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In vitro fertilization induces reproductive changes in male mouse offspring and has multigenerational effects
Eric A. Rhon-Calderon, Cassidy N. Hemphill, Alexandra J. Savage, Laren Riesche, Richard M. Schultz, Marisa S. Bartolomei
Eric A. Rhon-Calderon, Cassidy N. Hemphill, Alexandra J. Savage, Laren Riesche, Richard M. Schultz, Marisa S. Bartolomei
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Research Article Development Reproductive biology

In vitro fertilization induces reproductive changes in male mouse offspring and has multigenerational effects

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Abstract

In vitro fertilization (IVF) is a noncoital method of conception used to treat human infertility. Although IVF is viewed as largely safe, it is associated with adverse outcomes in the fetus, placenta, and adult offspring. Because studies focusing on the effect of IVF on the male reproductive system are limited, we used a mouse model to assess the morphological and molecular effects of IVF on male offspring. We evaluated 3 developmental stages: 18.5-day fetuses and 12- and 39-week-old adults. Regardless of age, we observed changes in testicular-to-body weight ratios, serum testosterone levels, testicular morphology, gene expression, and DNA methylation. Also, sperm showed changes in morphology and DNA methylation. To assess multigenerational phenotypes, we mated IVF-conceived and naturally conceived males with wild-type females. Offspring from IVF males exhibited decreased fetal-to-placental weight ratios and changes in placenta gene expression and morphology regardless of sex. At 12 weeks of age, offspring showed higher body weights and differences in glucose, triglyceride, insulin, total cholesterol, HDL-C, and LDL/VLDL-C levels. Both sexes showed changes in gene expression in liver, testes, and ovaries and decreased global DNA methylation. Collectively, our findings demonstrate that male IVF offspring exhibit abnormal testicular and sperm morphology and molecular alterations with a multigenerational impact.

Authors

Eric A. Rhon-Calderon, Cassidy N. Hemphill, Alexandra J. Savage, Laren Riesche, Richard M. Schultz, Marisa S. Bartolomei

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Figure 3

Sperm parameters and testicular DNA methylation.

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Sperm parameters and testicular DNA methylation.
(A) Sperm count using a...
(A) Sperm count using a bright-field microscope; (B) sperm morphology quantification using eosin 1% staining where sperm is categorized as normal (%normal), abnormal head (%head), abnormal tail (%tail), and abnormal midpiece (%midpiece); (C) testicular global DNA methylation; and (D) sperm global DNA methylation using LUMA for 12- and 39-week natural and IVF offspring. Infinium Mouse Methylation BeadChip sperm analysis, including (E) volcano plot for DMRs at 12 weeks, 12 weeks heatmap with (F) hypermethylated DMRs and (G) hypomethylated DMRs, (H) volcano plot for DMRs at 39 weeks, and 39 weeks heatmap with (I) hypermethylated DMRs and (J) hypomethylated DMRs. Seg, segmentation analysis. Each data point represents 1 individual from a minimum of 5 litters (n = 10–15/group). Data are expressed as mean ± SEM. Statistical analysis between groups was done by t test; *, **, and *** represent significant differences of P < 0.05, P < 0.01, and P < 0.001 respectively, when comparing IVF and Naturals. Variability was calculated using an F test, and # represents a significant difference (P < 0.05) in IVF compared with Naturals.

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