Abstract
Regenerative tissue engineering has the potential to revolutionize reconstructive approaches by providing either prefabricated tissue or responsive biomaterials with patient-specific geometry. The question to ask is how regeneration and repair are controlled in vivo and if a responsive biomaterial system can drive these processes? Does the cellular control lie at the cell-biomaterial nano-interface and do we have the tools to study this? The chemical and structural parameters and molecular linkages of the extracellular matrix that contribute to the internal mechanics of the cell and regulate a remodeling of an implanted biomaterial at the nano-interface have to be identified. This chapter is focused on introducing this concept of nano-scale regulated tissue regeneration by identifying numerous parameters of the biomaterial scaffold and cells so that the cell remodels the biomaterial without the addition of any growth factors, or other regulatory molecules by being influenced by composition, intermolecular linkages, nanostructure, nanomechanics of the biomaterial, and the biological/ chemical/ mechanical balance at the cell-biomaterial interface.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Altman, G.H., Diaz, F., Jakuba, C., Calabro, T., Horan, R.L., Chen, J., Lu, H., Richmond, J., Kaplan, D.L.: Silk-based biomaterials. Biomaterials 24, 401–416 (2003)
Anderson, J.M., Hiltner, A., Wiggins, M., Schubert, M.A., Collier, T.O., Kao, W.J., Mathur, A.B.: Recent Advances in Biomedical Polyurethane Biostability and Biodegradation. Polymer International 46, 163–171 (1998)
Badylak, S.: The extracellular matrix as a scaffold for tissue reconstruction. Cell and Developmental Biology 13, 377–383 (2002)
Badylak, S.: Xenogeneic extracellular matrix as a scaffold for tissue reconstruction. Transplant Immunology 12, 367–377 (2004)
Badylak, S., Kokini, K., Tullius, B., Simmons-Byrd, A., Morff, R.: Morphologic study of small intestinal submucosa as a body wall repair device. Journal of Surgical Research 103, 190–202 (2002)
Badylak, S., Kokini, K., Tullius, B., Whitson, B.: Strength over time of a resorbable bioscaffold for body wall repair in a dog model. Journal of Surgical Research 99, 282–287 (2001)
Balaban, N.Q., Schwarz, U.S., Riveline, D., Goichberg, P., Tzur, G., Sabanay, I., Mahalus, D., Safran, S., Bershadsky, A., Addadi, L., Geiger, B.: Force and focal adhesion assembly: a close relationship studied using elastic micropatterned substrates. Nature Cell Biology 3, 466–472 (2001)
Bos, K.J., Holmes, D.F., Meadows, R.S., Kadler, K.E., McLeod, D., Bishop, P.N.: Collagen fibril organization in mammalian vitreous by freeze etch/ rotary shadowing electron microscopy. Micron 32, 301–306 (2001)
Butler, C.E., Navarro, F.A., Orgill, D.P.: Reduction of abdominal adhesions using composite collagen-GAG implants for ventral hernia repair. Journal of Biomedical Materials Research: Applied Biomaterials 58, 75–80 (2001)
Chiarini, A., Petrini, P., Bozzini, S., Pra, I.D., Armato, U.: Silk fibroin/ poly(carbonate)-urethane as a substrate for cell growth: in vitro interactions with human cells. Biomaterials 24, 789–799 (2003)
Danielson, K.G., Baribault, H., Holmes, D.F., Graham, H., Kadler, K., Iozzo, R.V.: Targeted disruption of decorin leads to abnormal collagen fibril morphology and skin fragility. The Journal of Cell Biology 136(3), 729–743 (1997)
Foschi, D., Corsi, F., Cellerino, P., Rizzi, A., Morandi, E., Trabucchi, E.: Angiogenic effects of suture biomaterials. An experimental study in rats. Eur. Surg. Research 33(1), 16–20 (2001)
Gobin, A.S., Butler, C.E., Mathur, A.B.: Repair and regneration of the abdominal wall musculofascial defect using silk fibroin-chitosan blend. Tissue Engineering 12(12), 3383–3394 (2006)
Gobin, A.S., Froude, V.E., Mathur, A.B.: Structural and mechanical characteristics of silk fibroin and chitosan blend scaffolds for tissue regeneration. J. Biomed. Mat. Res. 74A(3), 465–473 (2005)
