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硝酸镓可抑制间充质细胞分化培养中的碱性磷酸酶活性。

Gallium nitrate inhibits alkaline phosphatase activity in a differentiating mesenchymal cell culture.

作者信息

Boskey A L, Ziecheck W, Guidon P, Doty S B

机构信息

Hospital for Special Surgery, Cornell University Medical College, New York, NY 10021.

出版信息

Bone Miner. 1993 Feb;20(2):179-92. doi: 10.1016/s0169-6009(08)80026-8.

Abstract

The effect of gallium nitrate on alkaline phosphatase activity in a differentiating chick limb-bud mesenchymal cell culture was monitored in order to gain insight into the observation that rachitic rats treated with gallium nitrate failed to show the expected increase in serum alkaline phosphatase activity. Cultures maintained in media containing 15 microM gallium nitrate showed drastically decreased alkaline phosphatase activities in the absence of significant alterations in total protein synthesis and DNA content. However, addition of 15 microM gallium nitrate to cultures 18 h before assay for alkaline phosphatase activity had little effect. At the light microscopic and electron microscopic level, gallium-treated cultures differed morphologically from gallium-free cultures: with gallium present, there were fewer hypertrophic chondrocytes and cartilage nodules were flatter and further apart. Because of altered morphology, staining with an antibody against chick cartilage alkaline phosphatase appeared less extensive; however, all nodules stained equivalently relative to gallium-free controls. Histochemical staining for alkaline phosphatase activity was negative in gallium-treated cultures, demonstrating that the alkaline phosphatase protein present was not active. The defective alkaline phosphatase activity in cultures maintained in the presence of gallium was also evidenced when cultures were supplemented with the alkaline phosphatase substrate, beta-glycerophosphate (beta GP). The data presented suggest that gallium inhibits alkaline phosphatase activity in this culture system and that gallium causes alterations in the differentiation of mesenchymal cells into hypertrophic chondrocytes.

摘要

监测硝酸镓对分化中的鸡胚肢体芽间充质细胞培养物中碱性磷酸酶活性的影响,以便深入了解用硝酸镓治疗的佝偻病大鼠血清碱性磷酸酶活性未能显示预期增加这一观察结果。在含有15微摩尔硝酸镓的培养基中培养的细胞,在总蛋白合成和DNA含量无显著变化的情况下,碱性磷酸酶活性急剧下降。然而,在测定碱性磷酸酶活性前18小时向培养物中添加15微摩尔硝酸镓几乎没有影响。在光学显微镜和电子显微镜水平上,经镓处理的培养物在形态上与无镓培养物不同:存在镓时,肥大软骨细胞较少,软骨结节更扁平且间距更大。由于形态改变,用抗鸡软骨碱性磷酸酶抗体染色的范围似乎变小;然而,相对于无镓对照,所有结节的染色程度相同。在经镓处理的培养物中,碱性磷酸酶活性的组织化学染色为阴性,表明存在的碱性磷酸酶蛋白无活性。当向培养物中添加碱性磷酸酶底物β-甘油磷酸酯(βGP)时,也证明了在镓存在下培养的细胞中碱性磷酸酶活性存在缺陷。所提供的数据表明,镓在该培养系统中抑制碱性磷酸酶活性,并且镓导致间充质细胞向肥大软骨细胞分化的过程发生改变。

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