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[L-抗坏血酸和骨代谢因子对ROS 17/2.8细胞碱性磷酸酶活性及45Ca2+掺入的影响]

[Effects of L-ascorbic acid and bone metabolism factors on alkaline phosphatase activity of and 45Ca2+ incorporation by ROS 17/2.8 cells].

作者信息

Kodama A, Hosoi K, Kurihara K, Atsumi T, Sugita K, Shioda Y, Fukuuchi H, Ueha T

机构信息

Department of Oral Physiology, Meikai University School of Dentistry, Saitama, Japan.

出版信息

Meikai Daigaku Shigaku Zasshi. 1990;19(1):109-16.

PMID:2134281
Abstract

Among several bioactive substances known as coupling factors, transforming growth factor-beta (TGF-beta), interleukin-1 (IL-1), and prostaglandin (PG) E1 and E2 increased not only the activity of alkaline phosphatase but also the rate of incorporation of 45Ca2+ into ROS 17/2.8 during a 3-day culture: the former two factors are known to be formed at the site where bone is resorbed, while PG's are known as one of the factors involved in bone resorption. Parathyroid hormone, another hormone that affects bone metabolism, elevated the incorporation of 45Ca2+ by and decreased the alkaline phosphatase activity of the cells. The facts indicate the possibility that the osteoblastic cells are involved in the transport of calcium ions when bones are being resorbed. On the other hand, when these osteosarcoma cells were cultured in DMEM containing ascorbate and beta-glycerophosphate, followed by staining with silver nitrate by the procedure of von Kossa, there appeared many groups of cells that were positively stained as dark brown spots. Cells were then cultured under the same conditions in the presence of radioactive calcium, and the radioactivity accumulated was measured. The result showed that the presence of both ascorbate and beta-glycerophosphate in the culture medium dramatically increased the accumulation of 45Ca2+. It appears from these facts that ROS 17/2.8 cells are capable of incorporating and/or accumulating calcium ion if they are cultured under appropriate conditions. These cells will probably be able to produce a calcified matrix in vitro.

摘要

在几种被称为偶联因子的生物活性物质中,转化生长因子-β(TGF-β)、白细胞介素-1(IL-1)以及前列腺素(PG)E1和E2不仅在3天的培养过程中提高了碱性磷酸酶的活性,还提高了45Ca2+掺入ROS 17/2.8细胞的速率:已知前两种因子在骨吸收部位形成,而前列腺素被认为是参与骨吸收的因子之一。甲状旁腺激素是另一种影响骨代谢的激素,它提高了45Ca2+的掺入量并降低了细胞的碱性磷酸酶活性。这些事实表明,在骨吸收过程中,成骨细胞可能参与了钙离子的转运。另一方面,当这些骨肉瘤细胞在含有抗坏血酸和β-甘油磷酸的DMEM中培养,然后按照冯·科萨(von Kossa)的方法用硝酸银染色时,出现了许多呈深棕色斑点阳性染色的细胞群。然后在相同条件下,在放射性钙存在的情况下培养细胞,并测量积累的放射性。结果表明,培养基中同时存在抗坏血酸和β-甘油磷酸显著增加了45Ca2+的积累。从这些事实看来,如果在适当条件下培养,ROS 17/2.8细胞能够掺入和/或积累钙离子。这些细胞可能能够在体外产生钙化基质。

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