Peroxiredoxin-controlled G-CSF signalling at the endoplasmic reticulum-early endosome interface.
J Cell Sci
; 124(Pt 21): 3695-705, 2011 Nov 01.
Article
en En
| MEDLINE
| ID: mdl-22045733
ABSTRACT
Reactive oxygen species (ROS) regulate growth factor receptor signalling at least in part by inhibiting oxidation-sensitive phosphatases. An emerging concept is that ROS act locally to affect signal transduction in different subcellular compartments and that ROS levels are regulated by antioxidant proteins at the same local level. Here, we show that the ER-resident antioxidant peroxiredoxin 4 (Prdx4) interacts with the cytoplasmic domain of the granulocyte colony-stimulating factor receptor (G-CSFR). This interaction occurs when the activated G-CSFR resides in early endosomes. Prdx4 inhibits G-CSF-induced signalling and proliferation in myeloid progenitors, depending on its redox-active cysteine core. Protein tyrosine phosphatase 1b (Ptp1b) appears to be a major downstream effector controlling these responses. Conversely, Ptp1b might keep Prdx4 active by reducing its phosphorylation. These findings unveil a new signal transduction regulatory circuitry involving redox-controlled processes in the ER and activated cytokine receptors in endosomes.
Texto completo:
1
Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Endosomas
/
Transducción de Señal
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Regulación hacia Abajo
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Factor Estimulante de Colonias de Granulocitos
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Retículo Endoplásmico
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Peroxirredoxinas
Límite:
Animals
/
Humans
Idioma:
En
Revista:
J Cell Sci
Año:
2011
Tipo del documento:
Article
País de afiliación:
Países Bajos