Journal Article (Letter)

DKFZ-2026-00172

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png Deletion of the angiopoietin receptor Tie2 enhances proliferation and sprouting of cardiac endothelial cells.

Anisimov, A. ; Lackman, M. H. ; Augustin, H. G.DKFZ* ; Mervaala, E. ; Alitalo, K. ; Karaman, S.

2026
Springer Science + Business Media B.V Dordrecht [u.a.]

Abstract: Endothelial cells (ECs) of the heart proliferate and form new vessels in response to vascular endothelial growth factor (VEGF), but VEGF has not benefited the therapy of cardiac ischemia because of its side effects. Here, we explored if deletion of the vascular steady-state homeostasis maintaining Tie1 and Tie2 receptor tyrosine kinases affects the proliferation and sprouting of cardiac ECs.We analyzed EC proliferation and histological and immunohistochemical stainings by confocal microscopy, plus scRNA and qPCR analyses of gene expression in the heart, kidneys, and lungs of Tie1fl/fl, Tie2fl/fl, and Tie1fl/fl;Tie2fl/fl mice, in which vascular endothelial cadherin-driven CreERT2 recombinase was used to delete Tie1, Tie2 or both receptors. These analyses were also performed in mice subjected to transverse aortic constriction (TAC). Boyden chamber assays were performed to assess the migration of cultured ECs in cultures with or without TIE receptor silencing.Genetic deletion of Tie1, Tie2, or Tie1/Tie2 in mice increased significantly the proliferation of cardiac but not renal or pulmonary ECs, as measured by EdU incorporation into DNA and quantification of the cell cycle marker cyclin D1. Tie1/Tie2 or Tie2 deletion, but not Tie1 deletion alone, induced EC sprouting in coronary vasculature and expression of endothelial tip cell markers, including expression of the FOXO1-regulated Angpt2 and Esm1 genes in cardiac versus kidney or lung ECs. Consistent with these findings, silencing of TIE2, but not TIE1, in cultured ECs resulted in increased migration of ECs. Similar results were obtained in mice subjected to TAC.Deletion of Tie2 alone or together with Tie1 increases the proliferation and sprouting of cardiac, but not renal or pulmonary ECs, without to neovessel formation in the heart.

Keyword(s): Animals (MeSH) ; Receptor, TIE-2: genetics (MeSH) ; Receptor, TIE-2: metabolism (MeSH) ; Receptor, TIE-2: deficiency (MeSH) ; Cell Proliferation (MeSH) ; Endothelial Cells: metabolism (MeSH) ; Endothelial Cells: cytology (MeSH) ; Mice (MeSH) ; Gene Deletion (MeSH) ; Receptor, TIE-1: genetics (MeSH) ; Receptor, TIE-1: metabolism (MeSH) ; Myocardium: metabolism (MeSH) ; Myocardium: cytology (MeSH) ; Neovascularization, Physiologic (MeSH) ; Cell Movement (MeSH) ; Mice, Knockout (MeSH) ; Angpt2 ; Proliferation ; Sprouting ; Tie2 receptor ; Tip cell markers ; Receptor, TIE-2 ; Tek protein, mouse ; Receptor, TIE-1

Note: Brief Communication

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Contributing Institute(s):

1. A190 Vaskuläre Onkologie und Metastasierung (A190)

Research Program(s):

1. 311 - Zellbiologie und Tumorbiologie (POF4-311) (POF4-311)

Appears in the scientific report 2026

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Database coverage:
; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; Current Contents - Life Sciences ; DEAL Springer ; DEAL Springer ; Essential Science Indicators ; IF >= 5 ; JCR ; Nationallizenz ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection

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