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A A Herrera

Publications and source records attributed to A A Herrera.

At least 19 recordsLinked to original sources
PubMed2003

Structural alterations at the neuromuscular junctions of matrix metalloproteinase 3 null mutant mice.

Matrix metalloproteinases are important regulators of extracellular matrix molecules and cell-cell signaling. Antibodies to matrix metalloproteinase 3 (MMP3) recognize molecules at the frog neuromuscular junction, and MMP3 can remove agrin from synaptic basal lamina (VanSaun & Werle, 2000). To gain insight into the possible roles of MMP3 at the neuromuscular junction, detailed observations were made on the structure and function of the neuromuscular junctions in MMP3 null mutant mice. Striking differences were found in the appearance of the postsynaptic apparatus of MMP3 null mutant mice. Endplates had an increased volume of AChR stained regions within the endplate structure, leaving only small regions devoid of AChRs. Individual postsynaptic gutters were wider, containing prominent lines that represent the AChRs concentrated at the tops of the junctional folds. Electron microscopy revealed a dramatic increase in the number and size of the junctional folds, in addition to ectopically located junctional folds. Electrophysiological recordings revealed no change in quantal content or MEPP frequency, but there was an increase in MEPP rise time in a subset of endplates. No differences were observed in the rate or extent of developmental synapse elimination. In vitro cleavage experiments revealed that MMP3 directly cleaves agrin. Increased agrin immunofluorescence was observed at the neuromuscular junctions of MMP3 null mutant mice. These results provide strong evidence that MMP3 is involved in the control of synaptic structure at the neuromuscular junction and they support the hypothesis that MMP3 is involved in the regulation of agrin at the neuromuscular junction.

Agrin↗
PubMed2000

The role of perisynaptic Schwann cells in development of neuromuscular junctions in the frog (Xenopus laevis).

Fluorescence microscopy was used to study the behavior of perisynaptic Schwann cells (PSCs) in relation to motor nerve terminals and postsynaptic clusters of acetylcholine receptors, during the development of the neuromuscular junction (NMJ) in the frog Xenopus laevis. Pectoral (supracoracoideus) muscles were labeled with monoclonal antibody 2A12 for Schwann cells, the dye FM4-64 for nerve terminals (NTs), alpha-bungarotoxin for acetylcholine receptors (AChRs), and Hoechst 33258 for cellular nuclei, in animals from tadpole stage 57 to fully grown adults. When muscle fibers first appeared in stage 57, NMJs consisted of tightly apposed NTs and AChRs and were only partially covered with PSCs or their processes. Within a few stages, PSCs fully occupied and overgrew the NMJs, extending fine sprouts between a few micrometers and hundreds of micrometers beyond the borders of the junction. Sprouts of PSCs were most abundant during the time when secondary myogenesis, synaptogenesis, and synaptic growth occurred at their highest rates. PSCs were recruited to NMJs during synaptic growth, at rates between 1.3 PSCs/100 microm junctional length early on and 0.4 PSCs/100 microm later. Shortly after metamorphosis, PSC sprouts disappeared and NMJs acquired the adult appearance, in which PSCs, NTs, and AChRs were mostly congruent. The results suggest that, although PSCs may not be required for initial nerve-muscle contacts, PSCs sprouts lead synaptic growth and play a role in the extension and maturation of developing NMJs.

Age Factors↗
PubMed1996

Precision of reinnervation and synaptic remodeling observed in neuromuscular junctions of living frogs.

Repeated in vivo observations were used to study regenerated nerve terminals in neuromuscular junctions of the adult frog Rana pipiens. Sartorius junctions in living animals were stained with the fluorescent vital dye RH414 and viewed with video fluorescence microscopy. Each junction was observed in the intact muscle and then again 7, 10, and 13 weeks after nerve crush. At 13 weeks, junctions were determined to be mono- or polyneuronally innervated using intracellular recording. Between 7 and 13 weeks, most identified junctions were reinnervated less precisely and completely than described previously. Although some of the original synaptic gutters were reoccupied by regenerated terminal branches, other gutters were only partially occupied, and many appeared abandoned. Junctions showing precise recapitulation of original terminal arborizations comprised a small number of the total examined, as did those where reinnervation was very imprecise. Striking differences in the precision of reinnervation were found within the muscle such that distal terminals regenerated more precisely and completely than did proximal terminals. Terminals in reinnervated muscles were more dynamic than terminals in unoperated muscles over equivalent times. In singly innervated junctions, terminal growth was favored over regression. In doubly innervated junctions, regressive events were more common. Imprecise reinnervation is explained in terms of multisite innervation of muscle fibers and the activity dependence of synaptic stability. We hypothesize that when axons reinnervate the second or third junctions on a fiber, they do so less precisely, because the activity restored by reinnervation of the first junction renders later sites less attractive or less stable.

