Inhibition of the stem cell factor-induced migration of mast cells by dexamethasone

被引:52
作者
Jeong, HJ
Na, HJ
Hong, SH
Kim, HM
机构
[1] Kyung Hee Univ, Dept Pharmacol, Coll Oriental Med, Seoul 130701, South Korea
[2] Wonkwang Univ, Coll Pharm, VestibuloCochlear Res Ctr, Jeonbuk 570749, South Korea
关键词
D O I
10.1210/en.2003-0115
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mast cell accumulation can be causally related to several allergic inflammations. Previous work has demonstrated that glucocorticoids decreased tissue mast cell number, and stem cell factor (SCF)-induced migration of mast cells required p38 MAPK activation. In the present study we investigated the effects of dexamethasone on SCF-induced migration of rat peritoneal mast cells (RPMCs). SCF significantly induced the migration of RPMCs at 4 h. Dexamethasone dose-dependently inhibited SCF-induced migration of RPMCs(similar to90.1% at 100 nM; P<0.05). The MAPK p38 inhibitor SB203580 (20 μM) also inhibited the SCF-induced migration. The ability of SCF to enhance morphological alteration and filamentous actin formation was also abolished by treatment with dexamethasone. Dexamethasone inhibited SCF-induced p38 MAPK activation to near-basal levels and induced MAPK phosphatase-1 expression. In addition, SCF-induced inflammatory cytokine production was significantly inhibited by treatment with dexamethasone or SB203580 (P<0.01). Our results show that dexamethasone potently regulates SCF-induced migration, p38 MAPK activation, and inflammatory cytokine production through the expression of MKP-1 protein in RPMCs. Such modulation may have functional consequences during dexamethasone treatment, especially mast cell-mediated allergic inflammation disorders.
引用
收藏
页码:4080 / 4086
页数:7
相关论文
共 53 条
  • [41] Nilsson G, 1999, BLOOD, V93, P2791
  • [42] T helper cell type 2 cytokine-mediated comitogenic responses and CCR3 expression during differentiation of human mast cells in vitro
    Ochi, H
    Hirani, WM
    Yuan, Q
    Friend, DS
    Austen, KF
    Boyce, JA
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 190 (02) : 267 - 280
  • [43] The p38 signal transduction pathway - Activation and function
    Ono, K
    Han, JH
    [J]. CELLULAR SIGNALLING, 2000, 12 (01) : 1 - 13
  • [44] Mucosal and enterocyte IL-6 production during sepsis and endotoxemia - role of transcription factors and regulation by the stress response
    Pritts, T
    Hungness, E
    Wang, Q
    Robb, B
    Hershko, D
    Hasselgren, PO
    [J]. AMERICAN JOURNAL OF SURGERY, 2002, 183 (04) : 372 - 383
  • [45] PTEIFFER JR, 1994, J IMMUNOL, V152, P270
  • [46] Tryptase-chymase double-positive human mast cells express the eotaxin receptor CCR3 and are attracted by CCR3-binding chemokines
    Romagnani, P
    De Paulis, A
    Beltrame, C
    Annunziato, F
    Dente, V
    Maggi, E
    Romagnani, S
    Marone, G
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 1999, 155 (04) : 1195 - 1204
  • [47] Migration of Langerhans cells in an in vitro organ culture system:: IL-6 and TNF-α are partially responsible for migration into the epidermis
    Saitoh, A
    Yasaka, N
    Osada, A
    Nakamura, K
    Furue, M
    Tamaki, K
    [J]. JOURNAL OF DERMATOLOGICAL SCIENCE, 1999, 19 (03) : 166 - 174
  • [48] Glucocorticoids inhibit proliferation and adhesion of the IL-3-dependent mast cell line, MC/9, to NIH/3T3 fibroblasts, with an accompanying decrease in IL-3 receptor expression
    Sakai, H
    Toyota, N
    Ito, F
    Takahashi, H
    Hashimoto, Y
    Iizuka, H
    [J]. ARCHIVES OF DERMATOLOGICAL RESEARCH, 1999, 291 (04) : 224 - 231
  • [49] Stem cell factor-induced migration of mast cells requires p38 mitogen-activated protein kinase activity
    Sundström, M
    Alfredsson, J
    Olsson, N
    Nilsson, G
    [J]. EXPERIMENTAL CELL RESEARCH, 2001, 267 (01) : 144 - 151
  • [50] THE MAST-CELL AND SYNOVIAL INFLAMMATION - OR, WHATS A NICE CELL LIKE YOU DOING IN A JOINT LIKE THIS
    WASSERMAN, SI
    [J]. ARTHRITIS AND RHEUMATISM, 1984, 27 (08): : 841 - 844