Skip to content
DraconiticResearch
Search Sources API
201,683 studies31 sourcesUpdated 22 min ago
PreprintarXiv licencearXiv

Boundary-contact repolarization provides a mechanism for directional guidance of neural crest cell collectives

Abstract

Neural crest cells (NCCs) provide a well-established system for investigating collective migration during embryonic development and exhibit migratory behaviors with parallels to cancer invasion. Previous studies establish roles for co-attraction, contact inhibition of locomotion, polarity persistence, and tissue confinement in guiding NCC migration. However, it remains unclear whether NCC migration in confined environments occurs through spatial restriction alone or also through a repolarization response induced by contact with boundaries of confinement. By developing a computational model that couples self-generated chemical transport with contact-mediated repolarization and mechanical interactions, we show that cell-boundary contact can reorient cell polarity and sustain directional migration under confinement, whereas no persistent collective direction emerges without confinement. Moreover, suppressing contact-mediated repolarization from non-permissive confinement boundaries while preserving the mechanical interactions prevents sustained directional migration, suggesting that spatial restriction alone is insufficient in the model. Together, these findings establish an experimentally testable mechanism through which self-generated chemical signals and contact with confining tissues jointly regulate collective guidance of NCCs. These insights provide a basis for investigating developmental migration defects and potential strategies to regulate collective tissue invasion.

Related

  1. Mechanism of Incommensurate Magnetic Order in BaCo2(AsO4)2: Interplay of Frustrated Further-Neighbor Exchanges and Bond-Directional Anisotropy
    Mohammad-Hossein Zare, Mehdi Biderang, Hamid Mosadeq
    arXivPreprintCC BY-NC-SA 4.0Full textCondensed matterarXiv
  2. A Boundary-Layer Mechanism for One-Third Scaling in Online Softmax Classification
    Marcel Kühn, Yoon Thelge, Bernd Rosenow
    arXivPreprintarXiv licenceFull textCondensed matterarXiv
  3. Mechanisms of spatial pattern transition in motile bacterial collectives
    Jean-Baptiste Saulnier, Michèle Romanos, Jonathan Schrohe +3
    Nature PhysicsPeer-reviewedCC BY 4.0Full textCell biologyMicrobiologyHALHAL
  4. Boundary crossings as a minimal mechanism for global connectivity in structured landscapes
    Fabio Nelli
    arXivPreprintCC BY 4.0Full textStatistical & nonlinear physicsarXiv
  5. Mechanism-Resolved Interface Momentum Transfer in Immersed-Boundary Lattice Boltzmann Simulations
    Hongju Jo
    arXivPreprintarXiv licenceFull textComputational physicsFluid dynamicsarXiv
BibTeX
@misc{paspunurwar2026boundarycontact,
  title = {{Boundary-contact repolarization provides a mechanism for directional guidance of neural crest cell collectives}},
  author = {Aditya Shankar Paspunurwar and Hector Gomez},
  howpublished = {arXiv},
  year = {2026},
  month = oct,
  doi = {10.48550/arxiv.2610.12721},
  eprint = {2610.12721},
  archivePrefix = {arXiv},
  url = {https://arxiv.org/abs/2610.12721},
}
RIS
TY  - UNPB
TI  - Boundary-contact repolarization provides a mechanism for directional guidance of neural crest cell collectives
AU  - Aditya Shankar Paspunurwar
AU  - Hector Gomez
PY  - 2026
DA  - 2026/10/08
PB  - arXiv
DO  - 10.48550/arxiv.2610.12721
UR  - https://arxiv.org/abs/2610.12721
AB  - Neural crest cells (NCCs) provide a well-established system for investigating collective migration during embryonic development and exhibit migratory behaviors with parallels to cancer invasion. Previous studies establish roles for co-attraction, contact inhibition of locomotion, polarity persistence, and tissue confinement in guiding NCC migration. However, it remains unclear whether NCC migration in confined environments occurs through spatial restriction alone or also through a repolarization response induced by contact with boundaries of confinement. By developing a computational model that couples self-generated chemical transport with contact-mediated repolarization and mechanical interactions, we show that cell-boundary contact can reorient cell polarity and sustain directional migration under confinement, whereas no persistent collective direction emerges without confinement. Moreover, suppressing contact-mediated repolarization from non-permissive confinement boundaries while preserving the mechanical interactions prevents sustained directional migration, suggesting that spatial restriction alone is insufficient in the model. Together, these findings establish an experimentally testable mechanism through which self-generated chemical signals and contact with confining tissues jointly regulate collective guidance of NCCs. These insights provide a basis for investigating developmental migration defects and potential strategies to regulate collective tissue invasion.
ER  -