Hynes M A, Van Wyk J J, Brooks P J, D'Ercole A J, Jansen M, Lund P K
Department of Pediatrics, University of North Carolina School of Medicine, Chapel Hill 27514.
Mol Endocrinol. 1987 Mar;1(3):233-42. doi: 10.1210/mend-1-3-233.
The GH dependence of somatomedin-C/insulin-like growth factor I (Sm-C/IGF-I) and insulin like growth factor II (IGF-II) mRNAs was investigated by Northern blot hybridizations of polyadenylated RNAs from liver, pancreas, and brain of normal rats, untreated hypophysectomized rats, and hypophysectomized rats 4 h or 8 h after an ip injection of human GH (hGH). Using a 32P-labeled human Sm-C/IGF-I cDNA as probe, four Sm-C/IGF-I mRNAs of 7.5, 4.7, 1.7, and 1.2 kilobases (kb) were detected in rat liver and pancreas but were not detectable in brain. In both liver and pancreas, the abundance of these Sm-C/IGF-I mRNAs was 8- to 10-fold lower in hypophysectomized rats than in normal rats. Within 4 h after injection of hGH into hypophysectomized animals, the abundance of liver and pancreatic Sm-C/IGF-I mRNAs was restored to normal. A human IGF-II cDNA was used as a probe for rat IGF-II mRNAs which were found to be very low in abundance in rat liver and showed no evidence of regulation by GH status. In pancreas, IGF-II mRNA abundance was below the detection limit of the hybridization procedures. The brain contained two IGF-II mRNAs of 4.7 and 3.9 kb that were 5-fold lower in abundance in hypophysectomized rats than in normal rats. These brain IGF-II mRNAs were not, however, restored to normal abundance at 4 or 8 h after ip hGH injection into hypophysectomized animals. To investigate further, the effect of GH status on abundance of Sm-C/IGF-I and IGF-II mRNAs in rat brain, a second experiment was performed that differed from the first in that hypophysectomized rats were given an injection of hGH into the lateral ventricle (intracerebroventricular injection) and a rat Sm-C/IGF-I genomic probe was used to analyze Sm-C/IGF-I mRNAs. In this experiment, a 7.5 kb Sm-C/IGF-I mRNA was detected in brain polyadenylated RNAs. The abundance of the 7.5 kb mRNA was 4-fold lower in hypophysectomized rats than in normal rats and was increased to 80% of normal within 4 h after icv administration of hGH to hypophysectomized animals. As in the first experiment, the abundance of the 4.7 and 3.9 kb brain IGF-II mRNAs was lower than normal in hypophysectomized rats. Brain IGF-II mRNAs were increased to 50% of normal in hypophysectomized rats given an icv injection of hGH but within 8 h after the injection rather than at 4 h as with Sm-C/IGF-I mRNAs.
通过对正常大鼠、未经处理的垂体切除大鼠以及腹腔注射人生长激素(hGH)4小时或8小时后的垂体切除大鼠的肝脏、胰腺和大脑中的多聚腺苷酸化RNA进行Northern印迹杂交,研究了生长激素(GH)对生长调节素-C/胰岛素样生长因子I(Sm-C/IGF-I)和胰岛素样生长因子II(IGF-II)mRNA的依赖性。使用32P标记的人Sm-C/IGF-I cDNA作为探针,在大鼠肝脏和胰腺中检测到了7.5、4.7、1.7和1.2千碱基(kb)的四种Sm-C/IGF-I mRNA,但在大脑中未检测到。在肝脏和胰腺中,垂体切除大鼠中这些Sm-C/IGF-I mRNA的丰度比正常大鼠低8至10倍。在垂体切除的动物中注射hGH后4小时内,肝脏和胰腺中Sm-C/IGF-I mRNA的丰度恢复正常。用人IGF-II cDNA作为大鼠IGF-II mRNA的探针,发现其在大鼠肝脏中的丰度非常低,且未显示出受GH状态调节的证据。在胰腺中,IGF-II mRNA的丰度低于杂交程序的检测限。大脑中含有4.7和3.9 kb的两种IGF-II mRNA,垂体切除大鼠中其丰度比正常大鼠低5倍。然而,在垂体切除的动物腹腔注射hGH后4或8小时,这些大脑IGF-II mRNA的丰度并未恢复到正常水平。为了进一步研究GH状态对大鼠大脑中Sm-C/IGF-I和IGF-II mRNA丰度的影响,进行了第二个实验,该实验与第一个实验的不同之处在于,给垂体切除的大鼠侧脑室注射hGH(脑室内注射),并使用大鼠Sm-C/IGF-I基因组探针分析Sm-C/IGF-I mRNA。在这个实验中,在大脑多聚腺苷酸化RNA中检测到了一种7.5 kb的Sm-C/IGF-I mRNA。垂体切除大鼠中7.5 kb mRNA的丰度比正常大鼠低4倍,在垂体切除的动物脑室内注射hGH后4小时内增加到正常水平的80%。与第一个实验一样,垂体切除大鼠中4.7和3.9 kb大脑IGF-II mRNA的丰度低于正常水平。给垂体切除的大鼠脑室内注射hGH后,大脑IGF-II mRNA增加到正常水平的50%,但在注射后8小时而不是4小时,与Sm-C/IGF-I mRNA的情况不同。