scholarly journals THE SMALL PYRAMIDAL NEURON OF THE RAT CEREBRAL CORTEX

1968 ◽  
Vol 39 (3) ◽  
pp. 604-619 ◽  
Author(s):  
Alan Peters ◽  
Charmian C. Proskauer ◽  
Ita R. Kaiserman-Abramof
Keyword(s):  
Cerebral Cortex ◽  
Dendritic Spines ◽  
Pyramidal Neuron ◽  
Synaptic Vesicles ◽  
Initial Segment ◽  
Axon Terminals ◽  
Axon Hillock ◽  
Synaptic Junctions ◽  
Cytological Features ◽  
Synaptic Complexes

The axon of the pyramidal neuron in the cerebral cortex arises either directly from the perikaryon or as a branch from a basal dendrite. When it arises from the perikaryon, an axon hillock is present. The hillock is a region in which there is a transition between the cytological features of the perikaryon and those of the initial segment of the axon. Thus, in the hillock there is a diminution in the number of ribosomes and a beginning of the fasciculation of microtubules that characterize the initial segment. Not all of the microtubules entering the hillock from the perikaryon continue into the initial segment. Distally, the axon hillock ends where the dense undercoating of the plasma membrane of the initial segment commences. Dense material also appears in the extracellular space surrounding the initial segment. The initial segment of the pyramidal cell axon contains a cisternal organelle consisting of stacks of flattened cisternae alternating with plates of dense granular material. These cisternal organelles resemble the spine apparatuses that occur in the dendritic spines of this same neuron. Axo-axonal synapses are formed between the initial segment and surrounding axon terminals. The axon terminals contain clear synaptic vesicles and, at the synaptic junctions, both synaptic complexes and puncta adhaerentia are present.

Synapses on the Axon Hillocks and Initial Segments of Pyramidal Cell Axons in the Cerebral Cortex

1969 ◽  
Vol 5 (2) ◽  
pp. 495-507
Author(s):  
E. G. JONES ◽  
T. P. S. POWELL
Keyword(s):  
Pyramidal Cell ◽  
Synaptic Vesicles ◽  
Initial Segment ◽  
Sensory Cortex ◽  
Axon Terminals ◽  
Dense Bodies ◽  
Inner Surface ◽  
Spine Apparatus ◽  
Membrane Bound ◽  
Somatic Sensory Cortex

The axon hillocks and initial segments of pyramidal cell axons can be clearly recognized in electron micrographs of the somatic sensory cortex. The initial segment is characterized by three features: bundles of neurotubules linked together by electron-dense bands, a layer of dense material attached to the inner surface of the plasma membrane, and small membrane-bound dense bodies. All of these elements and the few ribosomes usually present disappear at the commencement of the myelin sheath. The initial segment of the axon often contains a cluster of cisternae similar to the spine apparatus, and this part of the axon sometimes gives off small branches. Axon terminals end on both the axon hillock and the initial segment, and there is an increase in number on the latter as the distance from the hillock increases. All of these terminals are relatively large, contain a high proportion of small flattened or pleomorphic synaptic vesicles and terminate in symmetrical synaptic contacts. These morphological features suggest that the synapses may be inhibitory in function.

The site of termination of afferent fibres in the caudate nucleus

1971 ◽  
Vol 262 (845) ◽  
pp. 413-427 ◽  
Keyword(s):  
Cerebral Cortex ◽  
Caudate Nucleus ◽  
Dendritic Spines ◽  
Axon Terminal ◽  
Main Stem ◽  
Electron Microscopic ◽  
Axon Terminals ◽  
Terminal Degeneration ◽  
Contralateral Cortex ◽  
Cell Somata

An electron microscopic study has been made of the axon terminal degeneration in the caudate nucleus in the cat after lesions in either the cerebral cortex, the thalamus, the cerebral cortex and the thalamus, the midbrain or within the caudate nucleus. Degenerating axon terminals can be recognized after a survival period of 4 days as dark, shrunken profiles with indistinct vesicles. After shorter survival periods the degenerating terminals contain swollen vesicles and have pale cytoplasm. After lesions in all the above sites there is degeneration of fine myelinated and nonmyelinated fibres. The degenerating terminals of all the afferent fibres to the caudate nucleus have asymmetrical membrane thickenings and end mainly on dendritic spines with a small proportion in contact with peripheral dendrites; after damage of the cerebral cortex or thalamus a few of the degenerating terminals also end upon main stem dendrites and cell bodies. The projection from the ipsilateral cerebral cortex is greater than that from the thalamus, which in turn is heavier than that from the contralateral cortex or midbrain. After lesions within the caudate nucleus degenerating terminals with symmetrical membrane thickenings are found in a region extending approximately 450 pm from the damaged part of the nucleus. These terminals make contact with nerve cell somata, main stem and peripheral dendrites and the initial segments of axons. After such a lesion of the caudate nucleus degenerating axon terminals with symmetrical membrane thickenings are also seen in the globus pallidus and the substantia nigra.

