RESUMO
The growth cones of dissociated rat sympathetic neurons developing in culture were fixed with potassium permanganate to visualize vesicular stores of norepinephrine through the formation of granular precipitates. It was found that growth cones contain numerous small granular vesicles (SGV) 40-60 nm in diameter. The majority of the SGV was present in the varicosity of the growth cone but SGV also occurred in filopodia. The SGV appeared in clusters or scattered throughout the varicosity. Treatment of the cultured neurons, before fixation, with reserpine, which depletes catecholamine stores by blocking uptake into vesicles, resulted in the presence of small clear vesicles. In contrast, growth cones of nonadrenergic sensory neurons dissociated from dorsal root ganglia and fixed with permanganate lacked SGV and possessed small clear vesicles. These observations indicate that the growth cones of cultured sympathetic neurons contain norepinephrine, suggest that the norepinephrine is stored in synaptic vesicles, and raise the question whether this transmitter plays a role in early axon-target cell interactions during synapse formation.
Assuntos
Neurônios/ultraestrutura , Norepinefrina , Sistema Nervoso Simpático/citologia , Divisão Celular , Células Cultivadas , Grânulos Citoplasmáticos/análise , Pseudópodes/ultraestrutura , Reserpina/farmacologiaRESUMO
The maturation of cerebellar Purkinje cells of normal and nervous (nr/nr) mutant mice has been studied by light and electron microscopy. In the mutant, 90% of Purkinje cells selectively degenerate between postnatal days 23 and 50. Losses are greater in lateral than medial regions. Other cerebellar neurons appear normal. The first morphological abnormality recognized is the presence of rounded mitochondria in perikarya of some Purkinje cells of the mutant at 9 days after birth. By 15 days, all nr/nr Purkinje cells contain spherical mitochondria and begin to deviate from the normal maturational sequence. Elaboration of the extensive dendritic tree halts midway and newly formed axon collateral fibers degenerate. In the perikaryon, the basal polysomal accumulation and climbing fiber-somatic spine synapses are sometimes abnormally retained. Cisternae of the Golgi apparatus and rough endoplasmic reticulum cease to form aligned stacks, and decrease in number, while polysomes dissociate into free ribosomes. These changes are progressive, culminating in cell death. Although every nr/nr Purkinje cell demonstrates spherical mitochondria, some cells survive the critical period, retain a near-normal complement of organelles, and reacquire normal-appearing mitochondria. The disorder appears intrinsic to Purkinje cells since all major classes of synapses were identified before cell death.
Assuntos
Cerebelo/citologia , Mitocôndrias , Células de Purkinje/citologia , Animais , Axônios/citologia , Dendritos/citologia , Retículo Endoplasmático , Feminino , Complexo de Golgi , Masculino , Camundongos , Camundongos Endogâmicos BALB C , Microscopia Eletrônica , Mutação , Neurônios/citologia , Polirribossomos , Ribossomos , Sinapses/citologia , Fatores de TempoRESUMO
WI-38 and HeLa cells in mitosis have been selected from fixed monolayer cultures and serially sectioned for electron microscopy. Sections perpendicular to the spindle axis permit counting of the number of microtubules at each position on the spindle axis and hence the preparation of tubule distribution profiles. Errors intrinsic to this method are discussed. The changes in the tubule distributions from one mitotic stage to another provide evidence concerning the behavior of the spindle tubules during mitosis. The ratio of the number of tubules passing the chromosomes on the metaphase plate to the maximum number in each half spindle is about 1/2. This ratio changes little in early anaphase, and then decreases in late anaphase at about the same time that a zone of increased tubule number develops at the middle of the interzone. The region where the stem bodies form contains about 3/2 the number of tubules seen elsewhere in the interzone. This ratio is almost constant as the mid-body forms in telophase and then increases to 2/1 in early interphase before the final stages of cytokinesis occur.
