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甲状旁腺激素相关蛋白在伴高钙血症的胰腺内分泌细胞瘤中的表达与加工

Expression and processing of parathyroid hormone-related protein in a pancreatic endocrine cell tumour associated with hypercalcaemia.

作者信息

Ratcliffe W A, Bowden S J, Dunne F P, Hughes S, Emly J F, Baker J T, Pye J K, Williams C P

机构信息

Wolfson Research Laboratories, Queen Elizabeth Medical Centre, Birmingham, UK.

出版信息

Clin Endocrinol (Oxf). 1994 May;40(5):679-86. doi: 10.1111/j.1365-2265.1994.tb03021.x.

Abstract

We describe a patient with a neuroendocrine tumour of the pancreas associated with hypercalcaemia which was attributed to production of parathyroid hormone-related protein (PTHrP) by the tumour. Plasma PTHrP 1-86 was significantly raised, and fell following surgical resection of the tumour. PTHrP mRNA and peptide were identified in tumour tissue by in-situ hybridization and immunohistochemistry respectively. PTHrP was quantitated in an extract of tumour tissue by three region-specific immunoassays (PTHrP 1-34 45.2 pmol/g, PTHrP 37-67 81.7 pmol/g, PTHrP 1-86 27.3 pmol/g) and suggested the presence of excess of amino-terminal and mid-region immunoreactivity. On chromatography of the tumour extract the first peak eluted as 22 kDa and comprised approximately equimolar 1-34, 37-67 and 1-86 activities. The second and major peak of 16 kDa contained only 37-67 activity, while the third peak of 6 kDa contained only 1-34 activity. This suggested that the tumour contained a native or intact form of PTHrP together with two major subfragments containing 37-67 and 1-34 activity respectively. Thus chromatographic separation and quantitation of PTHrP by region-specific immunoassays have provided new information on in-vivo proteolytic processing by tumour tissue by indicating that a site of cleavage is located between residues 17 and 61. Our findings are compatible with cleavage at residue 37, a site previously indicated from in-vitro studies.

摘要

我们描述了一名患有胰腺神经内分泌肿瘤并伴有高钙血症的患者,高钙血症归因于肿瘤产生甲状旁腺激素相关蛋白(PTHrP)。血浆PTHrP 1 - 86显著升高,肿瘤手术切除后下降。分别通过原位杂交和免疫组织化学在肿瘤组织中鉴定出PTHrP mRNA和肽。通过三种区域特异性免疫测定法对肿瘤组织提取物中的PTHrP进行定量(PTHrP 1 - 34为45.2 pmol/g,PTHrP 37 - 67为81.7 pmol/g,PTHrP 1 - 86为27.3 pmol/g),提示存在过量的氨基末端和中间区域免疫反应性。对肿瘤提取物进行色谱分析时,第一个峰以22 kDa洗脱,包含大约等摩尔的1 - 34、37 - 67和1 - 86活性。第二个也是主要的16 kDa峰仅含有37 - 67活性,而第三个6 kDa峰仅含有1 - 34活性。这表明肿瘤含有一种天然或完整形式的PTHrP以及两个分别含有37 - 67和1 - 34活性的主要亚片段。因此,通过区域特异性免疫测定法对PTHrP进行色谱分离和定量,通过表明切割位点位于第17和61位残基之间,为肿瘤组织体内蛋白水解加工提供了新信息。我们的发现与在第37位残基处的切割相符,这是先前体外研究表明的一个位点。

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