A biomimetic porous hydrogel of gelatin and glycosaminoglycans cross-linked with transglutaminase and its application in the culture of hepatocytes

被引:44
作者
De Colli, M. [1 ]
Massimi, M. [1 ]
Barbetta, A. [2 ]
Di Rosario, B. L. [2 ]
Nardecchia, S. [2 ]
Devirgiliis, L. Conti [3 ]
Dentini, M. [2 ]
机构
[1] Univ Aquila, Dept Basic & Appl Biol, I-67100 Laquila, Italy
[2] Univ Roma La Sapienza, Dept Chem, I-00185 Rome, Italy
[3] Univ Roma La Sapienza, Dept Biol & Biotechnol C Darwin, I-00185 Rome, Italy
关键词
EXTRACELLULAR-MATRIX; HYALURONIC-ACID; CELL-CULTURE; SCAFFOLDS; LINKING; METABOLISM; C3A;
D O I
10.1088/1748-6041/7/5/055005
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The development of blended gelatin and glycosaminoglycan (GAG) scaffolds can potentially be used in many soft tissue engineering applications since these scaffolds mimic the structure and biological function of native extracellular matrix (ECM). In this study, we were able to obtain a gelatin-GAG scaffold by using a concentrated emulsion templating technique known as high internal phase emulsion (HIPE), in which a prevailing in volume organic phase is dispersed in the form of discrete droplets inside an aqueous solution of three biopolymers represented by gelatin, hyaluronic acid (HA) and chondroitin sulfate (CS) in the presence of a suitable surfactant. In order to preserve the bioactive potential of the biopolymers employed, the cross-linking procedure involved the use of transglutaminase (MTGase) that catalyzes the formation of covalent N-epsilon-(gamma-glutamyl) lysine amide bonds. Since neither HA nor CS possess the necessary primary amino groups toward which MTGase is active, they were functionalized with the dipeptide glycine-lysine (GK). In this way the introduction of foreign cross-linking bridging units with an unpredictable biocompatibility was avoided. These enzymatic cross-linked gelatin-GAG scaffolds were tested in the culture of primary rat and C3A hepatocytes. Results underlined the good performance of this novel support in maintaining and promoting hepatocyte functions in vitro.
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页数:13
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共 35 条
  • [1] Influence of retinoic acid on adhesion complexes in human hepatoma cells: A clue to its antiproliferative effects
    Ara, C
    Devirgiliis, LC
    Massimi, M
    [J]. CELL COMMUNICATION AND ADHESION, 2004, 11 (01) : 13 - +
  • [2] Tailoring the porosity and morphology of gelatin-methacrylate polyHIPE scaffolds for tissue engineering applications
    Barbetta, A
    Dentini, M
    Zannoni, EM
    De Stefano, ME
    [J]. LANGMUIR, 2005, 21 (26) : 12333 - 12341
  • [3] Scaffolds based on biopolymeric foams
    Barbetta, A
    Dentini, M
    De Vecchis, MS
    Filippini, P
    Formisano, G
    Caiazza, S
    [J]. ADVANCED FUNCTIONAL MATERIALS, 2005, 15 (01) : 118 - 124
  • [4] Enzymatic cross-linking versus radical polymerization in the preparation of gelatin polyHIPEs and their performance as scaffolds in the culture of hepatocytes
    Barbetta, Andrea
    Massimi, Mara
    Devirgiliis, Laura Conti
    Dentini, Mariella
    [J]. BIOMACROMOLECULES, 2006, 7 (11) : 3059 - 3068
  • [5] Primary Rat Hepatocyte Culture on 3D Nanofibrous Polymer Scaffolds for Toxicology and Pharmaceutical Research
    Bierwolf, Jeanette
    Lutgehetmann, Marc
    Feng, Kai
    Erbes, Johannes
    Deichmann, Steffen
    Toronyi, Eva
    Stieglitz, Christina
    Nashan, Bjoern
    Ma, Peter X.
    Pollok, Joerg M.
    [J]. BIOTECHNOLOGY AND BIOENGINEERING, 2011, 108 (01) : 141 - 150
  • [6] Emulsion-templated porous polymers as scaffolds for three dimensional cell culture: effect of synthesis parameters on scaffold formation and homogeneity
    Bokhari, Maria
    Carnachan, Ross J.
    Przyborski, Stefan A.
    Cameron, Neil R.
    [J]. JOURNAL OF MATERIALS CHEMISTRY, 2007, 17 (38) : 4088 - 4094
  • [7] Novel cell culture device enabling three-dimensional cell growth and improved cell function
    Bokhari, Maria
    Carnachan, Ross J.
    Cameron, Neil R.
    Przyborski, Stefan A.
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 354 (04) : 1095 - 1100
  • [8] Bulpitt P, 1999, J BIOMED MATER RES, V47, P152
  • [9] Enzymatic methods for in situ cell entrapment and cell release
    Chen, TH
    Small, DA
    McDermott, MK
    Bentley, WE
    Payne, GF
    [J]. BIOMACROMOLECULES, 2003, 4 (06) : 1558 - 1563
  • [10] New gelatin-based hydrogels via enzymatic networking
    Crescenzi, V
    Francescangeli, A
    Taglienti, A
    [J]. BIOMACROMOLECULES, 2002, 3 (06) : 1384 - 1391