CHARACTERIZATION OF BIOLOGIC PROPERTIES OF WOUND FLUID COLLECTED DURING EARLY STAGES OF WOUND-HEALING

被引:95
作者
CHEN, WYJ
ROGERS, AA
LYDON, MJ
机构
关键词
D O I
10.1111/1523-1747.ep12667378
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The clinical effects of occlusive dressings on wound healing are well documented. However, the underlying biologic mechanisms associated with moist healing are not well understood. Experimental studies and clinical experience have shown enhanced eschar and clot removal, re-epithelialization, and collagen synthesis under occlusion, suggesting the possibility of elevated activities of proteinases and other effectors, e.g., growth factors, in the moist wound environment. To gain an insight into the biology of early wounds under occlusion, we have carried out biologic and biochemical analyses on fluids from occluded full- and partial-thickness wounds. Metalloproteinase activities were detected in the wound fluid samples. When applied to cultured dermal fibroblasts, mitogenic activity was observed with fluids from full-thickness wounds. Wound fluid - stimulated accumulation of urokinase-type plasminogen activator by fibroblasts was also observed in a time-dependent manner. Stimulation of metalloproteinase accumulation by fibroblasts was also observed. We have further demonstrated the presence of platelet-derived growth factor-like and basic fibroblast growth factor - like factors in wound fluid by antibody neutralization of their biologic activities. Proteinase presence and proteinase stimulatory activity of wound fluid retained in the occluded wound may contribute to an enhanced proteolytic environment in these wounds in comparison to non-occluded "dry" wounds. The presence of growth factors and the potential abilities of proteinases to activate latent growth factors and generate chemotactic peptides through connective tissue breakdown may also contribute to the enhanced healing of occluded wounds.
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页码:559 / 564
页数:6
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共 45 条
[21]  
LYDON MJ, 1989, WOUNDS, V1, P95
[22]   CYTOKINE-MEDIATED PROTEOLYSIS IN TISSUE REMODELING [J].
MASURE, S ;
OPDENAKKER, G .
EXPERIENTIA, 1989, 45 (06) :542-549
[23]   METALLOPROTEINASES AND THEIR INHIBITORS IN MATRIX REMODELING [J].
MATRISIAN, LM .
TRENDS IN GENETICS, 1990, 6 (04) :121-125
[24]   2 PEPTIDES RELATED TO PLATELET-DERIVED GROWTH-FACTOR ARE PRESENT IN HUMAN WOUND FLUID [J].
MATSUOKA, J ;
GROTENDORST, GR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (12) :4416-4420
[25]   EPIDERMAL CYTOKINES AND THEIR ROLES IN CUTANEOUS WOUND-HEALING [J].
MCKAY, IA ;
LEIGH, IM .
BRITISH JOURNAL OF DERMATOLOGY, 1991, 124 (06) :513-518
[26]   GROWTH-FACTORS ARE RELEASED BY MECHANICALLY WOUNDED ENDOTHELIAL-CELLS [J].
MCNEIL, PL ;
MUTHUKRISHNAN, L ;
WARDER, E ;
DAMORE, PA .
JOURNAL OF CELL BIOLOGY, 1989, 109 (02) :811-822
[27]   INVITRO ANGIOGENESIS ON THE HUMAN AMNIOTIC MEMBRANE - REQUIREMENT FOR BASIC FIBROBLAST GROWTH-FACTOR INDUCED PROTEINASES [J].
MIGNATTI, P ;
TSUBOI, R ;
ROBBINS, E ;
RIFKIN, DB .
JOURNAL OF CELL BIOLOGY, 1989, 108 (02) :671-682
[28]   BASIC FIBROBLAST GROWTH-FACTOR IS EFFICIENTLY RELEASED FROM A CYTOLSOLIC STORAGE SITE THROUGH PLASMA-MEMBRANE DISRUPTIONS OF ENDOTHELIAL-CELLS [J].
MUTHUKRISHNAN, L ;
WARDER, E ;
MCNEIL, PL .
JOURNAL OF CELLULAR PHYSIOLOGY, 1991, 148 (01) :1-16
[29]   CHEMOTACTIC ATTRACTION OF HUMAN FIBROBLASTS TO TYPE-I, TYPE-2, AND TYPE-3 COLLAGENS AND COLLAGEN-DERIVED PEPTIDES [J].
POSTLETHWAITE, AE ;
SEYER, JM ;
KANG, AH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1978, 75 (02) :871-875
[30]   MESSENGER-RNA PHENOTYPING FOR STUDYING GENE-EXPRESSION IN SMALL NUMBERS OF CELLS - PLATELET-DERIVED GROWTH-FACTOR AND OTHER GROWTH-FACTORS IN WOUND-DERIVED MACROPHAGES [J].
RAPPOLEE, DA ;
WERB, Z .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1990, 2 (01) :3-10