The Lateral Giant Fiber to Motor Giant Fiber Synapse in Crayfish

1972 ◽  
Vol 30 ◽  
pp. 170-171
Author(s):  
Charles A. Stirling
Keyword(s):  
Synaptic Vesicles ◽  
Procambarus Clarkii ◽  
Synaptic Contact ◽  
Giant Fiber ◽  
Synaptic Junctions

The lateral giant (LG) to motor giant (MoG) synapses in crayfish (Procambarus clarkii) abdominal ganglia are the classic electrotonic synapses. They have previously been described as having synaptic vesicles and as having them on both the pre- and postsynaptic sides of symmetrical synaptic junctions. This positioning of vesicles would make these very atypical synapses, but in the present work on the crayfish Astacus pallipes the motor giant has never been found to contain any type of vesicle at its synapses with the lateral giant fiber.The lateral to motor giant fiber synapses all occur on short branches off the main giant fibers. Closely associated with these giant fiber synapses are two small presynaptic nerves which make synaptic contact with both of the giant fibers and with their small branches.

Synaptic organization of the gustatory NST

1994 ◽  
Vol 52 ◽  
pp. 150-151
Author(s):  
M. C. Whitehead
Keyword(s):  
Central Nervous System ◽  
Dendritic Spines ◽  
Fundamental Problem ◽  
Cell Types ◽  
Brain Regions ◽  
Excitatory Synapses ◽  
Solitary Tract ◽  
Synaptic Organization ◽  
Synaptic Junctions ◽  
Afferent Terminals

A fundamental problem in taste research is to determine how gustatory signals are processed and disseminated in the mammalian central nervous system. An important first step toward understanding information processing is the identification of cell types in the nucleus of the solitary tract (NST) and their synaptic relationships with oral primary afferent terminals. Facial and glossopharyngeal (LIX) terminals in the hamster were labelled with HRP, examined with EM, and characterized as containing moderate concentrations of medium-sized round vesicles, and engaging in asymmetrical synaptic junctions. Ultrastructurally the endings resemble excitatory synapses in other brain regions.Labelled facial afferent endings in the RC subdivision synapse almost exclusively with distal dendrites and dendritic spines of NST cells. Most synaptic relationships between the facial synapses and the dendrites are simple. However, 40% of facial endings engage in complex synaptic relationships within glomeruli containing unlabelled axon endings particularly ones termed "SP" endings. SP endings are densely packed with small, pleomorphic vesicles and synapse with both the facial endings and their postsynaptic dendrites by means of nearly symmetrical junctions.

Synaptic vesicles immunoisolated from rat cerebral cortex contain high levels of glutamate

Neuron ◽  
1989 ◽  
Vol 3 (6) ◽  
pp. 715-720 ◽  
Author(s):  
Peter M. Burger ◽  
Ehrenfried Mehl ◽  
Patricia L. Cameron ◽  
Peter R. Maycox ◽  
Marion Baumert ◽  
...  
Keyword(s):  
Cerebral Cortex ◽  
Synaptic Vesicles ◽  
Rat Cerebral Cortex

A study of the axon initial segment and proximal axon of neurons in the primate motor and somatic sensory cortices

1979 ◽  
Vol 285 (1006) ◽  
pp. 173-197 ◽  
Keyword(s):  
Initial Segment ◽  
Pyramidal Cells ◽  
Stellate Cells ◽  
Myelinated Axon ◽  
Full Length ◽  
Unmyelinated Axon ◽  
Parent Cell ◽  
Axon Terminals ◽  
Sensory Cortices ◽  
Axon Initial Segments

The axon initial segments of pyramidal cells and large and small stellate cells in the primate sensori-motor cortex have a typical membrane undercoating and bundles of neurotubules. Those of pyramidal cells are directed towards the white matter whereas those of large and small stellate cells often run obliquely or towards the cortical surface and may be curved. Cisternal organs in these initial segments are related to symmetrical axon terminals, frequently coming into close apposition to the non-synaptic part of these terminals adjacent to the synapse between the axon terminal and initial segment. The dense plates of cisternal organs and the membrane undercoating of the initial segment are specifically stained by ethanolic phosphotungstic acid (ethanolic PTA). Pyramidal initial segments have spines which receive only symmetrical synapses, as do the shafts of the initial segments of each cell type. The full length of the initial segment was studied for fourteen pyramidal and two large stellate cells. All gave rise to myelinated axons although two pyramidal cells had lengths of unmyelinated axon between the initial segment and myelinated axon. One of these lengths of unmyelinated axon made an asymmetric synapse on to a dendrite just after losing its initial segment features. Quantitative analysis of these complete initial segments showed that whereas the diameter of the initial segment and the axon it gave rise to were approximately proportional to the size of the parent cell soma over a considerable range of cell diameters, the length of the initial segment appeared to be unrelated to either its diameter or the size of its parent soma but varied between 30 and 55 μm apparently at random. Synapses were evenly distributed along the full length of the complete pyramidal initial segments, but the density of synapses on the initial segments of supragranular pyramids was about three times that on those of infragranular pyramids and cisternal organs were similarly more frequent in the initial segments of supragranular pyramids.

