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Title:
Expression and vitamin D-mediated regulation of matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs) in healthy skin and in diabetic foot ulcers | Archives of Dermatological Research
Description:
Diabetic foot ulcers (DFUs) are chronic wounds with high matrix metalloproteinase (MMP) activity, and are a frequent complication on diabetics. This work studied the expression of selected MMP and tissue inhibitor of metalloproteinases (TIMP) gene family members in DFU and normal skin biopsies, and in vitamin D-treated keratinocytes cultured from those biopsies. We report for the first time the expression of some of these genes in healthy skin. Our results suggest that vitamin D may modulate the expression of some MMP gene family members in keratinocytes. Gene expression in DFU and in non-diabetic healthy skin (control) biopsies was evaluated by RT-qPCR for MMP-1, MMP-3, MMP-8, MMP-9, MMP-10, MMP-19, TIMP-1 and TIMP-2, and also by immunohistochemistry for MMP-1 and MMP-9. Primary keratinocytes cultured from DFU and healthy skin biopsies were used for gene expression analyses of selected MMPs and TIMPs by RT-qPCR, both in the presence and absence of calcitriol. The expression of MMP-1, MMP-8, MMP-9, MMP-10, and TIMP-2 in healthy skin is reported here for the first time. DFUs showed increased MMP-1, MMP-9 and TIMP-1 expression, compared to healthy skin. Calcitriol down-regulated MMP-1 and MMP-10 expression in DFU-derived keratinocytes but not in those derived from healthy skin. Our data demonstrate the expression of certain MMPs that had not been previously described in healthy skin, and further support previous reports of MMP and TIMP up-regulation in DFUs. Our results point to calcitriol as a potential modulator for the expression of certain MMP members in DFUs.
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Keywords {🔍}
pubmed, article, google, scholar, cas, matrix, mmp, central, wound, expression, metalloproteinases, skin, diabetes, metalloproteinase, cell, biol, healing, vitamin, tissue, diabetic, healthy, timp, keratinocytes, foot, chronic, parks, dermatol, ulcers, res, type, inhibitors, wounds, activity, gene, invest, repair, human, research, mmps, timps, inhibitor, mol, clin, chem, privacy, cookies, function, content, analysis, data,
Topics {✒️}
josé antonio enciso-moreno & carmen month download article/chapter monica/kora augsburg study article lópez-lópez bruno rivas-santiago valentín trujillo-paez real-time quantitative pcr treviño-santa cruz full article pdf chronic wound fluid–thinking irma gonzález-curiel vitamin d-mediated regulation saarialho-kere dermatological research aims privacy choices/manage cookies diabetic foot ulcers sudbeck bd increased matrix metalloproteinase-9 diabetic foot ulceration edison state college impaired cell growth article archives chronic wound environments support previous reports gene family members diabetic peripheral neuropathy high-risk subjects unfolded protein response unwounded skin remodeling primary keratinocytes cultured metabolic diseases diabetic healthy skin related subjects calcium-dependent protease epidermal wound repair high matrix metalloproteinase activated matrix metalloproteinase-9 wound exudates obtained european economic area mycobacterium tuberculosis infection p38 mark pathway foxo1/stat1 interplay lipid-laden macrophages antioxid redox signal bisphosphonate-functionalised hydrogels epidermolysis bullosa simplex fully dominant allele san luis potosí cutaneous wound healing aberrant wound healing
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headline:Expression and vitamin D-mediated regulation of matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs) in healthy skin and in diabetic foot ulcers
description:Diabetic foot ulcers (DFUs) are chronic wounds with high matrix metalloproteinase (MMP) activity, and are a frequent complication on diabetics. This work studied the expression of selected MMP and tissue inhibitor of metalloproteinases (TIMP) gene family members in DFU and normal skin biopsies, and in vitamin D-treated keratinocytes cultured from those biopsies. We report for the first time the expression of some of these genes in healthy skin. Our results suggest that vitamin D may modulate the expression of some MMP gene family members in keratinocytes. Gene expression in DFU and in non-diabetic healthy skin (control) biopsies was evaluated by RT-qPCR for MMP-1, MMP-3, MMP-8, MMP-9, MMP-10, MMP-19, TIMP-1 and TIMP-2, and also by immunohistochemistry for MMP-1 and MMP-9. Primary keratinocytes cultured from DFU and healthy skin biopsies were used for gene expression analyses of selected MMPs and TIMPs by RT-qPCR, both in the presence and absence of calcitriol. The expression of MMP-1, MMP-8, MMP-9, MMP-10, and TIMP-2 in healthy skin is reported here for the first time. DFUs showed increased MMP-1, MMP-9 and TIMP-1 expression, compared to healthy skin. Calcitriol down-regulated MMP-1 and MMP-10 expression in DFU-derived keratinocytes but not in those derived from healthy skin. Our data demonstrate the expression of certain MMPs that had not been previously described in healthy skin, and further support previous reports of MMP and TIMP up-regulation in DFUs. Our results point to calcitriol as a potential modulator for the expression of certain MMP members in DFUs.
datePublished:2014-08-29T00:00:00Z
dateModified:2014-08-29T00:00:00Z
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Type 2 diabetes
Non-insulin dependent diabetes mellitus (NIDDM)
Matrix metalloproteinases (MMPs)
Tissue inhibitors of metalloproteinases (TIMPs)
Diabetic foot ulcers (DFUs)
Keratinocytes
Vitamin D
Calcitriol
Dermatology
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headline:Expression and vitamin D-mediated regulation of matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs) in healthy skin and in diabetic foot ulcers
description:Diabetic foot ulcers (DFUs) are chronic wounds with high matrix metalloproteinase (MMP) activity, and are a frequent complication on diabetics. This work studied the expression of selected MMP and tissue inhibitor of metalloproteinases (TIMP) gene family members in DFU and normal skin biopsies, and in vitamin D-treated keratinocytes cultured from those biopsies. We report for the first time the expression of some of these genes in healthy skin. Our results suggest that vitamin D may modulate the expression of some MMP gene family members in keratinocytes. Gene expression in DFU and in non-diabetic healthy skin (control) biopsies was evaluated by RT-qPCR for MMP-1, MMP-3, MMP-8, MMP-9, MMP-10, MMP-19, TIMP-1 and TIMP-2, and also by immunohistochemistry for MMP-1 and MMP-9. Primary keratinocytes cultured from DFU and healthy skin biopsies were used for gene expression analyses of selected MMPs and TIMPs by RT-qPCR, both in the presence and absence of calcitriol. The expression of MMP-1, MMP-8, MMP-9, MMP-10, and TIMP-2 in healthy skin is reported here for the first time. DFUs showed increased MMP-1, MMP-9 and TIMP-1 expression, compared to healthy skin. Calcitriol down-regulated MMP-1 and MMP-10 expression in DFU-derived keratinocytes but not in those derived from healthy skin. Our data demonstrate the expression of certain MMPs that had not been previously described in healthy skin, and further support previous reports of MMP and TIMP up-regulation in DFUs. Our results point to calcitriol as a potential modulator for the expression of certain MMP members in DFUs.
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Type 2 diabetes
Non-insulin dependent diabetes mellitus (NIDDM)
Matrix metalloproteinases (MMPs)
Tissue inhibitors of metalloproteinases (TIMPs)
Diabetic foot ulcers (DFUs)
Keratinocytes
Vitamin D
Calcitriol
Dermatology
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