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Status: Bibliographieeintrag

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Verfasst von:Olsavszky, Victor [VerfasserIn]   i
 Ulbrich, Friederike [VerfasserIn]   i
 Sticht, Carsten [VerfasserIn]   i
 Schmid, Christian David [VerfasserIn]   i
 Wohlfeil, Sebastian A. [VerfasserIn]   i
 Schledzewski, Kai [VerfasserIn]   i
 Dooley, Steven [VerfasserIn]   i
 Gaitantzi, Haristi [VerfasserIn]   i
 Breitkopf-Heinlein, Katja [VerfasserIn]   i
 Géraud, Cyrill [VerfasserIn]   i
 Goerdt, Sergij [VerfasserIn]   i
 Reiners-Koch, Philipp-Sebastian [VerfasserIn]   i
Titel:GATA4 and LMO3 balance angiocrine signaling and autocrine inflammatory activation by BMP2 in liver sinusoidal endothelial cells
Verf.angabe:Victor Olsavszky, Friederike Ulbrich, Sandhya Singh, Miriam Diett, Carsten Sticht, Christian David Schmid, Johanna Zierow, Sebastian A. Wohlfeil, Kai Schledzewski, Steven Dooley, Haristi Gaitantzi, Katja Breitkopf-Heinlein, Cyrill Géraud, Sergij Goerdt, Philipp-Sebastian Koch
E-Jahr:2017
Jahr:5 September 2017
Umfang:9 S.
Fussnoten:Gesehen am 27.08.2018 ; Available online 29 June 2017
Titel Quelle:Enthalten in: Gene
Ort Quelle:Amsterdam : Elsevier, 1976
Jahr Quelle:2017
Band/Heft Quelle:627(2017), Seite 491-499
ISSN Quelle:1879-0038
Abstract:Liver sinusoidal endothelial cells (LSEC) represent a unique, organ-specific type of discontinuous endothelial cells. LSEC instruct the hepatic vascular niche by paracrine-acting angiocrine factors. Recently, we have shown that LSEC-specific transcriptional regulator GATA4 induces expression of BMP2 in cultured endothelial cells (EC) in vitro. Furthermore, angiocrine Bmp2 signaling in the liver in vivo was demonstrated to control iron homeostasis. Here, we investigated GATA4-dependent autocrine BMP2 signaling in endothelial cells by gene expression profiling. GATA4 induced a large cluster of inflammatory endothelial response genes in cultured EC, which is similar to previously identified virus-induced and interferon-associated responses. Treating the cells with the BMP2 inhibitor Noggin counter-regulated the GATA4-dependent inflammatory phenotype of EC, indicating that BMP2 is indeed the major driver. In contrast to continuous EC, LSEC were less prone to activation by BMP2. Notably, GATA4-dependent induction of the inflammatory EC response gene cluster was attenuated by over-expression of the LSEC-specific transcriptional modifier LMO3 while hepatocyte activation was fully preserved, indicating conserved BMP2 synthesis. In summary, our data suggest that transcriptional counter-regulation by GATA4 and LMO3 in LSEC prevents autocrine induction of an inflammatory phenotype, while maintaining angiocrine BMP2-mediated cell-cell communication in the liver vascular niche.
DOI:doi:10.1016/j.gene.2017.06.051
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: http://dx.doi.org/10.1016/j.gene.2017.06.051
 Volltext: http://www.sciencedirect.com/science/article/pii/S0378111917305012
 DOI: https://doi.org/10.1016/j.gene.2017.06.051
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Bone morphogenetic protein (BMP)
 Endothelial cells
 GATA4
 Gene regulation
 Microarray
 Transcription/developmental factors
K10plus-PPN:1580411762
Verknüpfungen:→ Zeitschrift

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