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Effect of von Willebrand factor coexpression on the synthesis and secretion of factor VIII in Chinese hamster ovary cells.

作者信息

Kaufman R J, Wasley L C, Davies M V, Wise R J, Israel D I, Dorner A J

机构信息

Genetics Institute, Cambridge, Massachusetts 02140.

出版信息

Mol Cell Biol. 1989 Mar;9(3):1233-42. doi: 10.1128/mcb.9.3.1233-1242.1989.

DOI:10.1128/mcb.9.3.1233-1242.1989
PMID:2498645
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC362714/
Abstract

In plasma, antihemophilic factor (factor VIII) exists as a 200-kilodalton heavy-chain polypeptide in a metal ion association with an 80-kilodalton light-chain polypeptide. This complex is bound by hydrophobic and hydrophilic interactions to a large multimeric glycoprotein, von Willebrand factor (vWF). Accumulation of secreted human factor VIII activity expressed in Chinese hamster ovary cells requires the addition of serum in the growth medium, which provides vWF. Here we report that coexpression of vWF with factor VIII in Chinese hamster ovary cells resulted in increased stable accumulation of factor VIII activity in the absence of serum in the growth medium. In the coexpressing cells, the vWF cDNA transcription unit was transcribed to yield mRNA which was efficiently translated. vWF was properly processed and secreted to yield disulfide-bonded high-molecular-weight multimers similar to those observed in vWF secreted from human endothelial cells. Nuclear run-on assays showed that the factor VIII gene was transcribed at a level similar to that of the vWF gene, but the mRNA did not accumulate to high levels in the cytoplasm. In addition, although the translation efficiency of the factor VIII mRNA was similar to that of vWF, the processing and secretion of the factor VIII primary translation product was dramatically reduced compared with vWF. These results demonstrate that in Chinese hamster ovary cells both factor VIII mRNA accumulation and the processing and secretion of the primary factor VIII translation product are inefficient processes.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7afb/362714/acaad0abb1a7/molcellb00051-0373-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7afb/362714/db3f0b5ab422/molcellb00051-0370-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7afb/362714/20f16b99ef40/molcellb00051-0370-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7afb/362714/a51116bdae36/molcellb00051-0371-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7afb/362714/08563234e076/molcellb00051-0372-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7afb/362714/acaad0abb1a7/molcellb00051-0373-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7afb/362714/db3f0b5ab422/molcellb00051-0370-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7afb/362714/20f16b99ef40/molcellb00051-0370-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7afb/362714/a51116bdae36/molcellb00051-0371-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7afb/362714/08563234e076/molcellb00051-0372-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7afb/362714/acaad0abb1a7/molcellb00051-0373-a.jpg

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1
Effect of von Willebrand factor coexpression on the synthesis and secretion of factor VIII in Chinese hamster ovary cells.
Mol Cell Biol. 1989 Mar;9(3):1233-42. doi: 10.1128/mcb.9.3.1233-1242.1989.
2
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Abnormal binding of factor VIII is linked with the substitution of glutamine for arginine 91 in von Willebrand factor in a variant form of von Willebrand disease.在一种血管性血友病的变异形式中,因子VIII的异常结合与血管性血友病因子中精氨酸91被谷氨酰胺替代有关。
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Two novel type 2N von Willebrand disease-causing mutations that result in defective factor VIII binding, multimerization, and secretion of von Willebrand factor.两个导致2N型血管性血友病的新型突变,这些突变导致血管性血友病因子的凝血因子VIII结合、多聚化及分泌缺陷。
Blood. 2000 Mar 15;95(6):2000-7.
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The pro-polypeptide of von Willebrand factor is required for the formation of a functional factor VIII-binding site on mature von Willebrand factor.
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本文引用的文献

