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Ultrastructure of the stomatogastric ganglion neuropil of the crab, Cancer borealis
Author(s) -
Kilman Valerie L.,
Marder Eve
Publication year - 1996
Publication title -
journal of comparative neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.855
H-Index - 209
eISSN - 1096-9861
pISSN - 0021-9967
DOI - 10.1002/(sici)1096-9861(19961021)374:3<362::aid-cne5>3.0.co;2-#
Subject(s) - stomatogastric ganglion , neuropil , biology , axon , neuroscience , ultrastructure , ganglion , synaptic vesicle , neuron , vesicle , anatomy , central pattern generator , central nervous system , rhythm , genetics , membrane , philosophy , aesthetics
The stomatogastric ganglion (STG) of the crab, Cancer borealis , contains the neural networks responsible for rhythmic pattern generation of the foregut. Neuron counts indicate that the STG of C. borealis has 25–26 neurons, 4–5 fewer than that found in lobsters. We describe the ultrastructural features of the ganglion by focusing on those that may be involved in storage, release, or range of action of peptide modulators, including a lacunar system and multiple types of intercellular junctions. In the neuropil, we identify five synaptic profile classes that contain the invertebrate presynaptic apparatus (dense bars, small clear vesicles), two of which also contain dense core (modulator‐containing) vesicles. These latter two are comprised of multiple immunocytochemical classes that are not easily distinguished by structural criteria. In addition, we find neurohemal‐like profiles that contain primarily dense core vesicles. Our finding that multiple profile types in the STG possess modulator‐containing vesicles coincides with immunocytochemical results better than do previous ultrastructural studies that report only one such profile type. We show that a single modulatory input, stomatogastric nerve axon 1, makes only classical synapses and not neurohemal‐like profiles, although some modulators are found in both these profile types. These data provide the groundwork for understanding the architecture of modulatory input‐target interactions and suggest ways that the specificity of modulatory effects within a complex neuropil may be attained. © 1996 Wiley‐Liss, Inc.