Cytokine knockouts in reproduction: the use of gene ablation to dissect roles of cytokines in reproductive biology

被引:45
作者
Ingman, Wendy V. [1 ]
Jones, Rebecca L. [2 ]
机构
[1] Univ Adelaide, Res Ctr Reprod Hlth, Discipline Obstet & Gynaecol, Adelaide, SA 5005, Australia
[2] Univ Manchester, St Marys Hosp, Maternal & Fetal Hlth Res Grp, Manchester M13 0JH, Lancs, England
关键词
cytokines; gene ablation; animal model; IVF; contraception;
D O I
10.1093/humupd/dmm042
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Cytokines play many diverse and important roles in reproductive biology, and dissecting the complex interactions between these proteins and the different reproductive organs is a difficult task. One approach is to use gene ablation, or 'knockout', to analyse the effect of deletion of a single cytokine on mouse reproductive function. This review summarizes the essential roles of cytokines in reproductive biology that have been revealed by gene knockout studies, including development and regulation of the hypothalamo-pituitary-gondal axis, ovarian folliculogenesis, implantation and immune system modulation during pregnancy. However, successful utilization of this approach must consider the caveats associated with gene ablation studies, e.g. embryonic lethality, systemic effects of cytokine ablation on local reproductive processes and the limited exposure to pathogens in mice housed in laboratory conditions. New sophisticated technology that temporally or spatially regulates gene ablation can overcome some of these limitations. Discoveries on the roles of cytokines in reproductive function uncovered by gene ablation studies can now be applied to improve in vitro fertilization for infertile couples and in the development of contraceptive therapies.
引用
收藏
页码:179 / 192
页数:14
相关论文
共 170 条
[1]   Reproduction in mice lacking a functional type 1 IL-1 receptor [J].
Abbondanzo, SJ ;
Cullinan, EB ;
McIntyre, K ;
Labow, MA ;
Stewart, CL .
ENDOCRINOLOGY, 1996, 137 (08) :3598-3601
[2]   Suppressors of cytokine signalling (SOCS) in the immune system [J].
Alexander, WS .
NATURE REVIEWS IMMUNOLOGY, 2002, 2 (06) :410-416
[3]   Regulatory T cells mediate maternal tolerance to the fetus [J].
Aluvihare, VR ;
Kallikourdis, M ;
Betz, AG .
NATURE IMMUNOLOGY, 2004, 5 (03) :266-271
[4]   Follicular development and ovulation in macrophage colony-stimulating factor-deficient mice homozygous for the osteopetrosis (op) mutation [J].
Araki, M ;
Fukumatsu, Y ;
Katabuchi, H ;
Shultz, LD ;
Takahashi, K ;
Okamura, H .
BIOLOGY OF REPRODUCTION, 1996, 54 (02) :478-484
[5]   Assessment of requirements for IL-15 and IFN regulatory factors in uterine NK cell differentiation and function during pregnancy [J].
Ashkar, AA ;
Black, GP ;
Wei, QX ;
He, H ;
Liang, LC ;
Head, JR ;
Croy, BA .
JOURNAL OF IMMUNOLOGY, 2003, 171 (06) :2937-2944
[6]   Practical range of effective dose for Cre recombinase-expressing recombinant adenovirus without cell toxicity in mammalian cells [J].
Baba, Y ;
Nakano, M ;
Yamada, Y ;
Saito, I ;
Kanegae, Y .
MICROBIOLOGY AND IMMUNOLOGY, 2005, 49 (06) :559-570
[7]   The uterine NK cell population requires IL-15 but these cells are not required for pregnancy nor the resolution of a Listeria monocytogenes infection [J].
Barber, EM ;
Pollard, JW .
JOURNAL OF IMMUNOLOGY, 2003, 171 (01) :37-46
[8]   Adult consequences of fetal growth restriction [J].
Barker, David J. P. .
CLINICAL OBSTETRICS AND GYNECOLOGY, 2006, 49 (02) :270-283
[9]   In vivo adenovirus-mediated gene transduction into mouse endometrial glands: a novel tool to model endometrial cancer in the mouse [J].
Beauparlant, SL ;
Read, PW ;
Di Cristofano, A .
GYNECOLOGIC ONCOLOGY, 2004, 94 (03) :713-718
[10]   UTERINE EXPRESSION OF LEUKEMIA INHIBITORY FACTOR COINCIDES WITH THE ONSET OF BLASTOCYST IMPLANTATION [J].
BHATT, H ;
BRUNET, LJ ;
STEWART, CL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (24) :11408-11412