Collagen |
Electrospinning |
In vitro culture |
Scaffold with hydrogel or without hydrogel, with different cells |
TGF-β1, TGF-β3 |
Meniscus cell, BMSC, synovial cell, cell from the IPFP |
Collagen scaffolds with hydrogels loaded with IPFP cells yielded the highest cell densities with greater deposition of Col I and the highest mechanical properties compared to other cells. |
Baek et al. (2018)
|
Electrospinning |
Ex vivo repair model |
Collagen scaffold with meniscus cells |
- |
Meniscus cell |
Cell-seeded collagen scaffolds resulted in better integration of new tissue with native tissue. |
Baek et al. (2016)
|
Freeze-drying |
Partial meniscus repair |
Intra-articular injections of vehicle or gefitinib |
gefitinib |
- |
Intra-articular injection of gefitinib and implantation of a collagen scaffold enhanced meniscal regeneration. |
Pan et al. (2017)
|
Chemical crosslinking |
In vitro culture |
Scaffold with different PRP or whole blood |
PRP |
Meniscus cell |
PRP has a higher effect on meniscus cell growth and gene expression than whole blood |
Howard et al. (2014)
|
Photocrosslinking |
Partial meniscus repair |
Cells expanded with conditioned medium or growth medium |
TGF-β3 |
TMSC |
Chondrogenic induced cells in the scaffold have more cell proliferation, GAG and collagen deposition for the best meniscal repair |
(Heo et al., 2016; Koh et al., 2017) |
Silk |
Salt porogen leaching, freeze-drying |
In vitro culture |
Different layers of meniscal scaffold |
- |
Fibroblasts at the periphery and chondrocytes at the scaffold center |
Chondrocytes in the inner region enhanced Col I and Col II production, and fibroblasts in the outer region enhanced Col I production. |
Mandal et al. (2011a)
|
3D printing |
Subcutaneous implantation |
- |
- |
Fibrochondrocytes |
The scaffold supported to maintain cell phenotype. |
Bandyopadhyay & Mandal, (2019)
|
Processing into porous matrix |
Partial meniscus repair |
Meniscectomy |
- |
- |
The scaffold provided a degree of articular cartilage protection, improved tibiofemoral contact pressures. |
(Gruchenberg et al., 2014; S. Stein et al., 2019a; S. E. C. Stein et al., 2019b) |
Electrospinning |
Partial meniscus repair |
Meniscectomy |
Sr2+
|
- |
The SP-Sr group regenerated the meniscus, which provided better protection to the articular cartilage and slowed down the progression of arthritis. |
(Y. Li Y et al., 2020) |
Hyaluronic acid |
3D printing |
Partial meniscus repair |
Meniscectomy |
- |
- |
Fibrochondrocyte tissue growed inward and integrated firmly with the surroundings. |
Ghodbane et al. (2019b)
|
Photocrosslinking |
In vitro culture |
Agarose, gelatin, and PCL |
- |
Fibrochondrocyte |
Cells in MeHA were round, and the ratio of deposited Col II to Col I was close to the value of the inner area region of the native meniscus. |
Bahcecioglu et al. (2019b)
|
Electrospinning |
Subcutaneous implantation |
- |
- |
Fibrochondrocyte |
The stiffness of the fibers influenced cell behavior, and cellularity and collagen deposition were greater in the stiffer scaffold. |
Song et al. (2020)
|
Chitosan |
Gel casting |
In vitro culture |
Different ratios of chitosan and gelatin scaffolds |
- |
- |
All groups of scaffolds had good meniscal cytocompatibility and the scaffolds conforming to the mechanical strength of the different layers of the meniscus were prepared by different ratios of chitosan and gelatin. |
Sarem et al. (2013)
|
Crosslinking and dialyzing |
Total meniscus repair |
PVA/CS scaffold with different seed cells |
- |
ADSC and AC |
Extracellular matrix-rich meniscus tissue was regenerated in all experiment groups, but the meniscus in the AC group had the best protection of the femur and tibia. |
Moradi et al. (2017)
|
Extracellular matrix |
Freeze-drying |
Ex vivo repair model |
Different amounts of porcine MDM |
- |
- |
Endogenous meniscal cells and MSCs migrated to the scaffolds, 8% MDM scaffold promoted repair of partial meniscal defects. |
Ruprecht et al. (2019)
|
Freeze-drying |
Ex vivo repair model |
Meniscus suture |
PRP |
Fibrochondrocyte |
The scaffold promoted cell proliferation and infiltration, generated an amorphous extracellular matrix. |
Monibi et al. (2016)
|
Freeze-drying |
Subcutaneous implantation |
Sham-operated |
- |
- |
No sign of inflammation showed on the surrounding of tissues. |
Chen et al. (2015)
|
Freeze-drying |
Total meniscus repair |
DCB scaffold, ECM/DCB scaffold |
- |
- |
The ECM/DCB scaffold promoted fibrochondrocyte proliferation and secretion of collagen and GAG, and also promoted meniscal regeneration and prevented cartilage degeneration. |
Yuan et al. (2016)
|
Thermoresponsive gel |
In vitro culture |
- |
- |
Chondrocyte, fibroblast |
Cell infiltration and proliferation |
Wu et al. (2015)
|
Thermoresponsive gel |
Partial meniscus repair |
Collagen scaffold |
- |
BMSC |
ECM scaffolds induced fibrochondrogenesis of BMSCs and enhanced overall healing and cartilage protection of the meniscus |
Zhong et al. (2020)
|