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Disabled-2 small interfering RNA modulates cellular adhesive function and MAPK activity during megakaryocytic differentiation of K562 cells

  • Ching Ping Tseng*
  • , Chien Ling Huang
  • , Ching Hui Huang
  • , Ju Chien Cheng
  • , Arnold Stern
  • , Chin Hsiao Tseng
  • , Daniel Tsun Yee Chiu
  • *Corresponding author for this work
  • Chang Gung University
  • China Medical University Taichung
  • New York University
  • National Taiwan University

Research output: Contribution to journalJournal Article peer-review

62 Scopus citations

Abstract

Previous studies have shown that Disabled-2 (DAB2) is up-regulated during megakaryocytic differentiation of human K562 cells. To delineate the consequences of DAB2 induction, a DNA vector-based small interfering RNA (siRNA) was designed to intervene in DAB2 expression. We found that DAB2 siRNA specifically inhibited DAB2 induction, resulting in the modulation of cell-cell adhesion and mitogen-activated protein kinase (MAPK) phosphorylation. The morphological changes and β3 integrin expression associated with megakaryocytic differentiation were not affected. Since the MAPK pathway has been shown to involve DAB2 induction [Tseng et al., Biochem. Biophys. Res. Commun. 285 (2001) 129-135], our results suggest a reciprocal regulation between DAB2 and MAPK in the differentiation of K562 cells. In addition, we have demonstrated for the first time that DAB2 siRNA is a valuable tool for unveiling the biological consequences of DAB2 expression.

Original languageEnglish
Pages (from-to)21-27
Number of pages7
JournalFEBS Letters
Volume541
Issue number1-3
DOIs
StatePublished - 24 04 2003

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Disabled-2
  • K562 cell
  • Megakaryocytic differentiation
  • Mitogen-activated protein kinase
  • Small interfering RNA

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