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PHOSPHO1——一种在骨骼和软骨矿化部位特异性表达的新型磷酸酶。

PHOSPHO1-A novel phosphatase specifically expressed at sites of mineralisation in bone and cartilage.

作者信息

Houston Brian, Stewart Alan J, Farquharson Colin

机构信息

Roslin Institute, Midlothian, Scotland, United Kingdom.

出版信息

Bone. 2004 Apr;34(4):629-37. doi: 10.1016/j.bone.2003.12.023.

Abstract

Mineralisation of bone and cartilage is essential for skeletal development and function. We have previously reported a novel gene (PHOSPHO1); a member of the large haloacid dehalogenase superfamily of hydrolases which has an active site indicative of a phosphatase. Its high expression in skeletal tissues has led us to speculate that PHOSPHO1 may be involved in the mineralisation process. Therefore, in this study, we have determined that PHOSPHO1 is localized to sites of mineralisation in both cartilage and bone. Recombinant derived PHOSPHO1 protein was produced and affinity purified PHOSPHO1 antiserum was generated and used to immunostain a range of skeletal and soft avian tissues. In addition, PHOSPHO1 gene expression was determined in SaOS-2 and MG-63 osteoblast-like cells by RT-PCR. In diaphyseal cortical bone, immunohistochemistry localized PHOSPHO1 protein to the osteoid layer of the periosteum, forming surfaces of growing osteons, and newly formed osteocytes, whereas the endosteum and closed osteons were negative. In growth plate cartilage, immunoreactivity was limited to the early hypertrophic chondrocytes and the ossification groove of Ranvier. Cartilage remnants and trabecular bone within the primary spongiosa exhibited strong immunoreactivity on their mineralising surfaces. In 17-day-old embryonic calvaria, the osteoid present on the intramembranous and periosteal bone surfaces stained positively for PHOSPHO1. All soft tissues examined were negative. PHOSPHO1 gene expression was detected in mineralising SaOS-2 but not in the non-mineralising MG-63 osteoblast-like cells and gene expression levels were unchanged by dexamethasone, estradiol, 1,25-dihydroxyvitamin D3 or PTHrP treatment. Western analysis of chick growth plate cell lysate yielded bands (30.4 and 28.6 kD) corresponding to transcripts initiated at each of two possible initiation codons indicating the presence of alternative transcripts for PHOSPHO1 in growth cartilage. These results confirm that the PHOSPHO1 protein and gene expression profile is consistent with a role for PHOSPHO1 in bone and cartilage matrix mineralisation.

摘要

骨骼和软骨的矿化对于骨骼发育和功能至关重要。我们之前报道过一个新基因(PHOSPHO1),它是水解酶的大型卤代酸脱卤酶超家族的成员,其活性位点显示它是一种磷酸酶。它在骨骼组织中的高表达使我们推测PHOSPHO1可能参与矿化过程。因此,在本研究中,我们确定PHOSPHO1定位于软骨和骨骼的矿化部位。我们制备了重组来源的PHOSPHO1蛋白,并产生了亲和纯化的PHOSPHO1抗血清,用于对一系列禽类骨骼和软组织进行免疫染色。此外,通过RT-PCR测定了SaOS-2和MG-63成骨细胞样细胞中PHOSPHO1基因的表达。在骨干皮质骨中,免疫组织化学将PHOSPHO1蛋白定位于骨膜的类骨质层、生长骨单位的形成表面以及新形成的骨细胞,而骨内膜和封闭的骨单位呈阴性。在生长板软骨中,免疫反应仅限于早期肥大软骨细胞和Ranvier骨化沟。初级海绵骨内的软骨残余和小梁骨在其矿化表面表现出强烈的免疫反应。在17日龄胚胎颅骨中,膜内和骨膜骨表面的类骨质对PHOSPHO1染色呈阳性。所有检测的软组织均为阴性。在矿化的SaOS-2细胞中检测到PHOSPHO1基因表达,但在非矿化的MG-63成骨细胞样细胞中未检测到,并且地塞米松、雌二醇、1,25-二羟基维生素D3或甲状旁腺激素相关蛋白处理后基因表达水平未改变。对鸡生长板细胞裂解物的蛋白质免疫印迹分析产生了对应于两个可能起始密码子各自起始的转录本的条带(30.4和28.6 kD),表明生长软骨中存在PHOSPHO1的可变转录本。这些结果证实,PHOSPHO1蛋白和基因表达谱与PHOSPHO1在骨和软骨基质矿化中的作用一致。

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