Regulation of eosinophil apoptosis: Transduction of survival and death signals

被引:29
作者
Simon, HU
Alam, R
机构
[1] Univ Zurich, Swiss Inst Allergy & Asthma Res, CH-7270 Davos, Switzerland
[2] Univ Texas, Med Branch, Dept Internal Med, Galveston, TX 77550 USA
关键词
apoptosis; eosinophils; Fas receptor; inflammation; interleukin-5; nitric oxide; signal transduction;
D O I
10.1159/000024025
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Since eosinophils are prominent in allergic inflammation, investigators became interested in how these cells accumulate in tissues and their role within the inflammatory cascade. There is increasing evidence from several laboratories that eosinophil numbers are regulated in vivo, not only by eosinophil production in the bone marrow, but also by the amount of eosinophil apoptosis, Moreover, it has been directly demonstrated that eosinophil apoptosis is delayed in allergic inflammatory sites, and that this mechanism contributes to the expansion of these cells in tissue. In this article, we review recent studies that shed light on the intracellular pathways that control eosinophil apoptosis.
引用
收藏
页码:7 / 14
页数:8
相关论文
共 62 条
[1]   TRANSFORMING GROWTH-FACTOR-BETA ABROGATES THE EFFECTS OF HEMATOPOIETINS ON EOSINOPHILS AND INDUCES THEIR APOPTOSIS [J].
ALAM, R ;
FORSYTHE, P ;
STAFFORD, S ;
FUKUDA, Y .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (03) :1041-1045
[2]   Human ICE/CED-3 protease nomenclature [J].
Alnemri, ES ;
Livingston, DJ ;
Nicholson, DW ;
Salvesen, G ;
Thornberry, NA ;
Wong, WW ;
Yuan, JY .
CELL, 1996, 87 (02) :171-171
[3]  
[Anonymous], APOPTOSIS, DOI DOI 10.1007/BF01321019
[4]   New frontiers for IL-5 [J].
Bagley, CJ ;
Lopez, AF ;
Vadas, MA .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1997, 99 (06) :725-728
[5]   NITRIC-OXIDE AND ASTHMATIC INFLAMMATION [J].
BARNES, PJ ;
LIEW, FY .
IMMUNOLOGY TODAY, 1995, 16 (03) :128-130
[6]   Interleukin 5 signals through Shc and Grb2 in human eosinophils [J].
Bates, ME ;
Busse, WW ;
Bertics, PJ .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1998, 18 (01) :75-83
[7]   Bcl-x(L) can inhibit apoptosis in cells that have undergone Fas-induced protease activation [J].
Boise, LH ;
Thompson, CB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (08) :3759-3764
[8]   ACTIVATION OF THE STAT3 ACUTE-PHASE RESPONSE FACTOR TRANSCRIPTION FACTOR BY INTERLEUKIN-5 [J].
CALDENHOVEN, E ;
VANDIJK, T ;
RAAIJMAKERS, JAM ;
LAMMERS, JWJ ;
KOENDERMAN, L ;
DEGROOT, RP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (43) :25778-25784
[9]  
Cascino I, 1996, J IMMUNOL, V156, P13
[10]   PROTECTION FROM FAS-MEDIATED APOPTOSIS BY A SOLUBLE FORM OF THE FAS MOLECULE [J].
CHENG, JH ;
ZHOU, T ;
LIU, CD ;
SHAPIRO, JP ;
BRAUER, MJ ;
KIEFER, MC ;
BARR, PJ ;
MOUNTZ, JD .
SCIENCE, 1994, 263 (5154) :1759-1762