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骨硬化蛋白在金鱼再生鳞片中的表达及其在太空微重力下的增加。

Expression of sclerostin in the regenerating scales of goldfish and its increase under microgravity during space flight.

机构信息

Noto Marine Laboratory, Division of Marine Environmental Studies, Institute of Nature and Environmental Technology, Kanazawa University.

Department of Oral Morphology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences.

出版信息

Biomed Res. 2020;41(6):279-288. doi: 10.2220/biomedres.41.279.

Abstract

Osteocytes, osteoblasts (bone-forming cells), and osteoclasts (bone-resorbing cells) are the primary types of cells that regulate bone metabolism in mammals. Sclerostin produced in bone cells activates osteoclasts, inhibiting bone formation; excess production of sclerostin, therefore, leads to the loss of bone mass. Fish scales have been reported to have morphological and functional similarities to mammalian bones, making them a useful experimental system for analyzing vertebrate bone metabolism in vitro. However, whether fish scales contain cells producing sclerostin and/or osteocytes has not been determined. The current study demonstrated, for the first time, that sclerostin-containing cells exist in goldfish scales. Analysis of the distribution and shape of sclerostin-expressing cells provided evidence that osteoblasts produce sclerostin in goldfish scales. Furthermore, our results found that osteocyte-like cells exist in goldfish scales, which also produce sclerostin. Finally, we demonstrated that microgravity in outer space increased the level of sclerostin in the scales of goldfish, a finding suggesting that the induction of sclerostin is the mechanism underlying the activation of osteoclasts under microgravity.

摘要

成骨细胞(骨形成细胞)、骨细胞(骨代谢细胞)和破骨细胞(骨吸收细胞)是调节哺乳动物骨代谢的主要细胞类型。骨细胞产生的硬化蛋白激活破骨细胞,抑制骨形成;硬化蛋白过量产生,导致骨量丢失。鱼鳞片的形态和功能与哺乳动物骨骼相似,因此被广泛用作分析脊椎动物体外骨代谢的实验系统。然而,鱼鳞片中是否含有产生硬化蛋白和/或骨细胞的细胞尚未确定。本研究首次证明硬化蛋白阳性细胞存在于金鱼鳞片中。硬化蛋白表达细胞的分布和形态分析表明,成骨细胞在金鱼鳞片中产生硬化蛋白。此外,我们的研究结果发现,金鱼鳞片中存在骨细胞样细胞,这些细胞也产生硬化蛋白。最后,我们证明了外太空微重力增加了金鱼鳞片中硬化蛋白的水平,这一发现表明,硬化蛋白的诱导是微重力下破骨细胞激活的机制。

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