In vitro and in vivo studies on matrix metalloproteinases interacting with small intestine submucosa wound matrix

被引:38
作者
Shi, Lei [1 ]
Ramsay, Sarah [1 ]
Ermis, Ryan [1 ]
Carson, Dennis [1 ]
机构
[1] Healthpoint Biotherapeut, Res & Dev, Ft Worth, TX USA
关键词
MMP-1; MMP-2; MMP-9; Small intestine submucosa; Wound matrix; CHRONIC LEG ULCERS; EXTRACELLULAR-MATRIX; TISSUE INHIBITOR; GROWTH-FACTORS; COLLAGENASE; MATRIX-METALLOPROTEINASE-9; STERILIZATION; SCAFFOLD;
D O I
10.1111/j.1742-481X.2011.00843.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100227 [皮肤病学];
摘要
Small intestine submucosa (SIS), a bioactive extracellular matrix (ECM) containing critical components of the ECM including collagens, proteoglycans, and glycosaminoglycans, has been widely used for wound healing. The purpose of this study was to investigate the interaction between SIS and matrix metalloproteinases (MMPs). MMP-1, MMP-2, and MMP-9 displayed different binding affinities, indicated by a loss in activity in solution upon incubation with SIS at 53.%, 85.%, and 36.% over 24 hours, respectively. A cell migration study was conducted to evaluate the effects of MMPs and SIS on keratinocytes. The results indicated that MMPs inhibit keratinocyte migration in vitro, and that the inhibition can be significantly reduced by pre-incubating the MMP solution with SIS. To evaluate activity in vivo a diabetic mouse wound healing study was conducted. Biopsy samples were collected on different days for analysis of MMP levels by gelatin zymography. MMP activity was found to be attenuated by SIS treatment on day 3 after wounding. On day 7, the attenuation became less significant indicating that the MMP binding ability of SIS had become saturated. SIS was able to reduce MMP activity immediately, and may reduce the inhibitory effects of MMPs on keratinocyte migration.
引用
收藏
页码:44 / 53
页数:10
相关论文
共 43 条
[1]
Barendse-Hofmann M G, 2007, J Wound Care, V16, P455
[2]
Barone EJ, 1998, PLAST RECONSTR SURG, V102, P1023, DOI 10.1097/00006534-199809040-00015
[3]
TISSUE INHIBITOR OF METALLOPROTEINASES-1 IS DECREASES AND ACTIVATED GELATINASES ARE INCREASED IN CHRONIC WOUNDS [J].
BULLEN, EC ;
LONGAKER, MT ;
UPDIKE, DL ;
BENTON, R ;
LADIN, D ;
HOU, ZZ ;
HOWARD, EW .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1995, 104 (02) :236-240
[4]
Carson SN, 2003, WOUNDS, V15, P339
[5]
Molecular and mechanistic validation of delayed healing rat wounds as a model for human chronic wounds [J].
Chen, C ;
Schultz, GS ;
Bloch, M ;
Edwards, PD ;
Tebes, S ;
Mast, BA .
WOUND REPAIR AND REGENERATION, 1999, 7 (06) :486-494
[6]
Demling RH, 2004, WOUNDS, V16, P18
[7]
Dressel C, 2004, WIEN TIERARZTL MONAT, V91, P142
[8]
New functions for the matrix metalloproteinases in cancer progression [J].
Egeblad, M ;
Werb, Z .
NATURE REVIEWS CANCER, 2002, 2 (03) :161-174
[9]
Management of complicated gastroschisis with porcine small intestinal submucosa and negative pressure wound therapy [J].
Gabriel, Allen ;
Gollin, Gerald .
JOURNAL OF PEDIATRIC SURGERY, 2006, 41 (11) :1836-1840
[10]
Hodde J P, 1996, Tissue Eng, V2, P209, DOI 10.1089/ten.1996.2.209