Soluble expression of basic fibroblast growth factor and bone morphogenetic protein in Origami2 system and their synergistic effect to promote osteogenesis

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Soluble expression of basic fibroblast growth factor and bone morphogenetic protein in Origami2 system and their synergistic effect to promote osteogenesis

Basic Medicine | 更新时间：2026-01-09

- Soluble expression of basic fibroblast growth factor and bone morphogenetic protein in Origami2 system and their synergistic effect to promote osteogenesis
- Journal of Third Military Medical University Vol. 40, Issue 10, Pages: 882-888(2018)
- 作者机构：
  
  1.400038 重庆，陆军军医大学(第三军医大学)第一附属医院：全军矫形外科中心，组织工程国家地方联合工程实验室，重庆市再生重建医学工程技术研究中心，重庆市组织工程实验室
  2.400038 重庆，陆军军医大学(第三军医大学)第一附属医院：全军烧伤研究所，创伤、烧伤与复合伤国家重点试验室
- 作者简介：
- 基金信息：
  
  the Key Project of Military Logistics(BWS13C014-1);the Military Medical Innovation Plan of Southwest Hospital(SWH2016JSZD-01);the Preresearch Fund of Military Medicine of Third Military Medical University(SWH2013JS04)
- DOI：10.16016/j.1000-5404.201712042
  CLC： R322.71; R394-33; R394.3
- Received：05 December 2017，
  
  Revised：2018-03-09，
  
  Published：30 May 2018
- 稿件说明：
移动端阅览
Bing TU, Jixing YE, Yibo GAN, et al. Soluble expression of basic fibroblast growth factor and bone morphogenetic protein in Origami2 system and their synergistic effect to promote osteogenesis[J]. Journal of Third Military Medical University, 2018, 40(10): 882-888.
DOI：

Bing TU, Jixing YE, Yibo GAN, et al. Soluble expression of basic fibroblast growth factor and bone morphogenetic protein in Origami2 system and their synergistic effect to promote osteogenesis[J]. Journal of Third Military Medical University, 2018, 40(10): 882-888. DOI： 10.16016/j.1000-5404.201712042.

摘要

目的

2

建立优化高效的碱性成纤维细胞生长因子(basic fibroblast growth factor，bFGF)、骨形态发生蛋白2(bone morphogenetic protein，BMP-2)蛋白重组方法，阐明二者在促成骨中的协同效应。

方法

2

优化bFGF和BMP-2成熟肽的基因序列密码子，获得适用于大肠杆菌Origami2体系表达的bFGF及BMP-2成熟肽cDNA片段；利用PCR法将bFGF成熟肽cDNA片段插入原核表达质粒pColdⅡ中，构建重组原核表达质粒pColdⅡ-bFGF；利用PCR法将BMP-2成熟肽cDNA片段插入原核表达质粒pET-30a(+)中，构建重组原核表达质粒pET-30a(+)-BMP-2，转入大肠杆菌Origami2中表达纯化；运用双酶切、质粒测序及Western blot技术证明Origami2表达体系的构建效果；进行细胞增殖实验、碱性磷酸酶(alkaline phosphates

ALP)染色观察和体内成骨效率检测等，探索bFGF、BMP-2在促成骨中的协同效应。

结果

2

双酶切和质粒测序鉴定证明成功构建重组大肠杆菌pColdⅡ-bFGF/Origami2和pET30a(+)-BMP-2/Origami2表达体系，Western blot检测发现蛋白正确表达。经过Ni-NTA亲和层析纯化后bFGF及BMP-2纯度高达90%。通过对二者比例的优化筛选，发现40 ng/mL bFGF+40 ng/mL rhBMP-2时，大鼠骨髓间充质干细胞(bone marrow mesenchymal stem cells，BMSCs)增殖效率、ALP活性及体内成骨效率最高，是二者促成骨的最优效组合。

结论

2

成功构建高效表达的pColdⅡ-bFGF/Origami2和pET30a(+)-BMP-2/Origami2表达体系，实现了bFGF及BMP-2的高效表达。bFGF和BMP-2的优化联合应用具有促成骨协同效应。

Abstract

Objective

2

To establish recombinant expression systems for basic fibroblast growth factor (bFGF) and bone morphogenetic protein (BMP-2) and investigate the synergetic effect of bFGF and BMP-2 in promoting osteogenesis.

Methods

2

The codons encoding mature peptide sequences of bFGF and BMP-2 gene were optimized and their cDNA fragments capable of expressions in

E.coli

Origami2 system were obtained. Using PCR method

the mature peptide cDNA fragments of bFGF and BMP-2 were separately inserted in the prokaryotic expression plasmids pColdⅡ and pET-30a (+) to construct the recombinant expression plasmids pColdⅡ-bFGF and pET-30a (+)-BMP-2

respectively. The plasmids were transferred into

E.coli

Origami2 for expression and the products were purified. Doub

le enzyme digestion

sequencing analysis and Western blotting were used to verify the established Origami2 expression systems. The synergetic effect of the recombinant bFGF and BMP-2 proteins in promoting osteogenesis was tested by observing their effect on proliferation of rat one marrow mesenchymal stem cells (BMSCs)

ALP activity in mouse C2C12 myoblasts and osteogenesis of BMSCs in rat quadriceps femoris

in vivo

.

Results

2

Double enzyme digestion and sequencing analysis verified successful construction of recombinant

E.coli

pColdⅡ-bFGF/Origami2 and pET30a (+)-BMP-2/Origami2 expression systems. Western blotting demonstrated expressions of the two target proteins in the expression systems

and after purification with Ni-NTA affinity chromatography

the expressed bFGF and BMP-2 proteins reached a purity as high as 90%. At the optimized ratio

bFGF (40 ng/mL) combined with rhBMP2 (40 ng/mL) obviously promoted the proliferation of rat BMSCs

enhanced ALP activity in C2C12 myoblasts

and efficiently promoted ectopic osteogenesis of BMSCs in rat quadriceps femoris.

Conclusion

2

We successfully constructed pColdⅡ-bFGF/Origami2 and pET30a (+)-BMP-2/Origami2 expression systems for efficient expression of bFGF and BMP-2. At the optimized ratio

bFGF and BMP-2 produce a synergistic effect to promote osteogenesis of BMSCs.

关键词

Keywords

references

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