Animals↗
PubMed1995

Effects of testosterone on synaptic efficacy at neuromuscular junctions in a sexually dimorphic muscle of male frogs.

1. The effects of testosterone on synaptic efficacy were studied in the flexor carpi radialis, a sexually dimorphic forelimb muscle involved in frog clasping behaviour. Male Xenopus laevis frogs were castrated and then given either testosterone-filled implants (CT frogs) or empty implants (C frogs) for 2, 8 or 16 weeks. 2. Intracellular recordings were made from fibres in the shoulder region and in a region midway between the elbow and wrist. These regions are mainly innervated by spinal nerve 2 (SN2) and spinal nerve 3 (SN3), respectively. 3. In CT muscles, the percentage of fibres that failed to generate an action potential in response to a single nerve stimulus was greater than in C muscles. The percentage of such fibres was greater among SN2 fibres than among SN3 fibres. 4. The input resistance and membrane time constant were lower in CT muscles than in C muscles for SN2 fibres but not for SN3 fibres. The action potential threshold was lower in CT muscles than in C muscles. In SN2 fibres, the action potential threshold was higher than in SN3 fibres. 5. Quantal content with 1 Hz nerve stimulation and miniature endplate potential (MEPP) frequency did not differ between CT and C junctions. However, both parameters were lower at SN2 junctions than at SN3 junctions. The amplitude of MEPPs was lower in CT muscles than in C muscles only for SN2 junctions. 6. Facilitation of transmitter release with 70 or 10 Hz nerve stimulation was greater at CT junctions than at C junctions. Also, SN2 junctions showed greater facilitation than SN3 junctions. 7. We hypothesize that the more androgen-sensitive SN2 junctions, which have lower quantal content and greater facilitation, belong to motor units that are tonically active, fatigue resistant, and contract more slowly. The less androgen-sensitive SN3 junctions, which have higher quantal content and less facilitation, may belong to motor units that are phasically active, fatigable and contract more rapidly. Testosterone enhances these differences such that flexor carpi radialis junctions are better adapted to the functional demands of clasping.

Action Potentials↗
PubMed1994

Effects of testosterone on a sexually dimorphic frog muscle: repeated in vivo observations and androgen receptor distribution.

In the present study the sexually dimorphic, androgen-sensitive flexor carpi radialis muscle (FCR) in male Xenopus laevis was viewed repeatedly in vivo to assess the influence of testosterone on muscle fiber size over a period of up to 12 weeks. Regions of the muscle innervated by different spinal nerves responded differently to testosterone treatment. Muscle fibers innervated by spinal nerve 2 (SN2) hypertrophied within 7 days in frogs that had been castrated and given testosterone-filled implants. This initial hypertrophy was followed by a return to normal fiber size a week later, after which fiber size slowly increased again. In castrated males with empty implants, muscle fibers innervated by SN2 gradually atrophied. Fibers innervated by spinal nerve 3 (SN3) were not affected by androgen replacement or withdrawal. The sartorius, a control muscle that is neither sexually dimorphic nor particularly androgen sensitive, was also unaffected. The in vivo observations were confirmed by measurements of muscle fiber cross-sectional areas in frozen sections of whole forelimbs. At 8 and 12 weeks after castration, cross-sectional areas of fibers innervated by SN2 were significantly larger in frogs provided with testosterone than in castrates without testosterone. No difference was found in the SN3 region or in the anconeus caput scapulare (triceps), another control muscle. Immunocytochemistry employing an antibody against the androgen receptor (AR) indicated that the receptor is present in myonuclei of all muscles of the forelimb. While no difference in labeling intensity was detected, the number of AR-containing nuclei per muscle fiber cross-section was higher in fibers innervated by SN2 than in those innervated by SN3, and was yet lower in the triceps. This suggests that regulation of androgen sensitivity may occur via muscle fiber ARs, although an influence of the nerve may also contribute.

