In vitro studies of spontaneous and corticosteroid-induced apoptosis of lymphocyte populations from metamorphosing frogs RU486 inhibition

被引:22
作者
Barker, KS [1 ]
Davis, AT [1 ]
Li, B [1 ]
RollinsSmith, LA [1 ]
机构
[1] VANDERBILT UNIV,MED CTR,SCH MED,DEPT PEDIAT,NASHVILLE,TN 37232
关键词
D O I
10.1006/brbi.1997.0489
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Metamorphosis in the South African clawed frog, Xenopus laevis, results in significant changes in the immune system. It is characterized by a striking involution of the thymus and spleen followed by lymphocyte expansion in the postmetamorphic period. While thyroid hormones are generally thought to be the most important mediators of morphological changes during metamorphosis, corticosteroid hormones (CH) have also been shown to accelerate metamorphic changes. We have been studying the possible role of CH as effecters of changes in the immune system at metamorphosis. Because CH induce apoptosis of developing murine thymocytes, we examined in vitro levels of spontaneous and CH-inducible apoptosis of lymphocyte populations removed from the thymus and spleen of tadpoles before metamorphosis, during the period of naturally elevated corticosteroids at the climax of metamorphosis, and from postmetamorphic adults. We show here that spontaneous apoptosis of splenocytes or thymocytes measurable at the time of sacrifice or after culture for 24 h at 4 degrees C is very low at all stages of development and is nor increased at metamorphosis. Apoptosis induced by culture of lymphocytes for 24 h at 26 degrees C in 10 nM corticosterone (well below the peak level of 70 nM found at climax of metamorphosis) ranges from about 30-50% in the splenocyte population and 55-70% in the thymocyte population. Using the corticosteroid hormone receptor antagonist, RU486, we separated the CH-dependent component of apoptosis from apoptosis due to other factors. In the spleen, about 12-23% of lymphocytes are susceptible to corticosteroid-induced apoptosis at all larval stages as well as during climax of metamorphosis as measured by this short term culture assay. Another approximately 15% of cells undergo spontaneous apoptosis which is independent of CH. Although dissociated thymocytes exhibit very high levels of apoptosis (55-75%) during culture at 26 degrees C for 24 h, most of the apoptosis is independent of CH and map result from loss of ''survival signals'' due to the disruption of the thymic microenvironment. These studies support the hypothesis that naturally elevated levels of endogenous free CH delete a significant proportion of the larval splenocyte population during climax of metamorphosis by induction of apoptosis. This clearing of lymphocytes may prevent destructive autoimmune responses to the new set of adult-specific antigens that emerges at metamorphosis. (C) 1997 Academic Press.
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页码:119 / 131
页数:13
相关论文
共 36 条
[1]  
[Anonymous], [No title captured]
[2]   INDUCTION OF SKIN ALLOGRAFT TOLERANCE DURING METAMORPHOSIS OF TOAD XENOPUS-LAEVIS - POSSIBLE MODEL FOR STUDYING GENERATION OF SELF TOLERANCE TO HISTOCOMPATIBILITY ANTIGENS [J].
CHARDONNENS, X ;
DUPASQUI.L .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1973, 3 (09) :569-573
[3]  
COHEN JJ, 1992, ANNU REV IMMUNOL, V10, P267, DOI 10.1146/annurev.iy.10.040192.001411
[4]  
COHEN N, 1985, METAMORPHOSIS, P388
[5]  
Denver RJ, 1996, METAMORPHOSIS POSTEM, P433, DOI DOI 10.1016/B978-012283245-1/50014-2
[6]   IMMUNOGENETIC ASPECTS OF INVIVO ALLOTOLERANCE INDUCTION DURING THE ONTOGENY OF XENOPUS-LAEVIS [J].
DIMARZO, SJ ;
COHEN, N .
IMMUNOGENETICS, 1982, 16 (02) :103-116
[7]  
DIMARZO SJ, 1982, IMMUNOLOGY, V45, P39
[8]  
Du Pasquier L, 1990, Dev Immunol, V1, P85, DOI 10.1155/1990/67913
[9]   THYMUS DURING ONTOGENY OF TOAD XENOPUS-LAEVIS - GROWTH, MEMBRANE-BOUND IMMUNOGLOBULINS AND MIXED LYMPHOCYTE-REACTION [J].
DUPASQUIER, L ;
WEISS, N .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1973, 3 (12) :773-777
[10]   EVOLUTION OF THE MHC - ANTIGENICITY AND UNUSUAL TISSUE DISTRIBUTION OF XENOPUS (FROG) CLASS-II MOLECULES [J].
FLAJNIK, MF ;
FERRONE, S ;
COHEN, N ;
DUPASQUIER, L .
MOLECULAR IMMUNOLOGY, 1990, 27 (05) :451-462