Literature DB >> 5840798

Developmental changes in the structure of the synapse on the myelinated cell bodies of the chicken ciliary ganglion.

A Hess.   

Abstract

Electron micrographs, stained Epon-embedded sections, and silver stains of the ciliary ganglion of chickens 19 days prehatched, 4 days, 5 weeks, 6 months, and 1 to 2 years of age were studied. The majority of ganglion cells are large neurons; smaller cells are restricted to a dorsal, distal part of the ganglion. The following description applies to the large neurons. Three to twenty lamellae of loose, semicompact, and compact myelin ensheathe virtually every neuron. All these types of myelin form the sheath of a single neuron. The lamellae greatly increase in number and in compactness during the period between the 19-day embryo and the 4-day-old chick. During the period between the 4-day chick and the adult chicken, the myelin becomes only slightly thicker and denser. The calyx is a large synaptic terminal encircling virtually every neuron in the ganglion up to 5 weeks of age. At 6 months of age, the calyx appears to break up; only about half the number of neurons in the ganglion have this large terminal, while the remaining neurons have numerous relatively small, boutonlike synapses. This rather remarkable transformation in the structure of the calyx is virtually complete in the 1- to 2-year-old chickens. In these older chickens all the cells have boutons, and calyces are no longer present. The entering preterminal fiber, the calyx, the neuron, and the axon hillock can all have myelin lamellae on them. It is possible that this entire complex is effectively insulated by the myelin sheath. No synaptic discs or fusion of the membranes of the preterminal fiber and the postganglionic neuron are seen. The chick ciliary ganglion cells are the only myelinated neurons so far described which receive synapses. The neurons in the small-cell part of the ganglion do not have calyces and are not ensheathed by myelin lamellae at any age.

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Year:  1965        PMID: 5840798      PMCID: PMC2106688          DOI: 10.1083/jcb.25.3.1

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  12 in total

1.  DUAL MODE OF SYNAPTIC TRANSMISSION IN THE AVIAN CILIARY GANGLION.

Authors:  A R MARTIN; G PILAR
Journal:  J Physiol       Date:  1963-09       Impact factor: 5.182

2.  THE DIFFERENTIATION OF SYNAPTIC AREAS.

Authors:  R COUTEAUX
Journal:  Proc R Soc Lond B Biol Sci       Date:  1963-11-19

3.  Embedding in epoxy resins for ultrathin sectioning in electron microscopy.

Authors:  K C RICHARDSON; L JARETT; E H FINKE
Journal:  Stain Technol       Date:  1960-11

4.  Evidence for saltatory conduction in peripheral myelinated nerve fibres.

Authors:  A F Huxley; R Stämpfli
Journal:  J Physiol       Date:  1949-05-15       Impact factor: 5.182

5.  [Studies on the ciliary ganglion of birds; connections, age changes, and the effect of resection of the preganglionic fibers].

Authors:  C TERZUOLO
Journal:  Z Zellforsch Mikrosk Anat       Date:  1951

6.  Simple methods for "staining with lead" at high pH in electron microscopy.

Authors:  M J KARNOVSKY
Journal:  J Biophys Biochem Cytol       Date:  1961-12

7.  The fine structure of nerve cell bodies and their myelin sheaths in the eighth nerve ganglion of the goldfish.

Authors:  J ROSENBLUTH; S L PALAY
Journal:  J Biophys Biochem Cytol       Date:  1961-04

8.  The fine structure of synapses in the ciliary ganglion of the chick.

Authors:  A J DE LORENZO
Journal:  J Biophys Biochem Cytol       Date:  1960-02

9.  Improvements in epoxy resin embedding methods.

Authors:  J H LUFT
Journal:  J Biophys Biochem Cytol       Date:  1961-02

10.  THE ULTRASTRUCTURE OF MAUTHNER CELL SYNAPSES AND NODES IN GOLDFISH BRAINS.

Authors:  J D ROBERTSON; T S BODENHEIMER; D E STAGE
Journal:  J Cell Biol       Date:  1963-10       Impact factor: 10.539

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  24 in total

1.  Direct recording of nicotinic responses in presynaptic nerve terminals.

Authors:  J S Coggan; J Paysan; W G Conroy; D K Berg
Journal:  J Neurosci       Date:  1997-08-01       Impact factor: 6.167

2.  Neuronal acetylcholine receptors with alpha7 subunits are concentrated on somatic spines for synaptic signaling in embryonic chick ciliary ganglia.

Authors:  R D Shoop; M E Martone; N Yamada; M H Ellisman; D K Berg
Journal:  J Neurosci       Date:  1999-01-15       Impact factor: 6.167

3.  Population and structure of nerve cells in mouse submandibular ganglion.

Authors:  M Yamakado; T Yohro
Journal:  Anat Embryol (Berl)       Date:  1977-05-12

4.  The onset and development of transmission in the chick ciliary ganglion.

Authors:  L Landmesser; G Pilar
Journal:  J Physiol       Date:  1972-05       Impact factor: 5.182

5.  Synapse formation during embryogenesis on ganglion cells lacking a periphery.

Authors:  L Landmesser; G Pilar
Journal:  J Physiol       Date:  1974-09       Impact factor: 5.182

6.  Evidence for the vesicle hypothesis.

Authors:  J I Hubbard; S Kwanbunbumpen
Journal:  J Physiol       Date:  1968-02       Impact factor: 5.182

7.  The growth of synaptic endings in the mammalian brain: a study of the calyces of the trapezoid body.

Authors:  D K Morest
Journal:  Z Anat Entwicklungsgesch       Date:  1968-11-04

8.  [On a single cell nucleus enveloping the medullary sheath in the cerebral medulla of cats].

Authors:  H Haug
Journal:  Naturwissenschaften       Date:  1967-10

9.  PACAP/PAC1R signaling modulates acetylcholine release at neuronal nicotinic synapses.

Authors:  Phyllis C Pugh; Selwyn S Jayakar; Joseph F Margiotta
Journal:  Mol Cell Neurosci       Date:  2009-12-01       Impact factor: 4.314

10.  The effect of ions and second messengers on long-term potentiation of chemical transmission in avian ciliary ganglia.

Authors:  T R Scott; M R Bennett
Journal:  Br J Pharmacol       Date:  1993-09       Impact factor: 8.739

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