Fibrin-based biomaterials: Modulation of macroscopic properties through rational design at the molecular level

被引:202
作者
Brown, Ashley C. [1 ,2 ,3 ]
Barker, Thomas H. [2 ,3 ,4 ]
机构
[1] Georgia Inst Technol, Sch Chem & Biochem, Atlanta, GA 30332 USA
[2] Georgia Inst Technol, Wallace H Coulter Dept Biomed Engn, Atlanta, GA 30332 USA
[3] Emory Univ, Atlanta, GA 30332 USA
[4] Georgia Inst Technol, Parker H Petit Inst Bioengn & Biosci, Atlanta, GA 30332 USA
关键词
Fibrin; Biomaterial design; Fibrin glue; Wound repair; Tissue engineering; MESENCHYMAL STEM-CELLS; ALPHA-C-DOMAINS; HEPARIN-CONJUGATED FIBRIN; KNOB-HOLE INTERACTIONS; LINKED GAMMA-CHAINS; B-B INTERACTIONS; POLY(ETHYLENE GLYCOL); MECHANICAL-PROPERTIES; CROSS-LINKING; IN-VITRO;
D O I
10.1016/j.actbio.2013.09.008
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Fibrinogen is one of the primary components of the coagulation cascade and rapidly forms an insoluble matrix following tissue injury. In addition to its important role in hemostasis, fibrin acts as a scaffold for tissue repair and provides important cues for directing cell phenotype following injury. Because of these properties and the ease of polymerization of the material, fibrin has been widely utilized as a biomaterial for over a century. Modifying the macroscopic properties of fibrin, such as elasticity and porosity, has been somewhat elusive until recently, yet with a molecular-level rational design approach it can now be somewhat easily modified through alterations of molecular interactions key to the protein's polymerization process. This review outlines the biochemistry of fibrin and discusses methods for modification of molecular interactions and their application to fibrin based biomaterials. (C) 2013 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1502 / 1514
页数:13
相关论文
共 209 条
[1]  
Ahmann KA, 2010, TISSUE ENG PT A, V16, P3261, DOI [10.1089/ten.tea.2009.0708, 10.1089/ten.TEA.2009.0708]
[2]   Characterization and inhibition of fibrin hydrogel-degrading enzymes during development of tissue engineering scaffolds [J].
Ahmed, Tamer A. E. ;
Griffith, May ;
Hincke, Max .
TISSUE ENGINEERING, 2007, 13 (07) :1469-1477
[3]   Fibrin-polyethylene oxide interpenetrating polymer networks: New self-supported biomaterials combining the properties of both protein gel and synthetic polymer [J].
Akpalo, E. ;
Bidault, L. ;
Boissiere, M. ;
Vancaeyzeele, C. ;
Fichet, O. ;
Larreta-Garde, V. .
ACTA BIOMATERIALIA, 2011, 7 (06) :2418-2427
[4]   Magnetically-guided self-assembly of fibrin matrices with ordered nano-scale structure for tissue engineering [J].
Alsberg, Eben ;
Feinstein, Efraim ;
Joy, M. P. ;
Prentiss, Mara ;
Ingber, Donald E. .
TISSUE ENGINEERING, 2006, 12 (11) :3247-3256
[5]   A biodegradable composite scaffold for cell transplantation [J].
Ameer, GA ;
Mahmood, TA ;
Langer, R .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2002, 20 (01) :16-19
[6]   A Modular Fibrinogen Model that Captures the Stress-Strain Behavior of Fibrin Fibers [J].
Averett, Rodney D. ;
Menn, Bryant ;
Lee, Eric H. ;
Helms, Christine C. ;
Barker, Thomas ;
Guthold, Martin .
BIOPHYSICAL JOURNAL, 2012, 103 (07) :1537-1544
[7]   Factor Xa and thrombin, but not factor VIIa, elicit specific cellular responses in dermal fibroblasts [J].
Bachli, EB ;
Pech, CM ;
Johnson, KM ;
Johnson, DJD ;
Tuddenham, EGD ;
McVey, JH .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2003, 1 (09) :1935-1944
[8]   Factor XIII, clot structure, thrombosis [J].
Bagoly, Zsuzsa ;
Koncz, Zsuzsa ;
Harsfalvi, Jolan ;
Muszbek, Laszlo .
THROMBOSIS RESEARCH, 2012, 129 (03) :382-387
[9]   STRAIN ENHANCEMENT OF ELASTIC-MODULUS IN FINE FIBRIN CLOTS [J].
BALE, MD ;
FERRY, JD .
THROMBOSIS RESEARCH, 1988, 52 (06) :565-572
[10]   3-DIMENSIONAL RECONSTRUCTION OF FIBRIN CLOT NETWORKS FROM STEREOSCOPIC INTERMEDIATE VOLTAGE ELECTRON-MICROSCOPE IMAGES AND ANALYSIS OF BRANCHING [J].
BARADET, TC ;
HASELGROVE, JC ;
WEISEL, JW .
BIOPHYSICAL JOURNAL, 1995, 68 (04) :1551-1560