CELL DEATH DIFFER (ISSN: 1350-9047), 2017 Dec 11; N/D: N/D-N/D.
Tipo di articolo: Journal Article,
Impact factor: 8, Impact factor a 5 anni: 7.999
Url: Non disponibile.
Parole chiave: Non disponibili.
*** IBB - CNR *** Department of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, University of Torino, Torino, Italy., CIR Dental School, Department of Surgical Sciences, University of Torino, Torino, Italy., Department of Life Sciences and Systems Biology, University of Torino, Torino, Italy., Research Unit Internal Medicine, University Hospital of Zurich, Zurich, Switzerland., Department of Pediatric Oncology, Hematology and Immunology, University of Heidelberg, Heidelberg, Germany., Molecular Medicine Partnership Unit, Heidelberg University & European Molecular Biology Laboratory, Heidelberg, Germany., Department of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, University of Torino, Torino, Italy. firstname.lastname@example.org.,
Heme is required for cell respiration and survival. Nevertheless, its intracellular levels need to be finely regulated to avoid heme excess, which may catalyze the production of reactive oxygen species (ROS) and promote cell death. Here, we show that alteration of heme homeostasis in endothelial cells due to the loss of the heme exporter FLVCR1a, results in impaired angiogenesis. In vitro, FLVCR1a silencing in endothelial cells causes defective tubulogenesis and poor viability due to intracellular heme accumulation. Consistently, endothelial-specific Flvcr1a knockout mice show aberrant angiogenesis responsible for hemorrhages and embryonic lethality. Importantly, we demonstrate that impaired heme export leads to endothelial cell death by paraptosis and provide evidence that endoplasmic reticulum (ER) stress precedes heme-induced paraptosis. These findings highlight a crucial role for the cytosolic heme pool in the control of endothelial cell survival and in the regulation of the angiogenic process. Interfering with endothelial heme export represents a valuable model for a deeper understanding of the molecular mechanisms underlying heme-triggered paraptosis and, in the future, might provide a novel tool for the modulation of angiogenesis in pathophysiologic conditions.
Ntziachristos V, Cuénod CA, Fournier L, Balvay D, Pradel C, Siauve N, Clement O, Jouannot E, Lucidarme O, Vecchio SD, Salvatore M, Law B, Tung C-H, Jain RK, Fukumura D, Munn LL, Brown EB, Schellenberger E, Montet X, Weissleder R, Clerck ND, Postnov A * Tumor Imaging(121 visite) Textbook Of In Vivo Imaging In Vertebrates (ISSN: 9780-4700), 2007 Jul 16; 1: 277-309. Impact Factor:1.148 DettagliEsporta in BibTeXEsporta in EndNote
97 Records (90 escludendo Abstract e Conferenze). Impact factor totale: 415.528 (411.953 escludendo Abstract e Conferenze). Impact factor a 5 anni totale: 439.758 (435.125 escludendo Abstract e Conferenze).