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September 10, 2025Science Advances0 citationsOpen Access

Traction force and mechanosensitivity mediate species-specific implantation patterns in human and mouse embryos

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AGAmélie Luise GodeauASAnna SeriolaOTOren Tchaicheeyan

Key Points

  • Mouse embryos expand radially while human embryos generate multiple traction foci during implantation, highlighting a distinct mechanical behavior.
  • Displacement amplitudes were reduced in implantation-impaired human embryos and hindered mouse embryos lacking integrin-mediated force transmission.
  • External mechanical cues prompted a mechanosensitive response, with human embryos recruiting myosin to direct cell protrusions.
  • These findings emphasize the fundamental role of mechanical forces in determining species-specific implantation patterns.

Abstract

The invasion of human embryos in the uterus overcoming the maternal tissue barrier is a crucial step in embryo implantation and subsequent development. Although tissue invasion is fundamentally a mechanical process, most studies have focused on the biochemical and genetic aspects of implantation. Here, we fill the gap by using a deformable ex vivo platform to visualize traction during human embryo implantation. We demonstrate that embryos apply forces remodeling the matrix with species-specific displacement amplitudes and distinct radial patterns: principal displacement directions for mouse embryos, expanding on the surface while human embryos insert in the matrix generating multiple traction foci. Implantation-impaired human embryos showed reduced displacement, as well as mouse embryos with inhibited integrin-mediated force transmission. External mechanical cues induced a mechanosensitive response, human embryos recruited myosin, and directed cell protrusions, while mouse embryos oriented their implantation or body axis toward the external cue. These findings underscore the role of mechanical forces in driving species-specific invasion patterns during embryo implantation.

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Cite This Study

Godeau et al. (2025) studied this question.

synapsesocial.com/papers/68c1c64554b1d3bfb60f2899https://doi.org/10.1126/sciadv.adr5199
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