In vitro response of osteoarthritic chondrocytes and fibroblast-like synoviocytes to a 500-730 kDa hyaluronan amide derivative

被引:41
作者
Brun, Paola [1 ]
Zavan, Barbara [1 ]
Vindigni, Vincenzo [2 ]
Schiavinato, Antonella [3 ]
Pozzuoli, Assunta [4 ]
Iacobellis, Claudio [4 ]
Abatangelo, Giovanni [1 ]
机构
[1] Univ Padua, Dept Biomed Sci, I-35100 Padua, Italy
[2] Univ Padua, Clin Plast Surg, I-35100 Padua, Italy
[3] Fidia Farmaceutici, Qual & Dev, Abano Terme, Italy
[4] Univ Padua, Dipartimento Sci Chirurg Oncol & Gastroenterol, I-35100 Padua, Italy
关键词
hyaluronan; fibroblast-like synoviocytes; chondrocytes; CD44; IL-10; RHEUMATOID-ARTHRITIS; SODIUM HYALURONATE; MOLECULAR-WEIGHT; SYNOVIAL FIBROBLASTS; ARTICULAR CHONDROCYTES; RHEOLOGICAL PROPERTIES; KNEE OSTEOARTHRITIS; MODEL; ACID; CARTILAGE;
D O I
10.1002/jbm.b.32771
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
The aim of this study was to compare the effects of native hyaluronan (HA) with that of its hexadecylamide derivative (HYADD) on proliferation of fibroblast-like synoviocytes (FLS) and chondrocytes. The production of inflammatory and anti-inflammatory cytokines was also analyzed in FLS cultures. The proliferation of osteoarthritis (OA) chondrocytes was enhanced when cells were treated with 0.51.5 mg mL-1 of HA or HYADD (R) 4-G. This effect was completely suppressed by the anti-CD44 antibody. At 0.5 to 1 mg mL-1, HA and HYADD (R) 4-G did not influence the proliferation of normal or pathological FLS; however, at the higher concentration (1.5 mg mL-1), HYADD (R) 4-G did significantly inhibit cell proliferation. As to effects on inflammation, a significant increase in the expression of the IL-10 gene was observed when FLS were pretreated with tumor necrosis factor alpha and then cultured in the presence of 0.5 mg mL-1 HYADD (R) 4-G or HA. The effects of HA derivatives on FLS proliferation and production of anti-inflammatory cytokines indicate that they may be of therapeutic benefit in OA. The longer residence time in the joint cavity, the increased viscoelasticity, and the anti-inflammatory potential of HYADD (R) 4-G make it a better candidate than native HA for OA therapy. (c) 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2012.
引用
收藏
页码:2073 / 2081
页数:9
相关论文
共 60 条
[1]
Abatangelo G, 1999, CLIN ORTHOP RELAT R, V241, P278
[2]
Altman RD, 1998, J RHEUMATOL, V25, P2203
[3]
Long-term effect of sodium hyaluronate (Hyalgan®) on osteoarthritis progression in a rabbit model [J].
Amiel, D ;
Toyoguchi, T ;
Kobayashi, K ;
Bowden, K ;
Amiel, ME ;
Healey, RM .
OSTEOARTHRITIS AND CARTILAGE, 2003, 11 (09) :636-643
[4]
[Anonymous], 2011, US Patent, Patent No. [7863256, 7683256]
[5]
Apoptosis in rheumatoid arthritis [J].
Baier, A ;
Meineckel, I ;
Gay, S ;
Pap, T .
CURRENT OPINION IN RHEUMATOLOGY, 2003, 15 (03) :274-279
[6]
Balazs Endre A, 2004, Surg Technol Int, V12, P278
[7]
Induction of an Antiinflammatory Effect and Prevention of Cartilage Damage in Rat Knee Osteoarthritis by CF101 Treatment [J].
Bar-Yehuda, S. ;
Rath-Wolfson, L. ;
Del Valle, L. ;
Ochaion, A. ;
Cohen, S. ;
Patoka, R. ;
Zozulya, G. ;
Barer, F. ;
Atar, E. ;
Pina-Oviedo, S. ;
Perez-Liz, G. ;
Castel, D. ;
Fishman, P. .
ARTHRITIS AND RHEUMATISM, 2009, 60 (10) :3061-3071
[8]
Effect of hyaluronic acid amide derivative on equine synovial fluid viscoelasticity [J].
Borzacchiello, A. ;
Mayol, L. ;
Schiavinato, A. ;
Ambrosio, L. .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2010, 92A (03) :1162-1170
[9]
The effect of hyaluronan on CD44-mediated survival of normal and hydroxyl radical-damaged chondrocytes [J].
Brun, P ;
Panfilo, S ;
Gordini, DD ;
Cortivo, R ;
Abatangelo, G .
OSTEOARTHRITIS AND CARTILAGE, 2003, 11 (03) :208-216
[10]
Brun P, 1999, J BIOMED MATER RES, V46, P337, DOI 10.1002/(SICI)1097-4636(19990905)46:3<337::AID-JBM5>3.3.CO