The canine mast cell activation via CRP

被引:10
作者
Fujimoto, T
Sato, Y
Sasaki, N
Teshima, R
Hanaoka, K
Kitani, S
机构
[1] Univ Tokyo, Grad Sch Med, Dept Anesthesiol, Bunkyo Ku, Tokyo, Japan
[2] Univ Tokyo, Grad Sch Med, Dept Resp Med, Bunkyo Ku, Tokyo, Japan
[3] Univ Tokyo, Grad Sch Agr & Life Sci, Lab Vet Surg, Bunkyo Ku, Tokyo, Japan
[4] Natl Inst Hlth Sci, Div Biochem & Immunochem, Tokyo 158, Japan
[5] Tokyo Univ Fisheries, Hlth Sci Ctr, Tokyo 108, Japan
关键词
canine mast cell; C-reactive protein; chemotaxis; inflammation; pentraxin; G-proteins;
D O I
10.1016/S0006-291X(02)03009-7
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
We report here canine mastocytoma-derived cell (CMMC) activation via two pentraxin, limulus- and human-CRP. Mast cell chemotaxis was measured by Boyden's blindwell chamber. To confirm that the cell migration was chemotactic, "checkerboard" analysis was performed. We used Fura-2 to investigate CRP-mediated cytosolic calcium elevation. To examine whether CRP-induced stimulation is mediated through G-proteins, CMMC were incubated with pertussis toxin (PTx) before use in chemotaxis assay and Ca2+ mobilization. CMMC migration in response to CRP was both chemokinetic and chemotactic. Limulus-CRP induced a transient Ca2+-mobilization dose-dependently. Preincubation of the cells with PTx inhibited CRP chemotaxis and Ca2+-mobilization, suggesting that G-proteins of the Gi-class are involved in the chemotaxis. We suggest that CRP may participate in the migration of mast cells to inflamed tissues during an acute-phase response. CRP-mediated recruitment of mast cells might play an important role in hypersensitivity and inflammatory processes. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:212 / 217
页数:6
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