Abstract
Cartilage injuries may be caused by trauma, biomechanical imbalance, or degenerative changes of joint. Unfortunately, cartilage has limited capability to spontaneous repair once damaged and may lead to progressive damage and degeneration. Cartilage tissue-engineering techniques have emerged as the potential clinical strategies. An ideal tissue-engineering approach to cartilage repair should offer good integration into both the host cartilage and the subchondral bone. Cells, scaffolds, and growth factors make up the tissue engineering triad. One of the major challenges for cartilage tissue engineering is cell source and cell numbers. Due to the limitations of proliferation for mature chondrocytes, current studies have alternated to use stem cells as a potential source. In the recent years, a lot of novel biomaterials has been continuously developed and investigated in various in vitro and in vivo studies for cartilage tissue engineering. Moreover, stimulatory factors such as bioactive molecules have been explored to induce or enhance cartilage formation. Growth factors and other additives could be added into culture media in vitro, transferred into cells, or incorporated into scaffolds for in vivo delivery to promote cellular differentiation and tissue regeneration. Based on the current development of cartilage tissue engineering, there exist challenges to overcome. How to manipulate the interactions between cells, scaffold, and signals to achieve the moderation of implanted composite differentiate into moderate stem cells to differentiate into hyaline cartilage to perform the optimum physiological and biomechanical functions without negative side effects remains the target to pursue.
Original language | English |
---|---|
Pages (from-to) | 149-155 |
Number of pages | 7 |
Journal | Biomedical Engineering - Applications, Basis and Communications |
Volume | 21 |
Issue number | 3 |
DOIs | |
Publication status | Published - Jun 1 2009 |
Externally published | Yes |
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Keywords
- Cartilage
- Chondrocyte
- Growth factor
- Regenerative medicine
- Scaffold
- Stem cell
- Tissue engineering
ASJC Scopus subject areas
- Bioengineering
- Biophysics
- Biomedical Engineering
Cite this
Trends and challenges of cartilage tissue engineering. / Fang, Hsu Wei.
In: Biomedical Engineering - Applications, Basis and Communications, Vol. 21, No. 3, 01.06.2009, p. 149-155.Research output: Contribution to journal › Review article
}
TY - JOUR
T1 - Trends and challenges of cartilage tissue engineering
AU - Fang, Hsu Wei
PY - 2009/6/1
Y1 - 2009/6/1
N2 - Cartilage injuries may be caused by trauma, biomechanical imbalance, or degenerative changes of joint. Unfortunately, cartilage has limited capability to spontaneous repair once damaged and may lead to progressive damage and degeneration. Cartilage tissue-engineering techniques have emerged as the potential clinical strategies. An ideal tissue-engineering approach to cartilage repair should offer good integration into both the host cartilage and the subchondral bone. Cells, scaffolds, and growth factors make up the tissue engineering triad. One of the major challenges for cartilage tissue engineering is cell source and cell numbers. Due to the limitations of proliferation for mature chondrocytes, current studies have alternated to use stem cells as a potential source. In the recent years, a lot of novel biomaterials has been continuously developed and investigated in various in vitro and in vivo studies for cartilage tissue engineering. Moreover, stimulatory factors such as bioactive molecules have been explored to induce or enhance cartilage formation. Growth factors and other additives could be added into culture media in vitro, transferred into cells, or incorporated into scaffolds for in vivo delivery to promote cellular differentiation and tissue regeneration. Based on the current development of cartilage tissue engineering, there exist challenges to overcome. How to manipulate the interactions between cells, scaffold, and signals to achieve the moderation of implanted composite differentiate into moderate stem cells to differentiate into hyaline cartilage to perform the optimum physiological and biomechanical functions without negative side effects remains the target to pursue.
AB - Cartilage injuries may be caused by trauma, biomechanical imbalance, or degenerative changes of joint. Unfortunately, cartilage has limited capability to spontaneous repair once damaged and may lead to progressive damage and degeneration. Cartilage tissue-engineering techniques have emerged as the potential clinical strategies. An ideal tissue-engineering approach to cartilage repair should offer good integration into both the host cartilage and the subchondral bone. Cells, scaffolds, and growth factors make up the tissue engineering triad. One of the major challenges for cartilage tissue engineering is cell source and cell numbers. Due to the limitations of proliferation for mature chondrocytes, current studies have alternated to use stem cells as a potential source. In the recent years, a lot of novel biomaterials has been continuously developed and investigated in various in vitro and in vivo studies for cartilage tissue engineering. Moreover, stimulatory factors such as bioactive molecules have been explored to induce or enhance cartilage formation. Growth factors and other additives could be added into culture media in vitro, transferred into cells, or incorporated into scaffolds for in vivo delivery to promote cellular differentiation and tissue regeneration. Based on the current development of cartilage tissue engineering, there exist challenges to overcome. How to manipulate the interactions between cells, scaffold, and signals to achieve the moderation of implanted composite differentiate into moderate stem cells to differentiate into hyaline cartilage to perform the optimum physiological and biomechanical functions without negative side effects remains the target to pursue.
KW - Cartilage
KW - Chondrocyte
KW - Growth factor
KW - Regenerative medicine
KW - Scaffold
KW - Stem cell
KW - Tissue engineering
UR - http://www.scopus.com/inward/record.url?scp=68249150987&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=68249150987&partnerID=8YFLogxK
U2 - 10.4015/S1016237209001209
DO - 10.4015/S1016237209001209
M3 - Review article
AN - SCOPUS:68249150987
VL - 21
SP - 149
EP - 155
JO - Journal of Chinese Corrosion Engineering
JF - Journal of Chinese Corrosion Engineering
SN - 1016-2372
IS - 3
ER -