Maternal Exercise Rescues Fetal Akinesia‐Impaired Joint and Bone Development

Fetal movements exert mechanical forces that shape the developing skeleton. Conditions that impair fetal movement can cause skeletal defects, but interventions are limited. Here, we show that maternal wheel running exercise regulates fetal skeletal development in mice. In wild-type fetuses, maternal exercise stimulated joint morphogenesis and bone development. These changes could not be fully explained by altered placental transport. Therefore, we next evaluated the effects of maternal exercise in the Splotch-delayed (Sp<sup>d</sup>) mouse model of fetal akinesia, which features intact maternofetal communication, but homozygous mutants lack contractile limb skeletal muscle. Maternal exercise substantially rescued fetal akinesia-impaired joint and bone development and prevented disuse-induced resorption of the deltoid tuberosity. Further, bioreactor mechanical stimulation of explanted Sp<sup>d</sup> limbs, which remove systemic factors, similarly stimulated joint morphogenesis. Together, these findings identify maternal exercise as a regulator of fetal skeletal development, provide a platform for studying skeletal developmental mechanobiology, and suggest potential therapeutic implications for maternal exercise in skeletal conditions caused by impaired fetal movement.

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Publication Details

Journal
The FASEB Journal
Published
2025-12-13
DOI
https://doi.org/10.1096/fj.202503192r
Primary Topic
Neurogenetic and Muscular Disorders Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Maternal Exercise Rescues Fetal Akinesia‐Impaired Joint and Bone Development

Christopher J. Panebianco, Nidal Khatib, Joel D. Boerckel, Devin C. Gottlieb et al.
The FASEB Journal
Neurogenetic and Muscular Disorders Research
article

Maternal Exercise Rescues Fetal Akinesia‐Impaired Joint and Bone Development

Christopher J. Panebianco, Nidal Khatib, Joel D. Boerckel, Devin C. Gottlieb, Niamh C. Nowlan, Rebecca Anne Simmons, Nathaniel A. Dyment, Yuming Huang, Saima Ahmed, Maha Essaidi
article en

Abstract

Fetal movements exert mechanical forces that shape the developing skeleton. Conditions that impair fetal movement can cause skeletal defects, but interventions are limited. Here, we show that maternal wheel running exercise regulates fetal skeletal development in mice. In wild-type fetuses, maternal exercise stimulated joint morphogenesis and bone development. These changes could not be fully explained by altered placental transport. Therefore, we next evaluated the effects of maternal exercise in the Splotch-delayed (Sp<sup>d</sup>) mouse model of fetal akinesia, which features intact maternofetal communication, but homozygous mutants lack contractile limb skeletal muscle. Maternal exercise substantially rescued fetal akinesia-impaired joint and bone development and prevented disuse-induced resorption of the deltoid tuberosity. Further, bioreactor mechanical stimulation of explanted Sp<sup>d</sup> limbs, which remove systemic factors, similarly stimulated joint morphogenesis. Together, these findings identify maternal exercise as a regulator of fetal skeletal development, provide a platform for studying skeletal developmental mechanobiology, and suggest potential therapeutic implications for maternal exercise in skeletal conditions caused by impaired fetal movement.

The FASEB JournalVol. 39(24)
University College Dublin (IE), Children's Hospital of Philadelphia (US), Center for Human Reproduction (US), Imperial College London (GB), University of Pennsylvania (US)
National Science Foundation, University of Pennsylvania, European Commission, National Institutes of Health, Center for Undergraduate Research and Scholarship, Bowling Green State University, HORIZON EUROPE Framework Programme, National Institute of General Medical Sciences, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institute of Child Health and Human Development, Division of Civil, Mechanical and Manufacturing Innovation, Eunice Kennedy Shriver National Institute of Child Health and Human Development, HORIZON EUROPE European Research Council
Openalex Percentile: Top 39%
Neurogenetic and Muscular Disorders Research
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