Requirement of activation of JNK and p38 for environmental stress-induced erythroid differentiation and apoptosis and of inhibition of ERK for apoptosis
- PMID: 10419875
Requirement of activation of JNK and p38 for environmental stress-induced erythroid differentiation and apoptosis and of inhibition of ERK for apoptosis
Abstract
C-Jun amino terminal kinase/stress-activated protein kinases (JNK/SAPK) and p38 subgroups of mitogen-activated protein kinases have been suggested to play a critical role in apoptosis, cell growth, and/or differentiation. We found that a short exposure of SKT6 cells, which respond to erythropoietin (Epo) and induce erythroid differentiation, to osmotic or heat shock induced transient activation of JNK/SAPK and p38 and inactivation of ERK and resulted in erythroid differentiation without Epo, whereas long exposure of the cells to these stresses induced prolonged activation/inactivation of the same kinases and caused apoptosis. Inhibition of JNK/SAPK and p38 resulted in inhibition of stress-induced erythroid differentiation and apoptosis. Inhibition of ERK had no effect on stress-induced erythroid differentiation, but stimulated apoptosis. Activation of p38 and/or JNK/SAPK for a short time caused erythroid differentiation without Epo, although its prolonged activation induced apoptosis. Activation of ERK suppressed stress-induced apoptosis. These results indicate that short cellular stresses, inducing transient activation of JNK/SAPK and p38, lead to cell differentiation rather than apoptosis. Furthermore, activation of JNK/SAPK and p38 is required for both cell differentiation and apoptosis, and the duration of their activation may determine the cell fate, cell differentiation, and apoptosis. In contrast, inactivation of ERK is required for stress-induced apoptosis but not cell differentiation.
Similar articles
-
Activation of p38 MAP kinase and JNK but not ERK is required for erythropoietin-induced erythroid differentiation.Blood. 1998 Sep 15;92(6):1859-69. Blood. 1998. PMID: 9731042
-
JNK and p38 are activated by erythropoietin (EPO) but are not induced in apoptosis following EPO withdrawal in EPO-dependent HCD57 cells.Blood. 2000 Aug 1;96(3):933-40. Blood. 2000. PMID: 10910907
-
The cellular response to oxidative stress: influences of mitogen-activated protein kinase signalling pathways on cell survival.Biochem J. 1998 Jul 15;333 ( Pt 2)(Pt 2):291-300. doi: 10.1042/bj3330291. Biochem J. 1998. PMID: 9657968 Free PMC article.
-
The stress-activated protein kinase pathways.Cell Mol Life Sci. 1999 Aug 15;55(10):1230-54. doi: 10.1007/s000180050369. Cell Mol Life Sci. 1999. PMID: 10487205 Free PMC article. Review.
-
Mechanisms underlying sensing of cellular stress signals by mammalian MAP3 kinases.Mol Cell. 2024 Jan 4;84(1):142-155. doi: 10.1016/j.molcel.2023.11.028. Epub 2023 Dec 19. Mol Cell. 2024. PMID: 38118452 Review.
Cited by
-
Activation of p38 mitogen-activated protein kinase and c-Jun NH(2)-terminal kinase by double-stranded RNA and encephalomyocarditis virus: involvement of RNase L, protein kinase R, and alternative pathways.Mol Cell Biol. 2000 Jan;20(2):617-27. doi: 10.1128/MCB.20.2.617-627.2000. Mol Cell Biol. 2000. PMID: 10611240 Free PMC article.
-
Divergent calcium signaling in RBCs from Tropidurus torquatus (Squamata--Tropiduridae) strengthen classification in lizard evolution.BMC Physiol. 2007 Aug 23;7:7. doi: 10.1186/1472-6793-7-7. BMC Physiol. 2007. PMID: 17716375 Free PMC article.
-
Aberrant expression of IL-22 receptor 1 and autocrine IL-22 stimulation contribute to tumorigenicity in ALK+ anaplastic large cell lymphoma.Leukemia. 2008 Aug;22(8):1595-603. doi: 10.1038/leu.2008.129. Epub 2008 May 29. Leukemia. 2008. PMID: 18509351 Free PMC article.
-
Long circulating lectin conjugated paclitaxel loaded magnetic nanoparticles: a new theranostic avenue for leukemia therapy.PLoS One. 2011;6(11):e26803. doi: 10.1371/journal.pone.0026803. Epub 2011 Nov 16. PLoS One. 2011. PMID: 22110595 Free PMC article.
-
Signals transducers and activators of transcription (STAT)-induced STAT inhibitor-1 (SSI-1)/suppressor of cytokine signaling-1 (SOCS-1) suppresses tumor necrosis factor alpha-induced cell death in fibroblasts.Proc Natl Acad Sci U S A. 2000 May 9;97(10):5405-10. doi: 10.1073/pnas.090084797. Proc Natl Acad Sci U S A. 2000. PMID: 10792035 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous