CELLULAR-RESPONSES OF GUINEA-PIG MACROPHAGES TO C4A - INHIBITION OF C3A-INDUCED O2- GENERATION BY C4A

被引:24
作者
MURAKAMI, Y
YAMAMOTO, T
IMAMICHI, T
NAGASAWA, S
机构
[1] HOKKAIDO UNIV, FAC PHARMACEUT SCI, KITA KU, SAPPORO, HOKKAIDO 060, JAPAN
[2] KUMAMOTO UNIV, GRAD SCH MED SCI, DIV MOLEC PATHOL, KUMAMOTO 860, JAPAN
关键词
COMPLEMENT; ANAPHYLATOXINS; MACROPHAGES; CA2+ INFLUX; ACTIVE OXYGEN;
D O I
10.1016/0165-2478(93)90104-A
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have investigated the cellular responses of guinea-pig macrophages to human C4a. C4a induced a biphasic Ca2+ mobilization; a rapid temporary Ca2+ mobilization from intracellular Ca2+ pool followed by a weak Ca2+ influx of extracellular Ca2+. Although the C4a-treated macrophages did not respond again to C4a, that is, desensitization to C4a, the C4a-desensitized macrophages still responded to C3a to induce a Ca2+ mobilization. Furthermore, C4a failed to inhibit [I-125]-C3a binding to macrophages, suggesting that C4a receptors are different from C3a receptors. In contrast to C3a, C4a-induced Ca2+ mobilization didn't link to O2- generation but inhibited the C3a-induced O2- generation. These results suggest that C4a binds to a specific C4a receptor on guinea-pig macrophages to down-regulate the C3a receptor-mediated O2- generation in macrophages.
引用
收藏
页码:301 / 304
页数:4
相关论文
共 16 条
[1]   BIOLOGICAL-ACTIVITIES OF COMPLEMENT-DERIVED PEPTIDES [J].
DAMERAU, B .
REVIEWS OF PHYSIOLOGY BIOCHEMISTRY AND PHARMACOLOGY, 1987, 108 :151-206
[3]  
DISCIPIO RG, 1983, J BIOL CHEM, V258, P629
[4]   MOLECULAR CHARACTERIZATION OF THE COMPLEMENT ACTIVATING PROTEIN IN THE VENOM OF THE INDIAN COBRA (NAJA-N-SIAMENSIS) [J].
EGGERTSEN, G ;
LIND, P ;
SJOQUIST, J .
MOLECULAR IMMUNOLOGY, 1981, 18 (02) :125-133
[5]  
GOLDSTEIN IM, 1988, INFLAMMATION BASIC P, P55
[6]  
HUGLI TE, 1984, SPRINGER SEMIN IMMUN, V7, P193
[7]   PREPARATION OF IODINE-131 LABELLED HUMAN GROWTH HORMONE OF HIGH SPECIFIC ACTIVITY [J].
HUNTER, WM ;
GREENWOOD, FC .
NATURE, 1962, 194 (4827) :495-&
[8]  
IMAMICHI T, 1990, MOL IMMUNOL, V27, P829
[9]  
JANATOVA J, 1988, METHOD ENZYMOL, V162, P579
[10]  
MATSUBARA S, 1991, AM J PATHOL, V138, P1279