Ankrd17, an ubiquitously expressed ankyrin factor, is essential for the vascular integrity during embryogenesis

FEBS Letters

Volumn 583, Issue 17, 2009, Pages 2765-2771

  Hou, Shin Chen ^a,b   Chan, Li Wei ^b   Chou, Yu Chi ^b   Su, Ching Yuan ^b   Chen, Xin ^c   Shih, Yen Ling ^d   Tsai, Pei Chun ^d   Shen, C K James ^b   Yan, Yu Ting ^d  

^a NATIONAL DEFENSE MEDICAL CENTER   (Taiwan)

^b INSTITUTE OF MOLECULAR BIOLOGY   (Taiwan)

^c NATIONAL HEALTH RESEARCH INSTITUTES   (Taiwan)

^d INSTITUTE OF BIOMEDICAL SCIENCES   (Taiwan)

Author keywords

Ankyrin factor; Mouse gene targeting; SM actin gene; Smooth muscle cell; Vascular integrity

Indexed keywords

ANKYRIN; ANKYRIN REPEAT DOMAIN 17 PROTEIN; UNCLASSIFIED DRUG;

ANGIOGENESIS; ANIMAL TISSUE; ARTICLE; BLEEDING; CARDIOVASCULAR MALFORMATION; CELL DIFFERENTIATION; CONTROLLED STUDY; EMBRYO; EMBRYO DEATH; EMBRYO DEVELOPMENT; GENE EXPRESSION REGULATION; GENE TARGETING; MOUSE; NONHUMAN; PRIORITY JOURNAL; REGULATORY MECHANISM; UPREGULATION; VASCULAR SMOOTH MUSCLE;

ANIMALS; ANKYRINS; BLOOD VESSELS; CELL DIFFERENTIATION; EMBRYO, MAMMALIAN; EMBRYONIC DEVELOPMENT; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GENE TARGETING; HEMORRHAGE; MICE; MICE, KNOCKOUT; MUSCLE, SMOOTH, VASCULAR; MYOCYTES, SMOOTH MUSCLE; PROTEINS;

ANIMALIA; MUS;

EID: 69249215112     PISSN: 00145793     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.febslet.2009.07.025     Document Type: Article

References (32)

