Interleukin-4 elicits apoptosis of developing mast cells via a Stat6-dependent mitochondrial pathway.
Exp Hematol
; 32(1): 52-9, 2004 Jan.
Article
en En
| MEDLINE
| ID: mdl-14725901
ABSTRACT
OBJECTIVE:
The aim of this study was to assess the effects of interleukin-4 and signal transducer and activator of transcription (Stat)-6 on IL-3+SCF-induced mast cell development. PATIENTS ANDMETHODS:
Unseparated mouse bone marrow cells were cultured in IL-3+SCF, giving rise to mast cells and monocytes/macrophages. The addition of IL-4, the use of Stat6-deficient bone marrow cells, and expression of a constitutively active Stat6 mutant were employed to assess the effects of IL-4 and Stat6 on cell viability, proliferation, and differentiation. Bax-deficient and bcl-2 transgenic bone marrow cells were used to assess the importance of the mitochondria in IL-4-mediated effects.RESULTS:
IL-4 elicited apoptosis and limited the cell cycle progression of developing bone marrow cells, without affecting cell differentiation. Apoptosis required that IL-4 be present during the first 8 days of the 21-day culture period. Cell death correlated with loss of mitochondrial membrane potential. Accordingly, IL-4-mediated apoptosis was inhibited by Bax deletion or bcl-2 overexpression. Lastly, Stat6 activation was both necessary and sufficient to inhibit cell survival.CONCLUSION:
IL-4 exerts potent apoptotic effects on developing mast cells and monocyte/macrophages through mitochondrial damage and Stat6 activation.
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Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Transactivadores
/
Interleucina-4
/
Apoptosis
/
Mastocitos
/
Mitocondrias
Límite:
Animals
Idioma:
En
Revista:
Exp Hematol
Año:
2004
Tipo del documento:
Article
País de afiliación:
Estados Unidos