1
The importance of activation of antihemophilic globulin and proaccelerin by traces of thrombin in the generation of intrinsic prothrombinase activity.凝血酶痕量激活抗血友病球蛋白和加速素在内在凝血酶原酶活性生成中的重要性。
Blood. 1963 Feb;21:221-36.
2
Antihemophilic globulin assay following plasma infusions in hemophilia.血友病患者血浆输注后的抗血友病球蛋白测定
J Lab Clin Med. 1958 Jun;51(6):850-9.
3
Preparation and properties of bovine factor VIII (antihemophilic factor).牛因子VIII(抗血友病因子)的制备与特性
血管内皮和凝血:稳态、疾病和治疗,重点关注血管性血友病因子和因子 VIII 和 V。
Int J Mol Sci. 2022 Jul 27;23(15):8283. doi: 10.3390/ijms23158283.
4
A novel mouse model of type 2N VWD was developed by CRISPR/Cas9 gene editing and recapitulates human type 2N VWD.通过 CRISPR/Cas9 基因编辑,建立了一种新型的 2N 型血管性血友病(VWD)小鼠模型,可重现人类 2N 型 VWD。
Blood Adv. 2022 May 10;6(9):2778-2790. doi: 10.1182/bloodadvances.2021006353.
5
Genome-scale reconstructions of the mammalian secretory pathway predict metabolic costs and limitations of protein secretion.哺乳动物分泌途径的基因组规模重建预测了蛋白质分泌的代谢成本和限制。
Nat Commun. 2020 Jan 2;11(1):68. doi: 10.1038/s41467-019-13867-y.
6
Status of Recombinant Factor VIII Concentrate Treatment for Hemophilia a in Italy: Characteristics and Clinical Benefits.意大利重组凝血因子VIII浓缩物治疗甲型血友病的现状:特点与临床益处
Front Med (Lausanne). 2019 Dec 3;6:261. doi: 10.3389/fmed.2019.00261. eCollection 2019.
7
Correction of bleeding in experimental severe hemophilia A by systemic delivery of factor VIII-encoding mRNA.通过系统递送编码因子 VIII 的 mRNA 纠正实验性重度血友病 A 的出血。
Haematologica. 2020 Apr;105(4):1129-1137. doi: 10.3324/haematol.2018.210583. Epub 2019 Jul 9.
8
Effect of transmembrane pressure on Factor VIII yield in ATF perfusion culture for the production of recombinant human Factor VIII co-expressed with von Willebrand factor.跨膜压力对与血管性血友病因子共表达的重组人凝血因子VIII在ATF灌注培养中凝血因子VIII产量的影响。
Cytotechnology. 2016 Oct;68(5):1687-96. doi: 10.1007/s10616-015-9918-1. Epub 2015 Oct 13.
9
The important role of von Willebrand factor in platelet-derived FVIII gene therapy for murine hemophilia A in the presence of inhibitory antibodies.血管性血友病因子在存在抑制性抗体的情况下对小鼠甲型血友病进行血小板源性凝血因子VIII基因治疗中的重要作用。
J Thromb Haemost. 2015 Jul;13(7):1301-9. doi: 10.1111/jth.13001. Epub 2015 Jun 11.
10
Gene therapy for hemophilia.血友病的基因治疗。
Front Biosci (Landmark Ed). 2015 Jan 1;20(3):556-603. doi: 10.2741/4324.
Biochemistry. 1980 Feb 5;19(3):401-10. doi: 10.1021/bi00544a001.
4
Number and evolutionary conservation of alpha- and beta-tubulin and cytoplasmic beta- and gamma-actin genes using specific cloned cDNA probes.使用特异性克隆的cDNA探针检测α-和β-微管蛋白以及细胞质β-和γ-肌动蛋白基因的数量和进化保守性。
Cell. 1980 May;20(1):95-105. doi: 10.1016/0092-8674(80)90238-x.
5
Response to infusions of polyelectrolyte fractionated human factor VIII concentrate in human haemophilia A and von Willebrand's disease.人血友病A和血管性血友病患者对输注多电解质分级分离的人凝血因子VIII浓缩物的反应。
Br J Haematol. 1982 Oct;52(2):259-67. doi: 10.1111/j.1365-2141.1982.tb03888.x.
6
Porcine factor VIII:C prepared by affinity interaction with von Willebrand factor and heterologous antibodies: sodium dodecyl sulfate polyacrylamide gel analysis.通过与血管性血友病因子和异源抗体进行亲和相互作用制备的猪凝血因子VIII:C:十二烷基硫酸钠聚丙烯酰胺凝胶分析
Blood. 1982 Mar;59(3):615-24.
7
The role of phospholipid and factor VIIIa in the activation of bovine factor X.磷脂和凝血因子VIIIa在牛凝血因子X激活中的作用。
J Biol Chem. 1981 Apr 10;256(7):3433-42.
8
The effect of thrombin on human factor VIII. Cleavage of the factor VIII procoagulant protein during activation.凝血酶对人凝血因子VIII的作用。活化过程中凝血因子VIII促凝蛋白的裂解。
J Lab Clin Med. 1981 Jan;97(1):50-64.
9
Molecular cloning of a cDNA encoding human antihaemophilic factor.编码人抗血友病因子的cDNA的分子克隆
Nature. 1984;312(5992):342-7. doi: 10.1038/312342a0.
10
Structure of human factor VIII.人凝血因子VIII的结构
Nature. 1984;312(5992):337-42. doi: 10.1038/312337a0.