Literature DB >> 35772750

Short Communication: Maternal obesity alters ovine endometrial gene expression during peri-implantation development.

Sarah R McCoski1, Rebecca R Cockrum2, Alan D Ealy3.   

Abstract

Exposure to maternal obesity in utero is associated with marked developmental effects in offspring that may not be evident until adulthood. Mechanisms regulating the programming effects of maternal obesity on fetal development have been reported, but little is known about how maternal obesity affects the earliest periods of embryonic development. This work explored how obesity influences endometrial gene expression during the peri-implantation period using a sheep model. Ewes were assigned randomly to diets that produced an obese state or maintained a lean state. After 4 mo, obese and lean ewes were bred and then euthanized at day 14 post-breeding. The uterus was excised, conceptuses were flushed, and endometrial tissue was collected. Isolated RNA from endometrial tissues (n = 6 ewes/treatment) were sequenced using an Illumina-based platform. Reads were mapped to the Ovis aries genome (Oar_4.0). Differential gene expression was determined, and results were filtered (false discovery rate ≤ 0.05 and ≥2-fold change, ≥0.2 reads/kilobase/million reads). Differentially expressed genes (DEGs) were identified (n = 699), with 171 downregulated and 498 upregulated in obese vs. lean endometrium, respectively. The most pronounced gene ontology categories identified were cellular process, metabolic process, and biological regulation. Enrichments were detected within the DEGs for genes involved with immune system processes, negative regulation of apoptosis, cell growth, and cell adhesion. A literature search revealed that 125 DEGs were associated with either the trophoblast lineage or the placenta. Genes within this grouping were involved with wingless/integrated signaling, angiogenesis, and integrin signaling. In summary, these data indicate that the peri-implantation endometrium is responsive to maternal obesity. Transcript profile analyses suggest that the endometrial immune response, adhesion, and angiogenesis may be especially susceptible to obesity. Thus, alterations in uterine transcript profiles during early embryogenesis may be a mechanism responsible for developmental programming following maternal obesity exposure in utero.
© The Author(s) 2022. Published by Oxford University Press on behalf of the American Society of Animal Science. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  endometrium; ovine; pregnancy; transcriptomics

Mesh:

Year:  2022        PMID: 35772750      PMCID: PMC9246656          DOI: 10.1093/jas/skac090

Source DB:  PubMed          Journal:  J Anim Sci        ISSN: 0021-8812            Impact factor:   3.338


  48 in total

1.  Follicular dynamics, interval to ovulation and fertility after AI in short-term progesterone and PGF2α oestrous synchronization protocol in sheep.

Authors:  J F Cox; R Allende; E Lara; A Leiva; T Díaz; J Dorado; F Saravia
Journal:  Reprod Domest Anim       Date:  2012-04-04       Impact factor: 2.005

Review 2.  DOHaD (Developmental Origins of Health and Disease) and Birth Cohort Research.

Authors:  Hideoki Fukuoka
Journal:  J Nutr Sci Vitaminol (Tokyo)       Date:  2015       Impact factor: 2.000

3.  Serial measurement of uterine blood flow from mid to late gestation in growth restricted pregnancies induced by overnourishing adolescent sheep dams.

Authors:  J M Wallace; J S Milne; M Matsuzaki; R P Aitken
Journal:  Placenta       Date:  2008-06-24       Impact factor: 3.481

4.  Diet-induced obesity impairs endometrial stromal cell decidualization: a potential role for impaired autophagy.

Authors:  Julie S Rhee; Jessica L Saben; Allyson L Mayer; Maureen B Schulte; Zeenat Asghar; Claire Stephens; Maggie M-Y Chi; Kelle H Moley
Journal:  Hum Reprod       Date:  2016-04-06       Impact factor: 6.918

5.  Ovine osteopontin: II. Osteopontin and alpha(v)beta(3) integrin expression in the uterus and conceptus during the periimplantation period.

Authors:  G A Johnson; R C Burghardt; T E Spencer; G R Newton; T L Ott; F W Bazer
Journal:  Biol Reprod       Date:  1999-10       Impact factor: 4.285

6.  Prevalence of obesity in the United States, 2009-2010.

Authors:  Cynthia L Ogden; Margaret D Carroll; Brian K Kit; Katherine M Flegal
Journal:  NCHS Data Brief       Date:  2012-01

7.  WNT4 acts downstream of BMP2 and functions via β-catenin signaling pathway to regulate human endometrial stromal cell differentiation.

Authors:  Quanxi Li; Athilakshmi Kannan; Amrita Das; Franco J Demayo; Peter J Hornsby; Steven L Young; Robert N Taylor; Milan K Bagchi; Indrani C Bagchi
Journal:  Endocrinology       Date:  2012-11-09       Impact factor: 4.736

8.  Macrophage-derived LIF and IL1B regulate alpha(1,2)fucosyltransferase 2 (Fut2) expression in mouse uterine epithelial cells during early pregnancy.

Authors:  Melinda J Jasper; Alison S Care; Brad Sullivan; Wendy V Ingman; John D Aplin; Sarah A Robertson
Journal:  Biol Reprod       Date:  2010-09-23       Impact factor: 4.285

Review 9.  Inflammation and pregnancy: the role of the immune system at the implantation site.

Authors:  Gil Mor; Ingrid Cardenas; Vikki Abrahams; Seth Guller
Journal:  Ann N Y Acad Sci       Date:  2011-03       Impact factor: 5.691

10.  Interleukin-6 acts in the fashion of a classical chemokine on monocytic cells by inducing integrin activation, cell adhesion, actin polymerization, chemotaxis, and transmigration.

Authors:  Thomas Clahsen; Fred Schaper
Journal:  J Leukoc Biol       Date:  2008-09-02       Impact factor: 4.962

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