Tomomura A, Fukushige T, Noda T, Noikura T, Saheki T
Department of Biochemistry, Faculty of Medicine, Kagoshima University, Japan.
FEBS Lett. 1992 Apr 27;301(3):277-81. doi: 10.1016/0014-5793(92)80256-g.
We purified a serum calcium-decreasing factor, which showed chymotrypsin-like protease activity, from porcine pancreas to homogeneity. The factor administered to mice intravenously at a dose of 20 micrograms/kg b.w. decreased serum calcium by 15%. Treatment of the factor with the serine protease inhibitor, PMSF, caused a leftward shift in the dose-response curve, showing strengthened activity. It also caused a decrease in serum calcium and hydroxyproline levels in rats. At a dose of 10 ng/ml, the factor inhibited 45Ca release from cultured fetal long bone stimulated by parathyroid hormone (PTH) and PTH-related protein, but not by interleukin-1 alpha, prostaglandin E1 and 1,25-dihydroxy vitamin D3. No other well-known pancreatic proteases had these effects. In view of the results of experiments using protease inhibitor and pancreatic proteases, and in view of the specificity of this factor in vitro, we propose that the factor exerts its serum calcium-decreasing activity most probably not through proteolytic degradation of PTH, but through an inhibition of PTH action on bones by a yet undefined mechanism.
我们从猪胰腺中纯化出一种具有胰凝乳蛋白酶样蛋白酶活性的血清降钙因子,直至达到同质。以20微克/千克体重的剂量给小鼠静脉注射该因子,可使血清钙降低15%。用丝氨酸蛋白酶抑制剂苯甲基磺酰氟(PMSF)处理该因子,会使剂量反应曲线向左移动,表明活性增强。它还会导致大鼠血清钙和羟脯氨酸水平降低。在10纳克/毫升的剂量下,该因子抑制甲状旁腺激素(PTH)和PTH相关蛋白刺激培养的胎儿长骨释放45Ca,但不抑制白细胞介素-1α、前列腺素E1和1,25-二羟基维生素D3刺激的释放。其他知名的胰腺蛋白酶没有这些作用。鉴于使用蛋白酶抑制剂和胰腺蛋白酶的实验结果,以及该因子在体外的特异性,我们提出该因子发挥其血清降钙活性很可能不是通过对PTH的蛋白水解降解,而是通过一种尚未明确的机制抑制PTH对骨骼的作用。