Small intestinal submucosa: A tissue-derived extracellular matrix that promotes tissue-specific growth and differentiation of cells in vitro

Tissue Engineering

Volumn 4, Issue 2, 1998, Pages 157-174

  Voytik Harbin, Sherry L ^a   Brightman, Andrew O ^a   Waisner, Beverly Z ^b   Robinson, J Paul ^b   Lamar, Carlton H ^b  

^a PURDUE UNIVERSITY   (United States)

^b PURDUE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COLLAGEN TYPE 1; MATRIGEL; PLASTIC;

ANIMAL CELL; ARTICLE; CELL DIFFERENTIATION; CELL FUNCTION; CELL GROWTH; CELL INTERACTION; CELL STRUCTURE; EXTRACELLULAR MATRIX; FIBROBLAST; HUMAN; HUMAN CELL; MOUSE; NONHUMAN; PRIORITY JOURNAL; RAT; SMALL INTESTINE; SMOOTH MUSCLE; SQUAMOUS EPITHELIUM; STRUCTURE ACTIVITY RELATION; SUBMUCOSA; SWINE; TISSUE GROWTH;

EID: 0031804280     PISSN: 10763279     EISSN: None     Source Type: Journal    
DOI: 10.1089/ten.1998.4.157     Document Type: Article

References (50)

