p38 mitogen-activated protein kinase up-regulates NF-κB transcriptional activation through RelA phosphorylation during stretch-induced myogenesis

Biochemical and Biophysical Research Communications

Volumn 391, Issue 1, 2010, Pages 547-551

  Ji, Guoping ^a   Liu, Dongxu ^c   Liu, Jing ^b   Gao, Hui ^d   Yuan, Xiao ^b   Shen, Gang ^a  

^a SHANGHAI SECOND MEDICAL UNIVERSITY   (China)

^b QINGDAO UNIVERSITY   (China)

^c SHANDONG UNIVERSITY   (China)

^d TIANJIN STOMATOLOGICAL HOSPITAL   (China)

Author keywords

Cyclic stretch; Myogenesis; NF B; p38 MAPK

Indexed keywords

4 (4 FLUOROPHENYL) 2 (4 METHYLSULFINYLPHENYL) 5 (4 PYRIDYL)IMIDAZOLE; I KAPPA B ALPHA; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; MITOGEN ACTIVATED PROTEIN KINASE 14; MITOGEN ACTIVATED PROTEIN KINASE P38; SMALL INTERFERING RNA; SYNAPTOTAGMIN I; TRANSCRIPTION FACTOR RELA;

ANIMAL CELL; ARTICLE; CELL NUCLEUS; CONTROLLED STUDY; ENZYME ACTIVITY; GENE TRANSLOCATION; IN VITRO STUDY; MUSCLE DEVELOPMENT; MUSCLE STRETCHING; MYOBLAST; NONHUMAN; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN DEPLETION; PROTEIN PHOSPHORYLATION; PROTEIN PROTEIN INTERACTION; RECEPTOR DOWN REGULATION; RECEPTOR UPREGULATION; SIGNAL TRANSDUCTION; TRANSCRIPTION INITIATION;

ANIMALS; CELL LINE; ENZYME INHIBITORS; IMIDAZOLES; MECHANOTRANSDUCTION, CELLULAR; MICE; MUSCLE DEVELOPMENT; MYOBLASTS; P38 MITOGEN-ACTIVATED PROTEIN KINASES; PHOSPHORYLATION; PYRIDINES; TENSILE STRENGTH; TRANSCRIPTION FACTOR RELA; TRANSCRIPTIONAL ACTIVATION; UP-REGULATION;

EID: 73149121557     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2009.11.095     Document Type: Article

References (41)

