Evaluating the Histocompatibility of Fishskin Collagen Sponges as Biomaterial in vivo
1 Laboratory of Transplant Engineering, Wuhan Polytechnical University, Wuhan 430023, China
2 College of Chemical and Environmental Engineering, Wuhan Polytechnical University, Wuhan 430023, China
Abstract:This study investigated the cellular permeability, immunogenicity, inflammatory inductivity, biodegradation and deformation of grass carp skin collagen sponge in vivo to evaluate the histocompatibility and compared with pigskin collagen sponge. Fishskin acidsoluble collagen (FA), fishskin pepsinsoluble collagen (FP) and pigskin pepsinsoluble collagen (PP) sponges were prepared by selfassembly and had highly open porous structure with microfibrous. The collage sponges with 2×2×8 mm rod shape were implanted in the adductor longus muscles (n=6 each group) of SD rats. After 1 week, three kinds of materials were penetrated by nucleated cells. There was not significant difference of the inflammatory areas between group FP (7.93±0.77 mm2) and PP (7.49±1.03 mm2), but the area of group FA (9.81±1.42 mm2) was significantly greater. The cross sections of FP pallets were deformed but the borders were clear and the fibrous networks were complete. The fibrous networks of FA pallets were disrupted and the PP pallets’ were disappeared. Assessing the amount of specific IgG antibodies in sera of KM mice (n=5 each group) immunized with collagen solution by ELISA, the OD values of group FA, FP, and PP were (0.602±0.036), (0.518±0.019) and (0.390 ± 0.085). There was only significant difference of the amount of specific IgG between group FA and PP. These results indicated that the three kinds of materials are suitable for cellular immigration. The immune and inflammatory responses to FP sponge are similar to PP sponge. The biological stability of FP sponge is superior to that of FA and PP sponges. Experimental results suggest that fishskin pepsinsoluble collagen sponge has histocompatible advantages among the three kinds of materials.
[1]Marx RE. Bone and bone graft healing [J]. Oral and Maxillofacial Surgery Clinics of North America, 2007, 19(4): 455-466.
[2]Childs SG. Stimulators of bone healing. Biologic and biomechanical [J]. Orthopaedic Nursing, 2003, 22(6): 421-428.
[3]Williams DF. On the mechanisms of biocompatibility [J]. Biomaterials, 2008, 29(20): 2941-2953.
[4]Glowacki J, Mizuno S. Collagen scaffolds for tissue engineering [J]. Biopolymers, 2008, 89(5): 338-344.
[5]Williams DF. On the nature of biomaterials [J]. Biomaterials, 2009, 30(30): 5897-5909.
[6]Singh P, Benjakul S, Maqsood S, et al. Isolation and characterization of collagen extracted from the skin of striped catsh (Pangasianodon hypophthalmus) [J]. Food Chemistry, 2011, 124(1): 97-105.
[7]汪海波, 梁艳萍, 汪海婴, 等. 草鱼鱼鳞胶原蛋白的提取及其部分生物学性能 [J]. 水产学报, 2012, 36(4): 553-561.
[8]Pati F, Datta P, Adhikari B, et al. Collagen scaffolds derived from fresh water fish origin and their biocompatibility. J Biomed Mater Res Part A, 2012, 100〖A(4): 1068-1079.
[9]汪海波, 汪海婴, 梁艳萍, 等. 草鱼鱼鳞胶原蛋白的凝胶性能研究 [J]. 功能材料, 2012, 43(4): 433-437.
[10]方成, 刘立, 胡汉宁, 等. 大鼠双侧供肾左侧原位肾移植模型的建立及肾功能监测 [J]. 中国组织工程研究与临床康复, 2010, 14(53): 9933-9936.
[11]Bodine PV, Billiard J, Moran RA, et al. The Wnt antagonist secreted frizzledrelated protein-1 controls osteoblast and osteocyte apoptosis [J]. Journal of Cellular Biochemistry, 2005, 96(6): 1212-1230.
[12]Gautschi OP, Frey SP, Zellweger R. Bone morphogenetic proteins in clinical applications [J]. ANZ Journal of Surgery, 2007, 77(8): 626-631.
[13]Kawaguchi Y, Kondo E, Kitamura N, et al. In vivo effects of isolated implantation of salmonderived crosslinked atelocollagen sponge into an osteochondral defect [J]. J Mater Sci Mater Med, 2011, 22(2): 397-404.
[14]Kishore V, Uquillas JA, Dubikovsky A, et al. In vivo response to electrochemically aligned collagen bioscaffolds [J]. J Biomed Mater Res Part B, 2012, 100B(2): 400-408.[15]Matsumoto Y, Ikeda K, Yamaya Y, et al. The usefulness of the collagen and elastin sponge derived from salmon as an artificial dermis and scaffold for tissue engineering [J]. Biomed Res, 2011, 32(1): 29-36.
[16]刘新华, 但年华, 李正军, 等. 胶原基复合医用海绵的研究进展 [J]. 西部皮革, 2012, 35(8): 13-18.
[17]Roden RD Jr. Principles of bone grafting [J]. Oral and Maxillofacial Surgery Clinics of North America, 2010, 22(3): 295-300.
[18]李瑞, 王青山. 生物材料生物相容性的评价方法和发展趋势 [J]. 中国组织工程研究与临床康复, 2011, 15(29): 5471-5474.
[19]Yang Shoufeng, Leong KF, Du Zhaohui, et al. The design of scaffolds for use in tissue engineering. Part I. Traditional factors [J]. Tissue Engineering, 2001, 7(6): 679-689.
[20]Woolfson DN, Ryadnov MG. Peptidebased fibrous biomaterials: Some things old, new and borrowed [J]. Current Opinion in Chemical Biology, 2006, 10(6): 559-567.
[21]Blanco NM, Edwards J, Zamboni WA. Dermal substitute (Integra) for open nasal wounds [J]. Plastic and Reconstructive Surgery, 2004, 113(7): 2224-2225.
[22]Ikoma T, Kobayashi H, Tanaka J, et al. Physical properties of type I collagen extracted from fish scales of Pagrus major and Oreochromis Niloticas [J]. International Journal of Biological Macromolecules, 2003, 32(3-5): 199-204.
[23]Kishore V, Bullock W, Sun Xuanhao, et al. Tenogenic differentiation of human MSCs induced by the topography of electrochemically aligned collagen threads [J]. Biomaterials, 2012, 33(7): 2137-2144.
[24]Olde Damink LHH, Dijkstra PJ, Van Luyn MJA, et al. Crosslinking of dermal sheep collagen using hexamethylene diisocyanate [J]. Journal of Materials Science: Materials in Medicine, 1995, 6(7): 429-434.
[25]Lee JM, Edwards HHL, Pereira CA, et al. Crosslinking of tissuederived biomaterials in 1ethyl3(3dimethylaminopropyl)carbodiimide (EDC) [J]. Journal of Materials Science: Materials in Medicine, 1996, 7(9): 531-541.