The Insulin-Like Growth Factor (IGF) Receptor Type 1 (IGF1R) as an Essential Component of the Signalling Network Regulating Neurogenesis

被引:60
作者
Annenkov, Alexander [1 ]
机构
[1] Queen Mary Univ London, Barts & Royal London Sch Med & Dent, Bone & Joint Res Unit, William Harvey Res Inst, London EC1M 6BQ, England
关键词
Insulin-like growth factor receptor; Neurogenesis; Receptor tyrosine kinase; Neural stem cell; Intracellular signalling; Cell migration; Cadherin; Integrin; Focal adhesion; Adherence junction; NEURAL STEM-CELLS; CENTRAL-NERVOUS-SYSTEM; FOCAL ADHESION KINASE; FACTOR-I RECEPTOR; ACTIVATED PROTEIN-KINASE; ADULT-RAT BRAIN; OLIGODENDROCYTE PROGENITOR CELLS; CULTURED HIPPOCAMPAL-NEURONS; GLYCOGEN-SYNTHASE KINASE-3; EMBRYONIC CEREBRAL-CORTEX;
D O I
10.1007/s12035-009-8081-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The insulin-like growth factor receptor type 1 (IGF1R) signalling pathway is activated in the mammalian nervous system from early developmental stages. Its major effect on developing neural cells is to promote their growth and survival. This pathway can integrate its action with signalling pathways of growth and morphogenetic factors that induce cell fate specification and selective expansion of specified neural cell subsets. This suggests that during developmental and adult neurogenesis cellular responses to many signalling factors, including ligands of Notch, sonic hedgehog, fibroblast growth factor family members, ligands of the epidermal growth factor receptor, bone morphogenetic proteins and Wingless and Int-1, may be modified by co-activation of the IGF1R. Modulation of cell migration is another possible role that IGF1R activation may play in neurogenesis. Here, I briefly overview neurogenesis and discuss a role for IGF1R-mediated signalling in the developing and mature nervous system with emphasis on crosstalk between the signalling pathways of the IGF1R and other factors regulating neural cell development and migration. Studies on neural as well as on non-neural cells are highlighted because it may be interesting to test in neurogenic paradigms some of the models based on the information obtained in studies on non-neural cell types.
引用
收藏
页码:195 / 215
页数:21
相关论文
共 279 条
[1]   IGF-I has a direct proliferative effect in adult hippocampal progenitor cells [J].
Åberg, MAI ;
Åberg, ND ;
Palmer, TD ;
Alborn, AM ;
Carlsson-Skwirut, C ;
Bang, P ;
Rosengren, LE ;
Olsson, T ;
Gage, FH ;
Eriksson, PS .
MOLECULAR AND CELLULAR NEUROSCIENCE, 2003, 24 (01) :23-40
[2]   β-Catenin signaling promotes proliferation of progenitor cells in the adult mouse subventricular zone [J].
Adachi, Kazuhide ;
Mirzadeh, Zaman ;
Sakaguchi, Masanori ;
Yamashita, Toru ;
Nikolcheva, Tania ;
Gotoh, Yukiko ;
Peltz, Gary ;
Gong, Leyi ;
Kawase, Takeshi ;
Alvarez-Buylla, Arturo ;
Okano, Hideyuki ;
Sawamoto, Kazunobu .
STEM CELLS, 2007, 25 (11) :2827-2836
[3]   Structure and function of the type 1 insulin-like growth factor receptor [J].
Adams, TE ;
Epa, VC ;
Garrett, TPJ ;
Ward, CW .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2000, 57 (07) :1050-1093
[4]   Expression of Sox1, Sox2 and Sox9 is maintained in adult human cerebellar cortex [J].
Alcock, Joelle ;
Lowe, James ;
England, Tim ;
Bath, Philip ;
Sottile, Virginie .
NEUROSCIENCE LETTERS, 2009, 450 (02) :114-116
[5]   Notch signaling is required to maintain all neural stem cell populations - Irrespective of spatial or temporal niche [J].
Alexson, TO ;
Hitoshi, S ;
Coles, BL ;
Bernstein, A ;
van der Kooy, D .
DEVELOPMENTAL NEUROSCIENCE, 2006, 28 (1-2) :34-48
[6]   For the long run: Maintaining germinal niches in the adult brain [J].
Alvarez-Buylla, A ;
Lim, DA .
NEURON, 2004, 41 (05) :683-686
[7]  
Androutsellis-Theotokis A, 2006, NATURE, V442, P823, DOI 10.1038/nature04940
[8]  
Angenstein F, 2002, J NEUROSCI, V22, P8827
[9]   Chemoattractive activity of Sonic Hedgehog in the adult subventricular zone modulates the number of neural precursors reaching the olfactory bulb [J].
Angot, Elodie ;
Loulier, Karine ;
Nguyen-Ba-Charvet, Kim T. ;
Gadeau, Alain-Pierre ;
Ruat, Martial ;
Traiffort, Elisabeth .
STEM CELLS, 2008, 26 (09) :2311-2320
[10]  
Angst BD, 2001, J CELL SCI, V114, P629