1. Berkes C.A., and Tapscott S.J. MyoD and the transcriptional control of myogenesis. Semin. Cell Dev. Biol. 16 (2005) 585-595
2. Gossett L.A., Kelvin D.J., Sternberg E.A., and Olson E.N. A new myocyte-specific enhancer-binding factor that recognizes a conserved element associated with multiple muscle-specific genes. Mol. Cell. Biol. 9 (1989) 5022-5033
3. Naya F.J., and Olson E. MEF2: a transcriptional target for signaling pathways controlling skeletal muscle growth and differentiation. Curr. Opin. Cell Biol. 11 (1999) 683-688
4. Parker M.H., Seale P., and Rudnicki M.A. Looking back to the embryo: defining transcriptional networks in adult myogenesis. Nat. Rev. Genet. 4 (2003) 497-507
5. Zhan M., Jin B., Chen S.E., Reecy J.M., and Li J.P. TACE release of TNF-alpha mediates mechanotransduction-induced activation of p38 MAPK and myogenesis. J. Cell Sci. 15 (2007) 692-701
6. Puri P.L., and Sartorelli V. Regulation of muscle regulatory factors by DNA-binding, interacting proteins, and post-transcriptional modifications. J. Cell. Physiol. 185 (2000) 155-173
7. Cuenda A., and Cohen P. Stress-activated protein kinase-2/p38 and a rapamycin-sensitive pathway are required for C2C12 myogenesis. J. Biol. Chem. 274 (1999) 4341-4346
8. Zetser A., Gredinger E., and Bengal E. P38 mitogen-activated protein kinase pathway promotes skeletal muscle differentiation. Participation of the Mef2c transcription factor. J. Biol. Chem. 274 (1999) 5193-5200
9. Wu Z., Woodring P.J., Bhakta K.S., Tamura K., Wen F., Feramisco J.R., Karin M., Wang J.Y., and Puri P.L. p38 and extracellular signal-regulated kinases regulate the myogenic program at multiple steps. Mol. Cell. Biol. 20 (2000) 3951-3964
10. Cabane C., Englaro W., Yeow K., Ragno M., and Derijard B. Regulation of C2C12 myogenic terminal differentiation by MKK3/p38 alpha pathway. Am. J. Physiol. Cell Physiol. 284 (2003) C658-C666
11. Penn B.H., Bergstrom D.A., Dilworth F.J., Bengal E., and Tapscott S.J. A MyoD-generated feed-forward circuit temporally patterns gene expression during skeletal muscle differentiation. Genes Dev. 18 (2004) 2348-2353
12. de Angelis L., Zhao J., Andreucci J.J., Olson E.N., Cossu G., and McDermott J.C. Regulation of vertebrate myotome development by the p38 MAP kinase-MEF2 signaling pathway. Dev. Biol. 283 (2005) 171-179
13. Zhao M., New L., Kravchenko V.V., Kato Y., Gram H., Di Padova F., Olson E.N., Ulevitch R.J., and Han J. Regulation of the MEF2 family of transcription factors by p38. Mol. Cell. Biol. 19 (1999) 21-30
14. Guttridge D.C., Albanese C., Reuther J.Y., Pestell R.G., and Baldwin A.S. NF-kappaB controls cell growth and differentiation through transcriptional regulation of cyclin D1. Mol. Cell. Biol. 19 (1999) 5785-5799
15. Canicio J., Ruiz-Lozano P., Carrasco M., Palacin M., Chien K., Zorzano A., and Kaliman P. Nuclear factor kappa B-inducing kinase and I kappa B kinase-alpha signal skeletal muscle cell differentiation. J. Biol. Chem. 276 (2001) 20228-20233
16. May M.J., and Ghosh S. Rel/NF-kappa B and I kappa B proteins: an overview. Semin. Cancer Biol. 8 (1997) 63-73
17. Ghosh S., May M.J., and Kopp E.B. NF-kappa B and Rel proteins: evolutionarily conserved mediators of immune responses. Annu. Rev. Immunol. 16 (1998) 225-260
18. Baeuerle Z., Zabel U., and Baeuerle P.A. Purified human IκB can rapidly dissociate the complex of the NF-κB transcription factor with its cognate DNA. Cell 61 (1990) 255-265
19. Sizemore N., Leung S., and Stark G.R. Activation of phosphatidylinositol 3-kinase in response to interleukin-2 leads to phosphorylation and activation of the NF-B p65/RelA subunit. Mol. Cell. Biol. 19 (1999) 4798-4805
20. Boppart M.D., Hirshman M.F., Sakamoto K., Fielding R.A., and Goodyear L.J. Static stretch increases c-Jun NH2-terminal kinase activity and p38 phosphorylation in rat skeletal muscle. Am. J. Physiol. Cell Physiol. 280 (2001) C352-C358
21. Hornberger T.A., Mateja R.D., Chin E.R., Andrews J.L., and Esser K.A. Aging does not alter the mechanosensitivity of the p38, p70S6k, and JNK2 signaling pathways in skeletal muscle. J. Appl. Physiol. 98 (2005) 1562-1566
