Division of Neonatology, Department of Pediatrics, LAC+USC Medical Center, USC Keck School of Medicine and Children's Hospital Los Angeles, CA, USA.
Hastings Center for Pulmonary Research, USC Keck School of Medicine, Los Angeles, CA, USA.
Stem Cells. 2022 Jul 27;40(7):691-703. doi: 10.1093/stmcls/sxac031.
Lung maturation is not limited to proper structural development but also includes differentiation and functionality of various highly specialized alveolar cell types. Alveolar type 1 (AT1s) cells occupy nearly 95% of the alveolar surface and are critical for establishing efficient gas exchange in the mature lung. AT1 cells arise from progenitors specified during the embryonic stage as well as alveolar epithelial progenitors expressing surfactant protein C (Sftpcpos cells) during postnatal and adult stages. Previously, we found that Wnt5a, a non-canonical Wnt ligand, is required for differentiation of AT1 cells during the saccular phase of lung development. To further investigate the role of Wnt5a in AT1 cell differentiation, we generated and characterized a conditional Wnt5a gain-of-function mouse model. Neonatal Wnt5a gain-of-function disrupted alveologenesis through inhibition of cell proliferation. In this setting Wnt5a downregulated β-catenin-dependent canonical Wnt signaling, repressed AT2 (anti-AT2) and promoted AT1 (pro-AT1) lineage-specific gene expression. In addition, we identified 2 subpopulations of Sftpchigh and Sftpclow alveolar epithelial cells. In Sftpclow cells, Wnt5a exhibits pro-AT1 and anti-AT2 effects, concurrent with inhibition of canonical Wnt signaling. Interestingly, in the Sftpchigh subpopulation, although increasing AT1 lineage-specific gene expression, Wnt5a gain-of-function did not change AT2 gene expression, nor inhibit canonical Wnt signaling. Using primary epithelial cells isolated from human fetal lungs, we demonstrate that this property of Wnt5a is evolutionarily conserved. Wnt5a therefore serves as a selective regulator that ensures proper AT1/AT2 balance in the developing lung.
肺的成熟不仅限于适当的结构发育,还包括各种高度特化的肺泡细胞类型的分化和功能。肺泡 I 型(AT1)细胞占据了肺泡表面的近 95%,对于成熟肺中有效的气体交换至关重要。AT1 细胞来源于胚胎阶段指定的祖细胞,以及在出生后和成年阶段表达表面活性蛋白 C(Sftpcpos 细胞)的肺泡上皮祖细胞。以前,我们发现非经典 Wnt 配体 Wnt5a 在肺发育囊泡期 AT1 细胞的分化中是必需的。为了进一步研究 Wnt5a 在 AT1 细胞分化中的作用,我们构建并鉴定了条件性 Wnt5a 功能获得型小鼠模型。新生 Wnt5a 功能获得型通过抑制细胞增殖破坏肺泡发生。在这种情况下,Wnt5a 下调了 β-连环蛋白依赖性经典 Wnt 信号通路,抑制了 AT2(抗-AT2)并促进了 AT1(促-AT1)谱系特异性基因表达。此外,我们鉴定了 2 个 Sftpchigh 和 Sftpclow 肺泡上皮细胞亚群。在 Sftpclow 细胞中,Wnt5a 表现出促 AT1 和抗 AT2 作用,同时抑制经典 Wnt 信号通路。有趣的是,在 Sftpchigh 亚群中,尽管增加了 AT1 谱系特异性基因表达,但 Wnt5a 功能获得型并未改变 AT2 基因表达,也未抑制经典 Wnt 信号通路。使用从人胎肺分离的原代上皮细胞,我们证明了 Wnt5a 的这种特性在进化上是保守的。因此,Wnt5a 是一种选择性调节因子,可确保发育中的肺中适当的 AT1/AT2 平衡。