Schwann cell-derived factors modulate synaptic activities at developing neuromuscular synapses

被引:28
作者
Cao, Guan [1 ]
Ko, Chien-Ping [1 ]
机构
[1] Univ So Calif, Dept Biol Sci, Neurobiol Sect, Los Angeles, CA 90089 USA
关键词
glia; neuromuscular junctions; neuron-glia interactions; Schwann cell; synaptic transmission; synaptogenesis;
D O I
10.1523/JNEUROSCI.1329-07.2007
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Glial cells are active participants in the function, formation, and maintenance of the chemical synapse. To investigate the molecular basis of neuron - glia interactions at the peripheral synapse, we examined whether and how Schwann cell- derived factors modulate synaptic function at developing neuromuscular junctions ( NMJs). Schwann cell- conditioned medium ( SC- CM) from Xenopus Schwann cell cultures was collected and applied to Xenopus nerve - muscle cocultures. We found that SC- CM increased the frequency of spontaneous synaptic currents ( SSCs) within 3 - 15 min by an average of similar to 150- fold at developing neuromuscular synapses. The increase in SSC frequency by SC- CM is a presynaptic effect independent of neuronal excitability and requires the influx of Ca2+. In contrast to its potentiating effect on spontaneous transmitter release, SC- CM suppressed the evoked transmitter release. The SC- CM effect required the presence of motoneuron soma but not protein synthesis. Using molecular weight cutoff filters and dialysis membranes, we found that the molecular weight of functional factor( s) in SC- CM was within 500 and 5000 Da. The SC- CM effect was not attributable to currently known factors that modulate synaptic efficacy, including neurotrophins, glutamate, and ATP. SC- CM also enhanced spontaneous synaptic release at developing NMJs in Xenopus tadpoles in situ. Our results suggest that Schwann cells release small molecules that enhance spontaneous synaptic activities acutely and potently at developing neuromuscular synapses, and the glial cell- enhanced spontaneous neurotransmission may contribute to synaptogenesis.
引用
收藏
页码:6712 / 6722
页数:11
相关论文
共 77 条
[1]
Signaling between glia and neurons: focus on synaptic plasticity [J].
Allen, NJ ;
Barres, BA .
CURRENT OPINION IN NEUROBIOLOGY, 2005, 15 (05) :542-548
[2]
Tripartite synapses: glia, the unacknowledged partner [J].
Araque, A ;
Parpura, V ;
Sanzgiri, RP ;
Haydon, PG .
TRENDS IN NEUROSCIENCES, 1999, 22 (05) :208-215
[3]
Perisynaptic Schwann cells at neuromuscular junctions revealed by a novel monoclonal antibody [J].
Astrow, SH ;
Qiang, HH ;
Ko, CP .
JOURNAL OF NEUROCYTOLOGY, 1998, 27 (09) :667-681
[4]
Perisynaptic Schwann cells at the neuromuscular junction: Nerve- and activity-dependent contributions to synaptic efficacy, plasticity, and reinnervation [J].
Auld, DS ;
Robitaille, R .
NEUROSCIENTIST, 2003, 9 (02) :144-157
[5]
Control of synaptic strength by glial TNFα [J].
Beattie, EC ;
Stellwagen, D ;
Morishita, W ;
Bresnahan, JC ;
Ha, BK ;
Von Zastrow, M ;
Beattie, MS ;
Malenka, RC .
SCIENCE, 2002, 295 (5563) :2282-2285
[7]
Brown P, 2002, J PHYSIOL-LONDON, V540, P851
[8]
Differential regulation of transmitter release by presynaptic and glial Ca2+ internal stores at the neuromuscular synapse [J].
Castonguay, A ;
Robitaille, R .
JOURNAL OF NEUROSCIENCE, 2001, 21 (06) :1911-1922
[9]
Thrombospondins are astrocyte-secreted proteins that promote CNS synaptogenesis [J].
Christopherson, KS ;
Ullian, EM ;
Stokes, CCA ;
Mullowney, CE ;
Hell, JW ;
Agah, A ;
Lawler, J ;
Mosher, DF ;
Bornstein, P ;
Barres, BA .
CELL, 2005, 120 (03) :421-433
[10]
Seeking a function for spontaneous neurotransmission [J].
Chung, ChiHye ;
Kavalali, Ege T. .
NATURE NEUROSCIENCE, 2006, 9 (08) :989-990