Raisz L G, Bergmann P J, Dominguez J H, Price M A
Endocrinology. 1979 Jul;105(1):152-62. doi: 10.1210/endo-105-1-152.
Poly-L-lysine (PL II; mol wt, 1000-4000) was added to fetal rat bones cultured in a chemically defined medium (BGJ) containing bovine serum albumin in the presence and absence of parathyroid hormone (PTH). Bone resorption was measured by the release of previously incorporated 45Ca. The addition of PL II at concentrations of 3-100 microgram/ml enhanced the stimulation of bone resorption by submaximal doses of PTH but had little effect on 45Ca release from control unstimulated cultures. Higher concentrations of PL II produced inhibition of 45Ca release. Dialysis of PL II did not alter enhancement or inhibition by PL II. PL II did not increase sensitivity to PTH in serum-supplemented cultures. Higher molecular weight PL II preparations were less effective. PL II did not enhance the resorptive response to 1,25-dihydroxyvitamin D, prostaglandin E2, osteoclast-activating factor, or bacterial endotoxin. The mechanism of the selective ability of PL II to enhance the response to low concentrations of PTH is unknown but may be due to the ability of this basic polypeptide to interfere with binding of PTH to sites other than the hormone receptor or to block degradation of PTH by bone.
在含有牛血清白蛋白的化学限定培养基(BGJ)中培养胎鼠骨骼时,在有和没有甲状旁腺激素(PTH)的情况下添加了聚-L-赖氨酸(PL II;分子量为1000 - 4000)。通过先前掺入的45Ca的释放来测量骨吸收。以3 - 100微克/毫升的浓度添加PL II可增强次最大剂量PTH对骨吸收的刺激作用,但对未受刺激的对照培养物中45Ca的释放影响很小。更高浓度的PL II会抑制45Ca的释放。PL II的透析不会改变其增强或抑制作用。在补充血清的培养物中,PL II不会增加对PTH的敏感性。更高分子量的PL II制剂效果较差。PL II不会增强对1,25 - 二羟维生素D、前列腺素E2、破骨细胞激活因子或细菌内毒素的吸收反应。PL II选择性增强对低浓度PTH反应的机制尚不清楚,但可能是由于这种碱性多肽干扰PTH与激素受体以外位点结合的能力,或阻断骨骼对PTH降解的能力。