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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 6

Multigenerational impacts of IVF in placenta.

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Multigenerational impacts of IVF in placenta.
Percentage of placental ju...
Percentage of placental junctional and labyrinth zone at E18.5 using hematoxylin-eosin staining. Placenta cross sections from (A) hematoxylin-eosin–stained tissues (scale bar: 850 μm) from F2 E18.5 male placentas with the percentage of (B) labyrinth zone and (C) junctional zone shown. (D) Hematoxylin-eosin histological sections from F2 E18.5 female placentas with the percentage of (E) labyrinth zone and (F) junctional zone indicated. Quantitative analysis of labyrinth fetal endothelial cells using CD34 and counterstained with hematoxylin in natural and IVF placentas at E18.5: (G) representative images of male placentas from E18.5 natural and IVF and (H) quantification of E18.5 fetal endothelial cell positive staining as a percentage of total labyrinth area using ePathology software (5, 24) for male placentas. (I) Representative images of female placentas from F2 E18.5 natural and IVF and (J) quantification of E18.5 fetal endothelial cell positive staining in females. Original magnification is 4× (G and I). RNA-Seq using F2 male and female E18.5 placentas: volcano plots showing DEGs for (K) F2 male E18.5 placentas and (L) F2 female E18.5 placentas IVF versus natural. Heatmap for log2-transformed expression levels obtained from RNA-Seq of DEGs in (M) F2 male E18.5 placentas and (N) F2 female E18.5 placentas. For histology, each data point represents an individual placenta from a minimum of 4 different litters. The black line represents the mean of each group (n = 8/group/sex). Statistical significance was determined by t test; *P < 0.05 when compared groups against natural.

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