Gobin, A.S., West, J.L.: Effects of epidermal growth factor on fibroblast migration through biomimetic hydrogels. Biotechnology Progress 19(6), 1781–1785 (2003)
Higgins, S.P., Solan, A.K., Niklason, L.E.: Effects of polyglycolic acid on porcine smooth muscle cell growth and differentiation. Journal of Biomedical Materials Research 67(1), 295–302 (2003)
Horiuchi, K., Naito, I., Nakano, K., Nakatani, S., Nishida, K., Taguchi, T., Ohtsuka, A.: Three-dimensional ultrastructure of the brush border glycocalyx in the mouse small intestine: a high resolution scanning electron microscopic study. Archives of Histology and Cytology 68(1), 51–56 (2005)
Inoue, S., Magoshi, J., Tanaka, T., Magoshi, Y., Becker, M.: Atomic force microscopy: Bombyx mori silk fibroin molecules and their higher order structure. Journal of polymer science B: Polymer Physics 38, 1436–1439 (2000)
Inouye, K., Kurokawa, M., Nishikawa, S., Tsukada, M.: Use of Bombyx mori silk fibroin as a substratum for cultivation of animal cells. J. Biochem. Biophys. Methods 37, 159–164 (1998)
Iwasaki, S., Hosaka, Y., Iwasaki, T., Yamamoto, K., Nagayasu, A., Ueda, H., Kokai, Y., Takehana, K.: The modulation of collagen fibril assembly and its structure by decorin: An electron microscopic study. Archives of Histology and Cytology 71(1), 37–44 (2008)
Kadler, K.: Matrix Loading: Assembly of extracellular matrix collagen fibrils during embryogenesis. Birth Defects Research (Part C) 72, 1–11 (2004)
Kaplan, D., Adams, W., Farmer, B., Viney, C. (eds.): Silk Polymers Materials Science and Biotechnology. American Chemical Society, Washington (1994)
Li, J., Ogiso, M., Minoura, N.: Enzymatic degradation behavior of porous silk fibroin sheets. Biomaterials 24, 357–365 (2003)
Mathur, A.B., Collinsworth, A.M., Reichert, W.M., Kraus, W.E., Truskey, G.A.: Endothelial, cardiac muscle and skeletal muscle exhibit different viscous and elastic properties as determined by atomic force microscopy. Journal of Biomechanics 34(12), 1545–1553 (2001)
Mathur, A.B., Reichert, W.M., Truskey, G.A.: Flow and high affinity binding affect the elastic modulus of the nucleus, cell body, and the stress fibers of endothelial cells. Annals of Biomedical Engineering 35(7), 1120–1130 (2007)
Mathur, A.B., Tonelli, A.E., Rathke, T., Hudson, S.: The dissolution and characterization of bombyx mori silk fibroin in calcium nitrate-methanol solution and the regeneration of films. Biopolymers 42, 61–74 (1997)
Mathur, A.B., Truskey, G.A., Reichert, W.M.: Atomic force and total internal reflection fluorescence microscopy for the study of force transmission in endothelial cells. Biophysical Journal 78(4), 1725–1735 (2000)
Matthews, B.D., Pratt, B.L., Pollinger, H.S., Backus, C.L., Kercher, K.W., Sing, R.F., Heniford, B.T.: Assessment of adhesion formation to intra-abdominal polypropylene mesh and polytetrafluoroethylene mesh. Journal of Surgical Research 114, 126–132 (2003)
Miller, L., Putthanarat, S., Eby, R., Adams, W.: Investigation of the nanofibrillar morphology of silk fibers by small angle x-ray scattering and atomic force microscopy. International Journal of Biological Macromolecules 24, 159–165 (1999)
Minoura, N., Aiba, S., Gotoh, Y., Tsukada, M., Imai, Y.: Attachment and growth of cultured fibroblast cells on silk protein matrices. Journal of biomedical materials research 29, 1215–1221 (1995)
Miranti, C.K., Brugge, J.S.: Sensing the environment: a historical perspective on integrin signal transduction. Nature Cell Biology 4(4), E83–E90 (2002)
Morita, Y., Tomita, N., Aoki, H., Wakitani, S., Tamada, Y., Suguro, T., Ikeuchi, K.: Visco-elastic properteis of cartilage tissue regenerated wtih fibroin sponge. Bio-Medical Materials and Engineering 12, 291–298 (2002)
Panilaitis, B., Altman, G., Chen, J., Jin, H.-J., Karageorgiou, V., Kaplan, D.: Macrophage response to silk. Biomaterials 24, 3079–3085 (2003)
Pesen, D., Hoh, J.H.: Micromechanical architecture of the endothelial cell cortex. Biophysical Journal 88, 670–679 (2005)