RESUMO
The axostyle of the flagellate Saccinobaculus is a motile ribbon composed of microtubules, cross-bridged to form interconnected rows. We find a centriole-related row of dark-staining tubules near the nucleus at the anterior end of the axostyle. Other tubule rows bind parallel to this primary row, acquire ordered relationships, and become the tubules of the axostyle proper. The number of tubule rows is constant in Saccinobaculus lata from the region near the nucleus to within a few micrometers of the posterior tip of the cell. In Saccinobaculus ambloaxostylus a few tubule rows are added to the axostyle posterior to the nucleus, giving this axostyle a leaf spring construction. The tubules of S. lata are held in rows by links with a 140 A periodicity along the tubule axis; bridges between rows of tubules are also seen but are not apparently periodic. Each tubule in S. ambloaxostylus shows an axial periodicity of 150 A due to pairs of arms, one of which is always part of the intrarow link. Interrow bridges in this species run either from tubule to tubule or from tubule to the free arm, but as in S. lata they do not display an obvious axial periodicity. An average unit cell is presented for the axostyle of each species, and the relation of the intertubule links to the microtubule substructure is discussed.
Assuntos
Eucariotos/citologia , Microtúbulos , Organoides , Animais , Membrana Celular , Movimento Celular , Nucléolo Celular , Núcleo Celular , Grânulos Citoplasmáticos , Flagelos , Microscopia Eletrônica , Modelos Biológicos , Modelos EstruturaisRESUMO
When the sympathetic nerves that innervate rat sweat glands reach their targets, they are induced to switch from using norepinephrine as their neurotransmitter to acetylcholine. Catecholamines (such as norepinephrine) released by nerves growing to the sweat gland induce this phenotypic conversion by stimulating production of a cholinergic differentiation factor [sweat gland factor (SGF)] by gland cells. Here, culture of gland cells with sympathetic, but not sensory, neurons induced SGF production. Blockage of alpha 1- or beta-adrenergic receptors prevented acquisition of the cholinergic phenotype in sympathetic neurons co-cultured with sweat glands, and sweat glands from sympathectomized animals lacked SGF. Thus, reciprocal instructive interactions, mediated in part by small molecule neurotransmitters, direct the development of this synapse.
Assuntos
Glicoproteínas/biossíntese , Sistema Nervoso Parassimpático/fisiologia , Receptores Adrenérgicos/fisiologia , Glândulas Sudoríparas/inervação , Sistema Nervoso Simpático/fisiologia , Animais , Animais Recém-Nascidos , Sequência de Bases , Diferenciação Celular , Células Cultivadas , Meios de Cultivo Condicionados , Dados de Sequência Molecular , Neurregulinas , Neurônios/citologia , Neurônios/fisiologia , Neurônios Aferentes/citologia , Neurônios Aferentes/fisiologia , Sistema Nervoso Parassimpático/citologia , Fenótipo , Ratos , Glândulas Sudoríparas/citologia , Glândulas Sudoríparas/metabolismo , Simpatectomia , Sistema Nervoso Simpático/citologiaRESUMO
The sweat glands, a target of cholinergic sympathetic neurons, were replaced with parotid gland, a target of noradrenergic sympathetic neurons, in neonatal rats. This transplantation paradigm allowed sympathetic neurons that would normally innervate the sweat glands and develop a cholinergic phenotype to innervate the parotid gland instead. The innervation of the transplanted parotid gland did not develop a cholinergic phenotype, as assessed by choline acetyltransferase activity and acetylcholinesterase immunoreactivity, but continued to express intense catecholamine fluorescence. In addition, immunoreactivity for vasoactive intestinal peptide, normally expressed by the sympathetic innervation of the sweat glands but not the parotid, was observed in only a small percentage of the parotid-associated fibers. These results suggest that cellular interactions between neurons and their targets play an important role in the differentiation of mature neurotransmitter and neuropeptide phenotypes in vivo.
Assuntos
Sistema Nervoso Parassimpático/fisiologia , Peptídeos/fisiologia , Glândulas Sudoríparas/inervação , Sistema Nervoso Simpático/fisiologia , Animais , Catecolaminas/metabolismo , Fluorescência , Sistema Nervoso/metabolismo , Neuropeptídeos/metabolismo , Glândula Parótida/inervação , Glândula Parótida/transplante , Ratos , Ratos Endogâmicos LewRESUMO
The sympathetic innervation of rat sweat glands undergoes a target-induced switch from a noradrenergic to a cholinergic and peptidergic phenotype during development. Treatment of cultured sympathetic neurons with sweat gland extracts mimics many of the changes seen in vivo. Extracts induce choline acetyltransferase activity and vasoactive intestinal peptide expression in the neurons in a dose-dependent fashion while reducing catecholaminergic properties and neuropeptide Y. The cholinergic differentiation activity appears in developing glands of postnatal day 5 rats and is maintained in adult glands. It is a heat-labile, trypsin-sensitive, acidic protein that does not bind to heparin-agarose. Immunoprecipitation experiments with an antiserum directed against an N-terminal peptide of a cholinergic differentiation factor (CDF/LIF) from heart cells suggest that the sweat gland differentiation factor is not CDF/LIF. The sweat gland activity is a likely candidate for mediating the target-directed change in sympathetic neurotransmitter function observed in vivo.
