Morotti R A, Gutierrez M C, Askin F, Profitt S A, Wert S E, Whitsett J A, Greco M A
Department of Pathology, Children's Hospital, 700 Children's Drive, Columbus, OH 43205, USA.
Pediatr Dev Pathol. 2000 Sep-Oct;3(5):455-61. doi: 10.1007/s100240010092.
Congenital cystic adenomatoid malformation (CCAM) is an abnormality of branching morphogenesis of the lung. CCAM types 1, 2, and 3 exhibit a cellular composition that is different from that of CCAM type 4 when evaluated with bronchiolar and alveolar cell markers. Thyroid transcription factor 1 (TTF-1) regulates early lung development. To evaluate the potential role of TTF-1 in the development of CCAM, TTF-1 expression in CCAM was compared to that of fetal lungs at varying gestational ages. Twenty-three CCAM cases (17 type 1, two type 2, two type 3, and two type 4) and 11 fetal lungs (3 pseudoglandular, 4 canalicular, and 4 terminal sac stages) were analyzed using a rabbit polyclonal antiserum to rat TTF-1. Nuclear staining for TTF-1 was observed in ciliated and nonciliated cells of the bronchial and bronchiolar epithelia and in cells lining the distal air spaces by 12 weeks gestational age. By mid-gestation, proximal bronchial cells were TTF-1 negative, except for the basal cells, while TTF-1 staining was maintained in distal bronchiolar and alveolar cells. TTF-1 expression decreased in both bronchial, bronchiolar, and alveolar epithelia with advancing gestational age and cytodifferentiation. At term, TTF-1 expression persisted in a few bronchial and bronchiolar basal cells and in all alveolar type II cells, whereas type I cells were negative. In CCAM, TTF-1 was detected in the nuclei of epithelial cells lining the cysts. TTF-1 was expressed in a majority of the bronchiolar-like epithelial cells of the cysts in CCAM types 1, 2, and 3, where almost 100% of the cells were TTF-1 positive. In contrast, TTF-1 expression in the alveolar-like epithelium of CCAM type 4 cysts was restricted to type II cells and only 30%-60% of the lining cells were TTF-1 positive. These results support the hypothesis that CCAM types 1, 2, and 3 reflect abnormalities in lung morphogenesis and differentiation that are distinct from those for CCAM type 4. The role played by TTF-1 in the development of CCAM, if any, is not clear.
先天性囊性腺瘤样畸形(CCAM)是一种肺分支形态发生异常。当用细支气管和肺泡细胞标志物评估时,CCAM 1型、2型和3型的细胞组成与CCAM 4型不同。甲状腺转录因子1(TTF-1)调节肺的早期发育。为了评估TTF-1在CCAM发生中的潜在作用,将CCAM中TTF-1的表达与不同胎龄胎儿肺中的表达进行了比较。使用针对大鼠TTF-1的兔多克隆抗血清分析了23例CCAM病例(17例1型、2例2型、2例3型和2例4型)和11个胎儿肺(3个假腺期、4个小管期和4个终末囊期)。到孕12周时,在支气管和细支气管上皮的纤毛和非纤毛细胞以及远端气腔的衬里细胞中观察到TTF-1的核染色。到妊娠中期,近端支气管细胞TTF-1阴性,除了基底细胞,而TTF-1染色在远端细支气管和肺泡细胞中持续存在。随着胎龄增加和细胞分化,支气管、细支气管和肺泡上皮中的TTF-1表达均下降。足月时,TTF-1表达在少数支气管和细支气管基底细胞以及所有肺泡II型细胞中持续存在,而I型细胞为阴性。在CCAM中,在囊肿衬里的上皮细胞核中检测到TTF-1。TTF-1在CCAM 1型、2型和3型囊肿的大多数细支气管样上皮细胞中表达,其中几乎100%的细胞TTF-1阳性。相反CCAM 4型囊肿的肺泡样上皮中的TTF-1表达仅限于II型细胞,仅衬里细胞的30%-60%TTF-1阳性。这些结果支持这样的假说,即CCAM 1型、2型和3型反映了与CCAM 4型不同的肺形态发生和分化异常。TTF-1在CCAM发生中所起的作用(如果有的话)尚不清楚。