Animals↗
PubMed1993

Differential sensitivity to androgens within a sexually dimorphic muscle of male frogs (Xenopus laevis).

Male frogs use their forelimb flexor muscles to clasp females during the mating behavior known as amplexus. We investigated the effects of testosterone on a principal forelimb flexor, the flexor carpi radialis muscle (FCR), using morphological and histochemical techniques. Male Xenopus laevis were surgically manipulated to produce high or low levels of circulating testosterone for an 8-week period. After this treatment, measurement of fibers in muscle cross-sections revealed that average fiber size was positively correlated with testosterone level. This effect was not the same for all muscle fibers, however. Fibers in the shoulder region were more sensitive to testosterone than fibers in other regions of the muscle. Histochemical staining of cross-sections showed that the patterns of staining for myosin ATPase or succinic dehydrogenase (SDH) were not influenced by testosterone levels, but total SDH activity was increased by testosterone treatment. When sensitivity to testosterone was correlated with ATPase activity, fibers with high ATPase activity were found to be more sensitive to testosterone than fibers with low activity, regardless of position within the muscle. Most fibers with high ATPase activity were located in the shoulder region of the muscle. These fibers are innervated by different motor axons than are fibers in the elbow region of the muscle, and contractions of shoulder (but not elbow) region fibers, elicited by stimulation of motor axons, are slowed by testosterone treatment (Regnier and Herrera, 1993, J. Physiol. 461:565-581).

Animals↗
PubMed1993

Changes in contractile properties by androgen hormones in sexually dimorphic muscles of male frogs (Xenopus laevis).

1. Male frogs (Xenopus laevis) were castrated then given either empty or testosterone-filled implants to produce animals with low or high levels of circulating testosterone. Eight weeks later the contractile properties of an androgen-sensitive forelimb flexor, the flexor carpi radialis muscle (FCR), were measured in vitro. Another forelimb flexor muscle, the coracoradialis, and a hindlimb muscle, the iliofibularis, were analysed similarly. 2. Plasma testosterone levels were 0.9 +/- 0.3 ng/ml (+/- S.E.M.) in castrated frogs with blank implants (C) and 61.3 +/- 4.7 ng/ml in castrates with testosterone implants (CT). Unoperated males, sampled at various times of the year, ranged between 10.8 and 51.0 ng/ml. 3. With direct electrical stimulation of the FCR, contraction time of the isometric twitch was not affected by testosterone levels. Relaxation times were affected, however. Half- and 90% relaxation times were 27 and 42% longer, respectively, for CT compared to C muscles. 4. Testosterone also had no effect on the contraction time of twitches elicited by stimulation of the FCR nerve. Half- and 90% relaxation times were 51 and 76% longer, respectively, for CT compared to C muscles. 5. Tetanus tension, elicited by direct stimulation of the FCR at 50 Hz, was 86% greater in CT compared to C muscles. The average cross-sectional area of FCR muscle fibres was 84% greater in CT muscles. These results implied that testosterone treatment had no effect on specific muscle tension. 6. Stimulation of the FCR nerve at 50 Hz resulted in 53% less tension than the same stimulus applied directly to CT muscles. In C muscles the difference was only 14%. This suggested that testosterone treatment reduced synaptic efficacy. 7. In CT muscles, direct or nerve stimulation of fibres in the shoulder region of the FCR elicited twitches that contracted and relaxed more slowly than fibres in the elbow region. In C muscles there was no difference in contraction or relaxation time between fibres in the shoulder and elbow regions. 8. Testosterone treatment had little effect on contraction and relaxation times or tension levels of coracoradialis or iliofibularis muscles.

Animals↗
PubMed1993

Synapse formation and elimination during growth of the pectoral muscle in Xenopus laevis.

