Synovial mesenchymal stem cells from osteo- or rheumatoid arthritis joints exhibit good potential for cartilage repair using a scaffold-free tissue engineering.

Slides:



Advertisements
Similar presentations
Trichostatin A, a histone deacetylase inhibitor, suppresses synovial inflammation and subsequent cartilage destruction in a collagen antibody-induced.
Advertisements

The effect of platelet-rich plasma on the regenerative therapy of muscle derived stem cells for articular cartilage repair  Y. Mifune, T. Matsumoto, K.
M. M. J. Caron, P. J. Emans, M. M. E. Coolsen, L. Voss, D. A. M
Volume 29, Issue 6, Pages (June 2013)
Do adipose tissue-derived mesenchymal stem cells have the same osteogenic and chondrogenic potential as bone marrow-derived cells?  Gun-II Im, M.D., Yong-Woon.
Treatment of a full-thickness articular cartilage defect in the femoral condyle of an athlete with autologous bone-marrow stromal cells  R. Kuroda, M.D.,
Neo-cartilage engineered from primary chondrocytes is epigenetically similar to autologous cartilage, in contrast to using mesenchymal stem cells  N.
B. Bai, Y. Li  Osteoarthritis and Cartilage 
Chondro-protective effects of low intensity pulsed ultrasound
Chondrocytes extract from patients with osteoarthritis induces chondrogenesis in infrapatellar fat pad-derived stem cells  E. López-Ruiz, M. Perán, J.
BMP-2 induces the expression of chondrocyte-specific genes in bovine synovium- derived progenitor cells cultured in three-dimensional alginate hydrogel 
Muscle cell-derived factors inhibit inflammatory stimuli-induced damage in hMSC- derived chondrocytes  R.S. Rainbow, H. Kwon, A.T. Foote, R.C. Preda, D.L.
Implantation of bone marrow-derived buffy coat can supplement bone marrow stimulation for articular cartilage repair  L.H. Jin, B.H. Choi, Y.J. Kim, S.R.
Trichostatin A, a histone deacetylase inhibitor, suppresses synovial inflammation and subsequent cartilage destruction in a collagen antibody-induced.
Granulocyte macrophage – colony stimulating factor (GM-CSF) significantly enhances articular cartilage repair potential by microfracture  M.-D. Truong,
Combination of ADMSCs and chondrocytes reduces hypertrophy and improves the functional properties of osteoarthritic cartilage  M.R. Ahmed, A. Mehmood,
M. M. J. Caron, P. J. Emans, M. M. E. Coolsen, L. Voss, D. A. M
Synovial mesenchymal stem cells from osteo- or rheumatoid arthritis joints exhibit good potential for cartilage repair using a scaffold-free tissue engineering.
Mesenchymal stromal cells for cartilage repair in osteoarthritis
Intra-articular injection of microRNA-140 (miRNA-140) alleviates osteoarthritis (OA) progression by modulating extracellular matrix (ECM) homeostasis.
Intermittent cyclic mechanical tension promotes endplate cartilage degeneration via canonical Wnt signaling pathway and E-cadherin/β-catenin complex cross-talk 
X. Zhang, I. Prasadam, W. Fang, R. Crawford, Y. Xiao 
The effect of platelet-rich plasma on the regenerative therapy of muscle derived stem cells for articular cartilage repair  Y. Mifune, T. Matsumoto, K.
Acute inflammation with induction of anaphylatoxin C5a and terminal complement complex C5b-9 associated with multiple intra-articular injections of hylan.
Deiodinase 2 upregulation demonstrated in osteoarthritis patients cartilage causes cartilage destruction in tissue-specific transgenic rats  H. Nagase,
Neo-cartilage engineered from primary chondrocytes is epigenetically similar to autologous cartilage, in contrast to using mesenchymal stem cells  N.
Characterization of cells from pannus-like tissue over articular cartilage of advanced osteoarthritis  G.-H Yuan, M.D., Ph.D., M Tanaka, V.M.D., K Masuko-Hongo,
H. Bretschneider, M. Stiehler, A. Hartmann, E. Boger, C. Osswald, J
Evaluation of histological scoring systems for tissue-engineered, repaired and osteoarthritic cartilage  M. Rutgers, M.J.P. van Pelt, W.J.A. Dhert, L.B.
A review of the effects of insulin-like growth factor and platelet derived growth factor on in vivo cartilage healing and repair  M.B. Schmidt, Ph.D.,
Effect of glucosamine and its peptidyl-derivative on the production of extracellular matrix components by human primary chondrocytes  D. Stoppoloni, L.
Repair of full-thickness femoral condyle cartilage defects using allogeneic synovial cell- engineered tissue constructs  M. Pei, F. He, B.M. Boyce, V.L.
K.A. Payne, D.M. Didiano, C.R. Chu  Osteoarthritis and Cartilage 
G.-I. Im, H.-J. Kim  Osteoarthritis and Cartilage 
