Literature DB >> 12444050

Regulation of insulin-like growth factor binding protein-6 expression in the reproductive tract throughout the estrous cycle and during the development of the placenta in the ewe.

T S Gadd1, J C Osgerby, D C Wathes.   

Abstract

Insulin-like growth factors (IGF-I and IGF-II) are essential for normal uterine development and have been particularly implicated in fetal and placental growth. A family of six IGF binding proteins enhance or attenuate IGF-stimulated cell proliferation. In this study we have used in situ hybridization to map the distribution of IGFBP-6, one of the lesser known of the IGFBPs, in sections of the uterus collected from cyclic, anestrous, and ovariectomized nonpregnant ewes and from the uterus and placenta of early pregnant (13-55 days) and unilaterally pregnant ewes. In nonpregnant ewes IGFBP-6 mRNA (measured as arbitrary optical density units from autoradiographs) was abundant in the periepithelium and caruncles, with lower levels in the endometrial stroma and myometrium. In most regions IGFBP-6 mRNA showed cyclic variations with concentrations maximal around ovulation and the early luteal phase. In addition, 16 out of 25 ewes expressed IGFBP-6 mRNA in their endometrial glands between estrus and Day 2. Measurements of IGFBP-6 mRNA were high in anestrous ewes (equivalent values to ovulation) but low in ovariectomized ewes (equivalent values to mid to late luteal phase). In pregnant ewes IGFBP-6 mRNA was found in similar regions to those recorded during the cycle. In the periepithelium and caruncular stroma IGFBP-6 mRNA levels were higher during early pregnancy than in the midluteal phase. In the unilateral pregnant ewes there was no difference in IGFBP-6 mRNA measured between pregnant and nonpregnant horns. In conclusion, IGFBP-6 mRNA is differentially regulated during the estrous cycle and pregnancy and may be functionally important in modulating IGF activity in the uterus and placenta by virtue of its strong affinity and ability to regulate IGF-II mediated actions.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12444050     DOI: 10.1095/biolreprod67.6.1756

Source DB:  PubMed          Journal:  Biol Reprod        ISSN: 0006-3363            Impact factor:   4.285


  6 in total

1.  Rapid molecular evolution across amniotes of the IIS/TOR network.

Authors:  Suzanne E McGaugh; Anne M Bronikowski; Chih-Horng Kuo; Dawn M Reding; Elizabeth A Addis; Lex E Flagel; Fredric J Janzen; Tonia S Schwartz
Journal:  Proc Natl Acad Sci U S A       Date:  2015-05-19       Impact factor: 11.205

2.  Ovine feto-placental metabolism.

Authors:  J W Ward; F B P Wooding; A L Fowden
Journal:  J Physiol       Date:  2003-10-31       Impact factor: 5.182

3.  Data mining in networks of differentially expressed genes during sow pregnancy.

Authors:  Ligang Wang; Longchao Zhang; Yong Li; Wen Li; Weizhen Luo; Duxue Cheng; Hua Yan; Xiaojun Ma; Xin Liu; Xin Song; Jing Liang; Kebin Zhao; Lixian Wang
Journal:  Int J Biol Sci       Date:  2012-04-16       Impact factor: 6.580

4.  Metabolic and endocrine profiles and hepatic gene expression of Holstein cows fed total mixed ration or pasture with different grazing strategies during early lactation.

Authors:  Ana Laura Astessiano; Ana Meikle; Maite Fajardo; Jorge Gil; Diego Antonio Mattiauda; Pablo Chilibroste; Mariana Carriquiry
Journal:  Acta Vet Scand       Date:  2015-10-16       Impact factor: 1.695

5.  Negative energy balance in dairy cows is associated with specific changes in IGF-binding protein expression in the oviduct.

Authors:  M A Fenwick; S Llewellyn; R Fitzpatrick; D A Kenny; J J Murphy; J Patton; D C Wathes
Journal:  Reproduction       Date:  2008-01       Impact factor: 3.906

6.  Endometrial expression of the insulin-like growth factor system during uterine involution in the postpartum dairy cow.

Authors:  S Llewellyn; R Fitzpatrick; D A Kenny; J Patton; D C Wathes
Journal:  Domest Anim Endocrinol       Date:  2007-12-26       Impact factor: 2.290

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.