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体外对鸡胚颅骨骨吸收、胶原蛋白合成及钙化的系统评估:前列腺素E2的作用

Systematic assessment of bone resorption, collagen synthesis, and calcification in chick embryonic calvaria in vitro: effects of prostaglandin E2.

作者信息

Nagai M, Suzuki Y, Ota M

机构信息

Department of Biochemistry, Iwate Medical University, School of Dentistry, Morioka, Japan.

出版信息

Bone. 1993 Jul-Aug;14(4):655-9. doi: 10.1016/8756-3282(93)90088-r.

Abstract

A systematic method has been developed to assess bone resorption, matrix formation, and calcification in a single calvarial culture from 20-day-old chick embryos. The bones were prelabeled with 45Ca by an injection into the egg white before culture. In the last 2 h of incubation, the bones were further labeled with both 3H-proline and 3H-tetracycline. Bone resorption was assessed as 45Ca release into the medium. Collagen synthesis was measured by the incorporation of 3H-proline into collagenase-digestible protein (CDP). Since tetracycline has been commonly used as an in vivo marker for osteoid calcification, we assessed in vitro calcification as the uptake of 3H-tetracycline into bone. By using this method, we studied the effects of prostaglandin E2 (PGE2) and indomethacin, which inhibits biosynthesis of PGE2, on bone resorption and formation. The cultured bone synthesized approximately 300 ng of PGE2 during every 24 h of incubation, and indomethacin (10(-6) M) completely inhibited the synthesis. In indomethacin-treated cultures, % 45Ca release and the labeling of CDP were significantly reduced. These reductions were not seen when exogenous PGE2 (10(-9) M) comparable to its endogenous level was added along with the indomethacin. Furthermore, 10(-8) to 10(-5) M PGE2 increased % 45Ca release and the CDP labeling. In addition, the uptake of 3H-tetracycline into the cultured bone was also enhanced by PGE2. In devitalized calvaria, PGE2 had no effect on 3H-tetracycline uptake, suggesting that the stimulative effect on PGE2 was cell-mediated.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

已开发出一种系统方法,用于评估来自20日龄鸡胚的单个颅盖骨培养物中的骨吸收、基质形成和钙化情况。在培养前,通过向蛋清中注射45Ca对骨骼进行预标记。在培养的最后2小时,骨骼再用3H-脯氨酸和3H-四环素进行标记。骨吸收通过释放到培养基中的45Ca来评估。胶原蛋白合成通过3H-脯氨酸掺入胶原酶可消化蛋白(CDP)来测量。由于四环素一直被用作骨样钙化的体内标志物,我们将3H-四环素在骨中的摄取评估为体外钙化。通过使用这种方法,我们研究了前列腺素E2(PGE2)和抑制PGE2生物合成的吲哚美辛对骨吸收和形成的影响。培养的骨骼在每24小时的培养过程中合成约300 ng的PGE2,吲哚美辛(10(-6) M)完全抑制了合成。在吲哚美辛处理的培养物中,45Ca释放百分比和CDP标记显著降低。当与吲哚美辛一起添加与其内源性水平相当的外源性PGE2(10(-9) M)时,未观察到这些降低。此外,10(-8)至10(-5) M的PGE2增加了45Ca释放百分比和CDP标记。此外,PGE2还增强了3H-四环素在培养骨中的摄取。在失活的颅盖骨中,PGE2对3H-四环素摄取没有影响,这表明对PGE2的刺激作用是细胞介导的。(摘要截短至250字)

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