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钙离子和破骨细胞生成启动珊瑚衍生大孔构建体诱导骨形成。

Calcium ions and osteoclastogenesis initiate the induction of bone formation by coral-derived macroporous constructs.

机构信息

Bone Research Laboratory, School of Physiology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

出版信息

J Cell Mol Med. 2013 Nov;17(11):1444-57. doi: 10.1111/jcmm.12125. Epub 2013 Sep 23.

Abstract

Coral-derived calcium carbonate/hydroxyapatite macroporous constructs of the genus Goniopora with limited hydrothermal conversion to hydroxyapatite (7% HA/CC) initiate the induction of bone formation. Which are the molecular signals that initiate pattern formation and the induction of bone formation? To evaluate the role of released calcium ions and osteoclastogenesis, 7% HA/CC was pre-loaded with either 500 μg of the calcium channel blocker, verapamil hydrochloride, or 240 μg of the osteoclast inhibitor, biphosphonate zoledronate, and implanted in the rectus abdominis muscle of six adult Chacma baboons Papio ursinus. Generated tissues on days 15, 60 and 90 were analysed by histomorphometry and qRT-PCR. On day 15, up-regulation of type IV collagen characterized all the implanted constructs correlating with vascular invasion. Zoledronate-treated specimens showed an important delay in tissue patterning and morphogenesis with limited bone formation. Osteoclastic inhibition yielded minimal, if any, bone formation by induction. 7% HA/CC pre-loaded with the Ca(++) channel blocker verapamil hydrochloride strongly inhibited the induction of bone formation. Down-regulation of bone morphogenetic protein-2 (BMP-2) together with up-regulation of Noggin genes correlated with limited bone formation in 7% HA/CC pre-loaded with either verapamil or zoledronate, indicating that the induction of bone formation by coral-derived macroporous constructs is via the BMPs pathway. The spontaneous induction of bone formation is initiated by a local peak of Ca(++) activating stem cell differentiation and the induction of bone formation.

摘要

珊瑚衍生的碳酸钙/羟基磷灰石大孔结构的扇珊瑚属,经有限的热液转化为羟基磷灰石(7%HA/CC),可启动骨形成的诱导。那么,启动模式形成和骨形成诱导的分子信号是什么?为了评估释放的钙离子和破骨细胞生成的作用,将 7%HA/CC 预先加载 500μg 钙通道阻滞剂盐酸维拉帕米或 240μg 破骨细胞抑制剂唑来膦酸,并植入六只成年南非大狒狒(Papio ursinus)的腹直肌中。在第 15、60 和 90 天分析生成的组织,通过组织形态计量学和 qRT-PCR 进行分析。在第 15 天,所有植入的结构都表现出 IV 型胶原蛋白的上调,这与血管入侵有关。用唑来膦酸处理的标本表现出组织模式和形态发生的重要延迟,骨形成有限。破骨细胞抑制通过诱导产生最小的,如果有的话,骨形成。预先加载 Ca(++)通道阻滞剂盐酸维拉帕米的 7%HA/CC 强烈抑制骨形成的诱导。骨形态发生蛋白-2(BMP-2)的下调和 Noggin 基因的上调与预先加载维拉帕米或唑来膦酸的 7%HA/CC 中的有限骨形成相关,表明珊瑚衍生的大孔结构的骨形成诱导是通过 BMPs 途径进行的。骨形成的自发诱导是由局部钙峰激活干细胞分化和骨形成诱导引发的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45b9/4117557/4b829b0f2507/jcmm0017-1444-f1.jpg

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