Cell type specific signalling by hematopoietic growth factors in neural cells

被引:16
作者
Byts, Nadiya
Samoylenko, Anatoly
Woldt, Helge
Ehrenreich, Hannelore
Siren, Anna-Leena
机构
[1] Max Planck Inst Expt Med, Div Clin Neurosci, D-37075 Gottingen, Germany
[2] Univ Wurzburg, Dept Neurosurg, Sect Expt Neurosurg, D-97080 Wurzburg, Germany
关键词
thrombopoietin; granulocyte colony-stimulating factor; neurons; astrocytes; rat; phosphorylation;
D O I
10.1007/s11064-006-9149-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Correct timing and spatial location of growth factor expression is critical for undisturbed brain development and functioning. In terminally differentiated cells distinct biological responses to growth factors may depend on cell type specific activation of signalling cascades. We show that the hematopoietic growth factors thrombopoietin (TPO) and granulocyte colony-stimulating factor (GCSF) exert cell type specific effects on survival, proliferation and the degree of phosphorylation of Akt1, ERK1/2 and STAT3 in rat hippocampal neurons and cortical astrocytes. In neurons, TPO induced cell death and selectively activated ERK1/2. GCSF protected neurons from TPO- and hypoxia-induced cell death via selective activation of Akt1. In astrocytes, neither TPO nor GCSF had any effect on cell viability but inhibited proliferation. This effect was accompanied by activation of ERK1/2 and inhibition of STAT3 activity. A balance between growth factors, their receptors and signalling proteins may play an important role in regulation of neural cell survival.
引用
收藏
页码:1219 / 1230
页数:12
相关论文
共 57 条
[1]   The p44/42 mitogen-activated protein kinase cascade is involved in the induction and maintenance of astrocyte stellation mediated by protein kinase C [J].
Abe, K ;
Saito, H .
NEUROSCIENCE RESEARCH, 2000, 36 (03) :251-257
[2]   MEK1 protein kinase inhibition protects against damage resulting from focal cerebral ischemia [J].
Alessandrini, A ;
Namura, S ;
Moskowitz, MA ;
Bonventre, JV .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (22) :12866-12869
[3]   A potential role for erythropoietin in focal permanent cerebral ischemia in mice [J].
Bernaudin, M ;
Marti, HH ;
Roussel, S ;
Divoux, D ;
Nouvelot, A ;
MacKenzie, E ;
Petit, E .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1999, 19 (06) :643-651
[4]   STATs in oncogenesis [J].
Bowman, T ;
Garcia, R ;
Turkson, J ;
Jove, R .
ONCOGENE, 2000, 19 (21) :2474-2488
[5]   Isolation and culture of adult rat hippocampal neurons [J].
Brewer, GJ .
JOURNAL OF NEUROSCIENCE METHODS, 1997, 71 (02) :143-155
[6]   Emerging biological roles for erythropoietin in the nervous system [J].
Brines, M ;
Cerami, A .
NATURE REVIEWS NEUROSCIENCE, 2005, 6 (06) :484-494
[7]   Stat proteins and oncogenesis [J].
Bromberg, J .
JOURNAL OF CLINICAL INVESTIGATION, 2002, 109 (09) :1139-1142
[8]   Upregulation of gp130 and differential activation of STAT and p42/44 MAPK in the rat hippocampus following kainic acid-induced seizures [J].
Choi, JS ;
Kim, SY ;
Park, HJ ;
Cha, HJ ;
Choi, YS ;
Kang, JE ;
Chung, JW ;
Chun, MH ;
Lee, MY .
MOLECULAR BRAIN RESEARCH, 2003, 119 (01) :10-18
[9]   Thrombopoietin gene expression in the developing human central nervous system [J].
Dame, C ;
Wolber, EM ;
Freitag, P ;
Hofmann, D ;
Bartmann, P ;
Fandrey, J .
DEVELOPMENTAL BRAIN RESEARCH, 2003, 143 (02) :217-223
[10]   The carboxyl terminus of the granulocyte colony- stimulating factor receptor, truncated in patients with severe congenital neutropenia/acute myeloid leukemia, is required for SH2-containing phosphatase-1 suppression of Stat activation [J].
Dong, F ;
Qiu, YL ;
Yi, TL ;
Touw, IP ;
Larner, AC .
JOURNAL OF IMMUNOLOGY, 2001, 167 (11) :6447-6452