2006
DOI: 10.1186/1471-213x-6-51
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Defective ALK5 signaling in the neural crest leads to increased postmigratory neural crest cell apoptosis and severe outflow tract defects

Abstract: Background: Congenital cardiovascular diseases are the most common form of birth defects in humans. A substantial portion of these defects has been associated with inappropriate induction, migration, differentiation and patterning of pluripotent cardiac neural crest stem cells. While TGF-β-superfamily signaling has been strongly implicated in neural crest cell development, the detailed molecular signaling mechanisms in vivo are still poorly understood.

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Cited by 83 publications
(29 citation statements)
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“…Because our strategy to inhibit Wnt signaling competence was limited to the SHF, the defect in CNC patterning indicates that there is a nonautonomous signal acting downstream of ␤-catenin. Published data reveal that inactivation of Bmp ligands in SHF, and type I Bmp receptors in CNC resulted in defective cardiac cushion development, supporting the notion that Bmp signals from SHF regulate development of the CNC (17,(42)(43)(44).…”
Section: Wnt Signaling Is Critical For Development Of the Right Ventrmentioning
confidence: 74%
“…Because our strategy to inhibit Wnt signaling competence was limited to the SHF, the defect in CNC patterning indicates that there is a nonautonomous signal acting downstream of ␤-catenin. Published data reveal that inactivation of Bmp ligands in SHF, and type I Bmp receptors in CNC resulted in defective cardiac cushion development, supporting the notion that Bmp signals from SHF regulate development of the CNC (17,(42)(43)(44).…”
Section: Wnt Signaling Is Critical For Development Of the Right Ventrmentioning
confidence: 74%
“…40 Increased post-migratory neural crest cell apoptosis in mice defective for Alk5 leads to severe outflow tract defects. 41 Deregulation of TCL1B expression by epimutation could therefore contribute to CHD by secondary disruption of AKT signaling. The unavailability of additional tissue from these cases with TCL1B epimutations precluded further functional analyses.…”
Section: Discussionmentioning
confidence: 99%
“…99,100 Null mutants for the TGFβ receptor genes, Tgfbr1 and Tgfbr2, are embryonic lethal in mice, but tissue specific deletion of TGFβ receptor genes support a role for TGFβ signaling in development of the OFT. 101,102 Targeted deletion of Tgfbr1 or Tgfbr2 in neural crest cells leads to OFT defects (PTA, interrupted aortic arch and ventricular septal defect [VSD]), strongly suggesting that TGFβ signaling is necessary for cardiac neural crest cells to promote normal septation of the OFT. [101][102][103] Other mouse models with targeted deletions in BMP/TGFβ signaling Overview on developmental stages of the heart.…”
Section: Heart Development Is Coordinated By Multiple Signaling Networkmentioning
confidence: 99%
“…101,102 Targeted deletion of Tgfbr1 or Tgfbr2 in neural crest cells leads to OFT defects (PTA, interrupted aortic arch and ventricular septal defect [VSD]), strongly suggesting that TGFβ signaling is necessary for cardiac neural crest cells to promote normal septation of the OFT. [101][102][103] Other mouse models with targeted deletions in BMP/TGFβ signaling Overview on developmental stages of the heart. The cardiac crescent is formed around day 15 in humans.…”
Section: Heart Development Is Coordinated By Multiple Signaling Networkmentioning
confidence: 99%