胎儿大鼠肺发育过程中I型肺泡上皮细胞标记物的晚期出现。

Histochemistry Pub Date : 1994-10-01 DOI:10.1007/BF00269166
S I Danto, S M Zabski, E D Crandall
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引用次数: 3

摘要

最近利用免疫和分子探针对胎儿肺进行的研究发现,在这些细胞类型的形态发生之前,原始肺上皮细胞中存在I型和II型细胞表型标记。我们最近开发了针对成人I型细胞的单克隆抗体。为了进一步评估肺泡上皮细胞个体发育过程中I型细胞表型的时间外观,我们使用我们的一种单克隆抗体(mAb VIII B2)分析了胎儿肺发育。mAb VIII B2识别的表位首先出现在胎儿肺发育的小管阶段,约为。胚胎第19天(E19),偶有,微管淡淡染色。随着胎龄的增加,这种I型细胞探针的染色变得更加强烈和广泛,在此期间染色模式发生了变化。最初,远端上皮小管的所有细胞沿其顶端和底外侧表面均匀标记。随着肺泡上皮形态分化的进行,I型细胞的免疫反应性似乎仅限于原始I型细胞的顶端表面,其模式与成熟肺相似。我们同时用抗表面活性剂载脂蛋白a (α - sp - a)血清分析发育中的胎儿肺。与其他人的发现一致,SP-A的标记首先在E18的分散立方体细胞中检测到。仔细检查双标记标本表明,一些细胞对VIII B2和SP-A抗体都有反应,特别是在E20。E20肺切片的共聚焦显微镜分析证实了这一印象。检测到三种细胞群:仅用α - sp - a标记的细胞,仅用mAb VIII B2标记的细胞,以及两种标记的细胞的一小部分。(摘要删节250字)
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Late appearance of a type I alveolar epithelial cell marker during fetal rat lung development.

Recent studies in fetal lung using immunological and molecular probes have revealed type I and type II cell phenotypic markers in primordial lung epithelial cells prior to the morphogenesis of these cell types. We have recently developed monoclonal antibodies specific for adult type I cells. To evaluate further the temporal appearance of the type I cell phenotype during alveolar epithelial cell ontogeny, we analyzed fetal lung development using one of our monoclonal antibodies (mAb VIII B2). The epitope recognized by mAb VIII B2 first appears in the canalicular stage of fetal lung development, at approx. embryonic day 19 (E19), in occasional, faintly stained tubules. Staining with this type I cell probe becomes more intense and more widespread with increasing gestational age, during which time the pattern of staining changes. Initially, all cells of the distal epithelial tubules are uniformly labelled along their apical and basolateral surfaces. As morphological differentiation of the alveolar epithelium proceeds, type I cell immunoreactivity appears to become restricted to the apical surface of the primitive type I cells in a pattern approaching that seen in the mature lung. We concurrently analyzed developing fetal lung with an antiserum to surfactant apoprotein-A (alpha-SP-A). Consistent with the findings of others, labeling of SP-A was first detectable in scattered cuboidal cells at E18. Careful examination of the double-labeled specimens suggested that some cells were reactive with both the VIII B2 and SP-A antibodies, particularly at E20. Confocal microscopic analysis of such sections from E20 lung confirmed this impression. Three populations of cells were detected: cells labeled only with alpha-SP-A, cells labeled only with mAb VIII B2, and a smaller subset of cells labeled by both.(ABSTRACT TRUNCATED AT 250 WORDS)

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