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Sonic hedgehog is required for the assembly and remodeling of branchial arch blood vessels
H. Kolesova, H. Roelink, M. Grim
Jazyk angličtina Země Spojené státy americké
NLK
Free Medical Journals
od 1992 do Před 1 rokem
Wiley Online Library (archiv)
od 1996-01-01 do 2012-12-31
Wiley Free Content
od 1996 do Před 1 rokem
- MeSH
- branchiální krajina embryologie metabolismus MeSH
- cévy embryologie metabolismus MeSH
- financování organizované MeSH
- hybridizace in situ MeSH
- hybridomy MeSH
- imunohistochemie MeSH
- křepelky a křepelovití MeSH
- kultivované buňky MeSH
- myši MeSH
- proteiny hedgehog genetika imunologie metabolismus MeSH
- protilátky imunologie metabolismus MeSH
- ptačí proteiny genetika metabolismus MeSH
- transplantace buněk MeSH
- vývojová regulace genové exprese MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
Sonic hedgehog (Shh) is a morphogen involved in many developmental processes. Injection of cells (5E1) that produce a Shh-blocking antibody causes an attenuation of the Shh response, and this causes vascular malformations and impaired remodeling characterized by hemorrhages and protrusions of the anterior cardinal vein and outflow tract, delayed fusion of the dorsal aortae, impaired branching of the internal carotid artery, and delayed remodeling of the aortic arches. Distribution of smooth muscle cells in the vessel wall is unchanged. In 5E1-injected embryos, we also observed impaired assembly of endothelial cells into vascular tubes, particularly in the sixth branchial arch, around the anterior cardinal vein and around the dorsal aorta. In 5E1-treated embryos, increased numbers of macrophage-like cells, apoptotic cells, and a decreased level of proliferation were observed in head mesenchyme. Together, these observations show that Shh signaling is required at multiple stages for proper vessel formation and remodeling.
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- $a Sonic hedgehog (Shh) is a morphogen involved in many developmental processes. Injection of cells (5E1) that produce a Shh-blocking antibody causes an attenuation of the Shh response, and this causes vascular malformations and impaired remodeling characterized by hemorrhages and protrusions of the anterior cardinal vein and outflow tract, delayed fusion of the dorsal aortae, impaired branching of the internal carotid artery, and delayed remodeling of the aortic arches. Distribution of smooth muscle cells in the vessel wall is unchanged. In 5E1-injected embryos, we also observed impaired assembly of endothelial cells into vascular tubes, particularly in the sixth branchial arch, around the anterior cardinal vein and around the dorsal aorta. In 5E1-treated embryos, increased numbers of macrophage-like cells, apoptotic cells, and a decreased level of proliferation were observed in head mesenchyme. Together, these observations show that Shh signaling is required at multiple stages for proper vessel formation and remodeling.
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