1. Synapse formation and synapse elimination were studied in the pectoral muscle of Xenopus laevis. 2. Histology showed that fibres were not added during postmetamorphic growth. Most fibres were innervated at two widely separated junctions and this number did not change as frogs grew. 3. Intracellular recording revealed that fibres with two junctions could be mononeuronally innervated, or innervated in one of three different polyneuronal patterns. A growth-related shift in innervation pattern was observed, with the polyneuronal patterns replaced by mononeuronal innervation. 4. Endplate potentials (EPPs) evoked by low-frequency nerve stimulation were simultaneously measured at both junctions on individual fibres. For each fibre, the ratio of EPP amplitudes (smaller/larger) was calculated. When the two junctions were innervated by different motoneurones (A-B), the median EPP ratio was smaller than when the two junctions were innervated by the same motoneurone (A-A), although the difference was not significant. 5. The difference in the ratio of EPP amplitudes became significant, however, if junctions were conditioned by a train of fifty stimuli at 10 Hz. Immediately after such a train, EPP ratios for A-B fibres were significantly smaller than ratios for A-A fibres. This difference was due to greater synaptic depression at one of the junctions on A-B fibres. 6. We concluded that enhanced depression of the EPP upon repetitive stimulation is a physiological correlate of the competition that underlies synapse elimination.

Animals↗
PubMed1991

Postmetamorphic development of neuromuscular junctions and muscle fibers in the frog cutaneous pectoris.

Synaptic size, synaptic remodelling, polyneuronal innervation, and synaptic efficacy of neuromuscular junctions were studied as a function of growth in cutaneous pectoris muscles of postmetamorphic Rana pipiens. Recently metamorphosed frogs grew rapidly, and this growth was accompanied by hypertrophy of muscle fibers, myogenesis, and increases in the size and complexity of neuromuscular junctions. There were pronounced gradients in pre- and postsynaptic size across the width of the muscle, with neuromuscular junctions and muscle fibers near the medial edge being smaller than in more lateral regions. The incidence of polyneuronal innervation, measured physiologically and histologically, was also higher near the medial edge. Growth-associated declines in all measures of polyneuronal innervation indicated that synapse elimination occurs throughout life. Electrophysiology also demonstrated regional differences in synaptic efficacy and showed that doubly innervated junctions have lower synaptic efficacy than singly innervated junctions. Repeated, in vivo observations revealed extensive growth and remodelling of motor nerve terminals and confirmed that synapse elimination is a slow process. It was concluded that some processes normally associated with embryonic development persist long into adulthood in frog muscles.

Animals↗
PubMed1991

Elevated levels of polyneuronal innervation persist for as long as two years in reinnervated frog neuromuscular junctions.

When the nerve to an adult frog sartorius muscle is crushed, and axons are allowed to regenerate, the level of polyneuronal innervation at reinnervated neuromuscular junctions is higher than normal. With time, much of this polyneuronal innervation is reduced by the process of synapse elimination (Werle and Herrera, 1988). Using intracellular recording, we estimated the level of polyneuronal innervation in adult frog (Rana pipiens) sartorius muscles 2 years (range: 1.7-2.4 years) after crushing the sartorius nerve. We found that 27% (S.E. = 1.4%) of the junctions in muscles 2 years after reinnervation were polyneuronally innervated, whereas only 10% (S.E. = 1.2%) of the junctions in normal frog muscles were polyneuronally innervated. Thus, the synapse elimination that occurs following reinnervation does not restore the normal level of polyneuronal innervation. Histological comparisons of junctional structure between muscles 2 years after reinnervation and normal muscles revealed substantial differences. Reinnervated junctions had a greater length of synaptic gutter apposed by nerve terminal processes, more axonal inputs, more empty synaptic gutter, more instances of single synaptic gutters innervated by more than one axon, and longer lengths of nerve terminal processes that connect synaptic gutters within a junction. On the basis of this physiological and anatomical evidence, we conclude that nerve injury causes persistent changes in the pattern of muscle innervation.

Animals↗
PubMed1990

Mechanisms of elimination, remodeling, and competition at frog neuromuscular junctions.

