Artery formation in the intestinal wall and mesentery by intestine-derived Esm1+ endothelial cells

Arterial blood transport into peripheral organs is indispensable for developmental growth, homeostasis and tissue repair. While it is appreciated that defective formation or compromised function of arteries is associated with a range of human diseases, the cellular and molecular mechanisms mediating arterial development remain little understood for most organs. Here, we show with genetic approaches that a small subpopulation of endothelial cells inside the intestinal villi of the embryonic mouse, characterized by the expression of endothelial cell-specific molecule 1 (Esm1/endocan), gives rise to arterial endothelium in the intestinal wall but also in the distant mesenteric vasculature. This involves cell migration but also substantial changes in morphology and gene expression. Immunohistochemistry and single cell RNA-sequencing confirm that intestinal Esm1<sup>+</sup> cells have a distinct molecular profile and the capacity to undergo arterial differentiation. Genetic approaches establish that artery formation by the progeny of Esm1<sup>+</sup> cells requires integrin β1 and signaling by the growth factor VEGF-C and its receptor VEGFR3. The sum of these findings demonstrates that Esm1<sup>+</sup> cells inside the villus capillary network contribute to the formation of intestinal and mesenteric arteries during development.

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Publication Details

Journal
Nature Communications
Published
2025-09-25
DOI
https://doi.org/10.1038/s41467-025-64047-0
Citations
3
Primary Topic
Congenital heart defects research
Type
article
Field-Weighted Citation Impact
2.42
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article

Artery formation in the intestinal wall and mesentery by intestine-derived Esm1+ endothelial cells

Emma C. Watson, Frank Berkenfeld, Kai Kruse, Martin Stehling et al.
3 citations
Nature Communications
Congenital heart defects research
2.42
article

Artery formation in the intestinal wall and mesentery by intestine-derived Esm1+ endothelial cells

Emma C. Watson, Frank Berkenfeld, Kai Kruse, Martin Stehling, Mark L. Kahn, Esther Bovay, Ralf H. Adams, Vishal Mohanakrishnan, Mara E. Pitulescu
article en
3 citations

Abstract

Arterial blood transport into peripheral organs is indispensable for developmental growth, homeostasis and tissue repair. While it is appreciated that defective formation or compromised function of arteries is associated with a range of human diseases, the cellular and molecular mechanisms mediating arterial development remain little understood for most organs. Here, we show with genetic approaches that a small subpopulation of endothelial cells inside the intestinal villi of the embryonic mouse, characterized by the expression of endothelial cell-specific molecule 1 (Esm1/endocan), gives rise to arterial endothelium in the intestinal wall but also in the distant mesenteric vasculature. This involves cell migration but also substantial changes in morphology and gene expression. Immunohistochemistry and single cell RNA-sequencing confirm that intestinal Esm1<sup>+</sup> cells have a distinct molecular profile and the capacity to undergo arterial differentiation. Genetic approaches establish that artery formation by the progeny of Esm1<sup>+</sup> cells requires integrin β1 and signaling by the growth factor VEGF-C and its receptor VEGFR3. The sum of these findings demonstrates that Esm1<sup>+</sup> cells inside the villus capillary network contribute to the formation of intestinal and mesenteric arteries during development.

Nature CommunicationsVol. 16(1)
Max Planck Institute for Molecular Biomedicine (DE), University of Pennsylvania (US)
Openalex Percentile: Top 10%
Congenital heart defects research
2.42
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