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Nf1 has an essential role in endothelial cells

Abstract

Neurofibromatosis type 1 (NF1) or von Recklinghausen neurofibromatosis is a genetic disorder that occurs in 1 of 4000 births and is characterized by benign and malignant tumors. Cardiovascular defects also contribute to NF1, though the pathogenesis is still unclear. Deficiency in neurofibromin (encoded by Nf1) in mice results in mid-embryonic lethality owing to cardiac abnormalities previously thought to be secondary to cardiac neural-crest defects. Using tissue-specific gene inactivation, we show that endothelial-specific inactivation of Nf1 recapitulates key aspects of the complete null phenotype, including multiple cardiovascular abnormalities involving the endocardial cushions and myocardium. This phenotype is associated with an elevated level of ras signaling in Nf1−/− endothelial cells and greater nuclear localization of the transcription factor Nfatc1. Inactivation of Nf1 in the neural crest does not cause cardiac defects but results in tumors of neural-crest origin resembling those seen in humans with NF1. These results establish a new and essential role for Nf1 in endothelial cells and confirm the requirement for neurofibromin in the neural crest.

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Figure 1: Tissue-restricted transgenic expression of Cre recombinase in neural crest and endothelium.
Figure 2: Endothelial-specific Nf1 inactivation disrupts heart development.
Figure 3: Elevated ras signaling and increased Nfatc1 nuclear localization in hearts of Nf1−/− embryos.
Figure 4: Fate mapping of cardiac neural crest.
Figure 5: Nf1nc mice live longer than Nf1−/−embryos and develop tumors of neural-crest origin.

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Acknowledgements

We are grateful to M. Yanagisawa for providing Tek–cre mice; B. Zhou for providing the Nfatc1 expression plasmid; L. Rorke for reviewing pathologic specimens; and M. Weiss, C. Thompson, C. Simon, E. Morrisey, M. Kahn and members of J.A.E.'s laboratory for critically reading the manuscript and for helpful discussions. This work was supported by grants from the WW Smith Foundation, the American Heart Association and the US National Institutes of Health to J.A.E. L.F.P. is supported by grants from the US National Institute of Neurological Disorders and Stroke and the US Department of Defense. A.D.G. is supported by the Department of Cell and Developmental Biology predoctoral training grant from the US National Institutes of Health. Y.Z. is a recipient of a Young Investigator Award from the National Neurofibromatosis Foundation.

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Correspondence to Jonathan A. Epstein.

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Gitler, A., Zhu, Y., Ismat, F. et al. Nf1 has an essential role in endothelial cells. Nat Genet 33, 75–79 (2003). https://doi.org/10.1038/ng1059

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