Immunomodulatory effects of amniotic membrane matrix incorporated into collagen scaffolds
Rebecca A. Hortensius
Department of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, 61801
Search for more papers by this authorJill H. Ebens
Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, 61801
Search for more papers by this authorCorresponding Author
Brendan A. C. Harley
Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, 61801
Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, Illinois, 61801
Correspondence to: B.A.C. Harley, Department of Chemical and Biomolecular Engineering, Institute for Genomic Biology, University of Illinois at Urbana-Champaign, 110 Roger Adams Laboratory, 600 S. Mathews Ave. Urbana, IL 61801; e-mail: [email protected]Search for more papers by this authorRebecca A. Hortensius
Department of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, 61801
Search for more papers by this authorJill H. Ebens
Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, 61801
Search for more papers by this authorCorresponding Author
Brendan A. C. Harley
Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, 61801
Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, Illinois, 61801
Correspondence to: B.A.C. Harley, Department of Chemical and Biomolecular Engineering, Institute for Genomic Biology, University of Illinois at Urbana-Champaign, 110 Roger Adams Laboratory, 600 S. Mathews Ave. Urbana, IL 61801; e-mail: [email protected]Search for more papers by this authorAbstract
Adult tendon wound repair is characterized by the formation of disorganized collagen matrix which leads to decreases in mechanical properties and scar formation. Studies have linked this scar formation to the inflammatory phase of wound healing. Instructive biomaterials designed for tendon regeneration are often designed to provide both structural and cellular support. In order to facilitate regeneration, success may be found by tempering the body's inflammatory response. This work combines collagen-glycosaminoglycan scaffolds, previously developed for tissue regeneration, with matrix materials (hyaluronic acid and amniotic membrane) that have been shown to promote healing and decreased scar formation in skin studies. The results presented show that scaffolds containing amniotic membrane matrix have significantly increased mechanical properties and that tendon cells within these scaffolds have increased metabolic activity even when the media is supplemented with the pro-inflammatory cytokine interleukin-1 beta. Collagen scaffolds containing hyaluronic acid or amniotic membrane also temper the expression of genes associated with the inflammatory response in normal tendon healing (TNF-α, COLI, MMP-3). These results suggest that alterations to scaffold composition, to include matrix known to decrease scar formation in vivo, can modify the inflammatory response in tenocytes. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 104A: 1332–1342, 2016.
REFERENCES
- 1 James R, Kesturu G, Balian G, Chhabra AB. Tendon: Biology, biomechanics, repair, growth factors, and evolving treatment options. J Hand Surg Am 2008; 33: 102−112.
- 2 Lin TW, Cardenas L, Soslowsky LJ. Biomechanics of tendon injury and repair. J Biomech 2004; 37: 865−877.
- 3 Diegelmann RF, Evans MC. Wound healing: an overview of acute, fibrotic and delayed healing. Front Biosci 2004; 9: 283−289.
- 4 Eming SA, Krieg T, Davidson JM. Inflammation in wound repair: molecular and cellular mechanisms. J Invest Dermatol 2007; 127: 514−525.
- 5 Zgheib C, Xu J, Liechty KW. Targeting inflammatory cytokines and extracellular matrix composition to promote wound regeneration. Adv Wound Care (New Rochelle) 2014; 3: 344−355.
- 6 Larson BJ, Longaker MT, Lorenz HP. Scarless fetal wound healing: A basic science review. Plast Reconstr Surg 2010; 126: 1172−1180.
- 7 Olutoye OO, Yager DR, Cohen IK, Diegelmann RF. Lower cytokine release by fetal porcine platelets: A possible explanation for reduced inflammation after fetal wounding. J Pediatr Surg 1996; 31: 91−95.
- 8 Olutoye OO, Zhu X, Cass DL, Smith CW. Neutrophil recruitment by fetal porcine endothelial cells: Implications in scarless fetal wound healing. Pediatr Res 2005; 58: 1290−1294.
- 9 Naik-Mathuria B, Gay AN, Zhu X, Yu L, Cass DL, Olutoye OO. Age-dependent recruitment of neutrophils by fetal endothelial cells: implications in scarless wound healing. J Pediatr Surg 2007; 42: 166−171.
- 10 Liechty KW, Adzick NS, Crombleholme TM. Diminished interleukin 6 (IL-6) production during scarless human fetal wound repair. Cytokine 2000; 12: 671.
- 11 Liechty KW, Crombleholme TM, Cass DL, Martin B, Adzick NS. Diminished interleukin-8 (IL-8) production in the fetal wound healing response. J Surg Res 1998; 77: 80−84.
- 12 Beredjiklian PK, Favata M, Cartmell JS, Flanagan CL, Crombleholme TM, Soslowsky LJ. Regenerative versus reparative healing in tendon: A study of biomechanical and histological properties in fetal sheep. Ann Biomed Eng 2003; 31: 1143−1152.
