Regulation of PI3K signalling by the phosphatidylinositol transfer protein PITPα during axonal extension in hippocampal neurons

被引:44
作者
Cosker, Katharina E. [1 ]
Shadan, Sadaf
Van Diepen, Michiel [1 ]
Morgan, Clive
Li, Michelle
Allen-Baume, Victoria
Hobbs, Carl [2 ]
Doherty, Patrick [2 ]
Cockcroft, Shamshad
Eickholt, Britta J. [1 ]
机构
[1] Kings Coll London, MRC, Ctr Dev Neurobiol, London SE1 1UL, England
[2] Kings Coll London, Wolfson Ctr Age Related Dis, London SE1 1UL, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
PITP; axonal elongation; phosphoinositide; 3-kinase; hippocampal neurons;
D O I
10.1242/jcs.019166
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Phosphatidylinositol transfer proteins (PITPs) mediate the transfer of phosphatidylinositol ( PtdIns) or phosphatidylcholine (PtdCho) between two membrane compartments, thereby regulating the interface between signalling, phosphoinositide (PI) metabolism and membrane traffic. Here, we show that PITP alpha is enriched in specific areas of the postnatal and adult brain, including the hippocampus and cerebellum. Overexpression of PITP alpha, but not PITP beta or a PITP alpha mutant deficient in binding PtdIns, enhances laminin-dependent extension of axonal processes in hippocampal neurons, whereas knockdown of PITPa protein by siRNA suppresses laminin and BDNF-induced axonal growth. PITP alpha-mediated axonal outgrowth is sensitive to phosphoinositide 3-kinase (PI3K) inhibition and shows dependency on the Akt/GSK-3/CRMP-2 pathway. We conclude that PITP alpha controls the polarized extension of axonal processes through the provision of PtdIns for localized PI3K-dependent signalling.
引用
收藏
页码:796 / 803
页数:8
相关论文
共 41 条
[1]   UNC-6/Netrin induces neuronal asymmetry and defines the site of axon formation [J].
Adler, CE ;
Fetter, RD ;
Bargmann, CI .
NATURE NEUROSCIENCE, 2006, 9 (04) :511-518
[2]   The pathologies associated with functional titration of phosphatidylinositol transfer protein a activity in mice [J].
Alb, James G., Jr. ;
Phillips, Scott E. ;
Wilfley, Lindsey R. ;
Philpot, Benjamin D. ;
Bankaitis, Vytas A. .
JOURNAL OF LIPID RESEARCH, 2007, 48 (08) :1857-1872
[3]   Mice lacking phosphatidylinositol transfer protein-α exhibit spinocerebellar degeneration, intestinal and hepatic steatosis, and hypoglycemia [J].
Alb, JG ;
Cortese, JD ;
Phillips, SE ;
Albin, RL ;
Nagy, TR ;
Hamilton, BA ;
Bankaitis, VA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (35) :33501-33518
[4]   Current thoughts on the phosphatidylinositol transfer protein family [J].
Allen-Baume, V ;
Ségui, B ;
Cockcroft, S .
FEBS LETTERS, 2002, 531 (01) :74-80
[5]   Neuronal polarity: from extracellular signals to intracellular mechanisms [J].
Arimura, Nariko ;
Kaibuchi, Kozo .
NATURE REVIEWS NEUROSCIENCE, 2007, 8 (03) :194-205
[6]  
Bancroft J.D., 1990, THEORY PRACTICE HIST, V3rd
[7]   Differentiated neurons retain the capacity to generate axons from dendrites [J].
Bradke, F ;
Dotti, CG .
CURRENT BIOLOGY, 2000, 10 (22) :1467-1470
[8]   PTEN couples Sema3A signalling to growth cone collapse [J].
Chadborn, NH ;
Ahmed, AI ;
Holt, MR ;
Prinjha, R ;
Dunn, GA ;
Jones, GE ;
Eickholt, BJ .
JOURNAL OF CELL SCIENCE, 2006, 119 (05) :951-957
[9]   MIG-10/lamellipodin and AGE-1/Pl3K promote axon guidance and outgrowth in response to slit and netrin [J].
Chang, Chieh ;
Adler, Carolyn E. ;
Krause, Matthias ;
Clark, Scott G. ;
Gertler, Frank B. ;
Tessier-Lavigne, Marc ;
Bargmann, Cornelia I. .
CURRENT BIOLOGY, 2006, 16 (09) :854-862
[10]  
Cockcroft S, 1998, BIOESSAYS, V20, P423, DOI 10.1002/(SICI)1521-1878(199805)20:5<423::AID-BIES9>3.0.CO