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Symmetry and Fluctuation of Cell Movements in Neural Crest-derived Facial Mesenchyme

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Journal Development
Specialty Biology
Date 2021 Mar 24
PMID 33757991
Citations 2
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Abstract

In the face, symmetry is established when bilateral streams of neural crest cells leave the neural tube at the same time, follow identical migration routes and then give rise to the facial prominences. However, developmental instability exists, particularly surrounding the steps of lip fusion. The causes of instability are unknown but inability to cope with developmental fluctuations are a likely cause of congenital malformations, such as non-syndromic orofacial clefts. Here, we tracked cell movements over time in the frontonasal mass, which forms the facial midline and participates in lip fusion, using live-cell imaging of chick embryos. Our mathematical examination of cell velocity vectors uncovered temporal fluctuations in several parameters, including order/disorder, symmetry/asymmetry and divergence/convergence. We found that treatment with a Rho GTPase inhibitor completely disrupted the temporal fluctuations in all measures and blocked morphogenesis. Thus, we discovered that genetic control of symmetry extends to mesenchymal cell movements and that these movements are of the type that could be perturbed in asymmetrical malformations, such as non-syndromic cleft lip. This article has an associated 'The people behind the papers' interview.

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References
1.
Hu D, Marcucio R, Helms J . A zone of frontonasal ectoderm regulates patterning and growth in the face. Development. 2003; 130(9):1749-58. DOI: 10.1242/dev.00397. View

2.
Slater B, Londono C, McGuigan A . An algorithm to quantify correlated collective cell migration behavior. Biotechniques. 2013; 54(2):87-92. DOI: 10.2144/000113990. View

3.
Beaty T, Marazita M, Leslie E . Genetic factors influencing risk to orofacial clefts: today's challenges and tomorrow's opportunities. F1000Res. 2016; 5:2800. PMC: 5133690. DOI: 10.12688/f1000research.9503.1. View

4.
Oshima-Nakayama M, Yamada A, Kurosawa T, Aizawa R, Suzuki D, Saito Y . Cdc42 is crucial for facial and palatal formation during craniofacial development. Bone Rep. 2017; 5:1-6. PMC: 4926830. DOI: 10.1016/j.bonr.2016.01.001. View

5.
Grosen D, Bille C, Petersen I, Skytthe A, von Bornemann Hjelmborg J, Pedersen J . Risk of oral clefts in twins. Epidemiology. 2011; 22(3):313-9. PMC: 3089024. DOI: 10.1097/EDE.0b013e3182125f9c. View