» Articles » PMID: 9315904

In Vitro Synaptogenesis Between the Somata of Identified Lymnaea Neurons Requires Protein Synthesis but Not Extrinsic Growth Factors or Substrate Adhesion Molecules

Overview
Journal J Neurosci
Specialty Neurology
Date 1997 Oct 7
PMID 9315904
Citations 31
Authors
Affiliations
Soon will be listed here.
Abstract

Nerve growth factors, substrate and cell adhesion molecules, and protein synthesis are considered necessary for most developmental programs, including cell proliferation, migration, differentiation, axogenesis, pathfinding, and synaptic plasticity. Their direct involvement in synapse formation, however, has not yet been fully determined. The neurite outgrowth that precedes synaptogenesis is contingent on protein synthesis, the availability of externally supplied growth factors, and substrate adhesion molecules. It is therefore difficult to ascertain whether these factors are also needed for synapse formation. To examine this issue directly we reconstructed synapses between the cell somata of identified Lymnaea neurons. We show that when paired in the presence of brain conditioned medium (CM), mutual inhibitory chemical synapses between neurons right pedal dorsal 1 (RPeD1) and visceral dorsal 4 (VD4) formed in a soma-soma configuration (86%; n = 50). These synapses were reliable and target cell specific and were similar to those seen in the intact brain. To test whether synapse formation between RPeD1 and VD4 required de novo protein synthesis, the cells were paired in the presence of anisomycin (a nonspecific protein synthesis blocker). Chronic anisomycin treatment (18 hr) after cell pairing completely blocked synaptogenesis between RPeD1 and VD4 (n = 24); however, it did not affect neuronal excitability or responsiveness to exogenously applied transmitters (n = 7), nor did chronic anisomycin treatment affect synaptic transmission between pairs of cells that had formed synapses (n = 5). To test the growth and substrate dependence of synapse formation, RPeD1 and VD4 were paired in the absence of CM [defined medium; (n = 22)] on either plain plastic culture dishes (n = 10) or glass coverslips (n = 10). Neither CM nor any exogenous substrate was required for synapse formation. In summary, our data provide direct evidence that synaptogenesis in this system requires specific, cell contact-induced, de novo protein synthesis but does not depend on extrinsic growth factors or substrate adhesion molecules.

Citing Articles

The pond snail Lymnaea stagnalis.

Kuroda R, Abe M Evodevo. 2020; 11(1):24.

PMID: 33292457 PMC: 7716593. DOI: 10.1186/s13227-020-00169-4.


Gap Junction Coding Innexin in : Sequence Analysis and Characterization in Tissues and the Central Nervous System.

Mersman B, Jolly S, Lin Z, Xu F Front Synaptic Neurosci. 2020; 12:1.

PMID: 32158385 PMC: 7052179. DOI: 10.3389/fnsyn.2020.00001.


Dopamine-mediated calcium channel regulation in synaptic suppression in L. stagnalis interneurons.

Dong N, Lee D, Sun H, Feng Z Channels (Austin). 2018; 12(1):153-173.

PMID: 29589519 PMC: 5972806. DOI: 10.1080/19336950.2018.1457897.


Platycodon grandiflorus Root Extract Improves Learning and Memory by Enhancing Synaptogenesis in Mice Hippocampus.

Kim J, Jeon S, Kim K, Kim J, Song E, Jeon Y Nutrients. 2017; 9(7).

PMID: 28737698 PMC: 5537907. DOI: 10.3390/nu9070794.


The role of retinoic acid in the formation and modulation of invertebrate central synapses.

Rothwell C, de Hoog E, Spencer G J Neurophysiol. 2016; 117(2):692-704.

PMID: 27852736 PMC: 5292328. DOI: 10.1152/jn.00737.2016.


References
1.
Goodman C . The likeness of being: phylogenetically conserved molecular mechanisms of growth cone guidance. Cell. 1994; 78(3):353-6. DOI: 10.1016/0092-8674(94)90413-8. View

2.
Fuchs P, Henderson L, Nicholls J . Chemical transmission between individual Retzius and sensory neurones of the leech in culture. J Physiol. 1982; 323:195-210. PMC: 1250352. DOI: 10.1113/jphysiol.1982.sp014068. View

3.
Syed N, Richardson P, Bulloch A . Ciliary neurotrophic factor, unlike nerve growth factor, supports neurite outgrowth but not synapse formation by adult Lymnaea neurons. J Neurobiol. 1996; 29(3):293-303. DOI: 10.1002/(SICI)1097-4695(199603)29:3<293::AID-NEU2>3.0.CO;2-4. View

4.
Roubos E . Synaptology of the central nervous system of the freshwater snail Lymnaea stagnalis (L.), with particular reference to neurosecretion. Cell Tissue Res. 1979; 198(2):217-35. DOI: 10.1007/BF00232006. View

5.
Doherty P, Walsh F . Cell adhesion molecules, second messengers and axonal growth. Curr Opin Neurobiol. 1992; 2(5):595-601. DOI: 10.1016/0959-4388(92)90024-f. View