Transforming growth factor-beta 1, 2, 3 and receptor type I and II in diabetic foot ulcers

被引:138
作者
Jude, EB
Blakytny, R
Bulmer, J
Boulton, AJM
Ferguson, MWJ
机构
[1] Manchester Royal Infirm, Dept Med & Diabet, Manchester M13 9WL, Lancs, England
[2] Univ Manchester, Sch Biol Sci, Manchester, Lancs, England
关键词
diabetes mellitus; diabetic neuropathy; diabetic foot ulcer; chronic venous ulcer; transforming growth factor;
D O I
10.1046/j.1464-5491.2002.00692.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims To study the distribution of transforming growth factor-beta (TGF-beta) 1, 2 and 3, and TGF-beta receptor types I and II in diabetic foot ulcers, diabetic skin and normal skin by immunohistochemistry, immunofluorescence and Western blotting. We also compared the TGF-betas with those of chronic venous ulcers. Methods Skin biopsies were obtained from the leg or the foot of non-diabetic and diabetic subjects, and from the edge of diabetic foot ulcers and chronic venous ulcers. Distribution (by immunofluorescence and immunocytochemistry) of TGF-beta 1, 2 and 3 and TGF-beta receptors (RI and RII) was done by staining 8-mum skin sections using appropriate antibodies. Protein levels of TGF-beta were measured by Western blot analysis. Results TGF-beta expression was increased in the epithelium at the edge of diabetic foot ulcers, being more intense than diabetic and normal skin (P = 0.03, 0.02, respectively), as was its expression in venous ulcers compared with normal skin. However, TGF-beta1 expression was not increased in diabetic foot ulcers and chronic venous ulcers, and was comparable to diabetic and normal skin. There was also no increase for the receptors in diabetic foot ulcers. Conclusion The lack of TGF-beta1 up-regulation in both diabetic foot ulcers and venous ulcers may explain the impaired healing in these chronic wounds, and could represent a general pattern for chronicity.
引用
收藏
页码:440 / 447
页数:8
相关论文
共 31 条
  • [1] Multicenter study of the incidence of and predictive risk factors for diabetic neuropathic foot ulceration
    Abbott, CA
    Vileikyte, L
    Williamson, S
    Carrington, AL
    Boulton, AJM
    [J]. DIABETES CARE, 1998, 21 (07) : 1071 - 1075
  • [2] REGULATION OF PLATELET-DERIVED GROWTH-FACTOR-A AND GROWTH-FACTOR-B CHAIN GENE-EXPRESSION IN BONE-MARROW STROMAL CELLS
    ABBOUD, SL
    [J]. JOURNAL OF CELLULAR PHYSIOLOGY, 1995, 164 (02) : 434 - 440
  • [3] [Anonymous], 2000, FOOT DIABETES
  • [4] ONE SYSTEMIC ADMINISTRATION OF TRANSFORMING GROWTH-FACTOR-BETA-1 REVERSES AGE-IMPAIRED OR GLUCOCORTICOID-IMPAIRED WOUND-HEALING
    BECK, LS
    DEGUZMAN, L
    LEE, WP
    XU, Y
    SIEGEL, MW
    AMENTO, EP
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (06) : 2841 - 2849
  • [5] Blakytny Robert, 2000, Journal of Pathology, V190, P589, DOI 10.1002/(SICI)1096-9896(200004)190:5<589::AID-PATH553>3.0.CO
  • [6] 2-T
  • [7] BOULTON AJM, 1997, TXB DIABETES, P1
  • [8] Boyko EJ, 1996, DIABETIC MED, V13, P967, DOI 10.1002/(SICI)1096-9136(199611)13:11<967::AID-DIA266>3.3.CO
  • [9] 2-B
  • [10] Broadley K N, 1989, Biotechnol Ther, V1, P55