Kostyo J L, Cameron C M, Olson K C, Jones A J, Pai R C
Proc Natl Acad Sci U S A. 1985 Jun;82(12):4250-3. doi: 10.1073/pnas.82.12.4250.
The anterior pituitary gland produces a 20-kilodalton (kDa) variant of human growth hormone (hGH) that differs from the predominant 22-kDa form of hGH in that amino acid residues 32-46 are deleted. Previous work has suggested that the 20-kDa variant possesses the full growth-promoting and lactogenic activities of 22-kDa hGH but lacks its intrinsic diabetogenic and insulin-like activities. In the present study, recombinant DNA techniques were used to prepare biosynthetic 20-kDa hGH, and some of the biological properties of the purified hGH variant were examined. The biosynthetic 20-kDa hGH variant was found to share the propensity for aggregation exhibited by its native counterpart. Moreover, like the native variant, biosynthetic 20-kDa hGH possessed full growth-promoting activity in the weight gain test in hypophysectomized rats. However, contrary to previous work suggesting that native 20-kDa hGH lacks diabetogenic and insulin-like activities, biosynthetic 20-kDa hGH was found to have substantial diabetogenic activity when administered chronically to ob/ob mice and to possess approximately 20% the in vitro insulin-like activity of biosynthetic 22-kDa hGH on isolated epididymal adipose tissue of hypophysectomized rats. The diabetogenic and insulin-like activities of biosynthetic 20-kDa hGH cannot be ascribed to contamination of the hormone preparation with the 22-kDa form of hGH or with other diabetogenic or insulin-like pituitary peptides. Therefore, the results strongly suggest that diabetogenic and insulin-like activities are also intrinsic properties of the 20-kDa variant of hGH.
垂体前叶产生一种20千道尔顿(kDa)的人生长激素(hGH)变体,它与占主导地位的22-kDa hGH形式不同,在于其氨基酸残基32 - 46被删除。先前的研究表明,20-kDa变体具有22-kDa hGH的全部促生长和催乳活性,但缺乏其内在的致糖尿病和胰岛素样活性。在本研究中,使用重组DNA技术制备了生物合成的20-kDa hGH,并检测了纯化的hGH变体的一些生物学特性。发现生物合成的20-kDa hGH变体与其天然对应物一样具有聚集倾向。此外,与天然变体一样,生物合成的20-kDa hGH在垂体切除大鼠的体重增加试验中具有完全的促生长活性。然而,与先前认为天然20-kDa hGH缺乏致糖尿病和胰岛素样活性的研究相反,发现生物合成的20-kDa hGH长期给予ob/ob小鼠时具有显著的致糖尿病活性,并且对垂体切除大鼠的离体附睾脂肪组织具有约20%的生物合成22-kDa hGH的体外胰岛素样活性。生物合成的20-kDa hGH的致糖尿病和胰岛素样活性不能归因于激素制剂被22-kDa形式的hGH或其他致糖尿病或胰岛素样垂体肽污染。因此,结果强烈表明致糖尿病和胰岛素样活性也是hGH的20-kDa变体的内在特性。