Assuntos
Colina/fisiologia , Inibidores do Crescimento , Interleucina-6 , Neurônios/metabolismo , Glândulas Sudoríparas/inervação , Envelhecimento/fisiologia , Animais , Diferenciação Celular , Células Cultivadas , Colina O-Acetiltransferase/biossíntese , Glicoproteínas/análise , Glicoproteínas/fisiologia , Immunoblotting , Técnicas de Imunoadsorção , Fator Inibidor de Leucemia , Linfocinas/análise , Linfocinas/fisiologia , Miocárdio/química , Neurregulinas , Neurônios/citologia , Neuropeptídeo Y/metabolismo , Norepinefrina/fisiologia , Ratos , Glândulas Sudoríparas/crescimento & desenvolvimento , Glândulas Sudoríparas/fisiologia , Extratos de Tecidos/farmacologia , Tirosina 3-Mono-Oxigenase/metabolismo , Peptídeo Intestinal Vasoativo/metabolismoRESUMO
To determine whether postmigratory neural crest cells retain the capacity to give rise to multiple cell types, the clonal progeny of embryonic rat superior cervical ganglion (SCG) cells were examined in culture. Double labeling with BrdU and neurofilament antibodies demonstrated that neuron precursors from the E14.5 SCG continued to proliferate for several days in culture. Using the BAG retrovirus to examine the progeny of single cells, we obtained several kinds of distinct clones from SCG cultures after 3 days. At E14.5, during peak neurogenesis in vivo, neuron-containing clones composed of one to seven cells were common. At E17.5, after neurons have been born in vivo, most clones in vitro contained flat cells, primarily reflecting glial cell division. Even in cultures from E13.5 ganglia, mixed clones containing neurons and flat cells were rarely observed. These observations suggest that neuronal and nonneuronal cell precursors are specified during or before early gangliogenesis.
Assuntos
Diferenciação Celular , Gânglios Simpáticos/embriologia , Crista Neural/embriologia , Animais , Divisão Celular , Transformação Celular Viral , Células Cultivadas , Células Clonais , Gânglios Simpáticos/citologia , Técnicas In Vitro , Fatores de Crescimento Neural , Crista Neural/citologia , Neurônios/citologia , Neurônios/fisiologia , Ratos , Retroviridae , Células-Tronco/citologiaRESUMO
Leukemia inhibitory factor (LIF; also known as cholinergic differentiation factor) is a multifunctional cytokine that affects neurons, as well as many other cell types. To examine its neuronal functions in vivo, we have used LIF-deficient mice. In culture, LIF alters the transmitter phenotype of sympathetic neurons, inducing cholinergic function, reducing noradrenergic function, and altering neuropeptide expression. In vivo, a noradrenergic to cholinergic switch occurs in the developing sweat gland innervation, and changes in neuropeptide phenotype occur in axotomized adult ganglia. We find that the gland innervation of LIF-deficient mice is indistinguishable from normal. In contrast, neuropeptide induction in ganglia cultured as explants or axotomized in situ is significantly suppressed in LIF-deficient mice. Thus, LIF plays a role in transmitter changes induced by axotomy but not by developmental interactions with sweat glands.
