Neurofibromin modulation of ras activity is required for normal endocardial-mesenchymal transformation in the developing heart.

Endocardial cushions are the precursors of the cardiac valves and form by a process of epithelial-mesenchymal transformation. Secreted growth factors from myocardium induce endocardial cells to transform into mesenchyme and invade the overlying extracellular matrix. Here, we show that the product of the Nf1 neurofibromatosis gene is required to regulate this event. In the absence of neurofibromin, mouse embryo hearts develop overabundant endocardial cushions due to hyperproliferation and lack of normal apoptosis. Neurofibromin deficiency in explant cultures is reproduced by activation of ras signaling pathways, and the Nf1(-/-) mutant phenotype is prevented by inhibiting ras in vitro. These results indicate that neurofibromin normally acts to modulate epithelial-mesenchymal transformation and proliferation in the developing heart by down regulating ras activity.

[1]  C. Birchmeier,et al.  Scatter factor/hepatocyte growth factor and its receptor, the c-met tyrosine kinase, can mediate a signal exchange between mesenchyme and epithelia during mouse development , 1993, The Journal of cell biology.

[2]  M. Tassabehji,et al.  Tandem duplication within a neurofibromatosis type 1 (NF1) gene exon in a family with features of Watson syndrome and Noonan syndrome. , 1993, American journal of human genetics.

[3]  A. Moorman,et al.  Formation of the tricuspid valve in the human heart. , 1995, Circulation.

[4]  M. Wigler,et al.  The NF1 locus encodes a protein functionally related to mammalian GAP and yeast IRA proteins , 1990, Cell.

[5]  D. L. Weeks,et al.  Epithelial-mesenchymal transformation of embryonic cardiac endothelial cells is inhibited by a modified antisense oligodeoxynucleotide to transforming growth factor beta 3. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[6]  E. Effmann,et al.  Platelet-derived growth factor receptor alpha subunit deleted Patch mouse exhibits severe cardiovascular dysmorphogenesis. , 1995, Teratology.

[7]  F. McCormick,et al.  Ras signaling and NF1. , 1995, Current opinion in genetics & development.

[8]  B. Korf,et al.  The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2. , 1997, JAMA.

[9]  Y. Zhong,et al.  Requirement of Drosophila NF1 for activation of adenylyl cyclase by PACAP38-like neuropeptides. , 1997, Science.

[10]  D. Viskochil,et al.  Identification of NF1 mutations in both alleles of a dermal neurofibroma , 1996, Nature Genetics.

[11]  K. Miyazono,et al.  Extracellular Fibrillar Structure of Latent TGFβ Binding Protein-1: Role in TGFβ-dependent Endothelial-Mesenchymal Transformation during Endocardial Cushion Tissue Formation in Mouse Embryonic Heart , 1997, The Journal of cell biology.

[12]  G. Eichele,et al.  Developmental regulation of the orphan receptor COUP-TF II gene in spinal motor neurons. , 1994, Development.

[13]  N. Ratner,et al.  Nf1-deficient mouse Schwann cells are angiogenic and invasive and can be induced to hyperproliferate: reversion of some phenotypes by an inhibitor of farnesyl protein transferase , 1997, Molecular and cellular biology.

[14]  Raymond B. Runyan,et al.  Signal transduction of a tissue interaction during embryonic heart development. , 1990, Cell regulation.

[15]  D. Gutmann,et al.  O-20-295 RAS-GTP levels are elevated in human NF1 peripheral nerve tumors , 1996, Clinical Neurology and Neurosurgery.

[16]  A. Copp,et al.  Pax 3 is required for cardiac neural crest migration in the mouse : evidence from the splotch ( Sp 2 H ) mutant , 1996 .

[17]  P. O’Connell,et al.  The GAP-related domain of the neurofibromatosis type 1 gene product interacts with ras p21 , 1990, Cell.

[18]  N. Ratner,et al.  Schwann Cells Express NDF and SMDF/n-ARIA mRNAs, Secrete Neuregulin, and Show Constitutive Activation of erbB3 Receptors: Evidence for a Neuregulin Autocrine Loop , 1997, Experimental Neurology.

[19]  F. Collins,et al.  The neurofibromatosis type 1 gene and its protein product, neurofibromin , 1993, Neuron.

[20]  A. G. Gittenberger-de Groot,et al.  Cell origins and tissue boundaries during outflow tract development. , 1995, Trends in cardiovascular medicine.

[21]  C. Mickanin,et al.  Platelet endothelial cell adhesion molecule-1 (PECAM-1/CD31): alternatively spliced, functionally distinct isoforms expressed during mammalian cardiovascular development. , 1994, Development.

[22]  Raymond B. Runyan,et al.  Antibodies to the Type II TGFbeta receptor block cell activation and migration during atrioventricular cushion transformation in the heart. , 1996, Developmental biology.

