Hyaluronic acid-based polymers as cell carriers for tissue-engineered repair of bone and cartilage

被引:295
作者
Solchaga, LA
Dennis, JE
Goldberg, VM
Caplan, AI
机构
[1] Case Western Reserve Univ, Dept Biol, Skeletal Res Ctr, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Sch Med, Dept Orthopaed, Cleveland, OH 44106 USA
关键词
D O I
10.1002/jor.1100170209
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Culture-expanded bone marrow-derived mesenchymal progenitor cells differentiate into chondrocytes or osteoblasts when implanted subcutaneously in vivo in combination with an appropriate delivery vehicle. This in vivo implantation technique is used to test new materials as putative delivery vehicles in skeletal tissue-engineering models. HYAFF 11 and ACP sponges, two biomaterials based on hyaluronic acid modified by esterification of the carboxyl groups of the glucuronic acid, were tested as osteogenic or chondrogenic delivery vehicles for rabbit mesenchymal progenitor cells and compared with a well characterized porous calcium phosphate ceramic delivery vehicle. The implant materials were examined by scanning electron microscopy for differences in pore structure or cellular interactions, were quantified for their ability to bind and retain mesenchymal progenitor cells, and were examined histologically for their ability to support osteogene sis and chondrogenesis after subcutaneous implantation into nude mice. The ACP sponge bound the same number of cells as fibronectin-coated ceramic, whereas the HYAFF 11 sponge bound 90% more. When coated with fibronectin, ACP and HYAFF 11 bound, respectively, 100 and 130% more cells than the coated ceramics. HYAFF 11 sponge composites retained their integrity after the 3 or B-week incubation period in the animals and were processed for histomorphometric analysis. As a result of rapid degradation or resorption in vivo, ACP sponges could not be recovered after implantation and could not be analyzed. HYAFF 11 sponges presented more area available for cell attachment and more available volume for newly formed tissue. Following loading with mesenchymal progenitor cells and implantation, the pores of the sponges contained more bone and cartilage than the pores of ceramic cubes at either time point. Thus, relative to ceramic, HYAFF 11 sponges allow incorporation of twice as many cells and produce a 30% increase in the relative amount of bone and cartilage per unit area. Hence, the hyaluronic acid-based delivery vehicles are superior to porous calcium phosphate ceramic with respect to the number of cells loaded per unit volume of implant, and HYAFF 11 sponges are superior to the ceramics with regard to the amount of bone and cartilage formed. Additionally, hyaluronic acid-based vehicles have the advantage of degradation/resorption characteristics that allow complete replacement of the implant with newly formed tissue.
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页码:205 / 213
页数:9
相关论文
共 36 条
[1]   Biodegradable implants for the treatment of osteochondral defects in a goat model [J].
Athanasiou, K ;
Korvick, D ;
Schenck, R .
TISSUE ENGINEERING, 1997, 3 (04) :363-373
[2]   Histological evaluation of the course of healing of canine articular cartilage defects treated with cultured autologous chondrocytes [J].
Breinan, HA ;
Minas, T ;
Barone, L ;
Tubo, R ;
Hsu, HP ;
Shortkroff, S ;
Nehrer, S ;
Sledge, CB ;
Spector, M .
TISSUE ENGINEERING, 1998, 4 (01) :101-114
[3]   MESENCHYMAL STEM-CELLS IN IN BONE-DEVELOPMENT, BONE REPAIR, AND SKELETAL REGENERATION THERAPY [J].
BRUDER, SP ;
FINK, DJ ;
CAPLAN, AI .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1994, 56 (03) :283-294
[4]   Semisynthetic resorbable materials from hyaluronan esterification [J].
Campoccia, D ;
Doherty, P ;
Radice, M ;
Brun, P ;
Abatangelo, G ;
Williams, DF .
BIOMATERIALS, 1998, 19 (23) :2101-2127
[5]  
Dennis J E, 1992, Cell Transplant, V1, P23
[6]   In vivo osteogenesis assay: a rapid method for quantitative analysis [J].
Dennis, JE ;
Konstantakos, EK ;
Arm, D ;
Caplan, AI .
BIOMATERIALS, 1998, 19 (15) :1323-1328
[7]   Chondrocyte transplantation using a collagen bilayer matrix for cartilage repair [J].
Frenkel, SR ;
Toolan, B ;
Menche, D ;
Pitman, MI ;
Pachence, JM .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 1997, 79B (05) :831-836
[8]  
GOSHIMA J, 1991, CLIN ORTHOP RELAT R, V262, P298
[9]   IDENTIFICATION OF AN ALTERNATIVELY SPLICED SITE IN HUMAN-PLASMA FIBRONECTIN THAT MEDIATES CELL TYPE-SPECIFIC ADHESION [J].
HUMPHRIES, MJ ;
AKIYAMA, SK ;
KOMORIYA, A ;
OLDEN, K ;
YAMADA, KM .
JOURNAL OF CELL BIOLOGY, 1986, 103 (06) :2637-2647
[10]   Repair of partial-thickness defects in articular cartilage: Cell recruitment from the synovial membrane [J].
Hunziker, EB ;
Rosenberg, LC .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1996, 78A (05) :721-733