Differential expression of leptin and leptin's receptor isoform (Ob-Rb) mRNA between advanced and minimally affected osteoarthritic cartilage; effect.
Toward scaffold-based meniscus repair: effect of human serum, hyaluronic acid and TGF-ß3 on cell recruitment and re-differentiation  U. Freymann, M. Endres,
The support of matrix accumulation and the promotion of sheep articular cartilage defects repair in vivo by chitosan hydrogels  T. Hao, N. Wen, J.-K.
H.H. Lee, M.J. O'Malley, N.A. Friel, C.R. Chu 
Evaluation of autologous chondrocyte transplantation via a collagen membrane in equine articular defects – results at 12 and 18 months  D.D. Frisbie,
P. C. Kreuz, C. Gentili, B. Samans, D. Martinelli, J. P. Krüger, W
Human synovial fluid derived mesenchymal stem cells expanded under low oxygen conditions and in a serum-free environment exhibit enhanced lineage-specific.
The use of hyperosmotic saline for chondroprotection: implications for orthopaedic surgery and cartilage repair  N.M. Eltawil, S.E.M. Howie, A.H.R.W.
Treatment of a full-thickness articular cartilage defect in the femoral condyle of an athlete with autologous bone-marrow stromal cells  R. Kuroda, M.D.,
Intra-articular injection of human mesenchymal stem cells (MSCs) promote rat meniscal regeneration by being activated to express Indian hedgehog that.
M.M.-G. Sun, F. Beier  Osteoarthritis and Cartilage 
Expression of the semicarbazide-sensitive amine oxidase in articular cartilage: its role in terminal differentiation of chondrocytes in rat and human 
C. Candrian, S. Miot, F. Wolf, E. Bonacina, S. Dickinson, D. Wirz, M
Intra-individual comparison of human ankle and knee chondrocytes in vitro: relevance for talar cartilage repair  C. Candrian, M.D., E. Bonacina, B.Sc.,
Repair of full-thickness femoral condyle cartilage defects using allogeneic synovial cell- engineered tissue constructs  M. Pei, F. He, B.M. Boyce, V.L.
Destabilization of the medial meniscus leads to subchondral bone defects and site- specific cartilage degeneration in an experimental rat model  H. Iijima,
E. Farrell, P. Wielopolski, P. Pavljasevic, N. Kops, H. Weinans, M. R
Photo-crosslinked alginate hydrogels support enhanced matrix accumulation by nucleus pulposus cells in vivo  A.I. Chou, S.O. Akintoye, S.B. Nicoll  Osteoarthritis.
M. M. J. Caron, P. J. Emans, M. M. E. Coolsen, L. Voss, D. A. M
Lentiviral vector-mediated shRNAs targeting a functional isoform of the leptin receptor (Ob-Rb) inhibit cartilage degeneration in a rat model of osteoarthritis 
Synergistic effects of growth and differentiation factor-5 (GDF-5) and insulin on expanded chondrocytes in a 3-D environment  B. Appel, J. Baumer, D.
Differential cartilaginous tissue formation by human synovial membrane, fat pad, meniscus cells and articular chondrocytes  A. Marsano, M.Sc., S.J. Millward-Sadler,
T. Kurth, M. Sc. , E. Hedbom, Ph. D. , N. Shintani, Ph. D. , M
Utility of T2 mapping and dGEMRIC for evaluation of cartilage repair after allograft chondrocyte implantation in a rabbit model  J. Endo, A. Watanabe,
M. A. Cleary, R. Narcisi, K. Focke, R. van der Linden, P. A. J
Autologous chondrocyte implantation (ACI) for aged patients: development of the proper cell expansion conditions for possible therapeutic applications 
Growth characterization of neo porcine cartilage pellets and their use in an interactive culture model  Carsten Lübke, Ph.D., Jochen Ringe, M.Sc., Veit.
Joint instability leads to long-term alterations to knee synovium and osteoarthritis in a rabbit model  C. Egloff, D.A. Hart, C. Hewitt, P. Vavken, V.
An experimental study on costal osteochondral graft
Magnesium enhances adherence and cartilage formation of synovial mesenchymal stem cells through integrins  M. Shimaya, T. Muneta, S. Ichinose, K. Tsuji,
Do adipose tissue-derived mesenchymal stem cells have the same osteogenic and chondrogenic potential as bone marrow-derived cells?  Gun-II Im, M.D., Yong-Woon.
Identification of molecular markers for articular cartilage
Membrane culture and reduced oxygen tension enhances cartilage matrix formation from equine cord blood mesenchymal stromal cells in vitro  C. Co, M.K.
The detached osteochondral fragment as a source of cells for autologous chondrocyte implantation (ACI) in the ankle joint  S. Giannini, M.D., R. Buda,
Chondro-protective effects of low intensity pulsed ultrasound
Effect of expansion medium on ex vivo gene transfer and chondrogenesis in type II collagen–glycosaminoglycan scaffolds in vitro  R.M. Capito, Ph.D., M.
Presentation transcript:

