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Biomedical subjects

A Wernig

Publications and source records attributed to A Wernig.

At least 73 records · Page 4Linked to original sources

Light and electron microscopic identification of nerve terminal sprouting and retraction in normal adult frog muscle.

A combined light and electron microscopic study was performed on neuromuscular junctions of normal adult frogs. In a previous investigation signs of new synapse formation, as well as abandoned former synaptic sites, have been observed in normal muscles (Wernig, Pécot-Dechavassine & Stöver, 1980a, b). Here we performed a detailed light and electron microscopic correlation to investigate those parts of junctions which, after staining for cholinesterase (ChE) and presynaptic axon terminals, were suspected either to be newly formed or sites abandoned by the presynaptic nerve and the Schwann cell. Thin presynaptic nerve branches, enclosed by Schwann cell sheaths along most of their length, formed synaptic contacts with the muscle fibre only at small circumscribed areas. In these regions post-synaptic secondary folds (invariably present at mature synapses) were either missing or were less well developed. At these small contacts, binding sites for fluorescein-labelled alpha-bungarotoxin were usually present. At other sites the ChE reaction product was present but an axon could not be detected in silver-stained preparations. Electron microscopic observation revealed post-synaptic secondary folds filled with ChE reaction product while the presynaptic axon and Schwann cell were missing. The sites with ChE remnants can thus be regarded as abandoned former synaptic contacts. No binding of fluorescein-labelled alpha-bungarotoxin could be detected at such sites. These findings confirm earlier suggestions that synaptic contacts in frog muscle are normally undergoing continual remodelling. The lack of binding sites for fluorescein-labelled alpha-bungarotoxin at abandoned synaptic sites suggests that a neural or Schwann cell factor is important for the maintainance of synaptic acetylcholine receptors.

Animals↗

Different quantal responses within single frog neuromuscular junctions.

At frog neuromuscular junctions spontaneous miniature end-plate potentials (m.e.p.p.s) were recorded from several isolated spots within single synapses. This was done by consecutively placing an extracellular glass micro-electrode (focal electrode) at different recording sites, while the intracellular electrode remained in one place. After each set of recordings, muscles were stained to reveal both axon terminals and cholinesterase (ChE) such that the exact position of each recording site could be determined. In many nerve terminal branches a similar quantum size was found at several different spots. In other instances, however, mean quantum amplitudes varied by 10-60% at different spots along the same terminal branches. As a control, individual spots were recorded from repeatedly after repositioning the focal electrode. In these recordings mean m.e.p.p. amplitude varied by only 5-10%. It is concluded that quantum size within a single junction is similar at many spots, but deviates markedly at others. Correlation of this variation with the stained preparations suggested that spots where quanta significantly larger or smaller than normal were recorded were either at ChE rings or at the distal ends of nerve branches, respectively; at different nerve terminal branches within the same junction, quantum amplitudes were similar in many cases but deviated in others. The results are consistent with ultrastructural evidence that frog neuromuscular junctions are non-homogeneous structures which undergo continual remodelling.

Action Potentials↗

Abandoned synaptic sites in muscles of normal adult frog.

In previous investigations light microscopic cholinesterase (ChE) deposits without any nerve were found adjacent to normally occupied parts of a frog neuromuscular synapse [4, 9]. After identifying one such site at the light microscopic level ultrathin sections were cut and viewed with an electron microscope. ChE reaction product-filled secondary, clefts were observed in the region studied but a nerve was invariably missing. From this it is concluded that these loci are former synaptic sites from which nerve and Schwann cell have retracted, When incubating muscles with fluorescence-labelled alpha-bungarotoxin, all 23 abandoned sites found in 6 muscles remained bare of visible amounts of label. This indicate that receptor molecules eventually disappear from the synaptic membrane after retraction of the nerve and Schwann cell. No information as to the underlying time schedule of nerve retraction, turnover of ChE and alpha-bungarotoxin binding sites was obtained. Taken together with the evidence for synapse new formation in untreated frog muscles obtained previously [9, 11] the present observations indicate some ongoing remodeling of frog neuromuscular junction.

Animals↗

Light and electron microscopic identification of a nerve sprout in muscle of normal adult frog.

