Synapse Formation: Neuromuscular Junction Versus Central Nervous System

1996 ◽  
Vol 109 (13) ◽  
pp. 2959-2966
Author(s):  
G. Escher ◽  
C. Bechade ◽  
S. Levi ◽  
A. Triller

Agrin, a synaptic basal lamina protein synthesized by motoneurons is involved in the aggregation of nicotinic acetylcholine receptors (nAchRs) at the neuromuscular junction. Agrin transcripts are broadly expressed in the central nervous system (CNS) including non-cholinergic regions. This wide distribution of agrin mRNAs raises the question of its function in these areas. To approach this question, we analysed the expression and cellular distribution of agrin in primary cultures of rat embryonic dorsal horn neurons. Polymerase chain reaction analysis demonstrated that the four agrin isoform (B0, B8, B11, B19) mRNAs are expressed as early as 4 days in vitro, before the formation of functional synaptic contacts. Western blots also showed that agrin-like proteins are secreted in conditioned medium from 7 days cultures. We analysed the subcellular distribution of agrin by double immunolabeling and fluorescence microscopy. We found that agrin is synthesized by almost all neurons and was present in the somata and in the axons but not in dendrites within the sensitivity of the detection. This intra-axonal localisation of agrin could only be seen after permeabilization. Furthermore, agrin immunoreactive axons were found adjacent to gephyrin, the postsynaptic glycine receptor-associated protein. Altogether, our results suggest that, as established at the neuromuscular junction, agrin may be involved in pre- to postsynaptic interactions in the central nervous system.


1976 ◽  
Vol 4 (3) ◽  
pp. 199-202 ◽  
Author(s):  
T. A. Torda ◽  
P. W. Gage

Thiopentone and pentobarbitone reduce the time constant of decay of miniature end-plate currents when applied in anaesthetic concentrations to the neuromuscular junction. Such an effect at central synapses would lead to failure of synaptic transmission in the central nervous system and may reflect a common mode of action of many anaesthetic drugs.


1990 ◽  
Vol 153 (1) ◽  
pp. 141-153
Author(s):  
J. G. NICHOLLS ◽  
Y. LIU ◽  
B. W. PAYTON ◽  
D. P. KUFFLER

The physiological and fine structural events accompanying synapse formation have been followed while identified neurones of known function make contact in tissue culture. Particular pairs of identified neurones isolated from the central nervous system (CNS) of the leech form chemical synapses; other pairs of cells form nonrectifying electrical junctions, rectifying electrical junctions, mixed chemical and electrical synapses or no synapses at all, depending upon the partners that have been paired. Moreover, certain specific regions on the cell surface (such as the soma, initial cell segment or axon tips) preferentially develop chemical or electrical synapses. Of particular interest are the large, serotonergic Retzius cells that form mixed chemical and electrical synapses in culture, as in the animal. When these cells are juxtaposed at their initial segments, it has been shown that chemical synapses can develop reliably within 6h of contact in culture. Shortly after transmission can be detected physiologically, the principal features of synaptic structure are evident. The physiological and morphological characteristics resemble those of mature synapses studied within the central nervous system. Only at later times, after the chemical synapses have been formed, do electrical connections appear. By contrast, when other specialized regions of the Retzius cells are apposed (the tips of their axons), electrical synapses appear earlier. By comparing the connections that different types of serotonergic neurones make in culture we have been able to assess the role played by the transmitter in determining specificity: the results show that the transmitter does not determine what type of synapse is made on a particular partner. For example, Retzius cells make purely chemical synapses upon the sensory P neurone in culture; other serotonergic neurones (known as DL and VL) make purely electrical connections on this same pressure sensory neurone. Together, these results demonstrate that highly specific cell-cell recognition is a necessary feature of synapse formation after neurones have grown to their appropriate destinations.


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