Mechanisms governing synapse elimination, synaptic remodeling, and polyneuronal innervation were examined in anatomical and electrophysiological studies of frog neuromuscular junctions. There was a substantial level of polyneuronal innervation in adult junctions and this varied seasonally. Nerve terminal retraction and synapse elimination occurred during normal growth and following reinnervation. Synapse elimination was not inevitable, however. Repeated in vivo observations of some identified junctions showed that polyneuronal innervation could persist for over a year, while at other junctions it arose de novo by terminal sprouting. We concluded that polyneuronal innervation in adult muscles was governed by an equilibrium between processes of retraction and elimination on one hand, and sprouting and synaptogenesis on the other. Other observations revealed that structural remodeling was a common feature of adult junctions. Most often, remodeling involved the simultaneous growth and retraction of different parts of the same junction. The net result was usually junctional growth that, in small frogs, appeared to provide a good match between synaptic size and the electrical demands of transmission. In larger animals, pre- and postsynaptic sizes were not as well matched, providing morphological evidence for a growth-associated decline in synaptic efficacy. Finally, electrophysiology was used to describe some of the functional correlates and consequences of competitive interactions between the terminals of different axons. These results are explained by a hypothetical mechanism that involves trophic support provided by the muscle to the motoneuron, the overall level of nerve-muscle activity, and the synchrony of pre- and postsynaptic activity.

Animals↗
PubMed1990

The use and effects of vital fluorescent dyes: observation of motor nerve terminals and satellite cells in living frog muscles.

Several different fluorescent mitochondrial dyes were tested as vital stains for motor nerve terminals and other cells in frog skeletal muscles. It was found that 3,3' diethyloxadicarbocyanine iodide and 4-(4-diethylaminostyryl)-N-methylpyridinium iodide were most useful. Both dyes labelled motor nerve terminals with high reliability. Electrophysiological and morphological control experiments showed that these dyes could be used to repeatedly observe neuromuscular junctions in living animals without affecting synaptic growth or remodelling. The importance of appropriate controls was emphasized by the finding that illumination, if excessively intense or prolonged, can cause physiological and structural damage to nerve terminals. Additional observations indicated that these dyes may be useful for determining the mitochondrial content, and therefore oxidative capacity, of living muscle fibres. It was also found that the fluorescent dyes labelled cells identified as muscle satellite cells, and that these myoblast precursors could be visualized in fixed whole mounts with a nitroblue tetrazolium stain. Both methods were used to study reactive cells that were closely associated with muscle fibres in lesioned muscles. Mitochondrial dyes also labelled the microvasculature, associated axons and other cells.

Animals↗
PubMed1990

Repeated, in vivo observation of frog neuromuscular junctions: remodelling involves concurrent growth and retraction.

The fluorescent dye 4-(4-diethylaminostyryl)-N-methylpyridinium iodide was used as a vital stain to study remodelling of motor nerve terminals in sartorius muscles of living frogs (Rana pipiens). Identified terminals were observed twice in vivo at intervals of 87-192 days. After the second observation, muscles were fixed and stained with the nitroblue tetrazolium method for nerve terminals and with cholinesterase stain. Observations were made of 243 junctions in 26 frogs. Most nerve terminals grew during the observation interval, with an average increase in total terminal length of 29%. This growth involved substantial remodelling. Within single junctions, the change in size was the net result of differing degrees of growth or shrinkage in individual nerve terminal branches. At least one new terminal branch appeared in 25% of the junctions. Terminal retraction was also common, with branch shortening seen in 60% of junctions and the complete disappearance of a branch in 12%. In one case the original axonal input retracted completely and the junction was partially reinnervated by a terminal sprout from a junction on an adjacent fibre. Some discrepancies between histological and in vivo observations of remodelling were noted. These observations confirm that frog neuromuscular junctions are highly dynamic synapses, subject to profound structural remodelling throughout adult life.

Animals↗
PubMed1988

Synaptic competition and the elimination of polyneuronal innervation following reinnervation of adult frog sartorius muscles.

The elimination of polyneuronal innervation (synapse elimination) that occurs following reinnervation was studied in sartorius muscles of adult Rana pipiens. The percentage of neuromuscular junctions that were polyneuronally innervated declined from 47% at 40-80 days after nerve crush to 22% at greater than 250 days after nerve crush. We measured the size, synaptic strength, and position of competing nerve terminals at identified dually innervated neuromuscular junctions at these two different periods of synapse elimination. Our goal was to determine if any of these parameters play a role in the competition between nerve terminals that ultimately results in the elimination of polyneuronal innervation. Our data support the hypothesis that polyneuronal innervation will persist if competing nerve terminals are of similar synaptic efficacies but will be eliminated if the competing terminals are of different synaptic efficacies. We also tested, but failed to find any evidence, that the spatial proximity of competing nerve terminals at the same synaptic site influences the elimination of polyneuronal innervation.

