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

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.

1984 ◽  
Vol 33 (14) ◽  
pp. 2245-2252 ◽  
Author(s):  
M.P. Roisin ◽  
M.F. Isambert ◽  
J.P. Henry ◽  
M. Guillot ◽  
G. Lenoir

1969 ◽  
Vol 4 (3) ◽  
pp. 677-691
Author(s):  
J. M. ENGLAND ◽  
M. N. GOLDSTEIN

The uptake of exogenous [3H]dopamine, [3H]norepinephrine,[3H]epinephrine by dissociated chick embryo sympathetic neurons growing in tissue culture was studied by autoradiography. The neurons, growing in a medium containing nerve growth factor, rapidly and specifically took up all three catecholamines for at least 60 days, while no uptake was observed in several other cell types, including satellite cells and chick dorsal-root ganglion cells. The uptake was dependent on the concentration of the catecholamine and the duration of the pulse and was inhibited by cocaine and several sympathomimetic amines. Labelling was visualized only with fixatives which react with catecholamines to form water-insoluble compounds. Autoradiographs showed that the label was much denser over the axons than the cell bodies. The label was distributed uniformly along the axons and did not seem to be preferentially localized at the axon terminals or varicosities which contain aggregates of dense core granules. These observations indicate that a large portion of the exogenous 3[H]catecholamine is localized in an extragranular compartment and suggest that the differentiated function of the sympathetic neuronal cell membrane, which plays an important role in uptake, is retained after prolonged tissue culture.


Studies of the biosynthesis, storage and secretion of catecholamines by the adrenal medulla have served as models for similar studies of the adrenergic neuron. For example, the synthesis of noradrenaline and the intracellular distribution of the biosynthetic enzymes was first described in the adrenal medulla and subsequently shown to be the same in sympathetic nerves (Blaschko 1939; Kirshner 1957, 1959; Levin, Levenberg & Kaufman i960; Potter & Axelrod 1963; Nagatsu, Levitt & Udenfriend 1964; Stjarne & Lishajko 1966; Oka et al. 1967; Musacchio 1968; Laduron & Belpaire 1968). The storage vesicles of the adrenal medulla have counterparts in the synaptic vesicles (Blaschko & Welch 1953; Hillarp, Lagerstedt & Nilson 1953; von Euler & Hillarp 1956; Schumann 1958) and the incorporation of catecholamines into the storage vesicles, and the storage complex itself, seems to be similar in both tissues, (Kirshner 1962; Carlsson, Hillarp & Waldeck 1963; von Euler & Lishajko 1963; von Euler, Lishajko & Stjarne 1963; Stjarne 1964). Recently it has been demonstrated that proteins specifically localized in the storage vesicles of the adrenal medulla are also present in the storage vesicles of sympathetic nerve endings (Hopwood 1967, 1968; Geffen, Livett & Rush 1969; Banks, Helle & Major 1969; de Potter, de Schaepdryver, Moerman & Smith 1969). There are obvious differences between the two types of vesicles (Stjarne 1964; Potter 1967), but the similarities are such as to suggest that the vesicles from both tissues serve the same physiological functions—to synthesize and store adrenaline or noradrenaline and to release these compounds in response to neural stimulation. Secretion from the adrenal medulla appears to be a good model for release of neurotransmitters at synapses in the sense that it provides and suggests experimental approaches to the problem (Geffen et al. 1969; de Potter et al. 1969). In general, the secretion of substances which are synthesized in cells and stored in subcellular organelles have many features in common (Douglas 1968; Stormorken 1969) and release of neurotransmitters at synapses may be another example of this generalized biological process. During the past few years, evidence has been presented from several laboratories that secretion from the adrenal medulla occurs by exocytosis. The simultaneous release of catecholamines, adenine nucleotides, chromogranins and soluble dopamine β-hydroxylase contained within the storage vesicles and the retention of dopamine-β- hydroxylase firmly bound to the vesicle membrane have provided critical information on this secretory process.


1990 ◽  
Vol 40 (2) ◽  
pp. 351-355 ◽  
Author(s):  
Martin Grønberg ◽  
Ole Terland ◽  
Eystein S. Husebye ◽  
Torgeir Flatmark

2004 ◽  
Vol 279 (49) ◽  
pp. 51107-51121 ◽  
Author(s):  
Nitish R. Mahapatra ◽  
Manjula Mahata ◽  
Partha P. Hazra ◽  
Patrick M. McDonough ◽  
Daniel T. O'Connor ◽  
...  

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