- 13 Longaker MT, Chiu ES, Adzick NS, Stern M, Harrison MR, Stern R. Studies in fetal wound healing. V. A prolonged presence of hyaluronic acid characterizes fetal wound fluid. Ann Surg 1991; 213: 292−296.
- 14 Price RD, Myers S, Leigh IM, Navsaria HA. The role of hyaluronic acid in wound healing: Assessment of clinical evidence. Am J Clin Dermatol 2005; 6: 393–402.
- 15 Voigt J, Driver VR. Hyaluronic acid derivatives and their healing effect on burns, epithelial surgical wounds, and chronic wounds: A systematic review and meta-analysis of randomized controlled trials. Wound Repair Regen 2012; 20: 317−331.
- 16 Thomas SC, Jones LC, Hungerford DS. Hyaluronic acid and its effect on postoperative adhesions in the rabbit flexor tendon. A Preliminary Look. Clin Orthop Relat Res 1986; 281−289.
- 17 Tseng SC, Prabhasawat P, Barton K, Gray T, Meller D. Amniotic membrane transplantation with or without limbal allografts for corneal surface reconstruction in patients with limbal stem cell deficiency. Arch Ophthalmol 1998; 116: 431−441.
- 18 Azuara-Blanco A, Pillai CT, Dua HS. Amniotic membrane transplantation for ocular surface reconstruction. Br J Ophthalmol 1999; 83: 399–402.
- 19 Chen HJ, Pires RT, Tseng SC. Amniotic membrane transplantation for severe neurotrophic corneal ulcers. Br J Ophthalmol 2000; 84: 826−833.
- 20 Kim H, Son D, Choi TH, Jung S, Kwon S, Kim J, et al. Evaluation of an amniotic membrane-collagen dermal substitute in the management of full-thickness skin defects in a pig. Arch Plast Surg 2013; 40: 11−18.
- 21 Koob TJ, Rennert R, Zabek N, Massee M, Lim JJ, Temenoff JS, et al. Biological properties of dehydrated human amnion/chorion composite graft: Implications for chronic wound healing. Int Wound J 2013; 10: 493–500.
- 22 Samandari MH, Yaghmaei M, Ejlali M, Moshref M, Saffar AS. Use of amnion as a graft material in vestibuloplasty: A preliminary report. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2004; 97: 574−578.
- 23 Fairbairn NG, Randolph MA, Redmond RW. The clinical applications of human amnion in plastic surgery. J Plast Reconstr Aesthet Surg 2014; 67: 662−675.
- 24 Niknejad H, Peirovi H, Jorjani M, Ahmadiani A, Ghanavi J, Seifalian AM. Properties of the amniotic membrane for potential use in tissue engineering. Eur Cell Mater 2008; 15: 88–99.
- 25 Willett NJ, Thote T, Lin AS, Moran S, Raji Y, Sridaran S, Stevens HY, Guldberg RE. Intra-articular injection of micronized dehydrated human amnion/chorion membrane attenuates osteoarthritis development. Arthritis Res Ther 2014; 16: R47.
- 26 Farrell E, O'Brien FJ, Doyle P, Fischer J, Yannas I, Harley BA, O'Connell B, Prendergast PJ, Campbell VA. A collagen-glycosaminoglycan scaffold supports adult rat mesenchymal stem cell differentiation along osteogenic and chondrogenic routes. Tissue Eng 2006; 12: 459−468.
- 27 Yannas IV, Lee E, Orgill DP, Skrabut EM, Murphy GF. Synthesis and characterization of a model extracellular matrix that induces partial regeneration of adult mammalian skin. Proc Natl Acad Sci USA 1989; 86: 933−937.
- 28 Harley BA, Freyman TM, Wong MQ, Gibson LJ. A new technique for calculating individual dermal fibroblast contractile forces generated within collagen-GAG scaffolds. Biophys J 2007; 93: 2911−2922.
- 29 Harley BA, Kim HD, Zaman MH, Yannas IV, Lauffenburger DA, Gibson LJ. Microarchitecture of three-dimensional scaffolds influences cell migration behavior via junction interactions. Biophys J 2008; 95: 4013−4024.
- 30 Harley BA, Spilker MH, Wu JW, Asano K, Hsu HP, Spector M, et al. Optimal degradation rate for collagen chambers used for regeneration of peripheral nerves over long gaps. Cells Tissues Organs 2004; 176:153–165.
- 31 O'Brien FJ, Harley BA, Yannas IV, Gibson LJ. The effect of pore size on cell adhesion in collagen-GAG scaffolds. Biomaterials 2005; 26: 433−441.
- 32 Torres DS, Freyman TM, Yannas IV, Spector M. Tendon cell contraction of collagen-GAG matrices in vitro: effect of cross-linking. Biomaterials 2000; 21:1607–1619.
- 33 Murphy GF, Orgill DP, Yannas IV. Partial dermal regeneration is induced by biodegradable collagen-glycosaminoglycan grafts. Lab Invest 1990; 62: 305−313.
- 34 Yannas IV. Tissue and Organ Regeneration in Adults. New York: Springer; 2001.