[23]  B. Hogan,et al.  Cloning and characterization of developmental endothelial locus-1: An embryonic endothelial cell protein that binds the αvβ3 integrin receptor , 1997 .

[24]  D. Largaespada,et al.  Nf1 deficiency causes Ras-Dediated granulocyte/macrophage colony stimulating factor hypersensitivity and chronic myeloid leukaemia , 1996, Nature Genetics.

[25]  N. Copeland,et al.  Targeted disruption of the neurofibromatosis type-1 gene leads to developmental abnormalities in heart and various neural crest-derived tissues. , 1994, Genes & development.

[26]  A. Bernards,et al.  Neurofibromatosis type 1 and Ras-mediated signaling: filling in the GAPs. , 1995, Biochimica et biophysica acta.

[27]  Raymond B. Runyan,et al.  Epithelial-mesenchymal cell transformation in the embryonic heart can be mediated, in part, by transforming growth factor beta. , 1989, Developmental biology.

[28]  P. Maycox,et al.  Cell death in the Schwann cell lineage and its regulation by neuregulin. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[29]  M. Kirby,et al.  Neural crest cells contribute to normal aorticopulmonary septation. , 1983, Science.

[30]  M. Cayouette,et al.  Homozygous inactivation of the NF1 gene in bone marrow cells from children with neurofibromatosis type 1 and malignant myeloid disorders. , 1997, The New England journal of medicine.

[31]  J. Epstein Pax3, neural crest and cardiovascular development. , 1996, Trends in cardiovascular medicine.

[32]  Philippe Soriano The PDGF alpha receptor is required for neural crest cell development and for normal patterning of the somites. , 1997, Development.

[33]  R R Markwald,et al.  Molecular regulation of atrioventricular valvuloseptal morphogenesis. , 1995, Circulation research.

[34]  B. Hall,et al.  Signal transduction and TGF-beta superfamily receptors. , 1996, Biochemistry and cell biology = Biochimie et biologie cellulaire.

[35]  R. Markwald,et al.  A heart segmental defect in the anterior-posterior axis of a transgenic mutant mouse. , 1997, Developmental biology.

[36]  Raymond B. Runyan,et al.  Invasion of mesenchyme into three-dimensional collagen gels: a regional and temporal analysis of interaction in embryonic heart tissue. , 1983, Developmental biology.

[37]  J. Gusella,et al.  Rescue of a Drosophila NF1 mutant phenotype by protein kinase A. , 1997, Science.

[38]  D. Meryash,et al.  Neurofibromatosis with fully expressed Noonan syndrome. , 1988, American journal of medical genetics.

[39]  Joseph R. Nevins,et al.  Myc and Ras collaborate in inducing accumulation of active cyclin E/Cdk2 and E2F , 1997, Nature.

[40]  S. Pulst,et al.  Differential expression and tissue distribution of type I and type II neurofibromins during mouse fetal development. , 1994, Developmental biology.

[41]  J. Declue,et al.  Schwann cells from neurofibromin deficient mice exhibit activation of p21ras, inhibition of cell proliferation and morphological changes. , 1995, Oncogene.

[42]  M. Daston,et al.  Neurofibromin, a predominantly neuronal GTPase activating protein in the adult, is ubiquitously expressed during development , 1992, Developmental dynamics : an official publication of the American Association of Anatomists.

[43]  Margaret Robertson,et al.  The neurofibromatosis type 1 gene encodes a protein related to GAP , 1990, Cell.

[44]  A. Copp,et al.  Pax3 is required for cardiac neural crest migration in the mouse: evidence from the splotch (Sp2H) mutant. , 1997, Development.

[45]  B. Korf,et al.  The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2. , 1997, Journal of the American Medical Association (JAMA).

[46]  Carmen Birchmeier,et al.  Multiple essential functions of neuregulin in development , 1995, Nature.

[47]  S. Scherer,et al.  Axonal Interactions Regulate Schwann Cell Apoptosis in Developing Peripheral Nerve: Neuregulin Receptors and the Role of Neuregulins , 1996, The Journal of Neuroscience.

[48]  Robert A. Weinberg,et al.  Tumour predisposition in mice heterozygous for a targeted mutation in Nf1 , 1994, Nature Genetics.

[49]  R. Markwald,et al.  Induction of endocardial cushion tissue in the avian heart is regulated, in part, by TGFbeta-3-mediated autocrine signaling. , 1997, Developmental biology.

[50]  X. Estivill,et al.  Confirmation of a double-hit model for the NF1 gene in benign neurofibromas. , 1997, American journal of human genetics.

[51]  T. Jacks,et al.  Loss of NF1 results in activation of the Ras signaling pathway and leads to aberrant growth in haematopoietic cells , 1996, Nature Genetics.