Thrombospondin in Early Human Wound Tissue
We examined partial thickness incised human wounds of 2, 3, 5, 7, and 14 days of age for the presence of thrombospondin by immunostaining and light microscopy. At 2, 3, 5, and 7 days after wounding, thrombospondin is present primarily at the cut edges of the lateral and deep margins of the wound. It...
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Published in | Journal of investigative dermatology Vol. 89; no. 6; pp. 551 - 554 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Danvers, MA
Elsevier Inc
01.12.1987
Nature Publishing |
Subjects | |
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Abstract | We examined partial thickness incised human wounds of 2, 3, 5, 7, and 14 days of age for the presence of thrombospondin by immunostaining and light microscopy. At 2, 3, 5, and 7 days after wounding, thrombospondin is present primarily at the cut edges of the lateral and deep margins of the wound. It appears to be cleared from these extracellular matrix sites, and is no longer detectable in those sites in most 14-day-old wounds. Thrombospondin staining is present, however, in increased amounts around the vascular channels within and adjacent to the 7- and 14- day wounds in increased amounts relative to vascular channels distant from the wound. Our observations are consistent with known in vitro data regarding the binding of thrombospondin to fibrin and components of the extracellular matrix, as well as with data showing that proliferating endothelial cells secrete more thrombospondin than quiescent endothelial cells. These data support the hypothesis that thrombospondin plays a role in the early organization of the extracellular matrix of wounds. |
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AbstractList | We examined partial thickness incised human wounds of 2, 3, 5, 7, and 14 days of age for the presence of thrombospondin by immunostaining and light microscopy. At 2, 3, 5, and 7 days after wounding, thrombospondin is present primarily at the cut edges of the lateral and deep margins of the wound. It appears to be cleared from these extracellular matrix sites, and is no longer detectable in those sites in most 14-day-old wounds. Thrombospondin staining is present, however, in increased amounts around the vascular channels within and adjacent to the 7- and 14-day wounds in increased amounts relative to vascular channels distant from the wound. Our observations are consistent with known in vitro data regarding the binding of thrombospondin to fibrin and components of the extracellular matrix, as well as with data showing that proliferating endothelial cells secrete more thrombospondin than quiescent endothelial cells. These data support the hypothesis that thrombospondin plays a role in the early organization of the extracellular matrix of wounds. |
Author | Olerud, John E. Raugi, Gregory J. Gown, Allen M. |
Author_xml | – sequence: 1 givenname: Gregory J. surname: Raugi fullname: Raugi, Gregory J. organization: Veterans Administration Medical Center and Department of Medicine (Dermatology), University of Washington, Seattle, Washington, U.S.A – sequence: 2 givenname: John E. surname: Olerud fullname: Olerud, John E. organization: Department of Medicine (Dermatology) and Orthopaedics (Sports Medicine), University of Washington, Seattle, Washington, U.S.A – sequence: 3 givenname: Allen M. surname: Gown fullname: Gown, Allen M. organization: Department of Pathology, University of Washington, Seattle, Washington, U.S.A |
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Keywords | Skin disease Glycoproteins Skin Cicatrization Wound Thrombospondin |
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Snippet | We examined partial thickness incised human wounds of 2, 3, 5, 7, and 14 days of age for the presence of thrombospondin by immunostaining and light microscopy.... |
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SubjectTerms | Aged Biological and medical sciences Biopsy Dermatology Extracellular Matrix - analysis Glycoproteins - analysis Granulation Tissue - analysis Granulation Tissue - pathology Humans Male Medical sciences Middle Aged Skin - analysis Skin - pathology Skin involvement in other diseases. Miscellaneous. General aspects Thrombospondins Wound Healing |
Title | Thrombospondin in Early Human Wound Tissue |
URI | https://dx.doi.org/10.1111/1523-1747.ep12461198 http://dx.doi.org/10.1111/1523-1747.ep12461198 https://www.ncbi.nlm.nih.gov/pubmed/3680981 https://search.proquest.com/docview/77812352 |
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