Use of a Mouse In Vitro Fertilization Model to Understand the Developmental Origins of Health and Disease Hypothesis

Author:

Feuer Sky K.1,Liu Xiaowei1,Donjacour Annemarie1,Lin Wingka1,Simbulan Rhodel K.1,Giritharan Gnanaratnam12,Piane Luisa Delle13,Kolahi Kevin14,Ameri Kurosh5,Maltepe Emin5,Rinaudo Paolo F.1

Affiliation:

1. Department of Obstetrics, Gynecology and Reproductive Sciences (S.K.F., X.L., A.D., W.L., R.K.S., G.G., L.D.P., K.K., P.F.R.), University of California San Francisco, San Francisco, California 94143;

2. Nevada Center for Reproductive Medicine (G.G.), Reno, Nevada 89511;

3. Obstetric and Gynecology Department (L.D.P.), University of Turin, Turin, Italy;

4. Oregon Health & Science University (K.K.), Portland, Oregon 97239

5. Department of Pediatrics (K.A., E.M.), University of California San Francisco, San Francisco, California 94143;

Abstract

The Developmental Origins of Health and Disease hypothesis holds that alterations to homeostasis during critical periods of development can predispose individuals to adult-onset chronic diseases such as diabetes and metabolic syndrome. It remains controversial whether preimplantation embryo manipulation, clinically used to treat patients with infertility, disturbs homeostasis and affects long-term growth and metabolism. To address this controversy, we have assessed the effects of in vitro fertilization (IVF) on postnatal physiology in mice. We demonstrate that IVF and embryo culture, even under conditions considered optimal for mouse embryo culture, alter postnatal growth trajectory, fat accumulation, and glucose metabolism in adult mice. Unbiased metabolic profiling in serum and microarray analysis of pancreatic islets and insulin sensitive tissues (liver, skeletal muscle, and adipose tissue) revealed broad changes in metabolic homeostasis, characterized by systemic oxidative stress and mitochondrial dysfunction. Adopting a candidate approach, we identify thioredoxin-interacting protein (TXNIP), a key molecule involved in integrating cellular nutritional and oxidative states with metabolic response, as a marker for preimplantation stress and demonstrate tissue-specific epigenetic and transcriptional TXNIP misregulation in selected adult tissues. Importantly, dysregulation of TXNIP expression is associated with enrichment for H4 acetylation at the Txnip promoter that persists from the blastocyst stage through adulthood in adipose tissue. Our data support the vulnerability of preimplantation embryos to environmental disturbance and demonstrate that conception by IVF can reprogram metabolic homeostasis through metabolic, transcriptional, and epigenetic mechanisms with lasting effects for adult growth and fitness. This study has wide clinical relevance and underscores the importance of continued follow-up of IVF-conceived offspring.

Publisher

The Endocrine Society

Subject

Endocrinology

Reference64 articles.

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3. Long-term effects of culture of preimplantation mouse embryos on behavior;Ecker;Proc Natl Acad Sci USA,2004

4. Metabolism of the preimplantation embryo: 40 years on;Leese;Reproduction,2012

5. Preimplantation stress and development;Feuer;Birth Defects Res C,2012

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