Effects of granulocyte colony-stimulating factor on the proliferation and cell-fate specification of neural stem cells

Neuroscience

Volumn 164, Issue 4, 2009, Pages 1521-1530

  Liu, H ^a   Jia, D ^a,b   Fu, J ^a   Zhao, S ^a   He, G ^c   Ling, E A ^d   Gao, J ^e   Hao, A ^a  

^a BEIJING UNIVERSITY OF POSTS AND TELECOMMUNICATIONS   (China)

^b INSTITUTE OF MOLECULAR AND CELL BIOLOGY   (Singapore)

^c GUANGXI UNIVERSITY OF CHINESE MEDICINE   (China)

^d NATIONAL UNIVERSITY OF SINGAPORE   (Singapore)

^e SHANDONG UNIVERSITY   (China)

Author keywords

differentiation; G CSF; neural stem cells; proliferation; stat3

Indexed keywords

GRANULOCYTE COLONY STIMULATING FACTOR; STAT3 PROTEIN;

ANIMAL CELL; ARTICLE; CELL FATE; CELL PROLIFERATION; CONTROLLED STUDY; EMBRYO; GENE EXPRESSION; IN VITRO STUDY; MOUSE; NERVE CELL DIFFERENTIATION; NEURAL STEM CELL; NONHUMAN; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN PHOSPHORYLATION;

ANIMALS; ASTROCYTES; BASIC HELIX-LOOP-HELIX TRANSCRIPTION FACTORS; BRAIN; CELL DIFFERENTIATION; CELL PROLIFERATION; CELL SURVIVAL; CELLS, CULTURED; EMBRYO, MAMMALIAN; GRANULOCYTE COLONY-STIMULATING FACTOR; MICE; NEURONS; PHOSPHORYLATION; RECEPTORS, GRANULOCYTE COLONY-STIMULATING FACTOR; STAT3 TRANSCRIPTION FACTOR; STEM CELLS;

EID: 70449530620     PISSN: 03064522     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuroscience.2009.09.045     Document Type: Article

References (40)

