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N-甲基-D-天冬氨酸(NMDA)受体的特异性拮抗剂可阻止破骨细胞形成骨吸收所需的封闭区。

Specific antagonists of NMDA receptors prevent osteoclast sealing zone formation required for bone resorption.

作者信息

Itzstein C, Espinosa L, Delmas P D, Chenu C

机构信息

INSERM Unit 403, Hôpital E. Herriot, Pavillon F, Lyon Cedex 03, 69437, France.

出版信息

Biochem Biophys Res Commun. 2000 Feb 5;268(1):201-9. doi: 10.1006/bbrc.2000.2097.

Abstract

N-Methyl-d-aspartate (NMDA) glutamate receptors, widely distributed in the nervous system, have recently been identified in bone. They are expressed and are functional in osteoclasts. In the present work, we have studied the effects of specific antagonists of NMDA receptors on osteoclast activation and bone resorption. Using an in vitro assay of bone resorption, we showed that several antagonists of NMDA receptors binding to different sites of the receptor inhibit bone resorption. Osteoclast activation requires adhesion to the bone surface, cytoskeletal reorganization and survival. We demonstrated by autoradiography that the specific NMDA receptor channel blocker, MK 801, binds to osteoclasts. This antagonist had no effect on osteoclast attachment to bone and did not induce osteoclast apoptosis. In contrast, MK 801 rapidly decreased the percentage of osteoclasts with actin ring structures that are associated with actively resorbing osteoclasts. These results suggest that NMDA receptors expressed by osteoclasts may be involved in adhesion-induced formation of the sealing zone required for bone resorption.

摘要

N-甲基-D-天冬氨酸(NMDA)谷氨酸受体广泛分布于神经系统,最近在骨骼中也被发现。它们在破骨细胞中表达且具有功能。在本研究中,我们研究了NMDA受体特异性拮抗剂对破骨细胞活化和骨吸收的影响。通过骨吸收的体外测定,我们发现几种与受体不同位点结合的NMDA受体拮抗剂可抑制骨吸收。破骨细胞活化需要黏附于骨表面、细胞骨架重组和存活。我们通过放射自显影证明,特异性NMDA受体通道阻滞剂MK 801可与破骨细胞结合。该拮抗剂对破骨细胞黏附于骨无影响,也不诱导破骨细胞凋亡。相反,MK 801迅速降低了具有与活跃骨吸收相关的肌动蛋白环结构的破骨细胞百分比。这些结果表明,破骨细胞表达的NMDA受体可能参与黏附诱导的骨吸收所需封闭区的形成。

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