Literature DB >> 16995793

Novel geometries for tissue-engineered tendonous collagen constructs.

Yaling Shi1, Lawrence Rittman, Ivan Vesely.   

Abstract

A promising approach to addressing the performance limitations of currently available mechanical and bioprosthetic heart valves lies in tissue engineering. Tissue-engineered valves should incorporate the complex microstructure of the native valves to mimic their unique mechanics. This would include a layered topology, mesh networks, and branched collagen fiber bundles. Our approach to heart valve tissue engineering is to develop the functional components of the aortic valve cusps separately in vitro and, once they are mature, integrate them into a composite valve structure. Here we report on our efforts to create more complex collagenous structures, suitable for heart valve tissue engineering. Collagen fiber bundles were fabricated using the principle of directed collagen gel contraction, using neonatal rat aortic smooth muscle cells and acid-soluble type I rat-tail tendon collagen. The collagen gels were cast into rectangular or branched wells with porous end holders that constrained the gels longitudinally but allowed contraction to occur transverse to the long axis. Pairs of such constructs were placed in direct contact with each other and cultured further to determine whether they integrated to form continuous tissue. After 6-8 weeks of culture, highly compacted and aligned collagen fiber bundles formed. Mechanical testing revealed that linear constructs (2 free ends) with an 8:1 aspect ratio were significantly stronger than similar constructs with an aspect ratio of 2:1 (mean +/- SD, 298 +/- 90 kPa vs. 152 +/- 49 kPa; p < .001). Branching reduced mechanical strength considerably. Constructs fabricated with 4 free ends were significantly weaker than constructs with 3 ends (31 +/- 32 kPa vs. 116 +/- 66 kPa; p < .003). Histologic images demonstrated the integration of the crossed collagen bundles, with a bonding strength of 2.1 +/- 1.1 g (0.02 N). We found that the geometry of the molds into which the collagen constructs are cast can greatly affect their mechanical strength: multibranched constructs were the weakest, and long, linear constructs were the strongest. We also found that integration of collagen constructs occurs in vitro and that the fabrication of a composite structure in vitro is probably feasible.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16995793     DOI: 10.1089/ten.2006.12.2601

Source DB:  PubMed          Journal:  Tissue Eng        ISSN: 1076-3279


  10 in total

1.  Interaction of angiogenic microvessels with the extracellular matrix.

Authors:  Laxminarayanan Krishnan; James B Hoying; Hoa Nguyen; Helen Song; Jeffrey A Weiss
Journal:  Am J Physiol Heart Circ Physiol       Date:  2007-10-12       Impact factor: 4.733

2.  Initial fiber alignment pattern alters extracellular matrix synthesis in fibroblast-populated fibrin gel cruciforms and correlates with predicted tension.

Authors:  E A Sander; V H Barocas; R T Tranquillo
Journal:  Ann Biomed Eng       Date:  2010-10-29       Impact factor: 3.934

Review 3.  The heterogeneous biomechanics and mechanobiology of the mitral valve: implications for tissue engineering.

Authors:  K Jane Grande-Allen; Jun Liao
Journal:  Curr Cardiol Rep       Date:  2011-04       Impact factor: 2.931

4.  Engineered skeletal muscle tissue networks with controllable architecture.

Authors:  Weining Bian; Nenad Bursac
Journal:  Biomaterials       Date:  2008-12-12       Impact factor: 12.479

Review 5.  Tissue engineering of functional skeletal muscle: challenges and recent advances.

Authors:  Weining Bian; Nenad Bursac
Journal:  IEEE Eng Med Biol Mag       Date:  2008 Sep-Oct

6.  Mesoscopic hydrogel molding to control the 3D geometry of bioartificial muscle tissues.

Authors:  Weining Bian; Brian Liau; Nima Badie; Nenad Bursac
Journal:  Nat Protoc       Date:  2009-09-24       Impact factor: 13.491

7.  Electrospun polyhydroxybutyrate and poly(L-lactide-co-ε-caprolactone) composites as nanofibrous scaffolds.

Authors:  Donraporn Daranarong; Rodman T H Chan; Nico S Wanandy; Robert Molloy; Winita Punyodom; L John R Foster
Journal:  Biomed Res Int       Date:  2014-05-08       Impact factor: 3.411

8.  Type-1 Collagen differentially alters beta-catenin accumulation in primary Dupuytren's Disease cord and adjacent palmar fascia cells.

Authors:  Linda Vi; Anna Njarlangattil; Yan Wu; Bing Siang Gan; David B O'Gorman
Journal:  BMC Musculoskelet Disord       Date:  2009-06-19       Impact factor: 2.362

9.  Diabetic Conditions Confer Metabolic and Structural Modifications to Tissue-Engineered Skeletal Muscle.

Authors:  Francisca M Acosta; U-Ter Aonda Jia; Katerina Stojkova; Kennedy K Howland; Teja Guda; Settimio Pacelli; Eric M Brey; Christopher R Rathbone
Journal:  Tissue Eng Part A       Date:  2020-10-06       Impact factor: 3.845

10.  Adipogenic Differentiation Alters Properties of Vascularized Tissue-Engineered Skeletal Muscle.

Authors:  Francisca M Acosta; Kennedy K Howland; Katerina Stojkova; Elizabeth Hernandez; Eric M Brey; Christopher R Rathbone
Journal:  Tissue Eng Part A       Date:  2021-08-25       Impact factor: 3.845

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.