Chitosan-based scaffolds for the support of smooth muscle constructs in intestinal tissue engineering

被引:78
作者
Zakhem, Elie [1 ]
Raghavan, Shreya [1 ]
Gilmont, Robert R. [1 ]
Bitar, Khalil N. [1 ]
机构
[1] Wake Forest Sch Med, Wake Forest Inst Regenerat Med, Winston Salem, NC 27101 USA
基金
美国国家卫生研究院;
关键词
Rabbit circular smooth muscle (RCSM) constructs; Chitosan; Force generation; Scaffold; Concentric; SMALL-BOWEL RESECTION; IN-VITRO; CELLS; COLLAGEN; RELAXATION; OVERWEIGHT; WEIGHT; MODEL;
D O I
10.1016/j.biomaterials.2012.03.051
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Intestinal tissue engineering is an emerging field due to a growing demand for intestinal lengthening and replacement procedures secondary to massive resections of the bowel. Here, we demonstrate the potential use of a chitosan/collagen scaffold as a 3D matrix to support the bioengineered circular muscle constructs maintain their physiological functionality. We investigated the biocompatibility of chitosan by growing rabbit colonic circular smooth muscle cells (RCSMCs) on chitosan-coated plates. The cells maintained their spindle-like morphology and preserved their smooth muscle phenotypic markers. We manufactured tubular scaffolds with central openings composed of chitosan and collagen in a 1:1 ratio. Concentrically aligned 3D circular muscle constructs were bioengineered using fibrin-based hydrogel seeded with RCSMCs. The constructs were placed around the scaffold for 2 weeks, after which they were taken off and tested for their physiological functionality. The muscle constructs contracted in response to acetylcholine (Ach) and potassium chloride (KCl) and they relaxed in response to vasoactive intestinal peptide (VIP). These results demonstrate that chitosan is a biomaterial possibly suitable for intestinal tissue engineering applications. (c) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4810 / 4817
页数:8
相关论文
共 40 条
[1]   The intracellular pathway of the acetylcholine-induced contraction in cat detrusor muscle cells [J].
An, JY ;
Yun, HS ;
Lee, YP ;
Yang, SJ ;
Shim, JO ;
Jeong, JH ;
Shin, CY ;
Kim, JH ;
Kim, DS ;
Sohn, UD .
BRITISH JOURNAL OF PHARMACOLOGY, 2002, 137 (07) :1001-1010
[2]   ROLE OF THE ILEOCECAL VALVE AND SITE OF INTESTINAL RESECTION IN MALABSORPTION AFTER EXTENSIVE SMALL BOWEL RESECTION [J].
COSNES, J ;
GENDRE, JP ;
LEQUINTREC, Y .
DIGESTION, 1978, 18 (5-6) :329-336
[3]   Biochemical and cytochemical characterization of extracellular proteoglycans in the inner circular smooth muscle layer of dog small intestine [J].
de Toledo, OMS ;
Marquezini, MV ;
Jia, KB ;
Pinheiro, MD ;
Mora, OA .
IUBMB LIFE, 2002, 54 (01) :19-25
[4]   Chitosan: A versatile biopolymer for orthopaedic tissue-engineering [J].
Di Martino, A ;
Sittinger, M ;
Risbud, MV .
BIOMATERIALS, 2005, 26 (30) :5983-5990
[5]   SHORT-BOWEL SYNDROME - A COLLECTIVE REVIEW [J].
GALEA, MH ;
HOLLIDAY, H ;
CARACHI, R ;
KAPILA, L .
JOURNAL OF PEDIATRIC SURGERY, 1992, 27 (05) :592-596
[6]  
Gillian B., 1998, NUTRITION, V14, P813
[7]   Tissue-engineered small intestine improves recovery after massive small bowel resection [J].
Grikscheit, TC ;
Siddique, A ;
Ochoa, ER ;
Srinivasan, A ;
Alsberg, E ;
Hodin, RA ;
Vacanti, JP .
ANNALS OF SURGERY, 2004, 240 (05) :748-754
[8]   Tissue-engineered large intestine resembles native colon with appropriate in vitro physiology and architecture [J].
Grikscheit, TC ;
Ochoa, ER ;
Ramsanahie, A ;
Alsberg, E ;
Mooney, D ;
Whang, EE ;
Vacanti, JP .
ANNALS OF SURGERY, 2003, 238 (01) :35-41
[9]   In vitro small intestinal epithelial cell growth on a nanocomposite polycaprolactone scaffold [J].
Gupta, Ashish ;
Vara, Dina S. ;
Punshon, Geoffrey ;
Sales, Kevin M. ;
Winslet, Marc C. ;
Seifalian, Alexander M. .
BIOTECHNOLOGY AND APPLIED BIOCHEMISTRY, 2009, 54 :221-229
[10]   Development of a three-dimensional physiological model of the internal anal sphincter bioengineered in vitro from isolated smooth muscle cells [J].
Hecker, L ;
Baar, K ;
Dennis, RG ;
Bitar, KN .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2005, 289 (02) :G188-G196