Recent evidence from this laboratory indicates that axonal sprouting (and regression) occurs in neuromuscular junctions of normal adult frogs. In the present investigation, the appearance of a single nerve branch, which from light microscopy was assumed to be a sprout, was studied in ultrathin serial sections. In confirming the light microscopic evidence small synaptic contacts were found, which showed characteristics of new synapse formation. Unexpectedly, the Schwann cell surrounding the axon extended several microns distally from the axon tip. It appears that nerve sprouting (and regression) is a physiological event in adult frog muscles.

Animals↗

Muscle cells in a nerve trunk of a frog muscle.

Three muscle fibers were identified by electron microscopy within a nerve of a frog muscle. They resembled extrafusal muscle fibers but were located in an endoneurial rather than in an endomysial compartment. To call these endoneurial muscle fibers the obvious continuation of extrafusal fibers of a muscle spindle is certainly unwarranted; to label these fibers ectopic and to let the matter rest there is probably an understatement of sorts.

Animals↗

Sprouting and regression of the nerve at the frog neuromuscular junction in normal conditions and after prolonged paralysis with curare.

A light microscopical, histochemical and electron microscopical investigation of the frog neuromuscular junction has been performed on muscles from animals in different functional states of activity. The combined staining of axon terminals and cholinesterase (ChE) allows a precise description of the nerve terminal arborization and its synaptic contacts. Most terminal arborizations form long continuous contacts with the muscle cell. Distinquishable from these are nerve branches (usually of small diameter)d or distal endings of branches with one or several small and isolated contacts. It is assumed that these are sprouts with newly-formed synaptic sites. Other sprouts end without apparent synaptic contact. At the uttrastructural levet, nerve sprouts end without apparent synaptic contact. At the uttrastructural levet, nerve sprouts growing into empty, well-differentiated synaptic gutters or inducing the formation of new synaptic sites were observed. In other sites, ChE is apparently located at postsynaptic gutters with no nerve present. Similarly, in the electron microscope, well-differentiated synaptic gutters lacking any nerve or Schwann cell elements were observed. In addition, synaptic gutters only partially occupied by the nerve were frequently seen. These features have been interpreted as signs of regression of the nerve terminals. Nerve regression and sprouting were found in animals chronically paralysed with curare over several weeks as well as in untreated frogs (winter and summer frogs, laboratory frogs, fed and unfed). When quantitatively evaluating the occurence of presumed features of nerve sprouting and nerve regression, differences were found between different experimental groups. From this it is concluded that, in addition to developmental changes, the degree of nerve sprouting and regression is controlled by external factors such as muscle activity and seasonal variations. Signs of sprouting and nerve regression can be simultaneously present in a single synapse. It appears that the frog neuromuscular synapse is not a static structure, but is in a state of permenent remodelling.

Acetylcholinesterase↗

A combined silver and cholinesterase method for studying exact relations between the pre- and the postsynaptic elements at the frog neuromuscular junction.

Combination of Karnovsky's cholinesterase staining with silver impregnation of axons (modified Bodian's technique) offers a new means of studying the relation between the pre- and postsynaptic elements in the frog neuromuscular junction. The method can be applied to whole muscles so that synapses of individual superficial muscle fibers which have previously been investigated by electrophysiological techniques can be identified after staining. In this way synaptic activity can be correlated with such synaptic features as number of axon branches, length of the occupied synaptic gutter, axonal sprouts, etc. The distinction between occupied and unoccupied parts of the synaptic gutters is useful when studying reinnervation, regression, or growth of a synapse.

Animals↗

The labelling of motor end-plates in skeletal muscle of mice with 125I tetanus toxin.

Twelve hours after injection of 125I labelled tetanus toxin into the shank of one hindlimb of mice radioactivity was found in the end-plate region of soleus muscles. The ratio between the radioactivity of the end-plate and the end-plate-free region was 2.5 +/- 0.4 S.D. Autoradiographs showed intense labelling of end-plates and a slight but clear labelling of axons. When 125I tetanus toxin was injected 3 days after denervation of the soleus muscle the former end-plate region still accumulated a higher radioactivity (ratio 2.0 +/- 0.5 S.D.), however, autoradiographs showed a diffuse distribution of labelled tetanus toxin. It can be concluded that tetanus toxin binds to the presynaptic nerve terminal. This binding is not dependent on activity of the nerve terminal or transmitter release.

