Ghneim H K, Al-Saleh S S, Al-Shammary F J, Kordee Z S
Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud University, Riyadh, Saudi Arabia.
Cell Biochem Funct. 2003 Sep;21(3):275-82. doi: 10.1002/cbf.1023.
The level of adenosine deaminase (ADA; EC 3.5.4.4) was estimated at different passages in six confluent fibroblast cultures established from forearm skin biopsies of healthy adult normal volunteers. After determination of the zinc concentration in standard growth medium, ADA activity was estimated at different passages of subculture in media with different zinc concentrations. The results indicated that the specific activity of ADA in control confluent skin fibroblast cultures (passage 2) cultivated in standard growth medium containing 15.4 microM zinc (similar to that present in normal human plasma) was equal to 226.6+/-19.64 micromol min(-1) mg(-1) protein. The results showed that there were no significant changes in ADA specific activity in any of the control cultures as the zinc concentration of the medium was increased. To characterize the passage of subculture at which fibroblasts enter the ageing phase, three marker enzymes were assayed namely, phosphofructokinase, lactate dehydrogenase and glycogen phosphorylase. The result showed that the cells enter the ageing phase at passage 20 and beyond. Further investigation showed that ADA activity of serially subcultured confluent cultures cultivated in standard growth medium significantly dropped at passages 20, 25 and 30. ADA activity however was not significantly altered in cells at passage 2, 10 and 15 cultivated in standard growth medium and in the presence of higher zinc levels (23.1, 34.6, 53.8 and 73.1 microM). Furthermore there was significant lowering of ADA activities in cells at passages 20, 25 and 30 when cells were cultured in the presence of 15.4, 23.1 and 34.6 microM zinc. Such lowered activities of ADA were restored to normal when the cells were cultured in the presence of higher zinc concentration equal to 53.8 and 73.1 microM. From the results we concluded that it is possible to restore ADA activity in aged skin fibroblasts to normal levels by raising the zinc concentration in the culture medium to four or five times the control normal plasma zinc level.
在从健康成年正常志愿者前臂皮肤活检样本建立的六种汇合的成纤维细胞培养物中,在不同传代时对腺苷脱氨酶(ADA;EC 3.5.4.4)水平进行了评估。在测定标准生长培养基中的锌浓度后,在不同锌浓度的培养基中,对传代培养的不同传代时的ADA活性进行了评估。结果表明,在含有15.4 microM锌(类似于正常人血浆中的锌含量)的标准生长培养基中培养的对照汇合皮肤成纤维细胞培养物(第2代)中,ADA的比活性等于226.6±19.64微摩尔·分钟⁻¹·毫克⁻¹蛋白质。结果显示,随着培养基锌浓度的增加,任何对照培养物中的ADA比活性均无显著变化。为了表征成纤维细胞进入衰老阶段的传代培养次数,测定了三种标记酶,即磷酸果糖激酶、乳酸脱氢酶和糖原磷酸化酶。结果表明,细胞在第20代及以后进入衰老阶段。进一步研究表明,在标准生长培养基中连续传代培养的汇合培养物的ADA活性在第20、25和30代时显著下降。然而,在标准生长培养基中且锌水平较高(23.1、34.6、53.8和73.1 microM)的情况下,第2、10和15代细胞中的ADA活性没有显著改变。此外,当细胞在15.4、23.1和34.6 microM锌存在下培养时,第20、25和30代细胞中的ADA活性显著降低。当细胞在等于53.8和73.1 microM的更高锌浓度存在下培养时,这种降低的ADA活性恢复到正常水平。从结果中我们得出结论,通过将培养基中的锌浓度提高到对照正常血浆锌水平的四到五倍,可以将衰老皮肤成纤维细胞中的ADA活性恢复到正常水平。