Regulation of cell surface tissue transglutaminase:: Effects on matrix storage of latent transforming growth factor-β binding protein-1

被引:88
作者
Verderio, E
Gaudry, C
Gross, S
Smith, C
Downes, S
Griffin, M
机构
[1] Nottingham Trent Univ, Dept Life Sci, Nottingham NG11 8NS, England
[2] Univ Nottingham, Fac Med, Dept Biomed Sci, Nottingham NG7 2RD, England
[3] Unilever Res Colworth, Bedford, England
关键词
tissue transglutaminase; latent transforming growth factor-beta binding protein-1; extracellular matrix fibronectin;
D O I
10.1177/002215549904701108
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Using a cytochemical approach, we examined the role of tissue transglutaminase (tTgase, Type II) in the incorporation of latent TGF-beta binding protein-1 (LTBP-1) in the extracellular matrix of Swiss 3T3 fibroblasts in which tTgase expression can be modulated through a tetracycline-controlled promoter. Increased tTgase expression led to an increased rate of LTBP-1 deposition in the matrix, which was accompanied by an increased pool of deoxycholate-insoluble fibronectin. Matrix deposition of LTBP-1 could also be reduced by the competitive amine substrate putrescine. Immunolocalization at the fluorescence and electron microscopic level showed that extracellular tTgase is located at the basal and apical surfaces of cells and at cell-cell contacts, and that LTBP-1 is co-distributed with cell surface tTgase, suggesting an early contribution of tTgase to the binding of LTBP-1 to matrix proteins. LTPB-1 was also found to co-localize with both intracellular and extracellular fibronectin, and increased immunoreactivity for LTBP-1 and fibronectin was found in large molecular weight polymers in the deoxycholate-insoluble matrix of fibroblasts overexpressing tTgase. We conclude that regulation of tTgase expression is important for controlling matrix storage of latent TGF-beta 1 complexes and that fibronectin may be one extracellular component to which LTBP-1 is crosslinked when LTBP-1 and tTgase interact at tissue transglutaminase the cell surface.
引用
收藏
页码:1417 / 1432
页数:16
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