucose cotransporter (SGLT) reversed the effects of Dpp4 inhibition. Furthermore, injection of GIP peptide in unfed tadpoles initiated thyroid follicle formation—without requiring feeding—and injection of an incretin receptor antagonist suppressed follicle enlargement in the fed tadpoles. Lastly, GIP receptor knockout in neonatal mice showed smaller follicles in the thyroid, suggesting that the GI hormone-dependent thyroid morphogenesis is conserved in mammals. In conclusion, our study links external nutrients to thyroid morphogenesis and provides new insights into the function of GI hormone as a regulator of organ morphology in developing animals.
AB - Developing animals absorb nutrients either through the placenta or from ingested food; however, the mechanisms by which embryos use external nutrients for individual organ morphogenesis remain to be elucidated. In this study, we assessed nutrient-dependent thyroid follicle morphogenesis in Xenopus laevis and investigated the role of secreted gastrointestinal (GI) hormones post-feeding. We found that feeding triggers thyroid follicle formation, and the thyroid cells showed transient inactivation of cell proliferation after feeding. In addition, the thyroid cells with multi-lumina were frequently observed in the fed tadpoles. The expression of the particular GI hormone incretin, glucose-dependent insulinotropic polypeptide (GIP), responded to feeding in the intestines of Xenopus tadpoles. Inhibition of dipeptidyl peptidase 4 (Dpp4), a degradative enzyme of incretin, increased the size of the thyroid follicles by facilitating follicular lumina connection, whereas inhibition of the sodium-glucose cotransporter (SGLT) reversed the effects of Dpp4 inhibition. Furthermore, injection of GIP peptide in unfed tadpoles initiated thyroid follicle formation—without requiring feeding—and injection of an incretin receptor antagonist suppressed follicle enlargement in the fed tadpoles. Lastly, GIP receptor knockout in neonatal mice showed smaller follicles in the thyroid, suggesting that the GI hormone-dependent thyroid morphogenesis is conserved in mammals. In conclusion, our study links external nutrients to thyroid morphogenesis and provides new insights into the function of GI hormone as a regulator of organ morphology in developing animals.
KW - Xenopus laevis
KW - developmental stasis
KW - gastrointestinal hormone
KW - glucose-dependent insulinotropic polypeptide
KW - incretin
KW - nutrients
KW - thyroid follicle formation
KW - thyroid morphogenesis
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UR - http://www.scopus.com/inward/citedby.url?scp=85127654083&partnerID=8YFLogxK
U2 - 10.1016/j.cub.2022.01.075
DO - 10.1016/j.cub.2022.01.075
M3 - Article
C2 - 35196509
AN - SCOPUS:85127654083
SN - 0960-9822
VL - 32
SP - 1485-1496.e4
JO - Current Biology
JF - Current Biology
IS - 7
ER -