Cartilage tissue engineering and bioreactor systems for the cultivation and stimulation of chondrocytes
- PMID: 17318529
- DOI: 10.1007/s00249-007-0139-1
Cartilage tissue engineering and bioreactor systems for the cultivation and stimulation of chondrocytes
Abstract
Damage to and degeneration of articular cartilage is a major health issue in industrialized nations. Articular cartilage has a particularly limited capacity for auto regeneration. At present, there is no established therapy for a sufficiently reliable and durable replacement of damaged articular cartilage. In this, as well as in other areas of regenerative medicine, tissue engineering methods are considered to be a promising therapeutic component. Nevertheless, there remain obstacles to the establishment of tissue-engineered cartilage as a part of the routine therapy for cartilage defects. One necessary aspect of potential tissue engineering-based therapies for cartilage damage that requires both elucidation and progress toward practical solutions is the reliable, cost effective cultivation of suitable tissue. Bioreactors and associated methods and equipment are the tools with which it is hoped that such a supply of tissue-engineered cartilage can be provided. The fact that in vivo adaptive physical stimulation influences chondrocyte function by affecting mechanotransduction leads to the development of specifically designed bioreactor devices that transmit forces like shear, hydrostatic pressure, compression, and combinations thereof to articular and artificial cartilage in vitro. This review summarizes the basic knowledge of chondrocyte biology and cartilage dynamics together with the exploration of the various biophysical principles of cause and effect that have been integrated into bioreactor systems for the cultivation and stimulation of chondrocytes.
Similar articles
-
Concentric cylinder bioreactor for production of tissue engineered cartilage: effect of seeding density and hydrodynamic loading on construct development.Biotechnol Prog. 2003 Mar-Apr;19(2):510-21. doi: 10.1021/bp0256519. Biotechnol Prog. 2003. PMID: 12675595
-
[Research progress of bioreactor biophysical factors in cartilage tissue engineering].Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2013 Jul;27(7):810-3. Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2013. PMID: 24063168 Review. Chinese.
-
A new bioreactor for the controlled application of complex mechanical stimuli for cartilage tissue engineering.Proc Inst Mech Eng H. 2008 Jul;222(5):705-15. doi: 10.1243/09544119JEIM383. Proc Inst Mech Eng H. 2008. PMID: 18756689
-
Shear and Compression Bioreactor for Cartilage Synthesis.Methods Mol Biol. 2015;1340:221-33. doi: 10.1007/978-1-4939-2938-2_16. Methods Mol Biol. 2015. PMID: 26445842
-
Hydrostatic pressure in articular cartilage tissue engineering: from chondrocytes to tissue regeneration.Tissue Eng Part B Rev. 2009 Mar;15(1):43-53. doi: 10.1089/ten.teb.2008.0435. Tissue Eng Part B Rev. 2009. PMID: 19196119 Free PMC article. Review.
Cited by
-
Regenerative rehabilitation: The role of mechanotransduction in orthopaedic regenerative medicine.J Orthop Res. 2019 Jun;37(6):1263-1269. doi: 10.1002/jor.24205. Epub 2019 Jan 16. J Orthop Res. 2019. PMID: 30561813 Free PMC article. Review.
-
Development and Characterization of Acellular Extracellular Matrix Scaffolds from Porcine Menisci for Use in Cartilage Tissue Engineering.Tissue Eng Part C Methods. 2015 Sep;21(9):971-86. doi: 10.1089/ten.TEC.2015.0036. Epub 2015 Jun 10. Tissue Eng Part C Methods. 2015. PMID: 25919905 Free PMC article.
-
Effects of initial cell density and hydrodynamic culture on osteogenic activity of tissue-engineered bone grafts.PLoS One. 2013;8(1):e53697. doi: 10.1371/journal.pone.0053697. Epub 2013 Jan 11. PLoS One. 2013. PMID: 23326488 Free PMC article.
-
Development of an arbitrary waveform membrane stretcher for dynamic cell culture.Ann Biomed Eng. 2014 May;42(5):1062-73. doi: 10.1007/s10439-014-0976-x. Epub 2014 Jan 29. Ann Biomed Eng. 2014. PMID: 24473700 Free PMC article.
-
A novel system for studying mechanical strain waveform-dependent responses in vascular smooth muscle cells.Lab Chip. 2013 Dec 7;13(23):4573-82. doi: 10.1039/c3lc50894c. Lab Chip. 2013. PMID: 24096612 Free PMC article.
References
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources