Migration of keratinocytes is impaired on glycated collagen I

Keisuke Morita, Kazunori Urabe, Yoichi Moroi, Tetsuya Koga, Ryuji Nagai, Seiko Horiuchi, Masutaka Furue

研究成果: Contribution to journalArticle査読

20 被引用数 (Scopus)

抄録

Advanced glycation end products are the chemical modification of proteins induced by sugars in a hyperglycemic condition. Extracellular matrix proteins are prominent targets of nonenzymatic glycation because of their slow turnover rates. The aim of this study was to investigate the influence of nonenzymatic glycation of type I collagen on the migration of keratinocytes. The migration of keratinocytes was dramatically promoted on native type I collagen-coated dishes compared with that on uncoated dishes. When type collagen was glycated with glycolaldehyde, large amounts of advanced glycation end products were produced; the glycated collagen I-coated dishes did not promote the migration of keratinocytes. Glycated collagen I did not affect the proliferative capacity of keratinocytes. However, the adhesion of keratinocytes to glycated collagen I was profoundly diminished in a glycation intensity-dependent manner. α2β1 integrin is responsible for the migration and adhesion of keratinocytes to type I collagen. Pretreatment with glycated collagen I did not affect the expression level or functional activity of α2β1 integrin on keratinocytes. These findings suggest that in the presence of glycated collagen I, keratinocytes lose their adhesive and migratory abilities. As the glycation did not modify the α2β1 integrin on keratinocytes, it is suggested that glycation may diminish the binding capacity of type I collagen.

本文言語英語
ページ(範囲)93-101
ページ数9
ジャーナルWound Repair and Regeneration
13
1
DOI
出版ステータス出版済み - 1 2005

All Science Journal Classification (ASJC) codes

  • 外科
  • 皮膚病学

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