Assuntos
Gânglios Simpáticos/fisiologia , Inibidores do Crescimento/deficiência , Inibidores do Crescimento/fisiologia , Interleucina-6 , Linfocinas/deficiência , Linfocinas/fisiologia , Neurônios/fisiologia , Animais , Sequência de Bases , Células Cultivadas , Cruzamentos Genéticos , Primers do DNA , Feminino , Galanina , Deleção de Genes , Inibidores do Crescimento/genética , Fator Inibidor de Leucemia , Linfocinas/genética , Masculino , Camundongos , Camundongos Mutantes , Dados de Sequência Molecular , Neurocinina A/farmacologia , Neurônios/efeitos dos fármacos , Neuropeptídeos/farmacologia , Peptídeos/farmacologia , Fenótipo , Reação em Cadeia da Polimerase , Peptídeo Intestinal Vasoativo/análiseRESUMO
To determine the role of the p75 neurotrophin receptor (p75NTR) in sympathetic neuron development, we crossed transgenic mice with mutations in p75NTR, nerve growth factor (NGF) and neurotrophin-3 (NT-3). Neuron number is normal in sympathetic ganglia of adult p75NTR-/- mice. Mice heterozygous for a NGF deletion (NGF+/-) have 50% fewer sympathetic neurons. In the absence of p75NTR (p75NTR-/- NGF+/-), however, neuron number is restored to wild-type levels. When NT-3 levels are reduced (p75NTR-/- NGF+/- NT3 +/-), neuron number decreases compared to p75NTR-/- NGF+/- NT3+/+. Thus, without p75NTR, NT3 substitutes for NGF, suggesting that p75 alters the neurotrophin specificity of TrkA in vivo.
Assuntos
Gânglios Simpáticos/fisiologia , Fatores de Crescimento Neural/fisiologia , Neurônios/fisiologia , Receptores de Fator de Crescimento Neural/fisiologia , Adaptação Fisiológica , Alelos , Animais , Animais Recém-Nascidos , Contagem de Células , Camundongos , Camundongos Transgênicos , Fatores de Crescimento Neural/genética , Neurotrofina 3 , Receptor de Fator de Crescimento NeuralRESUMO
Studies of sympathetic neurons developing in cell culture revealed a surprising degree of transmitter plasticity and established the role of environmental factors in determining transmitter choice. The sympathetic neurons that innervate sweat glands undergo a change in neurotransmitter phenotype from noradrenergic to cholinergic during normal development similar to that observed in culture. Cross-innervation experiments indicate that the target sweat glands induce the switch and thereby specify the phenotype of the neurons that innervate them. Thus, both the transmitter plasticity and the role of environmental influences initially elucidated in culture are part of the developmental repertoire of sympathetic neurons in vivo. Further, these findings extend considerably our understanding of the role that targets may play during development; targets may not only determine how many neurons survive but also what their properties will be.
Assuntos
Neurotransmissores/fisiologia , Animais , Plasticidade Neuronal , Neurotransmissores/metabolismo , Fenótipo , Estimulação Química , Glândulas Sudoríparas/crescimento & desenvolvimento , Glândulas Sudoríparas/inervaçãoRESUMO
The sympathetic innervation of sweat glands undergoes a developmental change in transmitter phenotype from catecholaminergic to cholinergic. Acetylcholine elicits sweating and is necessary for development and maintenance of secretory responsiveness, the ability of glands to produce sweat after nerve stimulation or agonist administration. To determine whether catecholamines play a role in the development or function of this system, we examined the onset of secretory responsiveness in two transgenic mouse lines, one albino and the other pigmented, that lack tyrosine hydroxylase (TH), the rate-limiting enzyme in catecholamine synthesis. Although both lines lack TH, their catecholamine levels differ because tyrosinase in pigmented mice serves as an alternative source for catecholamine synthesis (Rios et al., 1999). At postnatal day 21 (P21), 28 glands on average are active in interdigital hind footpads of albino TH wild-type mice. In contrast, fewer than one gland is active in albino TH null mice, which lack catecholamines in gland innervation. Treatment of albino TH null mice with DOPA, a catecholamine precursor, from P11 to P21 increases the number of active glands to 14. Pigmented TH null mice, which have faint catecholamine fluorescence in the developing gland innervation, possess 12 active glands at P21, indicating that catecholamines made via tyrosinase, albeit reduced from wild-type levels, support development of responsiveness. Gland formation and the appearance of cholinergic markers occur normally in albino TH null mice, suggesting that catecholamines act directly on gland cells to trigger their final differentiation and to induce responsiveness. Thus, catecholamines, like acetylcholine, are essential for the development of secretory responsiveness.
