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锌对组织培养中骨蛋白合成的刺激作用。氨酰-tRNA合成酶的激活。

Zinc stimulation of bone protein synthesis in tissue culture. Activation of aminoacyl-tRNA synthetase.

作者信息

Yamaguchi M, Oishi H, Suketa Y

机构信息

Department of Environmental Biochemistry and Toxicology, Shizuoka College of Pharmacy, Japan.

出版信息

Biochem Pharmacol. 1988 Nov 1;37(21):4075-80. doi: 10.1016/0006-2952(88)90098-6.

Abstract

The present investigation was undertaken to clarify the effect of zinc on bone protein synthesis in tissue culture. Calvaria were removed from 3-week-old male rats and cultured for periods up to 96 hr in Dulbecco's Modified Eagle Medium (high glucose, 4500 mg/dl) supplemented with antibiotics and bovine serum albumin. The calvaria were incubated at 37 degrees in 5% CO2/95% air in the medium containing 10(-6)-10(-4) M zinc. Zinc content in bone cells was increased when the culture was treated with 10(-5) and 10(-4) M zinc for 48 hr. When calvaria cultured in the presence of 10(-4) M zinc were pulsed with [14C]uridine, the incorporation of [14C]uridine into the bone RNA was not increased significantly. In the pulse with [3H]leucine, the presence of 10(-5) to 10(-4) M zinc in the medium caused a significant increase in the incorporation of [3H]leucine into the acid-insoluble residues of bone tissue. This increase was blocked completely by treatment with 10(-7) M cycloheximide, an inhibitor of protein synthesis. When [3H]leucine was added into the reaction mixture containing the 5500 g supernatant fraction of the homogenate prepared from calvaria cultured in the presence of 10(-4) M zinc, the in vitro protein synthesis was increased about 2-fold. The activity of [3H]leucyl-tRNA synthetase in the 105,000 g supernatant fraction (cytosol) of the bone homogenate was increased about 2-fold by the culture with 10(-4) M zinc. The presence of 10(-4) M dipicolinate, a specific chelator of zinc, in the culture medium negated the effect of zinc on [3H]leucyl-tRNA synthetase activity. The addition of 10(-7) to 10(-6) M zinc into the reaction mixture containing enzyme extracts obtained from uncultured rat calvaria caused a 2-fold increase of [3H]leucyl-tRNA synthetase activity. These results clearly indicate that zinc induces the stimulation of protein synthesis at the translational level in bone cells. The present study further supports the view that zinc increases protein synthesis in bone cells and that the metal induces bone formation.

摘要

本研究旨在阐明锌对组织培养中骨蛋白合成的影响。从3周龄雄性大鼠中取出颅骨,在补充了抗生素和牛血清白蛋白的杜尔贝科改良伊格尔培养基(高糖,4500mg/dl)中培养长达96小时。颅骨在含有10(-6)-10(-4)M锌的培养基中于37℃、5%二氧化碳/95%空气环境下孵育。当培养物用10(-5)和10(-4)M锌处理48小时后,骨细胞中的锌含量增加。当在含有10(-4)M锌的培养基中培养的颅骨用[14C]尿苷脉冲标记时,[14C]尿苷掺入骨RNA的量没有显著增加。在用[3H]亮氨酸脉冲标记时,培养基中10(-5)至10(-4)M锌的存在导致[3H]亮氨酸掺入骨组织酸不溶性残渣的量显著增加。用蛋白质合成抑制剂10(-7)M环己酰亚胺处理可完全阻断这种增加。当将[3H]亮氨酸添加到含有从在10(-4)M锌存在下培养的颅骨制备的匀浆的5500g上清液部分的反应混合物中时,体外蛋白质合成增加约2倍。骨匀浆105,000g上清液部分(胞质溶胶)中[3H]亮氨酰-tRNA合成酶的活性通过用10(-4)M锌培养而增加约2倍。培养基中锌的特异性螯合剂10(-4)M二吡啶甲酸盐的存在消除了锌对[3H]亮氨酰-tRNA合成酶活性的影响。向含有从未培养的大鼠颅骨获得的酶提取物的反应混合物中添加10(-7)至10(-6)M锌导致[3H]亮氨酰-tRNA合成酶活性增加2倍。这些结果清楚地表明锌在骨细胞的翻译水平上诱导蛋白质合成的刺激。本研究进一步支持了锌增加骨细胞中蛋白质合成以及该金属诱导骨形成的观点。

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