- 35 Caliari SR, Harley BAC. The effect of anisotropic collagen-GAG scaffolds and growth factor supplementation on tendon cell recruitment, alignment, and metabolic activity. Biomaterials 2011; 32: 5330−5340.
- 36 Hortensius RA, Harley BA. The use of bioinspired alterations in the glycosaminoglycan content of collagen-GAG scaffolds to regulate cell activity. Biomaterials 2013; 34: 7645−7652.
- 37
Miki T,
Marongiu F,
Dorko K,
Ellis EC,
Strom SC. Isolation of amniotic epithelial stem cells. Curr Protoc Stem Cell Biol 2010;Chapter 1:Unit 1E 3.
10.1002/9780470151808.sc01e03s12 Google Scholar
- 38 Hopkinson A, Shanmuganathan VA, Gray T, Yeung AM, Lowe J, James DK, et al. Optimization of amniotic membrane (AM) denuding for tissue engineering. Tissue Eng Part C Methods 2008; 14: 371−381.
- 39 Samuel CS. Determination of collagen content, concentration, and sub-types in kidney tissue. Methods Mol Biol 2009; 466: 223−235.
- 40 Barbosa I, Garcia S, Barbier-Chassefiere V, Caruelle JP, Martelly I, Papy-Garcia D. Improved and simple micro assay for sulfated glycosaminoglycans quantification in biological extracts and its use in skin and muscle tissue studies. Glycobiology 2003; 13: 647−653.
- 41 Caliari SR, Ramirez MA, Harley BAC. The development of collagen-GAG scaffold-membrane composites for tendon tissue engineering. Biomaterials 2011; 32: 8990−8998.
- 42 O'Brien FJ, Harley BA, Yannas IV, Gibson L. Influence of freezing rate on pore structure in freeze-dried collagen-GAG scaffolds. Biomaterials 2004; 25: 1077−1086.
- 43 Olde Damink LHH, Dijkstra PJ, Van Luyn MJA, Van Wachem PB, Nieuwenhuis P, Feijen J. Cross-linking of dermal sheep collagen using a water-soluble carbodiimide. Biomaterials 1996; 17:765–773.
- 44 Harley BA, Leung JH, Silva EC, Gibson LJ. Mechanical characterization of collagen-glycosaminoglycan scaffolds. Acta Biomater 2007; 3: 463−474.
- 45 Kapoor A, Caporali EH, Kenis PJ, Stewart MC. Microtopographically patterned surfaces promote the alignment of tenocytes and extracellular collagen. Acta Biomater 2010; 6: 2580−2589.
- 46 Caliari SR, Harley BA. Composite growth factor supplementation strategies to enhance tenocyte bioactivity in aligned collagen-GAG scaffolds. Tissue Eng Part A 2013; 19: 1100−1112.
- 47 Galatz LM, Sandell LJ, Rothermich SY, Das R, Mastny A, Havlioglu N, et al. Characteristics of the rat supraspinatus tendon during tendon-to-bone healing after acute injury. J Orthop Res 2006; 24: 541−550.
- 48 Manning CN, Havlioglu N, Knutsen E, Sakiyama-Elbert SE, Silva MJ, Thomopoulos S, et al. The early inflammatory response after flexor tendon healing: a gene expression and histological analysis. J Orthop Res 2014; 32: 645−652.
- 49 Armstrong JR, Ferguson MW. Ontogeny of the skin and the transition from scar-free to scarring phenotype during wound healing in the pouch young of a marsupial, Monodelphis domestica. Dev Biol 1995; 169: 242−260.
- 50 Longaker MT, Whitby DJ, Ferguson MW, Lorenz HP, Harrison MR, Adzick NS. Adult skin wounds in the fetal environment heal with scar formation. Ann Surg 1994; 219: 65–72.
- 51 Krummel TM, Nelson JM, Diegelmann RF, Lindblad WJ, Salzberg AM, Greenfield LJ, et al. Fetal response to injury in the rabbit. J Pediatr Surg 1987; 22: 640−644.
- 52 Hu M, Sabelman EE, Cao Y, Chang J, Hentz VR. Three-dimensional hyaluronic acid grafts promote healing and reduce scar formation in skin incision wounds. J Biomed Mater Res B Appl Biomater 2003; 67: 586−592.
- 53 Wilshaw SP, Kearney JN, Fisher J, Ingham E. Production of an acellular amniotic membrane matrix for use in tissue engineering. Tissue Eng 2006; 12: 2117−2129.
- 54 Mozdzen LC, Rodgers RC, Banks JM, Bailey RC, Harley BA. Increasing the strength and bioactivity of collagen scaffolds using customizable arrays of 3D-printed polymer fibers. Under Rev 2015.
- 55 Caliari SR, Weisgerber DW, Ramirez MA, Kelkhoff DO, Harley BAC. The influence of collagen-glycosaminoglycan scaffold relative density and microstructural anisotropy on tenocyte bioactivity and transcriptomic stability. J Mech Behav Biomed Mater 2012; 11: 27–40.