Synovial mesenchymal stem cells from osteo- or rheumatoid arthritis joints exhibit good potential for cartilage repair using a scaffold-free tissue engineering approach  K. Koizumi, K. Ebina, D.A. Hart, M. Hirao, T. Noguchi, N. Sugita, Y. Yasui, R. Chijimatsu, H. Yoshikawa, N. Nakamura  Osteoarthritis and Cartilage  Volume 24, Issue 8, Pages 1413-1422 (August 2016) DOI: 10.1016/j.joca.2016.03.006 Copyright © 2016 Osteoarthritis Research Society International Terms and Conditions

Fig. 1 Relative gene expression levels of cell pellets composed of SMSCs at different passage number. Gene expression levels of cell pellets cultured in T-MEM for 2 weeks for (a) IL-1b, (b) IL-6, (c) IL-10, (d) MMP-3 and (e) ADAMTS-5, and of cell pellets cultured in C-MEM for 2 weeks for (f) COL2A1 (g) SOX9 and (h) ACAN normalized to GAPDH. Data are represented as mean ± 95% CI. (Bio(+)RA; N = 7, The other groups; N = 6). Osteoarthritis and Cartilage 2016 24, 1413-1422DOI: (10.1016/j.joca.2016.03.006) Copyright © 2016 Osteoarthritis Research Society International Terms and Conditions

Fig. 2 Proliferation assays for SMSCs derived from the four patient groups. Proliferation of SMSCs at passage 4 was assessed using the WST-1 assay and determination of PDT. (a) The margin between the absorbance values at 450 and 690 nm were normalized by the average margin at day 1 in each group. Data represent mean ± 95% CI. (b) PDT were calculated based on the cell number at passage 4 and 5, and the time between the passages. Data are represented as scatter plot. (Bio(+)RA; N = 7, The other groups; N = 6). Osteoarthritis and Cartilage 2016 24, 1413-1422DOI: (10.1016/j.joca.2016.03.006) Copyright © 2016 Osteoarthritis Research Society International Terms and Conditions

Fig. 3 Features of basic TEC composed of SMSCs from the four patient groups. (a) The WW and (b) wet mass of basic TEC comprised of the same number of SMSCs derived from the four patient groups, and at P5 cultured on 12-well culture dishes. Gene expression levels of basic TEC for (c) IL-1b, (d) IL-6, (e) IL-10, (f) MMP-3 and (g) ADAMTS-5 normalized to GAPDH are represented as scatter plot. (Bio(+)RA; N = 7, The other groups; N = 6). Osteoarthritis and Cartilage 2016 24, 1413-1422DOI: (10.1016/j.joca.2016.03.006) Copyright © 2016 Osteoarthritis Research Society International Terms and Conditions

Fig. 4 In vitro chondrogenic potential of basic TEC derived from SMSCs from the four patient groups. Macroscopic view of (a) basic TEC and (b) chondro-TEC. Chondro-TEC are a moderately transparent, thick and hard tissue (cartilage-like). (c) Low- and (d) high-magnification view of a typical chondro-TEC demonstrating cells with lacuna analogous to chondrocytes in cartilage, and with an abundant ECM strongly stained by Safranin O around them. Bar = 50 μm. (e) GAG content (data represent scatter plot, Bio(+)RA; N = 7, The other groups; N = 6) and gene expression levels for (f) COL2A1 (g) SOX9 (h) ACAN normalized to GAPDH (data represented in scatter plot, Bio(+)RA; N = 7, The other groups; N = 6). No significant differences between groups were detected. Osteoarthritis and Cartilage 2016 24, 1413-1422DOI: (10.1016/j.joca.2016.03.006) Copyright © 2016 Osteoarthritis Research Society International Terms and Conditions

Fig. 5 In vivo osteochondral repair in a rat model: implantation of basic TEC arising from SMSCs derived from the four patient groups. (a) Macroscopic view of the knees at sacrifice. There was no detectable apparent synovitis and inflammation. (b) Histology of the tissue after 8 weeks post-surgery stained with H&E, (c) Toluidine Blue (upper line; bar = 200 μm), their high-magnification images (lower line; bar = 30 μm) and (d) Immunohistochemical analysis of repair cartilage stained for type II collagen (Col II). The repair tissue arising from implantation with a TEC from any of the patient groups (N = 9 in each group) resulted in development of a hyaline cartilage-like repair with enriched ECM strongly stained by Toluidine Blue and expressing large quantities of Col II compared to the untreated group (N = 4). In some parts of repair tissue provided in the high-magnification images, the cells in the repair tissue contained lacuna (especially detected in the trauma group), clustering (presented in OA group), and arranged randomly or into columns (presented in intact and RA groups), which are found in articular cartilage tissue. (e) Immunohistochemical analysis of repair tissue stained for type I collagen (Col I) and (f) type X collagen (Col X) suggesting a deficiency of TEC-mediated cartilage in comparison to native articular cartilage. Osteoarthritis and Cartilage 2016 24, 1413-1422DOI: (10.1016/j.joca.2016.03.006) Copyright © 2016 Osteoarthritis Research Society International Terms and Conditions