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Endomucin is expressed in embryonic dorsal aorta and is able to inhibit cell adhesion

  • Masaya Ueno
  • , Katsuhide Igarashi
  • , Naoki Kimura
  • , Keisuke Okita
  • , Makiko Takizawa
  • , Ikuo Nobuhisa
  • , Tetsuo Kojima
  • , Toshio Kitamura
  • , Ulrike Samulowitz
  • , Dietmar Vestweber
  • , Taizo Shimomura
  • , Toshio Suda
  • , Kinichi Nakashima
  • , Tetsuya Taga

Research output: Contribution to journal › Article › peer-review

Abstract

Recent studies have suggested the existence of progenitors common to hematopoietic and endothelial cells, called hemangioblasts, in, for instance, embryonic dorsal aorta. To identify a membrane-bound or secretory molecule regulating early hematopoiesis, we screened a cDNA library from dorsal aortas of embryonic day (E) 10.5 mice by a signal sequence trap method and obtained a clone encoding a sialoprotein, endomucin-1. Immunohistochemistry revealed that the endomucin-1 transcript was specifically expressed in the endothelial cells of dorsal aorta of E10.5 mouse embryo. Overexpression of endomucin-1 strongly inhibited adhesion and aggregation of cells, including cultured endothelial cells from E10.5 dorsal aorta. These data suggest that endomucin-1 may play a role in detachment of hematopoietic cells from endothelium during early hematopoiesis.

Original languageEnglish
Pages (from-to)501-506
Number of pages6
JournalBiochemical and Biophysical Research Communications
Volume287
Issue number2
DOIs
Publication statusPublished - 2001 Sept 21
Externally publishedYes

Keywords

  • Aorta-gonad-mesonephros
  • Cell adhesion
  • Cell aggregation
  • Endomucin
  • Endothelial cells
  • Hemangioblasts
  • Hematopoiesis
  • Hematopoietic stem cells
  • Sialomucin
  • Signal sequence trap

ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Molecular Biology
  • Cell Biology

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