Action Potentials↗
PubMed1987

Synaptic competition and the persistence of polyneuronal innervation at frog neuromuscular junctions.

Mechanisms governing the elimination of polyneuronal innervation were examined by correlating the morphology and physiology of competing nerve terminals at identified dually innervated neuromuscular junctions in sartorius muscles of adult frogs (Rana pipiens). Synaptic efficacy (endplate potential amplitude per unit nerve terminal length) was presumed to reflect the ability of a terminal to compete for synaptic space. The synaptic efficacies of two terminals at the same synaptic site were found to be surprisingly equal, with a median difference of 33%. Much more variation would be expected if dually innervated junctions were randomly innervated by pairs of terminals having the same range of synaptic efficacy as that found at singly innervated junctions in the same muscle. This finding supports the hypothesis that the weaker input is eliminated from dually innervated junctions when there is a large discrepancy in competitive efficacy, and that both inputs may persist if competitive efficacies are relatively equal. We also tested but failed to find support for the hypothesis that spatial proximity between competing terminals intensifies competition for synaptic space during synapse elimination.

Animals↗
PubMed1986

A comparison of active zone structure in frog neuromuscular junctions from two fast muscles with different synaptic efficacy.

To search for ultrastructural correlates of differences in synaptic safety factor and neurotransmitter release, neuromuscular junctions from the cutaneous pectoris and cutaneous dorsi muscles of the grass frog Rana pipiens were freeze fractured. Synaptic efficacy in these muscles was determined by the extent to which isometric twitch tension could be blocked by lowering [Ca2+] in the bathing solution. We found that junctions in the cutaneous pectoris were significantly more effective than those of the cutaneous dorsi. Morphometric analysis of 16 junctions from each type of muscle showed significant differences in some aspects of active zone structure. Cutaneous pectoris terminals had longer active zone segments and active zones spaced more closely together. This resulted in 20% more active zone length per unit terminal length in the cutaneous pectoris. Cutaneous dorsi terminals had active zones that were more often segmented into two or more sections at a single junctional fold. Mean active zone length per junctional fold and the number of active zone particles per micrometre of active zone length were not significantly different. As a result of the somewhat larger terminal width in the cutaneous dorsi, the percentage of terminal width occupied by active zone was greater in the cutaneous pectoris. As an attempt to indirectly estimate active zone spacing with the light microscope, we applied rhodamine-conjugated alpha bungarotoxin to neuromuscular junctions from the cutaneous pectoris and cutaneous dorsi. No significant difference in the spacing of fluorescently labelled acetylcholine receptor bands was found between the two types of junctions. Our results indicated that the greater active zone length per unit terminal length in the cutaneous pectoris was associated with its increased synaptic efficacy. In addition the continuity and particle organization of active zones may have contributed to the observed differences in synaptic safety factor at frog neuromuscular junctions.

Animals↗
PubMed1986

Differences in synaptic efficacy at neuromuscular junctions in frog twitch muscles.

A comparison was made of neuromuscular junctions in cutaneous pectoris and cutaneous dorsi muscles of Rana pipiens in order to study mechanisms controlling synaptic efficacy. Other than a small difference in junctional size, the two muscles were structurally and functionally very similar. Despite these similarities, cutaneous pectoris junctions had substantially higher synaptic safety margins. With intracellular recording, it was apparent that the difference in safety margin was due to a large difference in transmitter release. In low-Ca2+ solutions, levels of evoked and spontaneous release were 4 times higher in the cutaneous pectoris. When corrected for differences in nerve terminal size at identified junctions, there remained a 3-fold difference in evoked release and a 6-fold difference in spontaneous release per unit terminal length. Differences in normal Ringer solution were 1.8- and 2.5-fold for evoked and spontaneous release, respectively. There was no simple relationship between synaptic efficacy and the total amount of nerve terminal supported by each motoneurone in different frog muscles. We concluded that there can be large differences in synaptic efficacy without correlated structural differences visible with the light microscope.

Animals↗