Antibacterial activity within degradation products of biological scaffolds composed of extracellular matrix

被引:164
作者
Brennan, Ellen P.
Reing, Janet
Chew, Douglas
Myers-Irvin, Julie M.
Young, E. J.
Badylak, Stephen F. [1 ]
机构
[1] Univ Pittsburgh, McGowan Inst Regenerat Med, Pittsburgh, PA USA
[2] Univ Pittsburgh, Dept Bioengn, Pittsburgh, PA USA
[3] Univ Pittsburgh, Dept Surg, Pittsburgh, PA USA
来源
TISSUE ENGINEERING | 2006年 / 12卷 / 10期
关键词
D O I
10.1089/ten.2006.12.2949
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Biological scaffolds composed of extracellular matrix (ECM) have been shown to be resistant to deliberate bacterial contamination in preclinical in vivo studies. The present study evaluated the degradation products resulting from the acid digestion of ECM scaffolds for antibacterial effects against clinical strains of Staphylococcus aureus and Escherichia coli. The ECM scaffolds were derived from porcine urinary bladder (UBM-ECM) and liver (L-ECM). These biological scaffolds were digested with acid at high temperatures, fractionated using ammonium sulfate precipitation, and tested for antibacterial activity in a standardized in vitro assay. Degradation products from both UBM-ECM and L-ECM demonstrated antibacterial activity against both S. aureus and E. coli. Specific ammonium sulfate fractions that showed antimicrobial activity varied for the 2 different ECM scaffold types. The results of this study suggest that several different low-molecular-weight peptides with antibacterial activity exist within ECM and that these peptides may help explain the resistance to bacterial infection provided by such biological scaffolds.
引用
收藏
页码:2949 / 2955
页数:7
相关论文
共 47 条
[1]
ISOLATION OF 3 ANTIBACTERIAL PEPTIDES FROM PIG INTESTINE - GASTRIC-INHIBITORY POLYPEPTIDE(7-42), DIAZEPAM-BINDING INHIBITOR(32-86) AND A NOVEL FACTOR, PEPTIDE-3910 [J].
AGERBERTH, B ;
BOMAN, A ;
ANDERSSON, M ;
JORNVALL, H ;
MUTT, V ;
BOMAN, HG .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1993, 216 (02) :623-629
[2]
AMINO-ACID-SEQUENCE OF PR-39 - ISOLATION FROM PIG INTESTINE OF A NEW MEMBER OF THE FAMILY OF PROLINE-ARGININE-RICH ANTIBACTERIAL PEPTIDES [J].
AGERBERTH, B ;
LEE, JY ;
BERGMAN, T ;
CARLQUIST, M ;
BOMAN, HG ;
MUTT, V ;
JORNVALL, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1991, 202 (03) :849-854
[3]
Experimental and clinical experience with tissue engineering techniques for urethral reconstruction [J].
Atala, A .
UROLOGIC CLINICS OF NORTH AMERICA, 2002, 29 (02) :485-+
[4]
Badylak S, 2003, HEART SURG FORUM, V6, pE20
[5]
Resorbable bioscaffold for esophageal repair in a dog model [J].
Badylak, S ;
Meurling, S ;
Chen, M ;
Spievack, A ;
Simmons-Byrd, A .
JOURNAL OF PEDIATRIC SURGERY, 2000, 35 (07) :1097-1103
[6]
THE USE OF XENOGENEIC SMALL-INTESTINAL SUBMUCOSA AS A BIOMATERIAL FOR ACHILLES-TENDON REPAIR IN A DOG-MODEL [J].
BADYLAK, SF ;
TULLIUS, R ;
KOKINI, K ;
SHELBOURNE, KD ;
KLOOTWYK, T ;
VOYTIK, SL ;
KRAINE, MR ;
SIMMONS, C .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1995, 29 (08) :977-985
[7]
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
[9]
Host protection against deliberate bacterial contamination of an extracellular matrix bioscaffold versus Dacron™ mesh in a dog model of orthopedic soft tissue repair [J].
Badylak, SF ;
Wu, CC ;
Bible, M ;
McPherson, E .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART B-APPLIED BIOMATERIALS, 2003, 67B (01) :648-654
[10]
Small intestinal submucosa: A rapidly resorbed bioscaffold for augmentation cystoplasty in a dog model [J].
Badylak, SF ;
Kropp, B ;
McPherson, T ;
Liang, H ;
Snyder, PW .
TISSUE ENGINEERING, 1998, 4 (04) :379-387