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实验条件对预先标记的胎鼠长骨中45钙释放的影响。

Effects of experimental conditions on the release of 45calcium from prelabeled fetal mouse long bones.

作者信息

van Beek E, Oostendorp-van de Ruit M, van der Wee-Pals L, Bloys H, van de Bent C, Papapoulos S, Löwik C

机构信息

Department of Endocrinology and Metabolic Diseases, University Hospital, Leiden, The Netherlands.

出版信息

Bone. 1995 Jul;17(1):63-9. doi: 10.1016/8756-3282(95)00135-z.

Abstract

Embryonic/neonatal bones in culture are commonly used for the study of osteoclastic resorption in vitro. For this purpose, the release of 45calcium (45Ca) from prelabeled bones is measured as an index of resorption. We studied 45Ca release from two types of long bone explants after different preparation methods: 17-day-old fetal mouse radii/ulnae with and without cartilage ends (intact radii/ulnae and shafts, respectively), and intact 18-day old metacarpals/metatarsals. In addition, we examined the effect of different culture conditions, such as cultures performed under the surface of the medium or at the interphase of medium and air, on 45Ca release and histology. When intact radii/ulnae were cultured under the surface of the medium, there was always a significant amount (10%) of net basal 45Ca release (corrected for physicochemical exchange) that was not due to osteoclastic resorption, as it could not be suppressed by inhibitors of resorption even at high concentrations. Moreover, histologically TRAcP-positive cells were almost absent after culture and the bone marrow/stromal cells in the center of the bone appeared necrotic, possibly due to a lack of oxygen. Under these culture conditions, osteoclasts could survive in shafts as well as in PTH-stimulated intact radii/ulnae, but a constant amount of 10% 45Ca, not due to resorption, was still released in the medium. When these explants were cultured at the interphase of medium and air, basal and stimulated 45Ca release originated from osteoclastic resorption. In contrast, in 18-day-old fetal mouse metacarpals/metatarsals, the experimental conditions applied did not affect 45Ca release, which was always due to resorption of the explants by osteoclasts.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

培养中的胚胎/新生骨骼常用于体外破骨细胞吸收的研究。为此,测量预先标记的骨骼中45钙(45Ca)的释放量作为吸收指标。我们研究了两种不同制备方法的长骨外植体中45Ca的释放:有和没有软骨端的17日龄胎鼠桡骨/尺骨(分别为完整的桡骨/尺骨和骨干),以及完整的18日龄掌骨/跖骨。此外,我们研究了不同培养条件,如在培养基表面或在培养基与空气界面进行培养,对45Ca释放和组织学的影响。当完整的桡骨/尺骨在培养基表面培养时,总有大量(10%)的净基础45Ca释放(经物理化学交换校正)不是由于破骨细胞吸收,因为即使在高浓度下,它也不能被吸收抑制剂抑制。此外,培养后组织学上几乎没有抗酒石酸酸性磷酸酶(TRAcP)阳性细胞,并且骨中心的骨髓/基质细胞似乎坏死,可能是由于缺氧。在这些培养条件下,破骨细胞可以在骨干以及甲状旁腺激素(PTH)刺激的完整桡骨/尺骨中存活,但培养基中仍会持续释放10%的45Ca,这并非由于吸收。当这些外植体在培养基与空气界面培养时,基础和刺激的45Ca释放源自破骨细胞吸收。相比之下,在18日龄胎鼠掌骨/跖骨中,所应用的实验条件不影响45Ca释放,其总是由于破骨细胞对外植体的吸收所致。(摘要截断于250字)

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