Rao, S., Sharma, C.: Use of chitosan as a biomaterial: studies on its safety and hemostatic potential. Journal of biomedical materials research 34(1), 21–28 (1997)
Rios, C.N., Skoracki, R.J., Miller, M.J., Satterfield, W.C., Mathur, A.B.: In vivo bone formation in silk fibroin and chitosan blend scaffolds via ectopically grafted periosteum as a cell source: a pilot study. Tissue Engineering (February 2009) (in Press)
Santin, M., Motta, A., Freddi, G., Cannas, M.: In vitro evaluation of the inflammatory potential of the silk fibroin. J. Biomed. Mater. Res. 46, 382–389 (1999)
Scott, J.E.: The first and second ’laws’ of chemical morphology, exemplified in mammalian extracellular matrices. European Journal of Histochemistry 46, 111–124 (2002)
Scott, J.E.: Elasticity in extracellular matrix ’shape modules’ of tendon, cartilage, etc. A sliding proteoglycan-filament model. Journal of Physiology 553(Pt 2), 335–343 (2003)
Scott, J.E., Dyne, K.M., Thomlinson, A.M., Ritchie, M., Bateman, J., Cetta, G., Valli, M.: Human cells unable to express decoron produced disorganized extracellular matrix lacking "shape modules" (interfibrillar proteoglycan bridges). Experimental Cell Research 243, 59–66 (1998)
Scott, J.E., Parry, D.A.D.: Control of collagen fibril diameters in tissues. International Journal of Biological Macromolecules 14, 1–2 (1992)
Sofia, S., McCarthy, M., Gronowicz, G., Kaplan, D.: Functionalized silk-based biomaterials for bone formation. Journal of Biomedical Materials Research 54, 139–148 (2001)
Squire, J.M., Chew, M., Nneji, G., Neal, C., Barry, J., Michel, C.: Quasi-periodic substructure in the microvessel endothelial glycocalyx: a possible explanation for molecular filtering. Journal of Structural Biology 136, 239–255 (2001)
Sugihara, A., Sugiura, K., Morita, H., Ninagawa, T., Tubouchi, K., Tobe, R., Izumiya, M., Horio, T., Abraham, N., Ikehara, S.: Promotive effects of a silk film on epidermal recovery from full-thickness skin wounds. P.S. E. B. M. 225, 58–64 (2000)
Tomihata, K., Ikada, Y.: In vitro and in vivo degradation of films of chitin and its deacetylated derivatives. Biomaterials 18(7), 567–575 (1997)
Ushiki, T.: Collagen fibers, reticular fibers, and elastic fibers. A comprehensive understanding from a morphological viewpoint. Archives of Histology and Cytology 65(2), 109–126 (2002)
Vink, H., Duling, B.R.: Identification of distinct luminal domains for macromolecules, erythrocytes, and leukocytes iwthin mammalian capillaries. Circulation Research 79, 581–589 (1996)
Vogel, V., Baneyx, G.: The tissue engineering puzzle: a molecular perspective. Annual Review in Biomedical Engineering 5, 441–463 (2003)
Walpita, D., Hay, E.: Studying actin-dependent processes in tissue culture. Nature Reviews 3, 137–141 (2002)
Weinbaum, S., Zhang, X., Han, Y., Vink, H., Cowin, S.C.: Mechanotransduction and flow across the endothelial glycocalyx. Proceedings of the National Academy of Sciences 100(13), 7988–7995 (2003)
Weis, S.M., Zimmerman, S.D., Shah, M., Covell, J.W., Omens, J.H., Ross, J.J., Dalton, N., Jones, Y., Reed, C.C., Iozzo, R.V., McCulloch, A.D.: A role for decorin in the remodeling of myocardial infarction. Matrix Biology 24(4), 313–324 (2005)
Woods, A., Smith, C.G., Rees, D.A., Wilson, G.: Stages in specialization of fibroblast adhesion and deposition of extracellular matrix. European Journal of Cell Biology 32(1), 108–116 (1983)
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2009 Springer Berlin Heidelberg
About this chapter
Cite this chapter
Mathur, A.B. (2009). Regenerative Wound Healing via Biomaterials. In: Gefen, A. (eds) Bioengineering Research of Chronic Wounds. Studies in Mechanobiology, Tissue Engineering and Biomaterials, vol 1. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-00534-3_18
Download citation
DOI: https://doi.org/10.1007/978-3-642-00534-3_18
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-00533-6
Online ISBN: 978-3-642-00534-3
eBook Packages: EngineeringEngineering (R0)