1. Risau W., and Flamme I. Vasculogenesis. Annu. Rev. Cell Dev. Biol. 11 (1995) 73-91
2. Darland D.C., Massingham L.J., Smith S.R., Piek E., Saint-Geniez M., and D'Amore P.A. Pericyte production of cell-associated VEGF is differentiation-dependent and is associated with endothelial survival. Dev. Biol. 264 (2003) 275-288
3. Owens G.K. Regulation of differentiation of vascular smooth muscle cells. Physiol. Rev. 75 (1995) 487-517
4. Owens G.K., Kumar M.S., and Wamhoff B.R. Molecular regulation of vascular smooth muscle cell differentiation in development and disease. Physiol. Rev. 84 (2004) 767-801
5. Coultas L., Chawengsaksophak K., and Rossant J. Endothelial cells and VEGF in vascular development. Nature 438 (2005) 937-945
6. Esner M., Meilhac S.M., Relaix F., Nicolas J.F., Cossu G., and Buckingham M.E. Smooth muscle of the dorsal aorta shares a common clonal origin with skeletal muscle of the myotome. Development 133 (2006) 737-749
7. Pouget C., Gautier R., Teillet M.A., and Jaffredo T. Somite-derived cells replace ventral aortic hemangioblasts and provide aortic smooth muscle cells of the trunk. Development 133 (2006) 1013-1022
8. Gittenberger-de Groot A.C., Vrancken Peeters M.P., Mentink M.M., Gourdie R.G., and Poelmann R.E. Epicardium-derived cells contribute a novel population to the myocardial wall and the atrioventricular cushions. Circ. Res. 82 (1998) 1043-1052
9. Hutson M.R., and Kirby M.L. Neural crest and cardiovascular development: a 20-year perspective. Birth Defects Res. C: Embryo Today 69 (2003) 2-13
10. Jiang X., Rowitch D.H., Soriano P., McMahon A.P., and Sucov H.M. Fate of the mammalian cardiac neural crest. Development 127 (2000) 1607-1616
11. Hellstrom M., Kalen M., Lindahl P., Abramsson A., and Betsholtz C. Role of PDGF-B and PDGFR-beta in recruitment of vascular smooth muscle cells and pericytes during embryonic blood vessel formation in the mouse. Development 126 (1999) 3047-3055
12. Hirschi K.K., Rohovsky S.A., and D'Amore P.A. PDGF, TGF-beta, and heterotypic cell-cell interactions mediate endothelial cell-induced recruitment of 10T1/2 cells and their differentiation to a smooth muscle fate. J. Cell Biol. 141 (1998) 805-814
13. Doi H., et al. Jagged1-selective notch signaling induces smooth muscle differentiation via a RBP-Jkappa-dependent pathway. J. Biol. Chem. 281 (2006) 28555-28564
14. High F.A., Lu M.M., Pear W.S., Loomes K.M., Kaestner K.H., and Epstein J.A. Endothelial expression of the Notch ligand Jagged1 is required for vascular smooth muscle development. Proc. Natl. Acad. Sci. USA 105 (2008) 1955-1959
15. High F.A., Zhang M., Proweller A., Tu L., Parmacek M.S., Pear W.S., and Epstein J.A. An essential role for Notch in neural crest during cardiovascular development and smooth muscle differentiation. J. Clin. Invest. 117 (2007) 353-363
16. Ronnov-Jessen L., and Petersen O.W. A function for filamentous alpha-smooth muscle actin: retardation of motility in fibroblasts. J. Cell Biol. 134 (1996) 67-80
17. Sobue K., Hayashi K., and Nishida W. Expressional regulation of smooth muscle cell-specific genes in association with phenotypic modulation. Mol. Cell. Biochem. 190 (1999) 105-118
18. Kawai-Kowase K., and Owens G.K. Multiple repressor pathways contribute to phenotypic switching of vascular smooth muscle cells. Am. J. Physiol. Cell Physiol. 292 (2007) C59-C69
19. Watt A.J., Jones E.A., Ure J.M., Peddie D., Wilson D.I., and Forrester L.M. A gene trap integration provides an early in situ marker for hepatic specification of the foregut endoderm. Mech. Dev. 100 (2001) 205-215
20. Nagy A., Gersenstein M., Vintersten K., and Behringer R. Manipulating the Mouse Embryo (2003), Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
21. Urness L.D., Sorensen L.K., and Li D.Y. Arteriovenous malformations in mice lacking activin receptor-like kinase-1. Nat. Genet. 26 (2000) 328-331
22. Forrester L.M., Nagy A., Sam M., Watt A., Stevenson L., Bernstein A., Joyner A.L., and Wurst W. An induction gene trap screen in embryonic stem cells: identification of genes that respond to retinoic acid in vitro. Proc. Natl. Acad. Sci. USA 93 (1996) 1677-1682
23. Krebs L.T., et al. Notch signaling is essential for vascular morphogenesis in mice. Gene Dev. 14 (2000) 1343-1352
24. Fischer A., Schumacher N., Maier M., Sendtner M., and Gessler M. The Notch target genes Hey1 and Hey2 are required for embryonic vascular development. Gene Dev. 18 (2004) 901-911
25. Wang H.U., Chen Z.F., and Anderson D.J. Molecular distinction and angiogenic interaction between embryonic arteries and veins revealed by ephrin-B2 and its receptor Eph-B4. Cell 93 (1998) 741-753
26. Dumont D.J., Gradwohl G., Fong G.H., Puri M.C., Gertsenstein M., Auerbach A., and Breitman M.L. Dominant-negative and targeted null mutations in the endothelial receptor tyrosine kinase, tek, reveal a critical role in vasculogenesis of the embryo. Gene Dev. 8 (1994) 1897-1909
27. Betsholtz C., Lindblom P., Bjarnegard M., Enge M., Gerhardt H., and Lindahl P. Role of platelet-derived growth factor in mesangium development and vasculopathies: lessons from platelet-derived growth factor and platelet-derived growth factor receptor mutations in mice. Curr. Opin. Nephrol. Hypertens. 13 (2004) 45-52
28. Wasteson P., Johansson B.R., Jukkola T., Breuer S., Akyurek L.M., Partanen J., and Lindahl P. Developmental origin of smooth muscle cells in the descending aorta in mice. Development 135 (2008) 1823-1832
29. Regan C.P., Manabe I., and Owens G.K. Development of a smooth muscle-targeted cre recombinase mouse reveals novel insights regarding smooth muscle myosin heavy chain promoter regulation. Circ. Res. 87 (2000) 363-369
30. Bergers G., and Song S. The role of pericytes in blood-vessel formation and maintenance. Neuro Oncol. 7 (2005) 452-464
31. Kono M., Mi Y., Liu Y., Sasaki T., Allende M.L., Wu Y.P., Yamashita T., and Proia R.L. The sphingosine-1-phosphate receptors S1P1, S1P2, and S1P3 function coordinately during embryonic angiogenesis. J. Biol. Chem. 279 (2004) 29367-29373
32. Liu Y., et al. Edg-1, the G protein-coupled receptor for sphingosine-1-phosphate, is essential for vascular maturation. J. Clin. Invest. 106 (2000) 951-961