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Expression profiles of micro RNA in proliferating and differentiating 32D murine myeloid cells

  • Bin Shi
  • , Marco Prisco
  • , George Calin
  • , Chang Gong Liu
  • , Giuseppe Russo
  • , Antonio Giordano
  • , Renato Baserga

Research output: Contribution to journalArticlepeer-review

Abstract

32D cells are murine myeloid cells that grow indefinitely in Interleukin-3 (IL-3). In these cells, the type 1 insulin-like growth factor (IGF-I) and granulocytic-colony stimulating factor (G-CSF) induce differentiation to granulocytes. 32D cells do not express insulin receptor substrate-1 (IRS-1) or IRS-2, docking proteins of the IGF-I receptor. Ectopic expression of IRS-1 in these cells inhibits differentiation, the cells become IL-3 independent and IGF-I dependent and can form tumors in mice. 32D and 32D-derived cells offer a good model in which to study the expression profiles of Micro Rna (miR) related to sustained proliferation or differentiation. We present here the data obtained with miR micro-arrays and identify the miR that are regulated by IGF-I or G-CSF and are associated with either differentiation or indefinite cell proliferation of 32D murine myeloid cells.

Original languageEnglish (US)
Pages (from-to)706-710
Number of pages5
JournalJournal of Cellular Physiology
Volume207
Issue number3
DOIs
StatePublished - Jun 2006
Externally publishedYes

ASJC Scopus subject areas

  • Physiology
  • Clinical Biochemistry
  • Cell Biology

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