Bergmann glial ensheathment of dendritic spines regulates synapse number without affecting spine motility

被引:29
作者
Bell, Jocelyn J. Lippman [1 ]
Lordkipanidze, Tamar [1 ]
Cobb, Natalie [1 ]
Dunaevsky, Anna [1 ]
机构
[1] Brown Univ, Dept Neurosci, Providence, RI 02912 USA
关键词
Synaptogenesis; Purkinje cell; cerebellum; GluR2; MAMMALIAN TARGET; ASTROCYTES; DYNAMICS; NEURON; CELLS; ULTRASTRUCTURE; MORPHOGENESIS; MTOR;
D O I
10.1017/S1740925X10000165
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
In the cerebellum, lamellar Bergmann glial (BG) appendages wrap tightly around almost every Purkinje cell dendritic spine. The function of this glial ensheathment of spines is not entirely understood. The development of ensheathment begins near the onset of synaptogenesis, when motility of both BG processes and dendritic spines are high. By the end of the synaptogenic period, ensheathment is complete and motility of the BG processes decreases, correlating with the decreased motility of dendritic spines. We therefore have hypothesized that ensheathment is intimately involved in capping synaptogenesis, possibly by stabilizing synapses. To test this hypothesis, we misexpressed GluR2 in an adenoviral vector in BG towards the end of the synaptogenic period, rendering the BG alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors (AMPARs) Ca2+-impermeable and causing glial sheath retraction. We then measured the resulting spine motility, spine density and synapse number. Although we found that decreasing ensheathment at this time does not alter spine motility, we did find a significant increase in both synaptic pucta and dendritic spine density. These results indicate that consistent spine coverage by BG in the cerebellum is not necessary for stabilization of spine dynamics, but is very important in the regulation of synapse number.
引用
收藏
页码:193 / 200
页数:8
相关论文
共 22 条
[1]
BOURGERON T, 2009, NEURON, V19, P231, DOI DOI 10.1016/J.CONB.2009.06.003
[2]
Dynamics of dendritic spines and their afferent terminals: spines are more motile than presynaptic boutons [J].
Deng, JB ;
Dunaevsky, A .
DEVELOPMENTAL BIOLOGY, 2005, 277 (02) :366-377
[3]
Spine motility with synaptic contact [J].
Dunaevsky, A ;
Blaszeski, R ;
Yuste, R ;
Mason, C .
NATURE NEUROSCIENCE, 2001, 4 (07) :685-686
[4]
Developmental regulation of spine motility in the mammalian central nervous system [J].
Dunaevsky, A ;
Tashiro, A ;
Majewska, A ;
Mason, C ;
Yuste, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (23) :13438-13443
[5]
Timing of neuronal and glial ultrastructure disruption during brain slice preparation and recovery in vitro [J].
Fiala, JC ;
Kirov, SA ;
Feinberg, MD ;
Petrak, LJ ;
George, P ;
Goddard, CA ;
Harris, KM .
JOURNAL OF COMPARATIVE NEUROLOGY, 2003, 465 (01) :90-103
[6]
Fiala JC, 2001, J AM MED INFORM ASSN, V8, P1
[7]
Bergmann glial cells form distinct morphological structures to interact with cerebellar neurons [J].
Grosche, J ;
Kettenmann, H ;
Reichenbach, A .
JOURNAL OF NEUROSCIENCE RESEARCH, 2002, 68 (02) :138-149
[8]
Microdomains for neuron-glia interaction:: parallel fiber signaling to Bergmann glial cells [J].
Grosche, J ;
Matyash, V ;
Möller, T ;
Verkhratsky, A ;
Reichenbach, A ;
Kettenmann, H .
NATURE NEUROSCIENCE, 1999, 2 (02) :139-143
[9]
Cooperative astrocyte and dendritic spine dynamics at hippocampal excitatory synapses [J].
Haber, Michael ;
Zhou, Lei ;
Murai, Keith K. .
JOURNAL OF NEUROSCIENCE, 2006, 26 (35) :8881-8891
[10]
Regulation of dendritic spine motility in cultured hippocampal neurons [J].
Korkotian, E ;
Segal, M .
JOURNAL OF NEUROSCIENCE, 2001, 21 (16) :6115-6124