Fibroblast growth-stimulating activity of S100A9 (MRP-14)

被引:37
|
作者
Shibata, F [1 ]
Miyama, K [1 ]
Shinoda, F [1 ]
Mizumoto, J [1 ]
Takano, K [1 ]
Nakagawa, H [1 ]
机构
[1] Toyama Med & Pharmaceut Univ, Fac Pharmaceut Sci, Dept Physiol Chem, Toyama 9300194, Japan
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 2004年 / 271卷 / 11期
关键词
carrageenan; fibroblast; growth; inflammation; S100A9;
D O I
10.1111/j.1432-1033.2004.04129.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fibroblasts play a critical role in chronic inflammation and wound healing. In this study, a fibroblast growth-stimulating factor was purified from the exudate of carrageenan-induced inflammation in rats. The purified protein was a disulfide-linked homodimer. Amino acid sequence analysis of the peptides generated by cleavage with cyanogen bromide and proteinase V8 resulted in identification of the protein as S100A9. Recombinant S100A9 as well as its disulfide-linked homodimer stimulated the proliferation of fibroblasts at a similar concentration of the purified protein. The concentration of S100A9 in the exudate was determined by immunoblot analysis. The total protein concentration in the exudate reached a maximum 4 days after carrageenan injection and then slightly decreased, whereas the concentration of S100A9 reached a maximum at day 3 and then decreased rapidly. These studies show that S100A9 is present at a high concentration in the exudate of carrageenan-induced inflammation in rats, and that S100A9 stimulates proliferation of fibroblasts, suggesting that it plays a role in chronic inflammation.
引用
收藏
页码:2137 / 2143
页数:7
相关论文
共 50 条
  • [1] Mitogenic activity of S100A9 (MRP-14)
    Shibata, F
    Ito, A
    Ohkuma, Y
    Mitsui, KI
    BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2005, 28 (12) : 2312 - 2314
  • [2] A comparison of human S100A12 with MRP-14 (S100A9)
    Robinson, MJ
    Hogg, N
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 275 (03) : 865 - 870
  • [3] Myeloid cell function in MRP-14 (S100A9) null mice
    Hobbs, JAR
    May, R
    Tanousis, K
    McNeill, E
    Mathies, M
    Gebhardt, C
    Henderson, R
    Robinson, MJ
    Hogg, N
    MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (07) : 2564 - 2576
  • [4] The heterodimeric complex of MRP-8 (S100A8) and MRP-14 (S100A9) - Antibody recognition, epitope definition and the implications for structure
    Hessian, PA
    Fisher, L
    EUROPEAN JOURNAL OF BIOCHEMISTRY, 2001, 268 (02): : 353 - 363
  • [5] Activity of a peptide identical to C-terminus region of the murine and human S100A9 protein (MRP-14) on in vivo neutrophilic migration
    Seixas, A. L. C.
    Pagano, R. L.
    Juliano, L.
    Juliano, M. A.
    Giorgi, R.
    FUNDAMENTAL & CLINICAL PHARMACOLOGY, 2004, 18 : 94 - 94
  • [6] Myeloid-Related Protein-14/MRP-14/S100A9/Calgranulin B is Associated with Inflammation in Proliferative Diabetic Retinopathy
    Abu El-Asrar, Ahmed M.
    Alam, Kaiser
    Siddiquei, Mohammad M.
    Van den Eynde, Kathleen
    Mohammad, Ghulam
    De Hertogh, Gert
    Opdenakker, Ghislain
    OCULAR IMMUNOLOGY AND INFLAMMATION, 2018, 26 (04) : 615 - 624
  • [7] THE S100 FAMILY PROTEIN MRP-14 (S100A9) HAS HOMOLOGY WITH THE CONTACT DOMAIN OF HIGH-MOLECULAR-WEIGHT KININOGEN
    HESSIAN, PA
    WILKINSON, L
    HOGG, N
    FEBS LETTERS, 1995, 371 (03) : 271 - 275
  • [8] Comparative evaluation of the antinociceptive effects of different peptide sequences that are homologous to the C-terminus of murine S100A9 protein (MRP-14)
    Dale, C. S.
    Pagano, R. L.
    Juliano, L.
    Juliano, M. A.
    Giorgi, R.
    FUNDAMENTAL & CLINICAL PHARMACOLOGY, 2004, 18 : 94 - 94
  • [9] Synthetic peptide identical to the C-terminus of the murine S100A9 (MRP-14) protein inhibits the function of adherent peritoneal cells
    Pagano, R. L.
    Sampaio, S. C.
    Juliano, L.
    Juliano, M. A.
    Giorgi, R.
    FUNDAMENTAL & CLINICAL PHARMACOLOGY, 2004, 18 : 93 - 93
  • [10] Novel insights into structure and function of MRP8 (S100A8) and MRP14 (S100A9)
    Kerkhoff, C
    Klempt, M
    Sorg, C
    BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 1998, 1448 (02): : 200 - 211