1. Bissell, M.J., Hall, H.G., and Parry, G. How does the extracellular matrix direct gene expression? J. Theor. Biol. 99, 31, 1982.
2. Bissell, M.J., and Aggeler, J. Dynamic reciprocity: How do extracellular matrix and hormones direct gene expression? In: Cabot, M.C., and McKeehan, W.L., eds. Mechanisms of Signal Transduction by Hormones and Growth Factors. New York: Alan R. Liss, 1987, pp. 251-262.
3. Adams, J.C., and Watt, F.M. Regulation of development and differentiation by the extracellular matrix. Development 117, 1183, 1993.
4. Lelievre, S., Weaver, V.M., and Bissell, M.J. Extracellular matrix signaling from the cellular membrane skeleton to the nuclear skeleton: A model of gene regulation. Recent Prog. Horm. Res. 51, 417, 1996.
5. Leighton, J. Radial histophysiologic gradient culture chamber: Rationale and preparation. In Vitro Cell. Dev. Biol. 27A, 786, 1991.
6. Douglas, W.H., McAteer, J.A., Dell'Orco, R.T., and Phelps, D. Visualization of cellular aggregates cultured on a three-dimensional collagen sponge matrix. In Vitro Cell. Dev. Biol. 16, 306, 1980.
7. Dehm, P., and Kefalides, N.A. The collagenous component of lens basement membrane. The isolation and characterization of an alpha chain size collagenous peptide and its relationship to newly synthesized lens components. J. Biol. Chem. 253, 6680, 1978.
8. Rojkind, M., Gatmaitan, Z., Mackensen, S., Giambrone, M.A., Ponce, P., and Reid, L.M. Connective tissue biomatrix: Its isolation and utilization for long-term cultures of normal rat hepatocytes. J. Cell Biol. 87, 255, 1980.
9. Liotta, L.A., Lee, C.W., and Morakis, D.J. New method for preparing large surfaces of intact human basement membrane for tumor invasion studies. Cancer Lett. 11, 141, 1980.
10. Armstrong, P.B., and Quigley, J.B. Transepithelial invasion and intramesenchymal infiltration of the chick embryo chorioallantois by tumor cell lines. Cancer Res. 42, 1826, 1982.
11. Knapp, P.M., Lingeman, J.E., Siegel, Y.I., Badylak, S.F., and Demeter, R.J. Biocompatibility of small-intestinal submucosa in urinary tract as augmentation cystoplasty graft and injectable suspension. J. Endourol. 8, 125, 1994.
12. Kropp, B.P., Rippy, M.K., Badylak, S.F., Adams, M.C., Keating, M.A., Rink, R.C., and Thor, K.B. Regenerative urinary bladder augmentation using small intestinal submucosa: Urodynamic and histopathological assessment in long-term canine bladder augmentation. J. Urol. 155, 2098, 1996.
13. Prevel, C.D., Eppley, B.L., Summerlin, D.J., Jackson, J.R., McCarty, M., and Badylak, S.F. Small intestinal submucosa (SIS): Utilization for repair of rodent abdominal wall defects. Ann. Plast. Surg. 35, 374, 1995.
14. Badylak, S.F., Tullius, R., Kokini, K., Shelbourne, K.D., Klootwyk, T., Voytik, S.L., Kraine, M.R., and Simmons, C. The use of xenogeneic small intestinal submucosa as a biomaterial for Achille's tendon repair in a dog model. J. Biomed. Mater. Res. 29, 977, 1995.
15. Aiken, S.W., Badylak, S.F., Toombs, J.P., Shelbourne, K.D., Hues, M.C., Lantz, G.C., and Van Sickle, D. Small intestinal submucosa as an intra-articular ligamentous graft material: A pilot study in dogs. V.C.O.T. 7, 124, 1994.
16. Lantz, G.C., Badylak, S.F., Hiles, M.C., Coffey, A.C., Geddes, L.A., Kokini, K., Sandusky, O.E., and Morff, R.J. Small intestinal submucosa as a vascular graft: A review. J. Invest. Surg. 6, 297, 1993.
17. Hodde, J.P., Badylak, S.F., Brightman, A.O., and Voytik-Harbin, S.L. Glycosaminoglycan content of small intestinal submucosa: A bioscaffold for tissue replacement. Tissue Eng. 2, 209, 1996.
18. McPherson, T., and Badylak, S.F. Characterization of fibronectin derived from porcine small intestinal submucosa. Tissue Eng. 4, 75, 1998.
19. Voytik-Harbin, S.L., Brightman, A.O., Waisner, B., Lamar, C.H., and Badylak, S.F. Identification of extractable growth factors from small intestinal submucosa. J. Cell. Biochem. 4, 478, 1997.
20. Carter, W.O., Narayanan, P.K., and Robinson, J.P. Intracellular hydrogen peroxide and Superoxide anion detection in endothelial cells. J. Leuk. Biol. 55, 253, 1994.
21. Singhvi, R., Stephanopoulos, G., and Wang, D. Review: Effects of substratum morphology on cell physiology. Biotechnol. Bioeng. 43, 764, 1994.
22. Martins-Green, M. The dynamics of cell-ECM interactions with implications for tissue engineering. In: Lanza, R.P., Langer, R., and Chick, W.L., eds. Principles of Tissue Engineering. Austin: R.G. Landes Company, 1997, pp. 23-46.
23. Freshney, R. Culture of Animal Cells. A Manual of Basic Technique. New York: Wiley-Liss, Inc., 1994.
24. Langer, R., Vacanti, J., Vacanti, C., Atala, A., Freed, L., and Vunjak-Novakovic, G. Tissue engineering: Biomedical applications. Tissue Eng. l, 151, 1995.
25. Horster, M. Tissue culture in nephrology: Potential and limits for the study of renal disease. Klin. Wochenschr. 58, 965, 1980.