Assuntos
Catecolaminas/metabolismo , Glândulas Sudoríparas/metabolismo , Acetilcolina/metabolismo , Acetilcolina/farmacologia , Animais , Catecolaminas/farmacologia , Di-Hidroxifenilalanina/metabolismo , Di-Hidroxifenilalanina/farmacologia , Melanócitos/citologia , Melanócitos/enzimologia , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Mutantes , Monofenol Mono-Oxigenase/metabolismo , Agonistas Muscarínicos/farmacologia , Neurônios/citologia , Neurônios/efeitos dos fármacos , Neurônios/metabolismo , Pilocarpina/farmacologia , Glândulas Sudoríparas/efeitos dos fármacos , Glândulas Sudoríparas/crescimento & desenvolvimento , Glândulas Sudoríparas/inervação , Tirosina 3-Mono-Oxigenase/genética , Tirosina 3-Mono-Oxigenase/metabolismoRESUMO
Myosin from chicken pectoralis muscle consists of isozymes that differ in their alkali light chains. It is possible to isolate alkali 1 (A1) and alkali 2 (A2) homodimers of native myosin by immunoadsorption methods, and to compare their steady-state kinetics as well as their assembly into synthetic filaments under a variety of ionic conditions. Bipolar filaments of the isozymes formed at low salt concentrations had a narrow length distribution and did not differ from controls made from unfractionated myosin. Chicken myosin also assembles into highly homogeneous minifilaments similar to those formed by rabbit myosin in a citrate/Tris buffer. Analytical ultracentrifugation and electron microscopy showed that A1-homodimer, A2-homodimer and unfractionated myosin assembled into 0.3 micron short, bipolar minifilaments, which were indistinguishable from one another in size and shape. The steady-state myosin ATPase activity of the two homodimeric isozymes was identical in K+(EDTA) and Ca2+ assay media. The actomyosin Mg2+ ATPase measured at 25 and 55 mM-KCl (pH 8.0) showed only minor differences in both Vmax and Kapp. Actomyosin activity was also determined for the more homogeneous minifilament preparations of the isozymes and these, as well, produced essentially indistinguishable kinetic parameters. Thus we find no evidence to support the hypothesis that a particular alkali light chain of myosin can affect either the structure of the filaments or the steady-state rate of ATP hydrolysis.
Assuntos
Adenosina Trifosfatases , Isoenzimas , Músculos/análise , Miosinas , Actomiosina/metabolismo , Adenosina Trifosfatases/metabolismo , Animais , Galinhas , Citoesqueleto/ultraestrutura , Isoenzimas/metabolismo , Cinética , Microscopia Eletrônica , Músculos/enzimologia , Músculos/ultraestrutura , Miosinas/metabolismoRESUMO
Choline uptake by the high affinity choline transporter (CHT) is the rate-limiting step in acetylcholine synthesis. Induction of CHT is therefore a critical step in cholinergic differentiation, and we examined the developmental expression of CHT in cholinergic sympathetic neurons that innervate rodent sweat glands. During postnatal development the earliest sympathetic axons in the rear footpads are noradrenergic, containing intense tyrosine hydroxylase immunoreactivity and lacking CHT-immunoreactivity (CHT-IR). By postnatal day 7 (P7) in mouse, and P10 in rat, weak CHT-IR appeared in axons associated with the sweat gland anlagen. CHT staining intensity increased during the following weeks in conjunction with plexus arborization and gland maturation. The pattern of CHT-immunoreactivity (CHT-IR) in the sweat gland innervation was similar to staining for the vesicular acetylcholine transporter and vasoactive intestinal peptide. Immunoblots of tissue from sympathectomized rats confirmed that most of the CHT in footpad was contained in sympathetic neurons. Although CHT expression has been reported in noradrenergic sympathetic neurons of the superior cervical ganglion, these data indicate that in the sympathetic neurons projecting to sweat glands CHT is present at detectable levels only after association with the glands.
