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 language | English (US) |
|---|---|
| Pages (from-to) | 706-710 |
| Number of pages | 5 |
| Journal | Journal of Cellular Physiology |
| Volume | 207 |
| Issue number | 3 |
| DOIs | |
| State | Published - Jun 2006 |
| Externally published | Yes |
ASJC Scopus subject areas
- Physiology
- Clinical Biochemistry
- Cell Biology
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