Gonadotropin-releasing hormone attenuates pregnancy-associated thymic involution and modulates the expression of antiproliferative gene product prohibitin

被引:47
作者
Dixit, VD
Sridaran, R
Edmonsond, MA
Taub, D
Thompson, WE
机构
[1] Morehouse Sch Med, Dept Obstet & Gynecol, Cooperat Reprod Sci Res Ctr, Atlanta, GA 30310 USA
[2] NIA, Dept Physiol, Cooperat Reprod Sci Res Ctr, Lab Immunol,NIH, Baltimore, MD 21224 USA
关键词
D O I
10.1210/en.2002-220955
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Thymic involution during pregnancy is believed to be a critical adaptive mechanism for regulation and control of the maternal immune system. These regulatory feedback mechanisms are important for the survival of the semiallogeneic fetus. In the present study, we examined the effects of GnRH on pregnancy-induced thymic involution by characterizing the expression patterns of prohibitin (PHB), an antiproliferative gene product, GnRH, and GnRH receptor (GnRH-R) proteins in the rat thymus and in mature splenic lymphocytes. GnRH agonist infusions in pregnant rats markedly attenuated pregnancy-induced thymic involution resulting in significant increases in thymic weight and thymocyte numbers. In addition, histological examination of the thymus revealed increase in cortical cellularity. Western blot analyses revealed a significant increase of total PHB protein content in thymi during pregnancy. Furthermore, distinct changes in PHB isoform expression were observed in the pregnant involuting thymi with greater expression of the basic PHB isoform. Basic isoform expression decreased in pregnant rats and was comparable with nonpregnant rat thymi upon GnRH agonist treatment. PHB is mainly expressed in mature cells of the thymic medulla, where it strongly colocalized with GnRH. We have observed GnRH-R immunoreactivity mainly in thymic medulla. Furthermore, as assessed by immunofluorescence double labeling with proliferating cell nuclear antigen, PHB was preferentially expressed in nonproliferating thymocytes. In this study, we demonstrated that GnRH, GnRH-R, and PHB show characteristic polarized expression in thymocytes. In addition, GnRH and PHB were coexpressed in mature splenic T cells. Our results suggest that PHB and GnRH are involved in thymic growth and may be important for maturation of T lymphocytes.
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页码:1496 / 1505
页数:10
相关论文
共 51 条
  • [1] Alonso MA, 2001, J CELL SCI, V114, P3957
  • [2] REGIONS OF EVOLUTIONARY CONSERVATION BETWEEN THE RAT AND HUMAN PROHIBITIN-ENCODING GENES
    ALTUS, MS
    WOOD, CM
    STEWART, DA
    ROSKAMS, AJI
    FRIEDMAN, V
    HENDERSON, T
    OWENS, GA
    DANNER, DB
    JUPE, ER
    DELLORCO, RT
    MCCLUNG, JK
    [J]. GENE, 1995, 158 (02) : 291 - 294
  • [3] The role of gonadectomy and testosterone replacement on thymic luteinizing hormone-releasing hormone production
    Azad, N
    LaPaglia, N
    Agrawal, L
    Steiner, J
    Uddin, S
    Williams, DW
    Lawrence, AM
    Emanuele, NV
    [J]. JOURNAL OF ENDOCRINOLOGY, 1998, 158 (02) : 229 - 235
  • [4] LUTEINIZING-HORMONE-RELEASING HORMONE SIGNALING AT THE LYMPHOCYTE INVOLVES STIMULATION OF INTERLEUKIN-2 RECEPTOR EXPRESSION
    BATTICANE, N
    MORALE, MC
    GALLO, F
    FARINELLA, Z
    MARCHETTI, B
    [J]. ENDOCRINOLOGY, 1991, 129 (01) : 277 - 286
  • [5] CYCLIN PCNA IS THE AUXILIARY PROTEIN OF DNA POLYMERASE-DELTA
    BRAVO, R
    FRANK, R
    BLUNDELL, PA
    MACDONALDBRAVO, H
    [J]. NATURE, 1987, 326 (6112) : 515 - 517
  • [6] Chen A, 2002, CANCER RES, V62, P1036
  • [7] Human peripheral blood mononuclear cells express gonadotropin-releasing hormone (GnRH), GnRH receptor, and interleukin-2 receptor γ-chain messenger ribonucleic acids that are regulated by GnRH in vitro
    Chen, HF
    Jeung, EB
    Stephenson, M
    Leung, PCK
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1999, 84 (02) : 743 - 750
  • [8] CHEN IT, 1995, ONCOGENE, V11, P1931
  • [9] THE THYMUS IN PREGNANCY - THE INTERPLAY OF NEURAL, ENDOCRINE AND IMMUNE INFLUENCES
    CLARKE, AG
    KENDALL, MD
    [J]. IMMUNOLOGY TODAY, 1994, 15 (11): : 545 - 551
  • [10] The prohibitin family of mitochondrial proteins regulate replicative lifespan
    Coates, PJ
    Jamieson, DJ
    Smart, K
    Prescott, AR
    Hall, PA
    [J]. CURRENT BIOLOGY, 1997, 7 (08) : 607 - 610