Literature DB >> 19361493

Sonic hedgehog maintains proliferation in secondary heart field progenitors and is required for normal arterial pole formation.

Laura A Dyer1, Margaret L Kirby.   

Abstract

The Sonic hedgehog (Shh)-null mouse was initially described as a phenotypic mimic of Tetralogy of Fallot with pulmonary atresia (Washington Smoak, I., Byrd, N.A., Abu-Issa, R., Goddeeris, M.M., Anderson, R., Morris, J., Yamamura, K., Klingensmith, J., and Meyers, E.N. 2005. Sonic hedgehog is required for cardiac outflow tract and neural crest cell development. Dev. Biol. 283, 357-372.); however, subsequent reports describe only a single outflow tract, leaving the phenotype and its developmental mechanism unclear. We hypothesized that the phenotype that occurs in response to Shh knockdown is pulmonary atresia and is directly related to the abnormal development of the secondary heart field. We found that Shh was expressed by the pharyngeal endoderm adjacent to the secondary heart field and that its receptor Ptc2 was expressed in a gradient in the secondary heart field, with the most robust expression in the caudal secondary heart field, closest to the Shh expression. In vitro culture of secondary heart field with the hedgehog inhibitor cyclopamine significantly reduced proliferation. In ovo, cyclopamine treatment before the secondary heart field adds to the outflow tract reduced proliferation only in the caudal secondary heart field, which coincided with the region of high Ptc2 expression. After outflow tract septation should occur, embryos treated with cyclopamine exhibited pulmonary atresia, pulmonary stenosis, and persistent truncus arteriosus. In hearts with pulmonary atresia, cardiac neural crest-derived cells, which form the outflow tract septum, migrated into the outflow tract and formed a septum. However, this septum divided the outflow tract into two unequal sized vessels and effectively closed off the pulmonary outlet. These experiments show that Shh is necessary for secondary heart field proliferation, which is required for normal pulmonary trunk formation, and that embryos with pulmonary atresia have an outflow tract septum.

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Year:  2009        PMID: 19361493      PMCID: PMC2810612          DOI: 10.1016/j.ydbio.2009.03.028

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  44 in total

Review 1.  Hedgehog signaling in animal development: paradigms and principles.

Authors:  P W Ingham; A P McMahon
Journal:  Genes Dev       Date:  2001-12-01       Impact factor: 11.361

2.  Shortened outflow tract leads to altered cardiac looping after neural crest ablation.

Authors:  T Mesud Yelbuz; Karen L Waldo; Donna H Kumiski; Harriett A Stadt; Raymond R Wolfe; Linda Leatherbury; Margaret L Kirby
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3.  A series of normal stages in the development of the chick embryo.

Authors:  V HAMBURGER; H L HAMILTON
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4.  Tbx1, a DiGeorge syndrome candidate gene, is regulated by sonic hedgehog during pharyngeal arch development.

Authors:  V Garg; C Yamagishi; T Hu; I S Kathiriya; H Yamagishi; D Srivastava
Journal:  Dev Biol       Date:  2001-07-01       Impact factor: 3.582

5.  Sonic hedgehog restricts adhesion and migration of neural crest cells independently of the Patched- Smoothened-Gli signaling pathway.

Authors:  S Testaz; A Jarov; K P Williams; L E Ling; V E Koteliansky; C Fournier-Thibault; J L Duband
Journal:  Proc Natl Acad Sci U S A       Date:  2001-10-09       Impact factor: 11.205

Review 6.  The incidence of congenital heart disease.

Authors:  Julien I E Hoffman; Samuel Kaplan
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7.  Fgf8 is required for pharyngeal arch and cardiovascular development in the mouse.

