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基质小泡中PHOSPHO1的存在及其在骨骼矿化之前的发育表达。

The presence of PHOSPHO1 in matrix vesicles and its developmental expression prior to skeletal mineralization.

作者信息

Stewart Alan J, Roberts Scott J, Seawright Elaine, Davey Megan G, Fleming Robert H, Farquharson Colin

机构信息

Roslin Institute, Roslin, Midlothian, EH25 9PS, United Kingdom.

Roslin Institute, Roslin, Midlothian, EH25 9PS, United Kingdom.

出版信息

Bone. 2006 Nov;39(5):1000-1007. doi: 10.1016/j.bone.2006.05.014. Epub 2006 Jul 11.

Abstract

PHOSPHO1 is a phosphoethanolamine/phosphocholine phosphatase that has previously been implicated in generating inorganic phosphate (P(i)) for matrix mineralization. In this study, we have investigated PHOSPHO1 mRNA expression during embryonic development in the chick. Whole-mount in situ hybridization indicated that PHOSPHO1 expression occurred prior to E6.5 and was initially restricted to the bone collar within the mid-shaft of the diaphysis of long bones but by E11.5 expression was observed over the entire length of the diaphysis. Alcian blue/alizarin red staining revealed that PHOSPHO1 expression seen in the primary regions of ossification preceded the deposition of mineral, suggesting that it is involved in the initial events of mineral formation. We isolated MVs from growth plate chondrocytes and confirmed the presence of high levels of PHOSPHO1 by immunoblotting. Expression of PHOSPHO1, like TNAP activity, was found to be up-regulated in MVs isolated from chondrocytes induced to differentiate by the addition of ascorbic acid. This suggests that both enzymes may be regulated by similar mechanisms. These studies provide for the first time direct evidence that PHOSPHO1 is present in MVs, and its developmental expression pattern is consistent with a role in the early stages of matrix mineralization.

摘要

PHOSPHO1是一种磷酸乙醇胺/磷酸胆碱磷酸酶,此前被认为与为基质矿化生成无机磷酸盐(P(i))有关。在本研究中,我们调查了鸡胚胎发育过程中PHOSPHO1 mRNA的表达情况。全胚胎原位杂交表明,PHOSPHO1的表达在胚胎第6.5天之前就已出现,最初局限于长骨干中段的骨环,但到胚胎第11.5天时,在骨干的整个长度上都观察到了表达。阿尔新蓝/茜素红染色显示,在骨化的主要区域观察到的PHOSPHO1表达先于矿物质的沉积,这表明它参与了矿物质形成的初始过程。我们从生长板软骨细胞中分离出微泡,并通过免疫印迹证实了高水平PHOSPHO1的存在。发现从添加抗坏血酸诱导分化的软骨细胞中分离出的微泡中,PHOSPHO1的表达与组织非特异性碱性磷酸酶(TNAP)活性一样上调。这表明这两种酶可能受相似机制调控。这些研究首次提供了直接证据,证明PHOSPHO1存在于微泡中,其发育表达模式与在基质矿化早期阶段所起的作用一致。

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