Literature DB >> 23077084

In vitro chondrogenesis by BMP6 gene therapy.

Gonca Karagöz Kayabaşi1, R Seda Tiğli Aydin, Menemşe Gümüşderelioğlu.   

Abstract

In this study, the promotion of in vitro chondrogenesis was investigated by using chitosan scaffolds and rat bone marrow-derived mesenchymal stem cells (rBMSCs) which are transfected by BMP6 (bone morphogenetic protein-6) encoding gene. For this purpose, plasmid DNA (pShuttle-rBMP6), the expression vector consisting of the coding sequence of the BMP6 was obtained, and then, it was entrapped in chitosan scaffolds to obtain a gene-activated matrix (GAM). The chitosan scaffolds performed the controlled and sustained release of plasmid DNA, thus they continuously provided the modification of rBMSCs to induce chondrogenic differentiation. In addition, the cells were transfected by lipid-based agent (Lipofectamine) and then, these modified cells were inoculated into the chitosan scaffolds. Furthermore, a group of chitosan scaffolds with nontransfected rBMSCs with recombinant BMP6 free in culture medium was used as control. Comparative results showed that, mitochondrial activities of modified rBMSCs by Lipofectamine and chitosan GAM were significantly higher than those of nontransfected rBMSCs. The observations from scanning electron microscopy analysis confirmed that BMP6 gene-modified rBMSCs differentiated to the chondrogenic phenotype. Highest amount of glycosaminoglycan contents of rBMSCs on GAM concluded that BMP6 gene-activated chitosan scaffold has a potential in the application of cartilage regeneration.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 23077084     DOI: 10.1002/jbm.a.34430

Source DB:  PubMed          Journal:  J Biomed Mater Res A        ISSN: 1549-3296            Impact factor:   4.396


  7 in total

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Authors:  Justin L Madrigal; Roberta Stilhano; Eduardo A Silva
Journal:  Tissue Eng Part B Rev       Date:  2017-03-10       Impact factor: 6.389

Review 2.  BMP gene delivery for skeletal tissue regeneration.

Authors:  Maxim Bez; Gadi Pelled; Dan Gazit
Journal:  Bone       Date:  2020-05-21       Impact factor: 4.398

3.  Non-viral gene-activated matrices: next generation constructs for bone repair.

Authors:  Erica G Tierney; Garry P Duffy; Sally-Ann Cryan; Caroline M Curtin; Fergal J O'Brien
Journal:  Organogenesis       Date:  2013-01-01       Impact factor: 2.500

4.  Effects of phosphorylatable short peptide-conjugated chitosan-mediated IL-1Ra and igf-1 gene transfer on articular cartilage defects in rabbits.

Authors:  Ronglan Zhao; Xiaoxiang Peng; Qian Li; Wei Song
Journal:  PLoS One       Date:  2014-11-12       Impact factor: 3.240

5.  IGF-1 Gene Transfer to Human Synovial MSCs Promotes Their Chondrogenic Differentiation Potential without Induction of the Hypertrophic Phenotype.

Authors:  Yasutoshi Ikeda; Morito Sakaue; Ryota Chijimatsu; David A Hart; Hidenori Otsubo; Kazunori Shimomura; Henning Madry; Tomoyuki Suzuki; Hideki Yoshikawa; Toshihiko Yamashita; Norimasa Nakamura
Journal:  Stem Cells Int       Date:  2017-06-27       Impact factor: 5.443

6.  miR-765 inhibits the osteogenic differentiation of human bone marrow mesenchymal stem cells by targeting BMP6 via regulating the BMP6/Smad1/5/9 signaling pathway.

Authors:  Tao Wang; Chao Zhang; Cihu Wu; Jianyun Liu; Hui Yu; Xiaoou Zhou; Jie Zhang; Xinping Wang; Shan He; Xiaoyuan Xu; Baicheng Ma; Xiangxin Che; Weidong Li
Journal:  Stem Cell Res Ther       Date:  2020-02-14       Impact factor: 6.832

Review 7.  Application of BMP in Bone Tissue Engineering.

Authors:  Liwei Zhu; Yuzhe Liu; Ao Wang; Zhengqing Zhu; Youbin Li; Chenyi Zhu; Zhenjia Che; Tengyue Liu; He Liu; Lanfeng Huang
Journal:  Front Bioeng Biotechnol       Date:  2022-03-31
  7 in total

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