Authors:  Radwan Abu-Issa; Graham Smyth; Ida Smoak; Ken-ichi Yamamura; Erik N Meyers
Journal:  Development       Date:  2002-10       Impact factor: 6.868

8.  Migration of cardiac neural crest cells in Splotch embryos.

Authors:  J A Epstein; J Li; D Lang; F Chen; C B Brown; F Jin; M M Lu; M Thomas; E Liu; A Wessels; C W Lo
Journal:  Development       Date:  2000-05       Impact factor: 6.868

9.  Conotruncal myocardium arises from a secondary heart field.

Authors:  K L Waldo; D H Kumiski; K T Wallis; H A Stadt; M R Hutson; D H Platt; M L Kirby
Journal:  Development       Date:  2001-08       Impact factor: 6.868

10.  An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome.

Authors:  Deborah U Frank; Lori K Fotheringham; Judson A Brewer; Louis J Muglia; Martin Tristani-Firouzi; Mario R Capecchi; Anne M Moon
Journal:  Development       Date:  2002-10       Impact factor: 6.868

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  62 in total

1.  BMP signaling modulates hedgehog-induced secondary heart field proliferation.

Authors:  Laura A Dyer; Frini A Makadia; Alexandria Scott; Kelly Pegram; Mary R Hutson; Margaret L Kirby
Journal:  Dev Biol       Date:  2010-10-14       Impact factor: 3.582

2.  Arterial pole progenitors interpret opposing FGF/BMP signals to proliferate or differentiate.

Authors:  Mary Redmond Hutson; Xiaopei Lily Zeng; Andrew J Kim; Emily Antoon; Stephen Harward; Margaret L Kirby
Journal:  Development       Date:  2010-08-11       Impact factor: 6.868

3.  Wnt/β-catenin and sonic hedgehog pathways interact in the regulation of the development of the dorsal mesenchymal protrusion.

Authors:  Laura E Briggs; Tara A Burns; Marie M Lockhart; Aimee L Phelps; Maurice J B Van den Hoff; Andy Wessels
Journal:  Dev Dyn       Date:  2015-12-29       Impact factor: 3.780

Review 4.  Understanding the role of Tbx1 as a candidate gene for 22q11.2 deletion syndrome.

Authors:  Shan Gao; Xiao Li; Brad A Amendt
Journal:  Curr Allergy Asthma Rep       Date:  2013-12       Impact factor: 4.806

Review 5.  Cilia and coordination of signaling networks during heart development.

Authors:  Karen Koefoed; Iben Rønn Veland; Lotte Bang Pedersen; Lars Allan Larsen; Søren Tvorup Christensen
Journal:  Organogenesis       Date:  2013-12-17       Impact factor: 2.500

6.  Loss of Wnt5a disrupts second heart field cell deployment and may contribute to OFT malformations in DiGeorge syndrome.

Authors:  Tanvi Sinha; Ding Li; Magali Théveniau-Ruissy; Mary R Hutson; Robert G Kelly; Jianbo Wang
Journal:  Hum Mol Genet       Date:  2014-11-19       Impact factor: 6.150

7.  Cadm4 restricts the production of cardiac outflow tract progenitor cells.

Authors:  Xin-Xin I Zeng; Deborah Yelon
Journal:  Cell Rep       Date:  2014-05-09       Impact factor: 9.423

8.  Gi proteins mediate activation of the canonical hedgehog pathway in the myocardium.

Authors:  Christian J Carbe; Lan Cheng; Sankar Addya; Jessica I Gold; Erhe Gao; Walter J Koch; Natalia A Riobo
Journal:  Am J Physiol Heart Circ Physiol       Date:  2014-05-09       Impact factor: 4.733

9.  Disheveled mediated planar cell polarity signaling is required in the second heart field lineage for outflow tract morphogenesis.

Authors:  Tanvi Sinha; Bing Wang; Sylvia Evans; Anthony Wynshaw-Boris; Jianbo Wang
Journal:  Dev Biol       Date:  2012-07-27       Impact factor: 3.582

Review 10.  The role of secondary heart field in cardiac development.

Authors:  Laura A Dyer; Margaret L Kirby
Journal:  Dev Biol       Date:  2009-10-14       Impact factor: 3.582

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