Animals↗

Localization of active sites in the neuromuscular junction of the frog.

Spontaneous quantal discharges at the frog neuromuscular junction were simultaneously monitored with three glass microelectrodes. Two extracellular electrodes were located at the synaptic cleft a few microns apart from each other so that each quantal discharge occurring nearby evoked signals in both electrodes. From the observed ratios of the signal amplitudes it is inferred that quantal discharges exclusively occur at discrete sites. The distance between active sites is in the same range as that between "active zones" seen from electron micrographs.

Action Potentials↗

Estimates of statistical release parameters from crayfish and frog neuromuscular junctions.

1. Transmitter release at crayfish and frog neuromuscular junctions was studied by recording synaptic potentials with extracellular or intracellular glass micro-electrodes. 2. The binomial release parameters n and p were calculated using the experimental observations for the mean number of quanta (m) released in a series of trials, the variance (var) of the quantum content distribution and the number of transmission failures (n-o). 3. In one series of experiments on frog neuromuscular junction, action potentials were blocked by tetrodotoxin. Transmitter release was limited to a circumscribed part of the nerve terminal by focal stimulation with a glass micro-electrode. Values for m were between 0-6 and 5-7 and calculated values for n ranged from 3 to 23. p was between 0-05 and 0-48. In a second series of experiments on frog neuromuscular junction transmitter release was evoked by conventional stimulation of the nerve trunk in Mg-Ringer. m was mostly between 20 and 60 and in the same experiments n was calculated to be between 70 and 125. Values for p ranged from 0-25 to 0-48. 4. It can be concluded from the present results that transmitter release at frog neuromuscular junction is described by binomial statistics as is the case for neuromuscular junction of crayfish. 5. In comparing the values for n for the two series of experiments on frog neuromuscular junction it appears that n is dependent on the length of the activated synaptic contact. The numbers for n calculated from frog neuromuscular junction are of the same order of magnitude as the number of 'active zones' seen in the corresponding length of the synaptic nerve terminal.

Action Potentials↗

Changes in statistical parameters during facilitation at the crayfish neuromuscular junction.

1. Transmitter release at excitatory neuromuscular junctions of the crayfish was studied at different frequencies of stimulation ranging from 1/sec to 20/sec.2. Over this frequency range the average number of quanta released per stimulus (m) increased with frequency by a factor of 6-7.3. Analysis of the fluctuations in quantal release using binomial statistics indicated that the increase in m was associated with increase in the average quantal release probability (p) at stimulation frequencies between 5/sec and 20/sec. Between 1/sec and 5/sec there was an apparent increase in the number of quanta available for release (n).

Animals↗

The effects of calcium and magnesium on statistical release parameters at the crayfish neuromuscular junction.

1. Transmitter release at excitatory neuromuscular junctions of crayfish muscle was studied at low temperature by recording synaptic potentials with extracellular micro-electrodes.2. Increasing the Ca concentration in the bathing solution produced an increase in the average number of quanta released per nerve stimulus (m). Increasing the Mg concentration resulted in a decrease in m.3. Statistical analysis of fluctuations in the quantal release from trial to trial, assuming binomial statistics, indicated that both the changes in m were due to changes in the average quantal release probability (p).

Animals↗

The binomial nature of transmitter release at the crayfish neuromuscular junction.

1. Transmitter release at excitatory junctions on the opener muscle of the crayfish dactyl was studied by recording junctional potentials with extracellular micro-electrodes.2. At low temperatures, evoked release was dispersed sufficiently in time for potentials produced by individual quanta to be counted, and the mean (m) and variance (sigma(2)) of the quantum content distribution for a series of trials measured directly. These values were used to calculate the average probability of quantal release (p), assuming a binomial distribution.3. For all values of m and p, the observed release pattern (number of 0, 1, 2, 3,... quantal releases during a series of trials) was approximated closely by the corresponding binomial distribution. However, Poisson predictions differed significantly from the observed quantal distribution for values of p > 0.2.

Animals↗