Differential expression of tissue inhibitors of metalloproteinases (TIMP-1, -2, -3, and -4) in normal and aberrant wound healing

• Published in: Human pathology Vol. 30; no. 7; pp. 795 - 802
• Main Authors: Vaalamo, Maarit, Leivo, Tomi, Saarialho-Kere, Ulpu
• Format: Journal Article
• Language: English
• Published: New York, NY Elsevier Inc 01.07.1999; Elsevier
• Subjects: Aged; Aged, 80 and over; Biological and medical sciences; connective tissue remodeling; Dermatology; Enzyme Inhibitors - metabolism; Epithelium - metabolism; Humans; Immunohistochemistry; In Situ Hybridization; Keratinocytes - metabolism; Medical sciences; Middle Aged; RNA, Messenger - metabolism; Skin - metabolism; Skin involvement in other diseases. Miscellaneous. General aspects; Skin Ulcer - metabolism; Time Factors; Tissue Inhibitor of Metalloproteinase-1 - biosynthesis; Tissue Inhibitor of Metalloproteinase-1 - genetics; Tissue Inhibitor of Metalloproteinase-2 - biosynthesis; Tissue Inhibitor of Metalloproteinase-2 - genetics; Tissue Inhibitor of Metalloproteinase-3 - biosynthesis; Tissue Inhibitor of Metalloproteinase-3 - genetics; Tissue Inhibitor of Metalloproteinase-4; Tissue Inhibitor of Metalloproteinases - biosynthesis; Tissue Inhibitor of Metalloproteinases - genetics; venous ulcer; Wound Healing; MMP; venous ulcer; BM; connective tissue remodeling; ECM; TIMP; Human; Immunohistochemistry; Skin disease; Enzyme; Pathogenesis; In situ; Lower limb; Hybridization; Metalloproteins; Wound; Leg; Pathology; Peptidases; Tissue; Dysfunction; Hydrolases; Ulcer; Inhibitor; Molecular biology; Cicatrization; Comparative study
• ISSN: 0046-8177; 1532-8392
• DOI: 10.1016/S0046-8177(99)90140-5

Wound healing is characterized by hemostasis, re-epithelialization, granulation tissue formation, and remodeling of the extracellular matrix. Matrix metalloproteinases and their specific inhibitors, TIMPs, contribute to these events. We investigated a total of 47 samples of normally healing wounds, chronic venous ulcers, ulcerative vasculitis, and suction blisters using immunohistochemistry and in situ hybridization, to clarify the role of TIMPs in normal and aberrant wound repair. Expression of TIMP-1 and -3 mRNAs was found in proliferating keratinocytes in 3- to 5-day-old normally healing wounds, whereas no epidermal expression was detected in chronic ulcers. However, TIMP-3 protein was found in the proliferating epidermis in 20 of 24 samples representing both full-thickness acute and chronic wounds. TIMP-1 and TIMP-3 also were abundantly expressed by spindle-shaped, fibroblast-like, and plump, macrophage-like stromal cells, as well as by endothelial cells. In normally healing wounds, TIMP-2 protein localized under the migrating epithelial tip and to the stromal tissue under the eschar more frequently than in chronic ulcers. Occasional staining for TIMP-4 protein was detected in stromal cells of chronic ulcers near blood vessels. Our results indicate that TIMP-1 and TIMP-3 may be involved both in the regeneration of the epidermis by stabilizing the basement membrane zone and in the regulation of stromal remodeling and angiogenesis of the wound bed. Lack of TIMP-2 near the migrating epithelial wound edges might contribute to uncontrolled activity of MMP-2 in chronic ulcers. We conclude also that TIMPs are temporally and spatially tightly regulated and that the imbalance between metalloproteinases and TIMPs-1, -2, and -3 may lead to delayed wound healing.