1. Byts N., Samoylenko A., Woldt H., Ehrenreich H., and Siren A.L. Cell type specific signalling by hematopoietic growth factors in neural cells. Neurochem Res 31 (2006) 1219-1230
2. Collins S.J., Ulmer J., Purton L.E., and Darlington G. Multipotent hematopoietic cell lines derived from C/EBPalpha(-/-) knockout mice display granulocyte macrophage-colony-stimulating factor, granulocyte- colony-stimulating factor, and retinoic acid-induced granulocytic differentiation. Blood 98 (2001) 2382-2388
3. de Koning J.P., Dong F., Smith L., Schelen A.M., Barge R.M., van der Plas D.C., Hoefsloot L.H., Lowenberg B., and Touw I.P. The membrane-distal cytoplasmic region of human granulocyte colony-stimulating factor receptor is required for STAT3 but not STAT1 homodimer formation. Blood 87 (1996) 1335-1342
4. de Koning J.P., Soede-Bobok A.A., Ward A.C., Schelen A.M., Antonissen C., van Leeuwen D., Lowenberg B., and Touw I.P. STAT3-mediated differentiation and survival and of myeloid cells in response to granulocyte colony-stimulating factor: role for the cyclin-dependent kinase inhibitor p27(Kip1). Oncogene 19 (2000) 3290-3298
5. Demetri G.D., and Griffin J.D. Granulocyte colony-stimulating factor and its receptor. Blood 78 (1991) 2791-2808
6. Gibson C.L., Bath P.M., and Murphy S.P. G-CSF reduces infarct volume and improves functional outcome after transient focal cerebral ischemia in mice. J Cereb Blood Flow Metab 25 (2005) 431-439
7. Grandbarbe L., Bouissac J., Rand M., Hrabe de Angelis M., Artavanis-Tsakonas S., and Mohier E. Delta-Notch signaling controls the generation of neurons/glia from neural stem cells in a stepwise process. Development 130 (2003) 1391-1402
8. Gu F., Hata R., Ma Y.J., Tanaka J., Mitsuda N., Kumon Y., Hanakawa Y., Hashimoto K., Nakajima K., and Sakanaka M. Suppression of Stat3 promotes neurogenesis in cultured neural stem cells. J Neurosci Res 81 (2005) 163-171
9. Guillemot F. Analysis of the role of basic-helix-loop-helix transcription factors in the development of neural lineages in the mouse. Biol cell 84 (1995) 3-6
10. Ihle J.N., and Kerr I.M. Jaks and stats in signaling by the cytokine receptor superfamily. Trends Genet 11 (1995) 69-74
11. Ihle J.N., Nosaka T., Thierfelder W., Quelle F.W., and Shimoda K. Jaks and stats in cytokine signaling. Stem Cells 15 Suppl 1 (1997) 105-111 discussion 112
12. Ito H., Nakajima A., Nomoto H., and Furukawa S. Neurotrophins facilitate neuronal differentiation of cultured neural stem cells via induction of mRNA expression of basic helix-loop-helix transcription factors Mash1 and Math1. J Neurosci Res 71 (2003) 648-658
13. Jen Y., Manova K., and Benezra R. Each member of the Id gene family exhibits a unique expression pattern in mouse gastrulation and neurogenesis. Dev Dyn 208 (1997) 92-106
14. Jung K.H., Chu K., Lee S.T., Kim S.J., Sinn D.I., Kim S.U., Kim M., and Roh J.K. Granulocyte colony-stimulating factor stimulates neurogenesis via vascular endothelial growth factor with STAT activation. Brain Res 1073- 1074 (2006) 190-201
15. Kageyama R., Ohtsuka T., Hatakeyama J., and Ohsawa R. Roles of bHLH genes in neural stem cell differentiation. Exp Cell Res 306 (2005) 343-348
16. Kirsch F., Kruger C., and Schneider A. The receptor for granulocyte-colony stimulating factor (G-CSF) is expressed in radial glia during development of the nervous system. BMC Dev Biol 8 (2008) 32
17. Komine-Kobayashi M., Zhang N., Liu M., Tanaka R., Hara H., Osaka A., Mochizuki H., Mizuno Y., and Urabe T. Neuroprotective effect of recombinant human granulocyte colony-stimulating factor in transient focal ischemia of mice. J Cereb Blood Flow Metab 26 (2006) 402-413
18. Lee S.T., Park J.E., Kim D.H., Kim S., Im W.S., Kang L., Jung S.H., Kim M.W., Chu K., and Kim M. Granulocyte-colony stimulating factor attenuates striatal degeneration with activating survival pathways in 3-nitropropionic acid model of Huntington's disease. Brain Res 1194 (2008) 130-137
19. Li Y., Chen J., Wang L., Lu M., and Chopp M. Treatment of stroke in rat with intracarotid administration of marrow stromal cells. Neurology 56 (2001) 1666-1672
20. Liu F., Wu H.Y., Wesselschmidt R., Kornaga T., and Link D.C. Impaired production and increased apoptosis of neutrophils in granulocyte colony-stimulating factor receptor-deficient mice. Immunity 5 (1996) 491-501