22. Rauch C., and Loughna P.T. Static stretch promotes MEF2A nuclear translocation and expression of neonatal myosin heavy chain in C2C12 myocytes in a calcineurin- and p38-dependent manner. Am. J. Physiol. Cell Physiol. 288 (2005) C593-C605
23. Chen K.D., Chen L.Y., Huang H.L., Lieu C.H., Chang Y.N., Chang M.D., and Lai Y.K. Involvement of p38 mitogen-activated protein kinase signaling pathway in the rapid induction of the 78-kDa glucose-regulated protein in 9 L rat brain tumor cells. J. Biol. Chem. 273 (1998) 749-755
24. Han J., Jiang Y., Li Z., Kravchenko V.V., and Ulevitch R.J. Activation of the transcription factor MEF2c by the MAP kinase p38 in inflammation. Nature 386 (1997) 296-299
25. Wang X.Z., and Ron D. Stress-induced phosphorylation and activation of the transcription factor CHOP (GADD153) by p38 MAP kinase. Science 272 (1996) 1347-1349
26. Kim H.J., Lee H.S., Chong Y.H., and Kang J.L. p38 mitogen-activated protein kinase up-regulates LPS-induced NF-κB activation in the development of lung injury and RAW 264.7 macrophages. Toxicology 225 (2006) 36-47
27. Baeza-Raja B., and Munoz-Canoves P. p38 MAPK-induced nuclear factor-κB activity is required for skeletal muscle differentiation: role of interleukin-6. Mol. Biol. Cell 15 (2004) 2013-2026
28. Kefaloyianni E., Gaitanaki C., and Beis I. ERK1/2 and p38-MAPK signalling pathways, through MSK1, are involved in NF-κB transactivation during oxidative stress in skeletal myoblasts. Cell. Signal. 18 (2006) 2238-2251
29. Richard C.H., Hirshman M.F., Li Y., Cai D., Farmer J.R., Aschenbach W.G., Witczak C.A., Shoelson S.E., and Goodyear L.J. Regulation of IκB kinase and NF-κB in contracting adult rat skeletal muscle. Am. J. Physiol. Cell Physiol. 289 (2005) C794-C801
30. Yuan X., Lin Z., Luo S., Ji G., Yuan C., and Wu Y. Effects of different magnitudes of cyclic stretch on Na + K + ATPase in skeletal muscle cells in vitro. J. Cell. Physiol. 212 (2007) 509-518
31. Yuan X., Luo S.J., Lin Z., and Wu Y. Cyclic stretch translocates the alpha2-subunit of the Na pump to plasma membrane in skeletal muscle cells in vitro. Biochem. Biophys. Res. Commun. 348 (2006) 750-757
32. Kerena A., Tamira Y., and Bengal E. The p38 MAPK signaling pathway: a major regulator of skeletal muscle development. Mol. Cell. Endocrinol. 252 1-2 (2007) 224-230
33. Li C., and Xu Q. Mechanical stress-initiated signal transduction in vascular smooth muscle cells in vitro and in vivo. Cell. Signal. 19 (2007) 881-891
34. Wozniak A.C., Kong J., Bock E., Pilipowicz O., and Anderson J.E. Signaling satellite-cell activation in skeletal muscle: markers, models, stretch, and potential alternate pathways. Muscle Nerve 31 (2005) 283-300
35. Tatsumi R., Sheehan S.M., Iwasaki H., Hattori A., and Allen R.E. Mechanical stretch induces activation of skeletal muscle satellite cells in vitro. Exp. Cell Res. 267 (2001) 107-114
36. Tatsumi R., Hattori A., Ikeuchi Y., Andersonand J.E., and Allen R.E. Release of hepatocyte growth factor from mechanically stretched skeletal muscle satellite cells and role of pH and nitric oxide. Mol. Biol. Cell 13 (2002) 2909-2918
37. Lluís F., Ballestar E., Suelves M., Esteller M., and Muñoz-Cánoves P. E47 phosphorylation by p38 MAPK promotes MyoD/E47 association and muscle-specific gene transcription. EMBO J. 24 (2005) 974-984
38. Vanden Berghe W., Plaisance S., Boone E., De Bosscher K., Schmitz M.L., Fiers W., and Haegeman G. p38 and extracellular signal-related protein kinase pathways are required for nuclear factor-kappaB p65 transactivation mediated by tumor necrosis factor. J. Biol. Chem. 273 6 (1998) 3285-3290
39. Purcell N.H., Tang G., Yu C., Mercurio F., DiDonato J.A., and Lin A. Activation of NF-kappa B is required for hypertrophic growth of primary rat neonatal ventricular cardiomyocytes. Proc. Natl. Acad. Sci. USA 98 (2001) 6668-6673
40. Saccani S., Pantano S., and Natoli G. P38-dependent marking of inflammatory genes for increased NF-κB recruitment. Nat. Immunol. 3 (2002) 69-75
41. Vermeulen L., De Wilde G., Van Damme P., Vanden Berghe W., and Haegeman G. Transcription activation of the NF-κB p65 subunit by mitogen- and stress-activated protein kinase-1 (MSK1). EMBO J. 22 (2003) 1313-1324