The tumor suppressor p53 plays a central role in negative growth control, including growth arrest and apoptosis. Interferons (IFNs) are capable of modulating a variety of cellular responses, including apoptosis. In this study, we have evaluated the influence of y-and a-interferon (IFN) on wild-type
Reversible macrophage differentiation induced in a new human myeloid cell line by gamma interferon.
✍ Scribed by Claudia Pintér; Ivana Magnani; Cinzia Paini; Alberto Clivio
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 550 KB
- Volume
- 19
- Category
- Article
- ISSN
- 1065-6995
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A new cell line was established from the bone marrow of a patient with chronic myeloid leukemia. The cells were attributed an intermediate myeloid phenotype on the basis of their cytochemical features and membrane antigen expression. These cells respond to both chemical and physiological activators of the signal transduction pathways with growth arrest and phenotype changes. Macrophage maturation can be induced in a fraction of the cells by gamma‐interferon (γ‐IFN). Cells are however recruited again into the cell cycle by recultivation in γ‐IFN‐free medium: variants unresponsive to γ‐IFN, and others which show either reversible or irreversible differentiation were isolated from the original cell line by cloning and sib‐selection. These clones can be used to investigate the relationship between γ‐IFN response pathways and cell proliferation.
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