Viability and function of autologous and allogeneic fibroblasts seeded in dermal substitutes after implantation

被引:60
作者
Morimoto, N
Saso, Y
Tomihata, K
Taira, T
Takahashi, Y
Ohta, M
Suzuki, S
机构
[1] Kyoto Univ, Grad Sch Med, Dept Plast & Reconstruct Surg, Sakyo Ku, Kyoto 6068507, Japan
[2] GUNZE Ltd, Dept Res & Dev, Kyoto, Japan
关键词
collagen sponge; autologous dermal substitute; allogeneic dermal substitute; PKH26; wound healing;
D O I
10.1016/j.jss.2004.11.012
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background. Fibroblast-seeded collagen sponges have been used for the treatment of skin defects and skin ulcers. However, the viability of the fibroblasts after implantation is still unknown. The objective of this study was to investigate the viability and distribution of autologous and allogeneic fibroblasts after implantation and to clarify which type is more effective for wound healing. Materials and methods. Skin samples of Hartley guinea pigs were retrieved and autologous fibroblasts were isolated and cultured. Fibroblasts isolated from the skin of a Strain2 guinea pig were used as allogeneic fibroblasts. Three full-thickness wounds were created on the backs of guinea pigs and an acellular collagen sponge, a collagen sponge seeded with autologous fibroblasts, and a collagen sponge seeded with allogeneic fibroblasts were transplanted. Before implantation, fibroblasts were labeled with PKH26. The guinea pigs were sacrificed 1, 2, and 3 weeks after implantation. The epithelization and contraction of the wounds were assessed, and the viability and distribution of the seeded fibroblasts were observed in cross sections. Results. Three weeks after implantation, the PKH26-labeled autologous and allogeneic fibroblasts remained viable. In the wounds covered with the autologous fibroblast-seeded collagen sponge, the epithelization was fastest, and the percent wound contraction was smallest. In contrast, in the wounds covered with allogeneic fibroblasts, the epithelization was slowest and the percent contraction was largest. Conclusion. The allogeneic fibroblasts seeded in the collagen sponge survived and remained viable on the grafted area, but did not accelerate wound healing. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:56 / 67
页数:12
相关论文
共 34 条
[1]
LIVING TISSUE FORMED INVITRO AND ACCEPTED AS SKIN-EQUIVALENT TISSUE OF FULL THICKNESS [J].
BELL, E ;
EHRLICH, HP ;
BUTTLE, DJ ;
NAKATSUJI, T .
SCIENCE, 1981, 211 (4486) :1052-1054
[2]
Viability of fibroblast-seeded ligament analogs after autogenous implantation [J].
Bellincampi, LD ;
Closkey, RF ;
Prasad, R ;
Zawadsky, JP ;
Dunn, MG .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1998, 16 (04) :414-420
[3]
The 1999 Clinical Research Award - Cultured skin substitutes combined with integra artificial skin to replace native skin autograft and allograft for the closure of excised full-thickness burns [J].
Boyce, ST ;
Kagan, RJ ;
Meyer, NA ;
Yakuboff, KP ;
Warden, GD .
JOURNAL OF BURN CARE & REHABILITATION, 1999, 20 (06) :453-461
[4]
SURVIVAL OF CULTURED ALLOGENEIC KERATINOCYTES TRANSPLANTED TO DEEP DERMAL BED ASSESSED WITH PROBE SPECIFIC FOR Y-CHROMOSOME [J].
BRAIN, A ;
PURKIS, P ;
COATES, P ;
HACKETT, M ;
NAVSARIA, H ;
LEIGH, I .
BRITISH MEDICAL JOURNAL, 1989, 298 (6678) :917-919
[5]
Rapid healing of venous ulcers and lack of clinical rejection with an allogeneic cultured human skin equivalent [J].
Falanga, V ;
Margolis, D ;
Alvarez, O ;
Auletta, M ;
Maggiacomo, F ;
Altman, M ;
Jensen, J ;
Sabolinski, M ;
Hardin-Young, J .
ARCHIVES OF DERMATOLOGY, 1998, 134 (03) :293-300
[6]
HANSBROUGH JF, 1992, SURGERY, V111, P438
[7]
Horan P K, 1990, Methods Cell Biol, V33, P469
[8]
STABLE CELL-MEMBRANE LABELING [J].
HORAN, PK ;
SLEZAK, SE .
NATURE, 1989, 340 (6229) :167-168
[9]
FIBROBLASTS IN ISOGENEIC SKIN EQUIVALENTS PERSIST FOR LONG PERIODS AFTER GRAFTING [J].
HULL, BE ;
SHER, SE ;
ROSEN, S ;
CHURCH, D ;
BELL, E .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1983, 81 (05) :436-438
[10]
Accelerated tissue regeneration through incorporation of basic fibroblast growth factor-impregnated gelatin microspheres into artificial dermis [J].
Kawai, K ;
Suzuki, S ;
Tabata, Y ;
Ikada, Y ;
Nishimura, Y .
BIOMATERIALS, 2000, 21 (05) :489-499