scholarly journals AXONAL AGRANULAR RETICULUM AND SYNAPTIC VESICLES IN CULTURED EMBRYONIC CHICK SYMPATHETIC NEURONS

1973 ◽  
Vol 57 (1) ◽  
pp. 88-108 ◽  
Author(s):  
Saul Teichberg ◽  
Eric Holtzman
Keyword(s):  
Synaptic Vesicles ◽  
Sympathetic Neurons ◽  
Size Spectrum ◽  
Embryonic Chick ◽  
Membrane Systems ◽  
Axon Terminals ◽  
Golgi Membranes ◽  
Storage Vesicles ◽  
Adrenergic Systems ◽  
Catecholamine Storage

Cultured chick embryonic sympathetic neurons contain an extensive axonal network of sacs and tubules of agranular reticulum. The reticulum is also seen branching into networks in axon terminals and varicosities. The axonal reticulum and perikaryal endoplasmic reticulum resemble one another in their content of cytochemically demonstrable enzyme activities (G6Pase and IDPase) and in their characteristic membrane thicknesses (narrower than plasma membrane or some Golgi membranes). From the reticulum, both along the axon and at terminals, there appear to form dense-cored vesicles ranging in size from 400 to 1,000 Å in diameter. These vesicles behave pharmacologically and cytochemically like the classes of large and small catecholamine storage vesicles found in several adrenergic systems; for example, they can accumulate exogenous 5-hydroxydopamine. In addition, dense-cored vesicles at the larger (1,000 Å) end of the size spectrum appear to arise within perikaryal membrane systems associated with the Golgi apparatus; this is true also of very large (800–3,500 Å) dense-cored vesicles found in some perikarya.

Altered excitability of goldfish mauthner cell following axotomy. I. Characterization and correlations with somatic and axonal morphological reactions

1986 ◽  
Vol 55 (6) ◽  
pp. 1424-1439 ◽  
Author(s):  
M. J. Titmus ◽  
D. S. Faber ◽  
S. J. Zottoli
Keyword(s):  
Cell Body ◽  
Initial Segment ◽  
Membrane Properties ◽  
Resting Potential ◽  
M Cells ◽  
M Cell ◽  
Spike Amplitude ◽  
Axon Hillock ◽  
The Mean ◽  
Lateral Dendrite

Axonal transection 7-10 mm distal to the cell body of the goldfish Mauthner (M) cell induced alterations in its excitability; namely, the antidromic spike recorded in the soma was converted from a single-component axon-hillock response to a larger amplitude, two-component impulse. The mean spike amplitude of the axotomized cells was approximately 50% greater (59.6 +/- 15.1 mV, n = 94) than that in controls (39.4 +/- 6.3 mV, n = 73). The onset of the induced increase in spike amplitude occurs at approximately 20 days postaxotomy, and the transition to a reactive spike is complete by approximately 30-35 days. Eighty-three percent of the M-cells axotomized for more than 30 days were physiologically reactive as judged by their large spike amplitudes and/or the presence of an additional spike component. Concomitant with the enhanced spike amplitudes, there was a depression of excitability in the initial segment-axon hillock region of the axotomized cells. This depression was suggested by a decrease in the initial segment (IS) spike height (from 39.4 +/- 6.3 mV, n = 73, in controls to 27.5 +/- 5.6 mV, n = 13, in axotomized cells), a decrease in its maximum rate of rise (from 153.6 +/- 24 V/s, n = 15, to 112.5 +/- 30 V/s, n = 29), and frequent failure of antidromic invasion into the initial segment and axon hillock. These changes in excitability could not be attributed to alterations in passive membrane properties, since the mean resting potential (77.8 +/- 5.2 mV, n = 37, control; 76.9 +/- 7.8 mV, n = 87, axotomized) and input resistance (170 +/- 21.3 K omega, n = 13, control; 176 +/- 26.6 K omega, n = 21, axotomized) were not altered significantly by axotomy. Threshold voltage was also unaffected (13.4 +/- 3.2 mV, n = 11, control; 11.9 +/- 2.5 mV, n = 11, axotomized). Sequential recordings of spike amplitudes from the axon hillock, soma, and lateral dendrite suggest that the generator of the axotomy-induced component is localized to the normally passive soma and proximal dendrite. In addition, the presumed soma-dendritic In addition, the presumed soma-dendritic component contributes very little if anything to the action potentials recorded in the axon. The onset and occurrence of alterations in excitability and cell body morphology (chromatolysis and nuclear associated changes) were compared in different M-cell populations and in the same identified M-cells. The comparisons suggested that these two events tend to occur in parallel.(ABSTRACT TRUNCATED AT 400 WORDS)

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