Assuntos
Proteínas de Membrana Transportadoras/biossíntese , Neurônios/metabolismo , Sistema Nervoso Simpático/crescimento & desenvolvimento , Sistema Nervoso Simpático/metabolismo , Animais , Axônios/metabolismo , Western Blotting , Colina O-Acetiltransferase/metabolismo , Feminino , Pé/inervação , Imuno-Histoquímica , Camundongos , Gravidez , Ratos , Ratos Sprague-Dawley , Gânglio Cervical Superior/metabolismo , Glândulas Sudoríparas/crescimento & desenvolvimento , Glândulas Sudoríparas/inervação , Glândulas Sudoríparas/metabolismo , Simpatectomia Química , Sistema Nervoso Simpático/citologia , Tirosina 3-Mono-Oxigenase/metabolismoRESUMO
The consequences of amino acid substitutions at the dimer interface for the strength of the interactions between the monomers and for the catalytic function of the dimeric enzyme alkaline phosphatase from Escherichia coli have been investigated. The altered enzymes R10A, R10K, R24A, R24K, T59A, and R10A/R24A, which have amino acid substitutions at the dimer interface, were characterized using kinetic assays, ultracentrifugation, and transverse urea gradient gel electrophoresis. The kinetic data for the wild-type and altered alkaline phosphatases show comparable catalytic behavior with k(cat) values between 51.3 and 69.5 s(-1) and Km values between 14.8 and 26.3 microM. The ultracentrifugation profiles indicate that the wild-type enzyme is more stable than all the interface-modified enzymes. The wild-type enzyme is dimeric in the pH range of pH 4.0 and above, and disassembled at pH 3.5 and below. All the interface-modified enzymes, however, are apparently monomeric at pH 4.0, begin assembly at pH 5.0, and are not fully assembled into the dimeric form until pH 6.0. The results from transverse urea gradient gel electrophoresis show clear and reproducible differences both in the position and the shape of the unfolding patterns; all these modified enzymes are more sensitive to the denaturant and begin to unfold at urea concentrations between 1.0 and 1.5 M; the wild-type enzyme remains in the folded high mobility form beyond 2.5 M urea. Alkaline phosphatase H370A, modified at the active site and not at the dimer interface, resembles the wild-type enzyme both in ultracentrifugation and electrophoresis studies. The results obtained suggest that substitution of a single amino acid at the interface sacrifices not only the integrity of the assembled dimer, but also the stability of the monomer fold, even though the activity of the enzyme at optimal pH remains unaffected and does not appear to depend on interface stability.
Assuntos
Fosfatase Alcalina/química , Aminoácidos/química , Escherichia coli/enzimologia , Conformação Proteica , Cromatografia em Gel , Dimerização , Eletroforese , Cinética , Modelos Moleculares , Ligação Proteica , Termodinâmica , UltracentrifugaçãoRESUMO
Purkinje cell degeneration (pcd), an autosomal recessive mutation in the mouse, causes the postnatal death of virtually all cerebellar Purkinje cells during the third and fourth postnatal week. We have compared the postnatal development of normal and pcd mutant Purkinje cells. The early deviations from normal development involve primarily the perikaryonal polysomes and endoplasmic reticulum. Many of the mutant Purkinje cells retain abnormally the basal accumulation of polysomes, a finding which permits the identification of affected animals at postnatal day 15, one week prior to the onset of behavioral abnormalities. In addition, the affected Purkinje cells possess unusual configurations of endoplasmic reticulum with associated electron-dense particles similar to but larger than ribosomes, mature and forming intracisternal A particles and nematosomes. Before the pcd Purkinje cells degenerate they appear to receive all their appropriate synaptic contacts. Some disruption, however, of parallel fiber: Purkinje spine synaptogenesis occurs at late stages of development. Some spines lack presynaptic elements, postsynaptic thickenings are present along the dendritic shafts and parallel fibers appear to make synaptic contacts directly onto the shafts. The spectrum of early morphological changes that has been observed in pcd mutant Purkinje cells is thus far unique to this cerebellar abnormality.
