Reelin and cyclin-dependent kinase 5-dependent signals cooperate in regulating neuronal migration and synaptic transmission

被引:90
作者
Beffert, U
Weeber, EJ
Morfini, G
Ko, J
Brady, ST
Tsai, LH
Sweatt, JD
Herz, J [1 ]
机构
[1] Univ Texas, SW Med Ctr, Dept Mol Genet, Dallas, TX 75390 USA
[2] Univ Illinois, Dept Anat & Cell Biol, Chicago, IL 60612 USA
[3] Baylor Coll Med, Div Neurosci, Houston, TX 77030 USA
[4] Harvard Univ, Sch Med, Howard Hughes Med Inst, Dept Pathol, Boston, MA 02115 USA
关键词
Alzheimer; long-term potentiation (LTP); Reelin; Cdk5; neuronal migration; signaling;
D O I
10.1523/JNEUROSCI.4084-03.2004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neuronal migration and positioning in the developing brain require the coordinated interaction of multiple cellular signaling pathways. The extracellular signaling molecule Reelin and the cytoplasmic serine/threonine kinase Cdk5 (cyclin-dependent kinase 5) are both required for normal neuronal positioning, lamination of the neocortex, and foliation of the cerebellum. They also modulate synaptic transmission in the adult brain. It is not known, however, to what extent Cdk5 participates in Reelin signaling and whether both pathways interact on the genetic or biochemical level. We have used genetically altered mice to generate compound functional defects of Reelin and Cdk5 signaling. Differential neurohistochemical staging combined with the biochemical analysis of Reelin- and Cdk5-dependent signaling in primary embryonic neurons and electrophysiology in hippocampal slices reveals evidence for genetic and functional interaction between both pathways. Inhibition of Reelin or Cdk5 signaling had no discernible biochemical effect on each other. Taken together, these findings suggest that both pathways function together in a parallel, rather than a simple, linear manner to coordinate neuronal migration and neurotransmission in the developing and mature brain.
引用
收藏
页码:1897 / 1906
页数:10
相关论文
共 44 条
[31]   Synergistic contributions of cyclin-dependant kinase 5/p35 and Reelin/Dab1 to the positioning of cortical neurons in the developing mouse brain [J].
Ohshima, T ;
Ogawa, M ;
Veeranna ;
Hirasawa, M ;
Longenecker, G ;
Ishiguro, K ;
Pant, HC ;
Brady, RO ;
Kulkarni, AB ;
Mikoshiba, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (05) :2764-2769
[32]   Conversion of p35 to p25 deregulates Cdk5 activity and promotes neurodegeneration [J].
Patrick, GN ;
Zukerberg, L ;
Nikolic, M ;
de la Monte, S ;
Dikkes, P ;
Tsai, LH .
NATURE, 1999, 402 (6762) :615-622
[33]   A LIS1/NUDEL/cytoplasmic dynein heavy chain complex in the developing and adult nervous system [J].
Sasaki, S ;
Shionoya, A ;
Ishida, M ;
Gambello, MJ ;
Yingling, J ;
Wynshaw-Boris, A ;
Hirotsune, S .
NEURON, 2000, 28 (03) :681-696
[34]  
SCHULZ PE, 1994, J NEUROSCI, V14, P5325
[35]   Cdk5 behind the wheel: a role in trafficking and transport? [J].
Smith, DS ;
Tsai, LH .
TRENDS IN CELL BIOLOGY, 2002, 12 (01) :28-36
[36]   Origins of peptide selectivity and phosphoinositide binding revealed by structures of disabled-1 PTB domain complexes [J].
Stolt, PC ;
Jeon, H ;
Song, HK ;
Herz, J ;
Eck, MJ ;
Blacklow, SC .
STRUCTURE, 2003, 11 (05) :569-579
[37]   Cdk5 is essential for synaptic vesicle endocytosis [J].
Tan, TC ;
Valova, VA ;
Malladi, CS ;
Graham, ME ;
Berven, LA ;
Jupp, OJ ;
Hansra, G ;
McClure, SJ ;
Sarcevic, B ;
Boadle, RA ;
Larsen, MR ;
Cousin, MA ;
Robinson, PJ .
NATURE CELL BIOLOGY, 2003, 5 (08) :701-710
[38]   AN ISOFORM OF THE NEURONAL CYCLIN-DEPENDENT KINASE-5 (CDK5) ACTIVATOR [J].
TANG, DM ;
YEUNG, J ;
LEE, KY ;
MATSUSHITA, M ;
MATSUI, H ;
TOMIZAWA, K ;
HATASE, O ;
WANG, JH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (45) :26897-26903
[39]   Reelin and brain development [J].
Tissir, F ;
Goffinet, AM .
NATURE REVIEWS NEUROSCIENCE, 2003, 4 (06) :496-505
[40]   Reeler/disabled-like disruption of neuronal migration in knockout mice lacking the VLDL receptor and ApoE receptor 2 [J].
Trommsdorff, M ;
Gotthardt, M ;
Hiesberger, T ;
Shelton, J ;
Stockinger, W ;
Nimpf, J ;
Hammer, RE ;
Richardson, JA ;
Herz, J .
CELL, 1999, 97 (06) :689-701