26. Lefebvre, V., Peeters-Joris, C., and Vaes, G. Production of collagens, collagenase and collagenase inhibitor during the dedifferentiation of articular chondrocytes by serial subcultures. Biochem. Biophys. Acta 1051, 266, 1990.
27. Gross, J., Highberger, J., and Schmitt, F. Collagen structures considered as states of aggregation of a kinetic unit. The tropocollagen particle. Proc. Natl. Acad. Sci. U.S.A. 40, 679, 1954.
28. Kleinman, H.K., McGarvey, M.L., Hassell, J.R., and Martin, G.R. Formation of a supramolecular complex is involved in the reconstitution of basement membrane components. Biochemistry 22, 4969, 1983.
29. Kleinman, H.K., McGarvey, M.L., Liotta, L.A., Robey, P.C., Tryggvason, K., and Martin, G.R. Isolation and characterization of type IV procollagen, laminin, and heparan sulfate proteoglycan from the EHS sarcoma. Biochemistry 21, 6188, 1982.
30. Kleinman, H.K., McGarvey, M.L., Hassell, J.R., Star, V.L., Cannon, F.B., Laurie, G.W., and Martin, G.R. Basement membrane complexes with biological activity. Biochemistry 25, 312, 1986.
31. Olsen, B. Matrix molecules and their ligands. In: Lanza, R.P., Langer, R., and Chick, W.L., eds. Principles of Tissue Engineering. Austin: R.G. Landes Company, 1997, pp. 47-65.
32. Madri, J.A., and Williams, S.K. Capillary endothelial cell cultures: Phenotypic modulation by matrix components. J. Cell Biol. 97, 153, 1983.
33. Kennedy, A., Frank, R.N., Sotolongo, L.B., Das, A., and Zhang, N.L. Proliferative response and macromolecular synthesis by ocular cells cultured on extracellular matrix materials. Curr. Eye Res. 9, 307, 1990.
34. Vernon, R.B., Lane, T.F., Angello, J.C., and Sage, H. Adhesions, shape, proliferation, and gene expression of mouse Leydig cells are influenced by extracellular matrix in vitro. Biol. Reprod. 44, 157, 1991.
35. Bergstraesser, L.M., and Weitzman, S.A. Culture of normal and malignant primary human mammary epithelial cells in a physiological manner simulates in vivo growth patterns and allows discrimination of cell type. Cancer Res. 53, 2644, 1993.
36. Elsdale, T., and Bard, J. Collagen substrata for studies on cell behavior. J. Cell Biol. 54, 626, 1972.
37. McGuire, P.G., and Orkin, R.W. Isolation of rat aortic endothelial cells by primary explant techniques and their phenotypic modulation by defined substrata. Lab. Invest. 57, 94, 1987.
38. Kubota, Y., Kleinman, H.K., Martin, G.R., and Lawley, T.J. Role of laminin and basement membrane in the morphological differentiation of human endothelial cells into capillary-like structures. J. Cell Biol. 107, 1589, 1988.
39. Folkman, J., and Haudenschild, C. Angiogenesis in vitro. Nature 288, 551, 1980.
40. Maciag, T., Kadish, J., Wilkins, L., Stemerman, M.B., and Weinstein, R. Organizational behavior of human umbilical vein endothelial cells. J. Cell Biol. 94, 511, 1982.
41. Montesano, R., Orci, L., and Vassalli, P. In vitro rapid organization of endothelial cells into capillary-like networks is promoted by collagen matrices. J. Cell Biol. 97, 1648, 1983.
42. Vernon, R., Angello, J., Iruela-Arispe, M., Lane, T., and Sage, E. Reorganization of basement membrane matrices by cellular traction promotes the formation of cellular networks in vitro. Lab. Invest. 66, 536, 1992.
43. Grant, D.S., Lelkes, P.I., Fukuda, K., and Kleinman, H.K. Intracellular mechanisms involved in basement membrane induced blood vessel differentiation in vitro. In Vitro Cell. Dev. Biol. 27A, 327, 1991.
44. Zimrin, A.B., Villeponteau, B., and Maciag, T. Models of in vitro angiogenesis: Endothelial cell differentiation on fibrin but not matrigel is transcriptionally dependent. Biochem. Biophys. Res. Commun. 213, 630, 1995.
45. Barcellos-Hoff, M.H., Aggeler, J., Ram, T.G., and Bissell, M.J. Functional differentiation and alveolar morphogenesis of primary mammary cultures on reconstituted basement membrane. Development 105, 223, 1989.
46. Yang, J., Richards, J., Guzman, R., Imagawa, W., and Nandi, S. Sustained growth in primary culture of normal mammary epithelial cells embedded in collagen gels. Proc. Natl. Acad. Sci. U.S.A. 77, 2088, 1980.
47. Kirkland, S.C. Polarity and differentiation of human rectal adenocarcinoma cells in suspension and collagen gel cultures. J. Cell. Sci. 91, 615, 1988.
48. Chambard, M., Gabrion, J., and Mauchamp, J. Influence of collagen gel on the orientation of epithelial cell polarity: Follicle formation from isolated thyroid cells and from preformed monolayers. J. Cell Biol. 91, 157, 1981.
49. Birukov, K.G., Frid, M.G., Rogers, J.D., Shirinsky, V.P., Koteliansky, V.E., Campbell, J.H., and Campbell, G.R. Synthesis and expression of smooth muscle phenotype markers in primary culture of rabbit aortic smooth muscle cells: Influence of seeding density and media and relation to cell contractility. Exp. Cell Res. 204, 46, 1993.
50. Baskin, L.S., Howard, P.S., Duckett, J.W., Snyder, H.M., and Macarak, E.J. Bladder smooth muscle cells in culture. I. Identification and characterization. J. Urol. 149, 190, 1993.