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Wnt7b regulates mesenchymal proliferation and vascular development in the lung.

机译:Wnt7b调节肺间质的增殖和血管发育。

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Although the Wnt signaling pathway regulates inductive interactions between epithelial and mesenchymal cells, little is known of the role that this pathway plays during lung development. Wnt7b is expressed in the airway epithelium, suggesting a possible role for Wnt-mediated signaling in the regulation of lung development. To test this hypothesis, we have mutated Wnt7b in the germline of mice by replacement of the first exon with the lacZ-coding region. Wnt7b(lacZ-/-) mice exhibit perinatal death due to respiratory failure. Defects in early mesenchymal proliferation leading to lung hypoplasia are observed in Wnt7b(lacZ-/-) embryos. In addition, Wnt7b(lacZ-/-) embryos and newborn mice exhibit severe defects in the smooth muscle component of the major pulmonary vessels. These defects lead to rupture of the major vessels and hemorrhage in the lungs after birth. These results demonstrate that Wnt7b signaling is required for proper lung mesenchymal growth and vascular development.
机译:尽管Wnt信号通路调节上皮细胞与间充质细胞之间的诱导性相互作用,但人们对该通路在肺发育过程中所起的作用知之甚少。 Wnt7b在气道上皮中表达,表明Wnt介导的信号传导可能在调节肺发育中发挥作用。为了验证这一假设,我们通过用lacZ编码区替换第一个外显子使小鼠种系中的Wnt7b突变。 Wnt7b(lacZ-/-)小鼠由于呼吸衰竭而表现出围产期死亡。 Wnt7b(lacZ-/-)胚胎中观察到早期间充质增殖的缺陷导致肺发育不全。此外,Wnt7b(lacZ-/-)胚胎和新生小鼠在主要肺血管的平滑肌成分中表现出严重缺陷。这些缺陷导致出生后主要血管破裂和肺部出血。这些结果表明,Wnt7b信号传导是正确的肺间充质生长和血管发育所必需的。

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