Assuntos
Doenças Cerebelares/genética , Células de Purkinje/ultraestrutura , Animais , Sobrevivência Celular , Doenças Cerebelares/patologia , Doenças Cerebelares/fisiopatologia , Cerebelo/crescimento & desenvolvimento , Retículo Endoplasmático/ultraestrutura , Corpos de Inclusão/ultraestrutura , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Endogâmicos , Microscopia Eletrônica , Mutação , Polirribossomos/ultraestrutura , Sinapses/ultraestruturaRESUMO
Footpads of normal adult mice are innervated by sympathetic and sensory fibers. The sympathetic fibers associated with sweat glands contain acetylcholinesterase and immunoreactivity for vasoactive intestinal peptide. Although catecholamine histofluorescence is absent, the gland innervation exhibits immunoreactivity for tyrosine hydroxylase. A distinct population of sympathetic fibers, which possess catecholamines and neuropeptide Y as well as tyrosinehydroxylase immunoreactivity, innervates blood vessels. Sensory fibers containing immunoreactivity for substance P and calcitonin gene-related peptide course beneath the epidermis and some form endings in it. Treatment of neonatal mice with the adrenergic neurotoxin, 6-hydroxydopamine, results in loss of sympathetic innervation of sweat glands and blood vessels, permits growth of sensory axons into sweat glands, but does not alter the peptidergic sensory innervation of the dermis and epidermis. Three mouse mutations, Tabby (Ta), crinkled (cr), and downless (dl), disrupt the interactions between the mesenchyme and epidermis that are required for normal development of specific epidermal derivatives, including sweat glands. The sympathetic innervation of blood vessels and sensory innervation of footpad skin of the three mutant mice that lack sweat glands is indistinguishable from normal. The sympathetic fibers that normally innervate sweat glands, however, are not present. These results indicate that in the absence of their normal target, the sympathetic fibers that innervate sweat glands are lacking. Furthermore, they suggest that, although sensory fibers may sprout into sympathetic targets in the footpad, the domains occupied by sensory fibers are not normally accessible to sympathetic axons.
Assuntos
Pé/inervação , Camundongos Endogâmicos C57BL/anatomia & histologia , Camundongos Mutantes/anatomia & histologia , Fibras Nervosas/fisiologia , Neurotransmissores/metabolismo , Glândulas Sudoríparas/anormalidades , Animais , Peptídeo Relacionado com Gene de Calcitonina/análise , Feminino , Masculino , Camundongos , Neurônios Aferentes/fisiologia , Valores de Referência , Sistema Nervoso Simpático/fisiologia , Tirosina 3-Mono-Oxigenase/análiseRESUMO
Sympathetic and sensory neurons form distinct axonal arborizations in several peripheral targets. The developmental mechanisms responsible for partitioning sympathetic and sensory axons between potential target tissues are poorly understood. We have used rodent footpads to study this process because three populations of peripheral axons innervate topographically segregated targets in the footpad; cholinergic sympathetic axons innervate sweat glands, noradrenergic sympathetic axons innervate blood vessels, and sensory axons form a plexus at the epidermal/dermal junction. To examine how nerve growth factor (NGF), a trophic and survival factor for sympathetic and some sensory neurons, may contribute to the generation of the patterned distribution of axons among targets, we studied transgenic mice (K14-NGF mice) in which NGF expression was significantly increased in the epidermis. Whereas the temporal sequence in which sensory and sympathetic fibers arrived in the footpad was not affected, the normal partitioning of axons between target tissues was disrupted. The two sympathetic targets in footpads, sweat glands, and blood vessels lacked substantial innervation and instead a dense plexus of catecholaminergic sympathetic fibers was found commingled with sensory fibers in the dermis. Those sympathetic fibers present in sweat glands expressed an abnormal dual catecholaminergic/cholinergic phenotype. Our findings indicate that overexpression of NGF in skin interferes with the segregation of sensory and sympathetic axonal arbors and suggests a role for target-derived NGF in the establishment of distinct axonal territories. Our data also suggest that by determining where axon arbors form, NGF can indirectly influence the phenotypic properties of sympathetic neurons.
