4.8 Article

EphB-ephrin-B2 interactions are required for thymus migration during organogenesis

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.1003747107

Keywords

collective cell migration; thymus organogenesis; ephrin-B2; Eph receptor; neural crest

Funding

  1. Medical Research Council (MRC) [G0601156]
  2. Cancer Research UK
  3. Leukaemia Research Fund
  4. Max-Planck Institute
  5. National Institutes of Health
  6. MRC [G0601156, MC_U117532048] Funding Source: UKRI
  7. Medical Research Council [G0700711B, MC_U117532048, G0601156] Funding Source: researchfish

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Thymus organogenesis requires coordinated interactions of multiple cell types, including neural crest (NC) cells, to orchestrate the formation, separation, and subsequent migration of the developing thymus from the third pharyngeal pouch to the thoracic cavity. The molecular mechanisms driving these processes are unclear; however, NC-derived mesenchyme has been shown to play an important role. Here, we show that, in the absence of ephrin-B2 expression on thymic NC-derived mesenchyme, the thymus remains in the cervical area instead of migrating into the thoracic cavity. Analysis of individual NC-derived thymic mesenchymal cells shows that, in the absence of ephrin-B2, their motility is impaired as a result of defective EphB receptor signaling. This implies a NC-derived cell-specific role of EphB-ephrin-B2 interactions in the collective migration of the thymic rudiment during organogenesis.

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