BONE-MARROW CELL RESPONSE FOLLOWING INDUCTION OF ACUTE-INFLAMMATION IN DIFFERENT STRAINS OF MICE

被引:6
作者
POZZULO, GN
SKAMENE, E
GERVAIS, F
机构
[1] McGill Center for the Study of Host Resistance, Montreal General Hospital Research Institute, Montreal, H3G 1A4, Quebec
关键词
D O I
10.1007/BF00920473
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The magnitude of the macrophage inflammatory response differs among inbred mouse strains. Mice of the A/J strain respond poorly to sterile inflammatory stimuli while those of the C57BL/6 strain show a strong response. Inflammatory macrophages found at the site of inflammation are the product of bone marrow (BM) myeloid stem cells. Mice of the A/J strain were found to have half the number of BM nucleated cells per femur than those of the C57BL/6 strain. The lower BM cellularity may be one reason for the poor macrophage inflammatory response observed in A/J mouse strain. Using A x B/B x A recombinant inbred mouse strains, we determined that the number of nucleated cells per femur found in normal mice was not a determining factor of the magnitude of the macrophage inflammatory response. One additional explanation for the poor macrophage inflammatory response in mice of the A/J strain is their deficiency in the C5 component of complement. Using a C5-sufficient A/J.C5 congenic strain, we have previously shown that the presence of C5 on the A/J background improved their inflammatory response. We compared A/J and A/J.C5 mouse strains to determine whether or not C5 had an impact on the BM cell response to inflammatory stimulus. The presence of C5 on the A/J background could contribute to the improvement of the inflammatory response in mice of the A/J.C5 strain by inducing a greater number of nucleated cells to exit the BM compartment early following induction of inflammation.
引用
收藏
页码:677 / 685
页数:9
相关论文
共 29 条
[1]  
ANNEMA A, 1992, EXP HEMATOL, V20, P69
[2]   REGULATION OF MYELOPOIESIS [J].
BENDER, JG ;
VANEPPS, DE ;
STEWART, CC .
COMPARATIVE IMMUNOLOGY MICROBIOLOGY AND INFECTIOUS DISEASES, 1987, 10 (02) :79-91
[3]   DERIVATION OF 2 DISTINCT ANAPHYLATOXIN ACTIVITIES FROM THIRD AND FIFTH COMPONENTS OF HUMAN COMPLEMENT [J].
COCHRANE, CG ;
MULLEREB.HJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1968, 127 (02) :371-&
[5]  
DIESSELHOFFDENDULK MMC, 1979, IMMUNOLOGY, V37, P7
[6]  
GERVAIS F, 1984, J IMMUNOL, V132, P2078
[7]  
GERVAIS F, 1989, J IMMUNOL, V142, P2057
[8]  
GOLDE DW, 1988, INFLAMMATION BASIC P, P253
[9]  
Hugh T.E, 1984, SPRINGER SEMIN IMMUN, V7, P193
[10]  
Hugh T. E., 1978, ADV IMMUNOL, V26, P1