Age-related differences in the temporal and spatial regulation of matrix metalloproteinases (MMPs) in normal skin and acute cutaneous wounds of healthy humans

被引:140
作者
Ashcroft, GS
Horan, MA
Herrick, SE
Tarnuzzer, RW
Schultz, GS
Ferguson, MWJ
机构
[1] Univ Manchester, Sch Biol Sci, Cells Immunol & Dev Div, Manchester M13 9PT, Lancs, England
[2] Univ S Manchester Hosp, Dept Geriatr Med, Manchester M20 2LR, Lancs, England
[3] Univ Florida, Dept Obstet & Gynaecol, Gainesville, FL 32610 USA
关键词
ageing; skin; proteinase; wound; human;
D O I
10.1007/s004410050963
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Despite the association of increasing age with chronic wound-healing disorders and an impaired rate of healing of acute cutaneous wounds, the role of matrix metalloproteinases (MMPs) is unknown. To determine the spatial and temporal patterns and activities of MMP-1, -2, -3 and -9, 132 healthy humans aged between 19 and 96 years underwent 4-mm punch biopsies followed by wound excision between day 1 and day 180 postwounding. Wounds showed an age-related increase in MMP-2 and MMP-9 immunostaining from day 3; this was associated with degradation of gelatin as shown by zymograms and with increased proteinase activity as shown by azocoll assays. Distinct spatial localisations for each MMP were observed: MMP-2 was found in epidermal structures; MMP-9 was observed in inflammatory cells up to day 21; MMP-1 was localised to keratinocytes at the wound margin. Normal old skin showed pro-MMP-2 bands on zymography and increased MMP-2 immunostaining. These results indicate that: (1) intrinsic ageing is associated with the up-regulation of MMPs previously associated with chronic wound healing; (2) wound-tissue proteinases are essentially active up to day 21 postwounding; and (3) intrinsic ageing may predispose to tissue breakdown disorders because of MMP-2 up-regulation in normal skin.
引用
收藏
页码:581 / 591
页数:11
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