Changes of IgE production in senescence-accelerated mice SAMPS

被引:0
|
作者
Aoki, K
Asano, K
Okamoto, KI
Yoshida, T
Kuroiwa, Y
机构
[1] SHOWA UNIV, SCH PHARMACEUT SCI, DEPT CLIN PHARM, SHINAGAWA KU, TOKYO 142, JAPAN
[2] SHOWA UNIV, SCH MED, DEPT MED BIOL, TOKYO 142, JAPAN
来源
IN VIVO | 1996年 / 10卷 / 04期
关键词
senescence-accelerated mice (SAMP8); IgE production; interferon gamma; interleukin; 4; T and B cells function;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The IgE production and proliferation activity of spleen B cells were studied in vivo in 2 similar to 3-month-old (designated as young) and 12 similar to 13-month-old (designated as old) senescence-accelerated mice (SAMP8) employing age-matched AKR mice, the origin of the SAM strain, as controls. After the secondary immunization with 2,4-dinitrophenyl-ovalbumin conjugate (DNP-OVA) with aluminium hydroxide gel (alum) as an adjuvant, the serum IgE levels were significantly reduced in old SAMP8 compared to young SAMP8 mice, but there were no changes in AKR. However, old SAMP8 mice had a proliferative activity of spleen B cells comparable to that found in young SAMP8; proliferative activity was measured by H-3-thymidine incorporation into the spleen after stimulation with water extract from wood chips of coniferous splash pine (pine wood extract) as a mitogen. These data indicate that a decline in IgE production is a characteristic phenomenon of SAMP8 mice and was not due to the functional deficiency of B cells with aging.
引用
收藏
页码:417 / 420
页数:4
相关论文
共 50 条
  • [1] AORTIC CHANGES IN SENESCENCE-ACCELERATED FEMALE MICE
    Onetti, Y.
    Jimenez-Altayo, F.
    Vila, E.
    Dantas, A. P.
    HYPERTENSION, 2010, 56 (06) : 1172 - 1172
  • [2] Longitudinal Changes in Motor and Muscle Function in Senescence-Accelerated Mice
    Kanazawa, Yuji
    Higuchi, Takashi
    Sugiyo, Shinichi
    INTERNATIONAL JOURNAL OF GERONTOLOGY, 2022, 16 (02) : 155 - 156
  • [3] VASCULAR CHANGES ON MESENTERIC ARTERIES FROM SENESCENCE-ACCELERATED MICE
    Jimenez-Altayo, F.
    Romo, M.
    Onetti, Y.
    Dantas, A. P.
    Vila, E.
    HYPERTENSION, 2010, 56 (06) : 1172 - 1172
  • [4] Oxidative status in senescence-accelerated mice
    Park, JW
    Choi, CH
    Kim, MS
    Chung, MH
    JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 1996, 51 (05): : B337 - B345
  • [5] Early atherogenesis in senescence-accelerated mice
    Fenton, M
    Huang, HL
    Hong, Y
    Hawe, E
    Kurz, DJ
    Erusalimsky, JD
    EXPERIMENTAL GERONTOLOGY, 2004, 39 (01) : 115 - 122
  • [6] Mechanisms of aging in senescence-accelerated mice
    Carter, TA
    Greenhall, JA
    Yoshida, S
    Fuchs, S
    Helton, R
    Swaroop, A
    Lockhart, DJ
    Barlow, C
    GENOME BIOLOGY, 2005, 6 (06)
  • [7] Analysis of spermatogenesis in senescence-accelerated mice
    Zakhidov, S. T.
    Gopko, A. V.
    Marshak, T. L.
    Kulibin, A. Yu.
    Zelenina, I. A.
    BIOLOGY BULLETIN, 2007, 34 (06) : 551 - 557
  • [8] Analysis of spermatogenesis in senescence-accelerated mice
    S. T. Zakhidov
    A. V. Gopko
    T. L. Marshak
    A. Yu. Kulibin
    I. A. Zelenina
    Biology Bulletin, 2007, 34 : 551 - 557
  • [9] Mechanisms of aging in senescence-accelerated mice
    Todd A Carter
    Jennifer A Greenhall
    Shigeo Yoshida
    Sebastian Fuchs
    Robert Helton
    Anand Swaroop
    David J Lockhart
    Carrolee Barlow
    Genome Biology, 6
  • [10] The neurosecretory system is hypertrophied in senescence-accelerated mice
    Crespo, D
    Megias, M
    Fernandez-Viadero, C
    Alonso, L
    Verduga, R
    REJUVENATION RESEARCH, 2006, 9 (02) : 297 - 301