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Evidence for the participation of the neuron-specific CDK5 activator p35 during laminin-enhanced axonal growth
被引:0
|作者:
Paglini, G
Pigino, G
Kunda, P
Morfini, G
Maccioni, R
Quiroga, S
Ferreira, A
Cáceres, A
机构:
[1] CONICET, Inst Mercedes & Martin Ferreyra, RA-5000 Cordoba, Argentina
[2] Univ Chile, Lab Biol Celular & Mol, Santiago 5000, Chile
[3] Univ Nacl Cordoba, CONICET, Dept Quim Biol, RA-5000 Cordoba, Argentina
[4] Northwestern Univ, Dept Cell & Mol Biol, Chicago, IL 60611 USA
[5] Northwestern Univ, Inst Neurosci, Chicago, IL 60611 USA
关键词:
cdk5;
p35;
neurons;
development;
axon;
growth;
cones;
MAP1b;
phosphorylation;
antisense oligonucleotides;
neuronal cultures;
D O I:
暂无
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Cultures of cerebellar macroneurons were used to study the pattern of expression, subcellular localization, and function of the neuronal cdk5 activator p35 during laminin-enhanced axonal growth. The results obtained indicate that laminin, an extracellular matrix molecule capable of selectively stimulating axonal extension and promoting MAP1B phosphorylation at a proline-directed protein kinase epitope, selectively stimulates p35 expression, increases its association with the subcortical cytoskeleton, and accelerates its redistribution to the axonal growth cones. Besides, suppression of p35, but not of a highly related isoform designated as p39, by antisense oligonucleotide treatment selectively reduces cdk5 activity, laminin-enhanced axonal elongation, and MAP1b phosphorylation. Taken collectively, the present results suggest that cdk5/p35 may serve as an important regulatory linker between environmental signals (e.g., laminin) and constituents of the intracellular machinery (e.g., MAP1B) involved in axonal elongation.
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页码:9858 / 9869
页数:12
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