Joyce-Brady M F, Brody J S
Pulmonary Center, Boston University School of Medicine, Massachusetts 02118.
Dev Biol. 1990 Feb;137(2):331-48. doi: 10.1016/0012-1606(90)90258-k.
We studied differentiation of the pulmonary epithelium in the periphery of fetal rat lung in vivo and in vitro by comparing the ontogeny of cell-surface glycoconjugates with that of surfactant phospholipids. Apical surface binding of the lectin Maclura pomifera agglutinin (MPA) and expression of a 200-kDa MPA-binding glycoprotein (MPA-gp200) was evident at 20 days gestation in type 2 cells, but did not correlate with ultrastructural features of type 2 cell differentiation. Epithelial cells isolated from peripheral lung of 18-day gestation fetal rats displayed hormone-sensitive surfactant synthesis prior to the hormone-insensitive expression of MPA-gp200. Expression of MPA-gp200 occurred in association with the appearance of many new apical surface proteins suggesting a hormone-independent process of polar membrane differentiation. Thus membrane and secretory differentiation are discordant and can be dissociated. In vivo binding of Ricinus communis 1 agglutinin (RCA1), an apical marker of the differentiated alveolar type 1 cell occurred in undifferentiated peripheral lung epithelial cells as early as 18 days gestation, disappeared from differentiating type 2 cells and appeared in differentiated type 1 cells. Both undifferentiated fetal epithelial cells at 18 days gestation and fully differentiated type 1 cells express multiple glycoproteins with terminal beta-linked galactose residues which bind RCA1. Some of these RCA1-binding glycoproteins appear to be similar. These observations suggest that alveolar epithelial type 1 cells may derive directly from undifferentiated peripheral lung epithelial cells as well as from fully differentiated type 2 cells. In addition, terminal differentiation of fetal lung peripheral epithelium into type 1 and type 2 cells may involve repression as well as induction of differentiation-related genes.
我们通过比较细胞表面糖缀合物与表面活性物质磷脂的个体发生过程,在体内和体外研究了胎鼠肺周边区域肺上皮细胞的分化。在妊娠20天时,凝集素桑橙凝集素(MPA)在2型细胞的顶端表面结合以及200-kDa MPA结合糖蛋白(MPA-gp200)的表达很明显,但与2型细胞分化的超微结构特征不相关。从妊娠18天胎鼠的周边肺组织分离出的上皮细胞,在MPA-gp200对激素不敏感的表达之前就表现出激素敏感的表面活性物质合成。MPA-gp200的表达与许多新的顶端表面蛋白的出现相关,提示极性膜分化是一个不依赖激素的过程。因此,膜分化和分泌分化不一致且可分离。蓖麻凝集素1(RCA1)是分化的肺泡1型细胞的顶端标志物,其在体内的结合早在妊娠18天时就在未分化的周边肺上皮细胞中出现,在分化的2型细胞中消失,而在分化的1型细胞中出现。妊娠18天的未分化胎儿上皮细胞和完全分化的1型细胞都表达多种带有末端β-连接半乳糖残基的糖蛋白,这些糖蛋白能结合RCA1。其中一些RCA1结合糖蛋白似乎是相似的。这些观察结果表明,肺泡1型上皮细胞可能直接来源于未分化的周边肺上皮细胞以及完全分化的2型细胞。此外,胎儿肺周边上皮细胞向1型和2型细胞的终末分化可能涉及分化相关基因的抑制以及诱导。