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GATA4-dependent organ-specific endothelial differentiation controls liver development and embryonic hematopoiesis
Cyrill Géraud, … , Kai Schledzewski, Sergij Goerdt
Cyrill Géraud, … , Kai Schledzewski, Sergij Goerdt
Published February 20, 2017
Citation Information: J Clin Invest. 2017;127(3):1099-1114. https://doi.org/10.1172/JCI90086.
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Research Article Hepatology Vascular biology Article has an altmetric score of 10

GATA4-dependent organ-specific endothelial differentiation controls liver development and embryonic hematopoiesis

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Abstract

Microvascular endothelial cells (ECs) are increasingly recognized as organ-specific gatekeepers of their microenvironment. Microvascular ECs instruct neighboring cells in their organ-specific vascular niches through angiocrine factors, which include secreted growth factors (angiokines), extracellular matrix molecules, and transmembrane proteins. However, the molecular regulators that drive organ-specific microvascular transcriptional programs and thereby regulate angiodiversity are largely elusive. In contrast to other ECs, which form a continuous cell layer, liver sinusoidal ECs (LSECs) constitute discontinuous, permeable microvessels. Here, we have shown that the transcription factor GATA4 controls murine LSEC specification and function. LSEC-restricted deletion of Gata4 caused transformation of discontinuous liver sinusoids into continuous capillaries. Capillarization was characterized by ectopic basement membrane deposition, formation of a continuous EC layer, and increased expression of VE-cadherin. Correspondingly, ectopic expression of GATA4 in cultured continuous ECs mediated the downregulation of continuous EC-associated transcripts and upregulation of LSEC-associated genes. The switch from discontinuous LSECs to continuous ECs during embryogenesis caused liver hypoplasia, fibrosis, and impaired colonization by hematopoietic progenitor cells, resulting in anemia and embryonic lethality. Thus, GATA4 acts as master regulator of hepatic microvascular specification and acquisition of organ-specific vascular competence, which are indispensable for liver development. The data also establish an essential role of the hepatic microvasculature in embryonic hematopoiesis.

Authors

Cyrill Géraud, Philipp-Sebastian Koch, Johanna Zierow, Kay Klapproth, Katrin Busch, Victor Olsavszky, Thomas Leibing, Alexandra Demory, Friederike Ulbrich, Miriam Diett, Sandhya Singh, Carsten Sticht, Katja Breitkopf-Heinlein, Karsten Richter, Sanna-Maria Karppinen, Taina Pihlajaniemi, Bernd Arnold, Hans-Reimer Rodewald, Hellmut G. Augustin, Kai Schledzewski, Sergij Goerdt

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Figure 11

Liver endothelial GATA4 controls hepatic colonization by hematopoietic stem and progenitor cells.

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Liver endothelial GATA4 controls hepatic colonization by hematopoietic s...
(A) FACS quantification of CD45loKit+ and CD45+Kit+/– hematopoietic progenitors in liver, blood, and YS of Stab2-Cre Gata4fl/fl embryos at E11.25 (liver: n = 14 mutants and 10 controls; blood: n = 15 mutants and 10 controls; YS: n = 8 mutants and 16 controls [YS controls: Stab2-Cretg/WT Gata4fl/WT, Stab2-CreWT/WT Gata4fl/fl, Stab2-CreWT/WT Gata4fl/WT]). (B) FACS quantification of CMPs, GMPs, and myeloid-erythroid progenitors (MEP) in the liver of Stab2-Cre Gata4fl/fl embryos at E11.25 (n = 7). (C) FACS quantification of CD45loKit+ and CD45+Kit+/– hematopoietic progenitors in the liver and blood of Lyve1-Cre Gata4fl/fl embryos at E13.25 (liver: n = 6; blood: n = 6 mutants and 5 controls). (D) FACS quantification of long-term HSCs (LT-HSC), short-term HSCs (ST-HSC), and MPPs in liver and blood of Stab2-Cre Gata4fl/fl (left panels) and Lyve1-Cre Gata4fl/fl (right panels) embryos at E13.25. LT-HSCs (Lin–Sca-1+Kit+CD150+CD48–), ST-HSCs (Lin–Sca-1+Kit+CD150–CD48–), and MPPs (Lin–Sca-1+Kit+CD150–CD48+) (Stab2-Cre Gata4fl/fl liver: n = 8; Stab2-Cre Gata4fl/fl peripheral blood: n = 7 mutants and 8 controls; Lyve1-Cre Gata4fl/fl liver: n = 6; Lyve1-Cre Gata4fl/fl peripheral blood: n = 6 mutants and 5 controls). Student’s t test; *P < 0.05, ***P < 0.001.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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