Davenport M L, D'Ercole A J, Azizkhan J C, Lund P K
Department of Pediatrics, University of North Carolina, Chapel Hill 27514.
Exp Lung Res. 1988;14(5):607-18. doi: 10.3109/01902148809087832.
Somatomedins/insulinlike growth factors (Sm/IGFs) are peptide growth factors that are synthesized in multiple tissues and have been implicated in organ growth. Poly(A +)RNAs from lungs of fetal and postnatal rats were examined by dot and Northern blot analyses to investigate the local synthesis of IGFs during lung organogenesis. Blots were successively hybridized with 32P-labeled human IGF-II and mouse Sm-C/IGF-I cDNAs followed by human ubiquitin cDNAs (a control). Multiple IGF-II mRNA species of 4.7, 3.9, 3.1, 2.2, 1.75, and 1.2 kb were observed. Prenatally, the 3.9 kb species was predominant. In adult lung, the 4.7 kb species was the major species, and the 1.2 kb species was not detectable. Multiple Sm-C/IGF-I mRNA species of estimated sizes 7.5, 4.7, 1.7, and 1.0 kb were observed and their relative abundance did not change discernibly throughout development. Densitometric quantification revealed that IGF-II mRNAs were 7-20 fold more abundant in fetal lung than adult lung. In addition, they were 5-8 times more abundant than Sm-C/IGF-I mRNAs in embryonic lung, and were slightly less abundant than Sm-C/IGF-I mRNAs in adult lung. These data suggest synthesis of both Sm-C/IGF-I and IGF-II throughout lung organogenesis. Developmental changes in IGF-II mRNA abundance during lung organogenesis imply regulation at the level of gene transcription and/or mRNA stability.
生长调节素/胰岛素样生长因子(Sm/IGFs)是在多种组织中合成的肽类生长因子,与器官生长有关。通过斑点杂交和Northern印迹分析检测了胎鼠和出生后大鼠肺组织中的多聚腺苷酸(Poly(A+))RNA,以研究肺器官发生过程中IGFs的局部合成情况。印迹先后与32P标记的人IGF-II和小鼠Sm-C/IGF-I cDNA杂交,随后与人泛素cDNA(作为对照)杂交。观察到了4.7、3.9、3.1、2.2、1.75和1.2 kb的多种IGF-II mRNA种类。在产前,3.9 kb的种类占主导。在成年肺中,4.7 kb的种类是主要种类,而1.2 kb的种类未检测到。观察到估计大小为7.5、4.7、1.7和1.0 kb的多种Sm-C/IGF-I mRNA种类,其相对丰度在整个发育过程中没有明显变化。密度定量分析显示,胎儿肺中IGF-II mRNA的丰度比成年肺高7至20倍。此外,它们在胚胎肺中的丰度比Sm-C/IGF-I mRNA高5至8倍,在成年肺中的丰度略低于Sm-C/IGF-I mRNA。这些数据表明在整个肺器官发生过程中都有Sm-C/IGF-I和IGF-II的合成。肺器官发生过程中IGF-II mRNA丰度的发育变化意味着在基因转录和/或mRNA稳定性水平上的调节。