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Semaphorins guide the entry of dendritic cells into the lymphatics by activating myosin II.

The recirculation of leukocytes is essential for proper immune responses. However, the molecular mechanisms that regulate the entry of leukocytes into the lymphatics remain unclear. Here we show that plexin-A1, a principal receptor component for class III and class VI semaphorins, was crucially involved in the entry of dendritic cells (DCs) into the lymphatics. Additionally, we show that the semaphorin Sema3A, but not Sema6C or Sema6D, was required for DC transmigration and that Sema3A produced by the lymphatics promoted actomyosin contraction at the trailing edge of migrating DCs. Our findings not only demonstrate that semaphorin signals are involved in DC trafficking but also identify a previously unknown mechanism that induces actomyosin contraction as these cells pass through narrow gaps.

Pubmed ID: 20512151


  • Takamatsu H
  • Takegahara N
  • Nakagawa Y
  • Tomura M
  • Taniguchi M
  • Friedel RH
  • Rayburn H
  • Tessier-Lavigne M
  • Yoshida Y
  • Okuno T
  • Mizui M
  • Kang S
  • Nojima S
  • Tsujimura T
  • Nakatsuji Y
  • Katayama I
  • Toyofuku T
  • Kikutani H
  • Kumanogoh A


Nature immunology

Publication Data

July 21, 2010

Associated Grants

  • Agency: NINDS NIH HHS, Id: R01 NS065048
  • Agency: NINDS NIH HHS, Id: R01 NS065048-02
  • Agency: NINDS NIH HHS, Id: R01NS065048

Mesh Terms

  • Actomyosin
  • Adoptive Transfer
  • Animals
  • Cell Migration Assays, Leukocyte
  • Cell Movement
  • Cells, Cultured
  • Dendritic Cells
  • Gene Knock-In Techniques
  • Immunity
  • Lymphatic Vessels
  • Mice
  • Mice, Knockout
  • Muscle Contraction
  • Myosin Type II
  • Nerve Tissue Proteins
  • Neuropilin-1
  • Receptors, Cell Surface
  • Semaphorins
  • Signal Transduction