Mesenchymal-epithelial crosstalk shapes intestinal regionalisation via Wnt and Shh signalling

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Mesenchymal-epithelial crosstalk shapes intestinal regionalisation via Wnt and Shh signalling. / Maimets, Martti; Pedersen, Marianne Terndrup; Guiu, Jordi; Dreier, Jes; Thodberg, Malte; Antoku, Yasuko; Schweiger, Pawel J; Rib, Leonor; Bressan, Raul Bardini; Miao, Yi; Garcia, K. Christopher; Sandelin, Albin; Serup, Palle; Jensen, Kim B.

I: Nature Communications, Bind 13, 715, 2022.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Maimets, M, Pedersen, MT, Guiu, J, Dreier, J, Thodberg, M, Antoku, Y, Schweiger, PJ, Rib, L, Bressan, RB, Miao, Y, Garcia, KC, Sandelin, A, Serup, P & Jensen, KB 2022, 'Mesenchymal-epithelial crosstalk shapes intestinal regionalisation via Wnt and Shh signalling', Nature Communications, bind 13, 715. https://doi.org/10.1038/s41467-022-28369-7

APA

Maimets, M., Pedersen, M. T., Guiu, J., Dreier, J., Thodberg, M., Antoku, Y., Schweiger, P. J., Rib, L., Bressan, R. B., Miao, Y., Garcia, K. C., Sandelin, A., Serup, P., & Jensen, K. B. (2022). Mesenchymal-epithelial crosstalk shapes intestinal regionalisation via Wnt and Shh signalling. Nature Communications, 13, [715]. https://doi.org/10.1038/s41467-022-28369-7

Vancouver

Maimets M, Pedersen MT, Guiu J, Dreier J, Thodberg M, Antoku Y o.a. Mesenchymal-epithelial crosstalk shapes intestinal regionalisation via Wnt and Shh signalling. Nature Communications. 2022;13. 715. https://doi.org/10.1038/s41467-022-28369-7

Author

Maimets, Martti ; Pedersen, Marianne Terndrup ; Guiu, Jordi ; Dreier, Jes ; Thodberg, Malte ; Antoku, Yasuko ; Schweiger, Pawel J ; Rib, Leonor ; Bressan, Raul Bardini ; Miao, Yi ; Garcia, K. Christopher ; Sandelin, Albin ; Serup, Palle ; Jensen, Kim B. / Mesenchymal-epithelial crosstalk shapes intestinal regionalisation via Wnt and Shh signalling. I: Nature Communications. 2022 ; Bind 13.

Bibtex

@article{31e26bded82e48e4be65bb2328c8acbd,
title = "Mesenchymal-epithelial crosstalk shapes intestinal regionalisation via Wnt and Shh signalling",
abstract = "Organs are anatomically compartmentalised to cater for specialised functions. In the small intestine (SI), regionalisation enables sequential processing of food and nutrient absorption. While several studies indicate the critical importance of non-epithelial cells during development and homeostasis, the extent to which these cells contribute to regionalisation during morphogenesis remains unexplored. Here, we identify a mesenchymal-epithelial crosstalk that shapes the developing SI during late morphogenesis. We find that subepithelial mesenchymal cells are characterised by gradients of factors supporting Wnt signalling and stimulate epithelial growth in vitro. Such a gradient impacts epithelial gene expression and regional villus formation along the anterior-posterior axis of the SI. Notably, we further provide evidence that Wnt signalling directly regulates epithelial expression of Sonic Hedgehog (SHH), which, in turn, acts on mesenchymal cells to drive villi formation. Taken together our results uncover a mechanistic link between Wnt and Hedgehog signalling across different cellular compartments that is central for anterior-posterior regionalisation and correct formation of the SI.",
author = "Martti Maimets and Pedersen, {Marianne Terndrup} and Jordi Guiu and Jes Dreier and Malte Thodberg and Yasuko Antoku and Schweiger, {Pawel J} and Leonor Rib and Bressan, {Raul Bardini} and Yi Miao and Garcia, {K. Christopher} and Albin Sandelin and Palle Serup and Jensen, {Kim B}",
note = "{\textcopyright} 2022. The Author(s).",
year = "2022",
doi = "10.1038/s41467-022-28369-7",
language = "English",
volume = "13",
journal = "Nature Communications",
issn = "2041-1723",
publisher = "nature publishing group",

}

RIS

TY - JOUR

T1 - Mesenchymal-epithelial crosstalk shapes intestinal regionalisation via Wnt and Shh signalling

AU - Maimets, Martti

AU - Pedersen, Marianne Terndrup

AU - Guiu, Jordi

AU - Dreier, Jes

AU - Thodberg, Malte

AU - Antoku, Yasuko

AU - Schweiger, Pawel J

AU - Rib, Leonor

AU - Bressan, Raul Bardini

AU - Miao, Yi

AU - Garcia, K. Christopher

AU - Sandelin, Albin

AU - Serup, Palle

AU - Jensen, Kim B

N1 - © 2022. The Author(s).

PY - 2022

Y1 - 2022

N2 - Organs are anatomically compartmentalised to cater for specialised functions. In the small intestine (SI), regionalisation enables sequential processing of food and nutrient absorption. While several studies indicate the critical importance of non-epithelial cells during development and homeostasis, the extent to which these cells contribute to regionalisation during morphogenesis remains unexplored. Here, we identify a mesenchymal-epithelial crosstalk that shapes the developing SI during late morphogenesis. We find that subepithelial mesenchymal cells are characterised by gradients of factors supporting Wnt signalling and stimulate epithelial growth in vitro. Such a gradient impacts epithelial gene expression and regional villus formation along the anterior-posterior axis of the SI. Notably, we further provide evidence that Wnt signalling directly regulates epithelial expression of Sonic Hedgehog (SHH), which, in turn, acts on mesenchymal cells to drive villi formation. Taken together our results uncover a mechanistic link between Wnt and Hedgehog signalling across different cellular compartments that is central for anterior-posterior regionalisation and correct formation of the SI.

AB - Organs are anatomically compartmentalised to cater for specialised functions. In the small intestine (SI), regionalisation enables sequential processing of food and nutrient absorption. While several studies indicate the critical importance of non-epithelial cells during development and homeostasis, the extent to which these cells contribute to regionalisation during morphogenesis remains unexplored. Here, we identify a mesenchymal-epithelial crosstalk that shapes the developing SI during late morphogenesis. We find that subepithelial mesenchymal cells are characterised by gradients of factors supporting Wnt signalling and stimulate epithelial growth in vitro. Such a gradient impacts epithelial gene expression and regional villus formation along the anterior-posterior axis of the SI. Notably, we further provide evidence that Wnt signalling directly regulates epithelial expression of Sonic Hedgehog (SHH), which, in turn, acts on mesenchymal cells to drive villi formation. Taken together our results uncover a mechanistic link between Wnt and Hedgehog signalling across different cellular compartments that is central for anterior-posterior regionalisation and correct formation of the SI.

U2 - 10.1038/s41467-022-28369-7

DO - 10.1038/s41467-022-28369-7

M3 - Journal article

C2 - 35132078

VL - 13

JO - Nature Communications

JF - Nature Communications

SN - 2041-1723

M1 - 715

ER -

ID: 291942979