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一种用于引发钙化的弹性蛋白合成五肽。

A synthetic polypentapeptide of elastin for initiating calcification.

作者信息

Hollinger J O, Schmitz J P, Yaskovich R, Long M M, Prasad K U, Urry D W

机构信息

United States Army Institute of Dental Research, Washington, D.C. 20307-5300.

出版信息

Calcif Tissue Int. 1988 Apr;42(4):231-6. doi: 10.1007/BF02553748.

DOI:10.1007/BF02553748
PMID:3135088
Abstract

A polypentapeptide (PPP) of tropoelastin having a repeating amino acid sequence of (Val-Pro-Gly-Val-Gly)n was evaluated for its potential to initiate in vivo calcification and to enhance bone formation in nonhealing calvarial wounds (8.0 mm) in 396 adult Walter Reed rats. There were four configurations of the PPP (molecular weight range of 50-100K dalton) consisting of 1-dry PPP; 2-coacervate PPP; 3-gamma irradiated, cross-linked PPP; 4-calcified, gamma irradiated, cross-linked PPP. These four iterations plus a control group of animals constituted the five treatment classes that were evaluated at days 1, 3, 7, 21, 42, and 147. Seventy two rats were used for each treatment and 36 rats for the control. Following euthanatization, specimens were placed into 70% ethanol, embedded in polymethyl methacrylate, sectioned at 3.5 micrometers, and alternating sections were stained with Masson-Goldner trichrome and von Kossa stains. Histomorphometric analysis was accomplished using a Zeiss Universal microscope (250 X) and Videoplan Image Analysis System to evaluate five random histologic fields from margin to margin of the craniotomy. Trabecular bony volume and area of calcification islands were quantitated. A Student's t test for unpaired data to determine treatment differences (within the same temporal groups) revealed that there was no significant difference between treatments and control for trabecular bony volume; however, there was a significant difference between experimentals and control for calcification islands (P less than 0.05) such that calcifications islands for the experimentals were greater than the control. There was not a significant difference between experimental treatments.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对一种原弹性蛋白的聚五肽(PPP)进行了评估,其氨基酸重复序列为(Val-Pro-Gly-Val-Gly)n,研究其在396只成年沃尔特·里德大鼠的非愈合颅骨伤口(8.0毫米)中引发体内钙化和促进骨形成的潜力。PPP有四种构型(分子量范围为50 - 100K道尔顿),分别为:1 - 干燥PPP;2 - 凝聚层PPP;3 - γ射线辐照交联PPP;4 - 钙化、γ射线辐照交联PPP。这四种变体加上一组对照动物构成了五个治疗组,在第1、3、7、21、42和147天进行评估。每组治疗用72只大鼠,对照组用36只大鼠。安乐死后,将标本放入70%乙醇中,嵌入聚甲基丙烯酸甲酯,切成3.5微米厚的切片,交替切片用马森 - 戈尔纳三色染色法和冯·科萨染色法染色。使用蔡司万能显微镜(250倍)和图像分析系统进行组织形态计量分析,以评估开颅术边缘到边缘的五个随机组织学视野。对小梁骨体积和钙化岛面积进行定量。采用学生t检验(用于非配对数据以确定治疗差异(在同一时间组内))显示,小梁骨体积在治疗组和对照组之间无显著差异;然而,钙化岛在实验组和对照组之间存在显著差异(P小于0.05),即实验组的钙化岛大于对照组。实验治疗组之间无显著差异。(摘要截断于250字)

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本文引用的文献

1
In vivo calcification induced by a proteolipid complex (lysozyme-acidic phospholipid).由蛋白脂质复合物(溶菌酶-酸性磷脂)诱导的体内钙化。
Biomater Med Devices Artif Organs. 1982;10(2):71-83. doi: 10.3109/10731198209118773.
2
A review of the primary mechanism of endochondral calcification with special emphasis on the role of cells, mitochondria and matrix vesicles.软骨内钙化的主要机制综述,特别强调细胞、线粒体和基质小泡的作用。
Clin Orthop Relat Res. 1982 Sep(169):219-42.
3
Calcium phosphate ceramics as hard tissue prosthetics.磷酸钙陶瓷作为硬组织修复体
Clin Orthop Relat Res. 1981 Jun(157):259-78.
4
Elastin structure, biosynthesis, and relation to disease states.弹性蛋白的结构、生物合成及其与疾病状态的关系。
N Engl J Med. 1981 Mar 5;304(10):566-79. doi: 10.1056/NEJM198103053041004.
5
Parathyroid hormone-responsive clonal cell lines from rat osteosarcoma.来自大鼠骨肉瘤的甲状旁腺激素反应性克隆细胞系。
Endocrinology. 1980 Nov;107(5):1494-503. doi: 10.1210/endo-107-5-1494.
6
Isolation and sequence of the vitamin K-dependent protein from human bone. Undercarboxylation of the first glutamic acid residue.人骨中维生素K依赖蛋白的分离与测序。首个谷氨酸残基的羧化不足。
J Biol Chem. 1980 Sep 25;255(18):8685-91.
7
Beta-tricalcium phosphate delivery system for bone morphogenetic protein.用于骨形态发生蛋白的β-磷酸三钙递送系统
Clin Orthop Relat Res. 1984 Jul-Aug(187):277-80.
8
Chemotactic activity of the gamma-carboxyglutamic acid containing protein in bone.骨骼中含γ-羧基谷氨酸蛋白的趋化活性。
Calcif Tissue Int. 1983;35(2):164-8. doi: 10.1007/BF02405025.
9
Demineralized bone-matrix-induced osteogenesis.脱矿骨基质诱导成骨
Clin Orthop Relat Res. 1984 Sep(188):239-51.
10
Coacervation and ion-binding studies on aortic elastin.主动脉弹性蛋白的凝聚和离子结合研究。
Biochim Biophys Acta. 1973 Jun 15;310(2):481-6. doi: 10.1016/0005-2795(73)90132-3.