21. Lo L., Dormand E., Greenwood A., and Anderson D.J. Comparison of the generic neuronal differentiation and neuron subtype specification functions of mammalian achaete-scute and atonal homologs in cultured neural progenitor cells. Development 129 (2002) 1553-1567
22. Morstyn G., and Burgess A.W. Hemopoietic growth factors: a review. Cancer Res 48 (1988) 5624-5637
23. Nicholson S.E., Novak U., Ziegler S.F., and Layton J.E. Distinct regions of the granulocyte colony-stimulating factor receptor are required for tyrosine phosphorylation of the signaling molecules JAK2, Stat3, and p42, p44MAPK. Blood 86 (1995) 3698-3704
24. Nicola N.A. Hemopoietic cell growth factors and their receptors. Annu Rev Biochem 58 (1989) 45-77
25. Ohtsuka T., Ishibashi M., Gradwohl G., Nakanishi S., Guillemot F., and Kageyama R. Hes1 and Hes5 as notch effectors in mammalian neuronal differentiation. EMBO J 18 (1999) 2196-2207
26. Ohtsuka T., Sakamoto M., Guillemot F., and Kageyama R. Roles of the basic helix-loop-helix genes Hes1 and Hes5 in expansion of neural stem cells of the developing brain. J Biol Chem 276 (2001) 30467-30474
27. Ota M., and Ito K. Induction of neurogenin-1 expression by Sonic hedgehog: its role in development of trigeminal sensory neurons. Dev Dyn 227 (2003) 544-551
28. Pitzer C., Kruger C., Plaas C., Kirsch F., Dittgen T., Muller R., Laage R., Kastner S., Suess S., Spoelgen R., Henriques A., Ehrenreich H., Schabitz W.R., Bach A., and Schneider A. Granulocyte-colony stimulating factor improves outcome in a mouse model of amyotrophic lateral sclerosis. Brain 131 (2008) 3335-3347
29. Ross S.E., Greenberg M.E., and Stiles C.D. Basic helix-loop-helix factors in cortical development. Neuron 39 (2003) 13-25
30. Rusthoven J., Bramwell V., and Stephenson B. Use of granulocyte colony-stimulating factor (G-CSF) in patients receiving myelosuppressive chemotherapy for the treatment of cancer. Provincial Systemic Treatment Disease Site Group. Cancer Prev Control 2 (1998) 179-190
31. Schabitz W.R., and Schneider A. New targets for established proteins: exploring G-CSF for the treatment of stroke. Trends Pharmacol Sci 28 (2007) 157-161
32. Schneider A., Kruger C., Steigleder T., Weber D., Pitzer C., Laage R., Aronowski J., Maurer M.H., Gassler N., Mier W., Hasselblatt M., Kollmar R., Schwab S., Sommer C., Bach A., Kuhn H.G., and Schabitz W.R. The hematopoietic factor G-CSF is a neuronal ligand that counteracts programmed cell death and drives neurogenesis. J Clin Invest 115 (2005) 2083-2098
33. Shyu W.C., Lin S.Z., Yang H.I., Tzeng Y.S., Pang C.Y., Yen P.S., and Li H. Functional recovery of stroke rats induced by granulocyte colony-stimulating factor-stimulated stem cells. Circulation 110 (2004) 1847-1854
34. Solaroglu I., Cahill J., Jadhav V., and Zhang J.H. A novel neuroprotectant granulocyte-colony stimulating factor. Stroke 37 (2006) 1123-1128
35. Spiekermann K., Roesler J., Emmendoerffer A., Elsner J., and Welte K. Functional features of neutrophils induced by G-CSF and GM-CSF treatment: differential effects and clinical implications. Leukemia 11 (1997) 466-478
36. Tian S.S., Tapley P., Sincich C., Stein R.B., Rosen J., and Lamb P. Multiple signaling pathways induced by granulocyte colony-stimulating factor involving activation of JAKs, STAT5, and/or STAT3 are required for regulation of three distinct classes of immediate early genes. Blood 88 (1996) 4435-4444
37. Toth Z.E., Leker R.R., Shahar T., Pastorino S., Szalayova I., Asemenew B., Key S., Parmelee A., Mayer B., Nemeth K., Bratincsak A., and Mezey E. The combination of granulocyte colony-stimulating factor and stem cell factor significantly increases the number of bone marrow-derived endothelial cells in brains of mice following cerebral ischemia. Blood 111 (2008) 5544-5552
38. Ward A.C., Hermans M.H., Smith L., van Aesch Y.M., Schelen A.M., Antonissen C., and Touw I.P. Tyrosine-dependent and -independent mechanisms of STAT3 activation by the human granulocyte colony-stimulating factor (G-CSF) receptor are differentially utilized depending on G-CSF concentration. Blood 93 (1999) 113-124
39. Ward A.C., Monkhouse J.L., Csar X.F., Touw I.P., and Bello P.A. The Src-like tyrosine kinase Hck is activated by granulocyte colony-stimulating factor (G-CSF) and docks to the activated G-CSF receptor. Biochem Biophys Res Commun 251 (1998) 117-123
40. Zhou Q., and Anderson D.J. The bHLH transcription factors OLIG2 and OLIG1 couple neuronal and glial subtype specification. Cell 109 (2002) 61-73