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一种用于体外破骨细胞分化的快速筛选方法,该方法可测量分泌到培养基中的抗酒石酸酸性磷酸酶5b的活性。

Rapid screening method for osteoclast differentiation in vitro that measures tartrate-resistant acid phosphatase 5b activity secreted into the culture medium.

作者信息

Alatalo S L, Halleen J M, Hentunen T A, Mönkkönen J, Väänänen H K

机构信息

Institute of Biomedicine, Department of Anatomy, University of Turku, Kiinamyllynkatu 10, FIN-20520 Turku, Finland.

出版信息

Clin Chem. 2000 Nov;46(11):1751-4.

Abstract

BACKGROUND

Osteoclasts secrete tartrate-resistant acid phosphatase (TRAP; EC 3.1.3.2) 5b into the circulation. We studied the release of TRAP 5b from osteoclasts using a mouse in vitro osteoclast differentiation assay.

METHODS

We developed and characterized a polyclonal antiserum in rabbits, using purified human osteoclastic TRAP 5b as antigen. The antiserum was specific for TRAP in Western analysis of mouse osteoclast culture medium and was used to develop an immunoassay. We cultured mouse bone marrow-derived osteoclast precursor cells for 3-7 days with or without clodronate in the presence of vitamin D and analyzed the number of osteoclasts formed and the amount of TRAP 5b activity released into the culture medium.

RESULTS

TRAP 5b activity was not secreted from osteoclast precursor cells. Addition of clodronate-containing liposomes decreased in a dose-dependent manner the number of osteoclasts and TRAP 5b activity released in 6-day cultures. The amount of TRAP 5b activity in the medium detected by the immunoassay correlated significantly with the number of osteoclasts formed (r = 0.94; P<0.0001; n = 120).

CONCLUSIONS

The TRAP 5b immunoassay can be used to replace the laborious and time-consuming microscopic counting of osteoclasts in the osteoclast differentiation assay and to test the effects of potential therapeutic agents on osteoclast differentiation, enabling fast screening of large amounts of potential therapeutic agents.

摘要

背景

破骨细胞将抗酒石酸酸性磷酸酶(TRAP;EC 3.1.3.2)5b分泌到循环系统中。我们使用小鼠体外破骨细胞分化试验研究了TRAP 5b从破骨细胞中的释放情况。

方法

我们以纯化的人破骨细胞TRAP 5b为抗原,在兔体内制备并鉴定了一种多克隆抗血清。该抗血清在对小鼠破骨细胞培养基进行蛋白质免疫印迹分析时对TRAP具有特异性,并用于开发一种免疫测定法。我们在维生素D存在的情况下,将小鼠骨髓来源的破骨细胞前体细胞培养3至7天,添加或不添加氯膦酸盐,并分析形成的破骨细胞数量以及释放到培养基中的TRAP 5b活性量。

结果

破骨细胞前体细胞不分泌TRAP 5b活性。添加含氯膦酸盐的脂质体以剂量依赖性方式减少了6天培养物中形成的破骨细胞数量和释放的TRAP 5b活性。通过免疫测定法检测到的培养基中TRAP 5b活性量与形成的破骨细胞数量显著相关(r = 0.94;P<0.0001;n = 120)。

结论

TRAP 5b免疫测定法可用于替代破骨细胞分化试验中繁琐且耗时的破骨细胞显微镜计数,并测试潜在治疗剂对破骨细胞分化的影响,从而能够快速筛选大量潜在治疗剂。

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