Assuntos
Fibras Adrenérgicas/química , Epiderme/inervação , Regulação da Expressão Gênica no Desenvolvimento/fisiologia , Proteínas de Membrana Transportadoras , Camundongos Transgênicos/fisiologia , Fatores de Crescimento Neural/genética , Proteínas de Transporte Vesicular , Acetilcolinesterase/metabolismo , Fibras Adrenérgicas/enzimologia , Animais , Biomarcadores , Proteínas de Transporte/análise , Extremidades/inervação , Camundongos , Morfogênese/fisiologia , Plasticidade Neuronal/fisiologia , Glândulas Sudoríparas/inervação , Sistema Nervoso Simpático/citologia , Sistema Nervoso Simpático/crescimento & desenvolvimento , Sinapses/química , Sinapses/enzimologia , Transgenes/fisiologia , Peptídeo Intestinal Vasoativo/análise , Proteínas Vesiculares de Transporte de AcetilcolinaRESUMO
We have examined the expression of tyrosine hydroxylase and neuropeptide Y in ciliary ganglia of normal adult rats and of adult rats in which the environment of these neurons was altered by sympathectomy at birth. Following neonatal 6-hydroxydopamine treatment, the proportion of tyrosine hydroxylase-immunoreactive and neuropeptide Y-immunoreactive neurons in ciliary ganglia was significantly increased. In ciliary neurons of both control and sympathectomized rats, neuropeptide Y immunoreactivity was preferentially co-localized with tyrosine hydroxylase. Immunoblot analysis confirmed the presence of tyrosine hydroxylase and its increase following sympathectomy. In situ hybridization studies revealed that many ciliary neurons contain mRNA for tyrosine hydroxylase and for neuropeptide Y. Like tyrosine hydroxylase immunoreactivity, the number of ciliary neurons containing tyrosine hydroxylase mRNA and the amount of mRNA per cell were increased in 6-hydroxydopamine-treated rats. In contrast, neuropeptide Y mRNA levels were the same in control and 6-hydroxydopamine-treated rats. Nerve growth factor is a candidate for mediating the effects of sympathectomy and most ciliary neurons in control and sympathectomized rats expressed immunoreactivity for the low-affinity nerve growth factor receptor. In addition, ciliary neurons from 6-hydroxydopamine-treated animals possessed increased nerve growth factor receptor immunoreactivity. These studies indicate that both tyrosine hydroxylase and neuropeptide Y in the ciliary ganglion are regulated by alterations in their environment. Their expression was enhanced by chemical sympathectomy which does not affect ciliary neurons directly but, rather, removes sympathetic innervation of shared targets, including the iris. In situ hybridization analysis suggests that the increased tyrosine hydroxylase and neuropeptide Y levels result from different mechanisms and provides evidence that neuropeptide levels can be regulated without changes in mRNA levels.
Assuntos
Gânglios Parassimpáticos/metabolismo , Neurônios/metabolismo , Neuropeptídeo Y/metabolismo , Simpatectomia Química , Tirosina 3-Mono-Oxigenase/metabolismo , Animais , Anticorpos Monoclonais , Gânglios Parassimpáticos/citologia , Immunoblotting , Imuno-Histoquímica , Neurônios/citologia , Oxidopamina , Ratos , Ratos Endogâmicos , Valores de ReferênciaRESUMO
The distribution of putative nicotinic receptors on cultured neurons from the rat superior cervical ganglion was determined by electron microscopic autoradiography using a radioactively labeled snake venom neurotoxin, toxin F. In a previous study, we demonstrated that toxin F blocks nicotinic transmission in these cultures of sympathetic neurons and in intact superior cervical ganglia. [125I]toxin F bound to two sites in these cultures: one site that was also recognized by the neuromuscular blocker, alpha-bungarotoxin, and a second site that was not. Since alpha-bungarotoxin neither blocks nicotinic transmission nor prevents the blocking effects of toxin F, the site specific to the binding of toxin F most probably represents neuronal nicotinic receptors. The total number of each of the toxin F binding sites was unaffected by culture conditions that are known to influence the extent to which these sympathetic neurons synthesize norepinephrine or acetylcholine. Autoradiographic analysis performed under saturating binding conditions (80 nM [125I]toxin F) revealed that the density of [125I]toxin F binding at synaptic membranes was about 5000 sites/micron 2, either in the absence of any competing ligand or in the presence of 2 microM alpha-bungarotoxin. In the presence of 2 microM unlabeled toxin F, there was no detectable binding at synapses. The density of these toxin F-specific sites was at least 80-fold higher at synaptic membranes than elsewhere. On the other hand, the data suggest that the toxin F binding site shared with alpha-bungarotoxin is exclusively extrasynaptic. Two micromolar alpha-bungarotoxin decreased the density of [125I]toxin F binding at non-synaptic sites by approximately two-thirds. These experiments support the hypothesis that toxin F blocks cholinergic transmission in cultures of sympathetic neurons by binding to nicotinic receptors and suggests that these receptors are highly clustered at synaptic membranes.