Molecular identification of venous progenitors in the dorsal aorta reveals an aortic origin for the cardinal vein in mammals

Henrik Lindskog, Yung Hae Kim, Eric B. Jelin, Yupeng Kong, Salvador Guevara, Tyson N. Kim, Rong A. Wang

Research output: Contribution to journalArticle

36 Citations (Scopus)

Abstract

Coordinated arterial-venous differentiation is crucial for vascular development and function. The origin of the cardinal vein (CV) in mammals is unknown, while conflicting theories have been reported in chick and zebrafish. Here, we provide the first molecular characterization of endothelial cells (ECs) expressing venous molecular markers, or venous-fated ECs, within the emergent dorsal aorta (DA). These ECs, expressing the venous molecular markers Coup-TFII and EphB4, cohabited the early DA with ECs expressing the arterial molecular markers ephrin B2, Notch and connexin 40. These mixed ECs in the early DA expressed either the arterial or venous molecular marker, but rarely both. Subsequently, the DA exhibited uniform arterial markers. Real-time imaging of mouse embryos revealed EC movement from the DA to the CV during the stage when venous-fated ECs occupied the DA. We analyzed mutants for EphB4, which encodes a receptor tyrosine kinase for the ephrin B2 ligand, as we hypothesized that ephrin B2/EphB4 signaling may mediate the repulsion of venous-fated ECs from the DA to the CV. Using an EC quantification approach, we discovered that venous-fated ECs increased in the DA and decreased in the CV in the mutants, whereas the rest of the ECs in each vessel were unaffected. This result suggests that the venous-fated ECs were retained in the DA and missing in the CV in the EphB4 mutant, and thus that ephrin B2/EphB4 signaling normally functions to clear venous-fated ECs from the DA to the CV by cell repulsion. Therefore, our cellular and molecular evidence suggests that the DA harbors venous progenitors that move to participate in CV formation, and that ephrin B2/EphB4 signaling regulates this aortic contribution to the mammalian CV.

Original languageEnglish (US)
Pages (from-to)1120-1128
Number of pages9
JournalDevelopment (Cambridge)
Volume141
Issue number5
DOIs
StatePublished - Mar 1 2014
Externally publishedYes

Fingerprint

Aorta
Mammals
Veins
Endothelial Cells
Ephrin-B2
Receptor Protein-Tyrosine Kinases
Zebrafish
Cell Movement
Blood Vessels
Embryonic Structures
Ligands

Keywords

  • Angiogenesis
  • Arterial-venous differentiation
  • Coup-TFII
  • EphB4
  • Ephrin B2
  • Mouse
  • Notch
  • Vascular development

ASJC Scopus subject areas

  • Developmental Biology
  • Molecular Biology

Cite this

Molecular identification of venous progenitors in the dorsal aorta reveals an aortic origin for the cardinal vein in mammals. / Lindskog, Henrik; Kim, Yung Hae; Jelin, Eric B.; Kong, Yupeng; Guevara, Salvador; Kim, Tyson N.; Wang, Rong A.

In: Development (Cambridge), Vol. 141, No. 5, 01.03.2014, p. 1120-1128.

Research output: Contribution to journalArticle

Lindskog, Henrik ; Kim, Yung Hae ; Jelin, Eric B. ; Kong, Yupeng ; Guevara, Salvador ; Kim, Tyson N. ; Wang, Rong A. / Molecular identification of venous progenitors in the dorsal aorta reveals an aortic origin for the cardinal vein in mammals. In: Development (Cambridge). 2014 ; Vol. 141, No. 5. pp. 1120-1128.
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AU - Kim, Yung Hae

AU - Jelin, Eric B.

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AU - Guevara, Salvador

AU - Kim, Tyson N.

AU - Wang, Rong A.

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AB - Coordinated arterial-venous differentiation is crucial for vascular development and function. The origin of the cardinal vein (CV) in mammals is unknown, while conflicting theories have been reported in chick and zebrafish. Here, we provide the first molecular characterization of endothelial cells (ECs) expressing venous molecular markers, or venous-fated ECs, within the emergent dorsal aorta (DA). These ECs, expressing the venous molecular markers Coup-TFII and EphB4, cohabited the early DA with ECs expressing the arterial molecular markers ephrin B2, Notch and connexin 40. These mixed ECs in the early DA expressed either the arterial or venous molecular marker, but rarely both. Subsequently, the DA exhibited uniform arterial markers. Real-time imaging of mouse embryos revealed EC movement from the DA to the CV during the stage when venous-fated ECs occupied the DA. We analyzed mutants for EphB4, which encodes a receptor tyrosine kinase for the ephrin B2 ligand, as we hypothesized that ephrin B2/EphB4 signaling may mediate the repulsion of venous-fated ECs from the DA to the CV. Using an EC quantification approach, we discovered that venous-fated ECs increased in the DA and decreased in the CV in the mutants, whereas the rest of the ECs in each vessel were unaffected. This result suggests that the venous-fated ECs were retained in the DA and missing in the CV in the EphB4 mutant, and thus that ephrin B2/EphB4 signaling normally functions to clear venous-fated ECs from the DA to the CV by cell repulsion. Therefore, our cellular and molecular evidence suggests that the DA harbors venous progenitors that move to participate in CV formation, and that ephrin B2/EphB4 signaling regulates this aortic contribution to the mammalian CV.

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