Study of mechanism on loss of some components from basement membrane in epithelial-interstitial junction in cutaneous pseudoepitheliomatous hyperplasia lesion

OBJECTIVE: To investigate the relationship between the formation of pseudoepitheliomatous hyperplasia (PEH) and the mechanism of loss of some components from the basement membrane in epithelial interstitial junction (EIJ) in the treatment of cutaneous wounds, when formation of PEH lesion was induced

Bibliographische Detailangaben
Veröffentlicht in:Zhongguo wei zhong bing ji jiu yi xue = Chinese critical care medicine = Zhongguo weizhongbing jijiuyixue. - 1998. - 16(2004), 1 vom: 05. Jan., Seite 36-41
1. Verfasser: Jiang, Du-yin (VerfasserIn)
Weitere Verfasser: Fu, Xiao-bing, Sheng, Zhi-yong, Cheng, Wei, Zhou, Gang, Sun, Tong-zhu
Format: Aufsatz
Sprache:Chinese
Veröffentlicht: 2004
Zugriff auf das übergeordnete Werk:Zhongguo wei zhong bing ji jiu yi xue = Chinese critical care medicine = Zhongguo weizhongbing jijiuyixue
Schlagworte:English Abstract Journal Article Research Support, Non-U.S. Gov't CTNNB1 protein, human Cadherins Cytoskeletal Proteins Proliferating Cell Nuclear Antigen Trans-Activators beta Catenin Keratins mehr... 68238-35-7 Matrix Metalloproteinases EC 3.4.24.-
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245 1 0 |a Study of mechanism on loss of some components from basement membrane in epithelial-interstitial junction in cutaneous pseudoepitheliomatous hyperplasia lesion 
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500 |a Date Revised 15.11.2006 
500 |a published: Print 
500 |a Citation Status MEDLINE 
520 |a OBJECTIVE: To investigate the relationship between the formation of pseudoepitheliomatous hyperplasia (PEH) and the mechanism of loss of some components from the basement membrane in epithelial interstitial junction (EIJ) in the treatment of cutaneous wounds, when formation of PEH lesion was induced 
520 |a METHODS: Morphological change in epithelial tissue was observed with histopathologic method and electronic microscopy in 11 specimens of PEH lesions and 6 specimens of normal skin adjacent to PEH (PEH-N) from 11 patients with injured skin. The expression characteristics and distribution of pan-cytokeratin (p-CK), matrix metalloproteinase-2 (MMP-2), MMP-3, MMP-9, proliferating cell nuclear antigen (PCNA), epithelial cadherin(E-Cad) and beta-catenin(beta-Cat) in EMJ were detected with immunohistochemical methods 
520 |a RESULTS: Epithelial cells expressing P-CK presented squamous epithelialization and extended into deep layer of mesenchyma. In epithelium-mesenchyma junction, where IV type collagen and laminin were weakly expressed, the protein contents of p-CK, E-Cad, MMP-2, MMP-3 MMP-9 were decreased, whilst the immunochemical staining of beta-Cat and PCNA was apparently increased. In the junction, epithelial basal cells were observed to migrate and to depart from basal membrane; epithelial islands and isolated epithelial cells expressing p-CK in mesenchyma could be observed. Ultrastructural observation revealed deformation of epithelial basal cells, increment of nucleus/cytoplasm ratio, loosened intercellular junctions, decrement of electronic density of BM and derangement of BM structure could be observed 
520 |a CONCLUSION: Reduction in the capability of epithelial basal cells adhesion, differentiation and formation of basement membrane and cytokeratin in PEH associated with wound may be the crucial cause which controls epithelial cells migration into mesenchyma. That the contents of ColIV and LN were decreased may not be associated with MMPs, but with enhancement of the ratio of beta-Cat/E-Cad signal might be the important mechanism of dedifferentiation of epithelial basal cells and the loss of ability of structure formation and cellular migration 
650 4 |a English Abstract 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 7 |a CTNNB1 protein, human  |2 NLM 
650 7 |a Cadherins  |2 NLM 
650 7 |a Cytoskeletal Proteins  |2 NLM 
650 7 |a Proliferating Cell Nuclear Antigen  |2 NLM 
650 7 |a Trans-Activators  |2 NLM 
650 7 |a beta Catenin  |2 NLM 
650 7 |a Keratins  |2 NLM 
650 7 |a 68238-35-7  |2 NLM 
650 7 |a Matrix Metalloproteinases  |2 NLM 
650 7 |a EC 3.4.24.-  |2 NLM 
700 1 |a Fu, Xiao-bing  |e verfasserin  |4 aut 
700 1 |a Sheng, Zhi-yong  |e verfasserin  |4 aut 
700 1 |a Cheng, Wei  |e verfasserin  |4 aut 
700 1 |a Zhou, Gang  |e verfasserin  |4 aut 
700 1 |a Sun, Tong-zhu  |e verfasserin  |4 aut 
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