Morphologic assessment of extracellular matrix scaffolds for patch tracheoplasty in a canine model

被引:57
作者
Gilbert, Thomas W.
Gilbert, Sebastien
Madden, Matthew
Reynolds, Susan D.
Badylak, Stephen F. [1 ]
机构
[1] Univ Pittsburgh, McGowan Inst Regenerat Med, Dept Surg, Heart Lung & Esophageal Inst,Med Ctr, Pittsburgh, PA 15219 USA
关键词
D O I
10.1016/j.athoracsur.2008.04.071
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. The optimal management of benign tracheal stricture remains surgical resection. Resection is not always an option because of the challenges posed by anastomotic tension and a tenuous blood supply. Regenerative medicine approaches, such as extracellular matrix (ECM) scaffold technology, may alleviate some of the limitations to tracheal replacement. ECM scaffolds facilitate site-specific tissue remodeling when used to reconstruct a variety of soft-tissue structures. Methods. A 1-cm wide x 2-cm-long defect was created in the ventral trachea of 15 dogs and repaired with one of three acellular biologic scaffolds: urinary bladder matrix (UBM), UBM crosslinked with carbodiimide (UBMC), and decellularized tracheal matrix (DTM). The grafts were evaluated periodically using bronchoscopy and by macroscopic and microscopic morphologic examination at either 2 months or 6 months. Results. The UBM, UBMC, and DTM groups showed no evidence of stenosis or tracheomalacia. The UBM, UBMC, and DTM groups all showed deposition of organized collagenous tissue at the site of scaffold placement and an intact epithelial layer. Scattered areas of mucociliary differentiation were present at the edges of the graft site. There was no evidence cartilage observed within the remodeled tissue at 6 months. Conclusions. ECM scaffolds promote healing of significantly sized tracheal defects without stricture and with some, but not all, of the necessary structures required for tracheal reconstruction, including complete coverage with ciliated epithelium and dense organized collagenous tissue.
引用
收藏
页码:967 / 974
页数:8
相关论文
共 26 条
[1]   Esophageal reconstruction with ECM and muscle tissue in a dog model [J].
Badylak, SF ;
Vorp, DA ;
Spievack, AR ;
Simmons-Byrd, A ;
Hanke, J ;
Freytes, DO ;
Thapa, A ;
Gilbert, TW ;
Nieponice, A .
JOURNAL OF SURGICAL RESEARCH, 2005, 128 (01) :87-97
[2]   The extracellular matrix as a biologic scaffold material [J].
Badylak, Stephen F. .
BIOMATERIALS, 2007, 28 (25) :3587-3593
[3]  
Billiar K, 2001, J BIOMED MATER RES, V56, P101, DOI 10.1002/1097-4636(200107)56:1<101::AID-JBM1074>3.0.CO
[4]  
2-6
[5]   Number and proliferation of basal and parabasal cells in normal human airway epithelium [J].
Boers, JE ;
Ambergen, AW ;
Thunnissen, FBJM .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1998, 157 (06) :2000-2006
[6]   Antibacterial activity within degradation products of biological scaffolds composed of extracellular matrix [J].
Brennan, Ellen P. ;
Reing, Janet ;
Chew, Douglas ;
Myers-Irvin, Julie M. ;
Young, E. J. ;
Badylak, Stephen F. .
TISSUE ENGINEERING, 2006, 12 (10) :2949-2955
[7]   The basement membrane component of biologic scaffolds derived from extracellular matrix [J].
Brown, B ;
Lindberg, K ;
Reing, J ;
Stolz, DB ;
Badylak, SF .
TISSUE ENGINEERING, 2006, 12 (03) :519-526
[8]   MANAGEMENT OF SUBGLOTTIC STENOSIS IN INFANCY AND CHILDHOOD - REVIEW OF A CONSECUTIVE SERIES OF CASES MANAGED BY SURGICAL RECONSTRUCTION [J].
COTTON, R .
ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY, 1978, 87 (05) :649-657
[9]   Surgisis patch tracheoplasty in a rodent model for tracheal stenosis [J].
De Ugarte, DA ;
Puapong, D ;
Roostaeian, J ;
Gillis, N ;
Fonkalsrud, EW ;
Atkinson, JB ;
Dunn, JCY .
JOURNAL OF SURGICAL RESEARCH, 2003, 112 (01) :65-69
[10]  
FREYTES DO, 2008, J BIOMED MAT RES A