Activin increases the number of synaptic contacts and the length of dendritic spine necks by modulating spinal actin dynamics

被引:51
作者
Shoji-Kasai, Yoko
Ageta, Hiroshi
Hasegawa, Yoshihisa
Tsuchida, Kunihiro
Sugino, Hiromu
Inokuchi, Kaoru [1 ]
机构
[1] Univ Tokushima, Inst Enzyme Res, Tokushima 7708503, Japan
[2] Mitsubishi Kagaku Inst Life Sci, MITILS, Tokyo 1948511, Japan
[3] Kitasato Univ, Sch Vet Med & Anim Sci, Lab Anim Sci, Towada, Aomori 0348628, Japan
[4] Yokohama Natl Univ, Grad Sch Environm & Informat Sci, Yokohama, Kanagawa 2408501, Japan
[5] Japan Sci & Technol Agcy, CREST, Kawaguchi, Saitama 3320012, Japan
关键词
activin; spine; morphology;
D O I
10.1242/jcs.012450
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Long-lasting modifications in synaptic transmission depend on de novo gene expression in neurons. The expression of activin, a member of the transforming growth factor beta (TGF-beta) superfamily, is upregulated during hippocampal long-term potentiation (LTP). Here, we show that activin increased the average number of presynaptic contacts on dendritic spines by increasing the population of spines that were contacted by multiple presynaptic terminals in cultured neurons. Activin also induced spine lengthening, primarily by elongating the neck, resulting in longer mushroom-shaped spines. The number of spines and spine head size were not significantly affected by activin treatment. The effects of activin on spinal filamentous actin (F-actin) morphology were independent of protein and RNA synthesis. Inhibition of cytoskeletal actin dynamics or of the mitogen-activated protein (MAP) kinase pathway blocked not only the activin-induced increase in the number of terminals contacting a spine but also the activin-induced lengthening of spines. These results strongly suggest that activin increases the number of synaptic contacts by modulating actin dynamics in spines, a process that might contribute to the establishment of late-phase LTP.
引用
收藏
页码:3830 / 3837
页数:8
相关论文
共 49 条
[1]   INDUCTION OF BETA-A ACTIVIN EXPRESSION BY SYNAPTIC ACTIVITY AND DURING NEOCORTICAL DEVELOPMENT [J].
ANDREASSON, K ;
WORLEY, PF .
NEUROSCIENCE, 1995, 69 (03) :781-796
[2]   STRUCTURAL-CHANGES ACCOMPANYING MEMORY STORAGE [J].
BAILEY, CH ;
KANDEL, ER .
ANNUAL REVIEW OF PHYSIOLOGY, 1993, 55 :397-426
[3]   Synergistic activity of activin A and basic fibroblast growth factor on tyrosine hydroxylase expression through Smad3 and ERK1/ERK2 MAPK signaling pathways [J].
Bao, YL ;
Tsuchida, K ;
Liu, B ;
Kurisaki, A ;
Matsuzaki, T ;
Sugino, H .
JOURNAL OF ENDOCRINOLOGY, 2005, 184 (03) :493-504
[4]   Increasing numbers of synaptic puncta during late-phase LTP: N-cadherin is synthesized, recruited to synaptic sites, and required for potentiation [J].
Bozdagi, O ;
Shan, W ;
Tanaka, H ;
Benson, DL ;
Huntley, GW .
NEURON, 2000, 28 (01) :245-259
[5]   Smad-dependent and Smad-independent pathways in TGF-β family signalling [J].
Derynck, R ;
Zhang, YE .
NATURE, 2003, 425 (6958) :577-584
[6]   Dendritic spine changes associated with hippocampal long-term synaptic plasticity [J].
Engert, F ;
Bonhoeffer, T .
NATURE, 1999, 399 (6731) :66-70
[7]   ACTIN MATRIX OF DENDRITIC SPINES, SYNAPTIC PLASTICITY, AND LONG-TERM POTENTIATION [J].
FIFKOVA, E ;
MORALES, M .
INTERNATIONAL REVIEW OF CYTOLOGY-A SURVEY OF CELL BIOLOGY, 1992, 139 :267-307
[8]   Glutamate receptors regulate actin-based plasticity in dendritic spines [J].
Fischer, M ;
Kaech, S ;
Wagner, U ;
Brinkhaus, H ;
Matus, A .
NATURE NEUROSCIENCE, 2000, 3 (09) :887-894
[9]   Rapid actin-based plasticity in dendritic spines [J].
Fischer, M ;
Kaech, S ;
Knutti, D ;
Matus, A .
NEURON, 1998, 20 (05) :847-854
[10]  
FUJITA S, 1989, BIOSIGNAL TRANSDUCTI, P159