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1.
J Physiol ; 558(Pt 2): 503-12, 2004 Jul 15.
Artículo en Inglés | MEDLINE | ID: mdl-15169845

RESUMEN

Dendritic spines are the site of most excitatory connections in the hippocampus. We have investigated the diffusibility of a membrane-bound green fluorescent protein (mGFP) within the inner leaflet of the plasma membrane using Fluorescence Recovery After Photobleaching. In dendritic spines the diffusion of mGFP was significantly retarded relative to the dendritic shaft. In parallel, we have assessed the motility of dendritic spines, and found an inverse correlation between spine motility and the rate of diffusion of mGFP. We then tested the influence of glutamate receptor activation or blockade, and the involvement of the actin cytoskeleton (using latrunculin A) on spine motility and mGFP diffusion. These results show that glutamate receptors regulate the mobility of molecules in the inner leaflet of the plasma membrane through an action upon the actin cytoskeleton, suggesting a novel mechanism for the regulation of postsynaptic receptor density and composition.


Asunto(s)
Espinas Dendríticas/fisiología , Hipocampo/citología , Hipocampo/fisiología , Receptores AMPA/metabolismo , Actinas/metabolismo , Animales , Membrana Celular/metabolismo , Difusión , Recuperación de Fluorescencia tras Fotoblanqueo , Proteínas Fluorescentes Verdes/genética , Proteínas Fluorescentes Verdes/metabolismo , Ratones , Ratones Transgénicos , Técnicas de Cultivo de Órganos
2.
Eur J Neurosci ; 15(12): 1976-82, 2002 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-12099903

RESUMEN

The growth-associated protein GAP-43 (or neuromodulin or B-50) plays a critical role during development in mechanisms of axonal growth and formation of synaptic networks. At later times, GAP-43 has also been implicated in the regulation of synaptic transmission and properties of plasticity such as long-term potentiation. In a molecular approach, we have analyzed transgenic mice overexpressing different mutated forms of GAP-43 or deficient in GAP-43 to investigate the role of the molecule in short-term and long-term plasticity. We report that overexpression of a mutated form of GAP-43 that mimics constitutively phosphorylated GAP-43 results in an enhancement of long-term potentiation in CA1 hippocampal slices. This effect is specific, because LTP was affected neither in transgenic mice overexpressing mutated forms of non-phosphorylatable GAP-43 nor in GAP-43 deficient mice. The increased LTP observed in transgenic mice expressing a constitutively phosphorylated GAP-43 was associated with an increased paired-pulse facilitation as well as an increased summation of responses during high frequency bursts. These results indicate that, while GAP-43 is not necessary for LTP induction, its phosphorylation may regulate presynaptic properties, thereby affecting synaptic plasticity and the induction of LTP.


Asunto(s)
Proteína GAP-43/deficiencia , Hipocampo/crecimiento & desarrollo , Hipocampo/metabolismo , Potenciación a Largo Plazo/genética , Neuronas/metabolismo , Mutación Puntual/genética , Regulación hacia Arriba/genética , Secuencia de Aminoácidos/genética , Animales , Estimulación Eléctrica , Antagonistas de Aminoácidos Excitadores/farmacología , Potenciales Postsinápticos Excitadores/efectos de los fármacos , Potenciales Postsinápticos Excitadores/genética , Antagonistas del GABA/farmacología , Proteína GAP-43/genética , Expresión Génica/efectos de los fármacos , Expresión Génica/fisiología , Hipocampo/citología , Potenciación a Largo Plazo/efectos de los fármacos , Ratones , Ratones Transgénicos , Neuronas/citología , Neuronas/efectos de los fármacos , Técnicas de Cultivo de Órganos , Fenotipo , Forbol 12,13-Dibutirato/farmacología , Fosforilación , Mutación Puntual/efectos de los fármacos , Proteína Quinasa C/efectos de los fármacos , Proteína Quinasa C/metabolismo , Receptores de N-Metil-D-Aspartato/antagonistas & inhibidores , Receptores de N-Metil-D-Aspartato/metabolismo , Transmisión Sináptica/efectos de los fármacos , Transmisión Sináptica/genética , Regulación hacia Arriba/efectos de los fármacos
3.
J Cell Biol ; 155(1): 101-12, 2001 Oct 01.
Artículo en Inglés | MEDLINE | ID: mdl-11571311

RESUMEN

The pathogenic bacterium Listeria monocytogenes is able to invade nonphagocytic cells, an essential feature for its pathogenicity. This induced phagocytosis process requires tightly regulated steps of actin polymerization and depolymerization. Here, we investigated how interactions of the invasion protein InlB with mammalian cells control the cytoskeleton during Listeria internalization. By fluorescence microscopy and transfection experiments, we show that the actin-nucleating Arp2/3 complex, the GTPase Rac, LIM kinase (LIMK), and cofilin are key proteins in InlB-induced phagocytosis. Overexpression of LIMK1, which has been shown to phosphorylate and inactivate cofilin, induces accumulation of F-actin beneath entering particles and inhibits internalization. Conversely, inhibition of LIMK's activity by expressing a dominant negative construct, LIMK1(-), or expression of the constitutively active S3A cofilin mutant induces loss of actin filaments at the phagocytic cup and also inhibits phagocytosis. Interestingly, those constructs similarly affect other actin-based phenomenons, such as InlB-induced membrane ruffling or Listeria comet tail formations. Thus, our data provide evidence for a control of phagocytosis by both activation and deactivation of cofilin. We propose a model in which cofilin is involved in the formation and disruption of the phagocytic cup as a result of its local progressive enrichment.


Asunto(s)
Listeria monocytogenes/fisiología , Proteínas de Microfilamentos/metabolismo , Fagocitosis/fisiología , Proteínas Quinasas/metabolismo , Factores Despolimerizantes de la Actina , Actinas/metabolismo , Animales , Proteínas Bacterianas/metabolismo , Extensiones de la Superficie Celular/metabolismo , Chlorocebus aethiops , Citoesqueleto/metabolismo , Quinasas Lim , Listeria monocytogenes/genética , Proteínas de la Membrana/metabolismo , Proteínas de Microfilamentos/genética , Microscopía Fluorescente , Fosforilación , Proteínas Quinasas/genética , Proteínas Proto-Oncogénicas c-met/metabolismo , Células Vero , Proteínas de Unión al GTP rac/metabolismo
4.
EMBO J ; 20(16): 4332-6, 2001 Aug 15.
Artículo en Inglés | MEDLINE | ID: mdl-11500359

RESUMEN

The phosphoinositide lipid PI(4,5)P(2) is now established as a key cofactor in signaling to the actin cytoskeleton and in vesicle trafficking. PI(4,5)P(2) accumulates at membrane rafts and promotes local co-recruitment and activation of specific signaling components at the cell membrane. PI(4,5)P(2) rafts may thus be platforms for local regulation of morphogenetic activity at the cell membrane. Raft PI(4,5)P(2) is regulated by lipid kinases (PI5-kinases) and lipid phosphatases (e.g. synaptojanin). In addition, GAP43-like proteins have recently emerged as a group of PI(4,5)P(2) raft-modulating proteins. These locally abundant proteins accumulate at inner leaflet plasmalemmal rafts where they bind to and co-distribute with PI(4,5)P(2), and promote actin cytoskeleton accumulation and dynamics. In keeping with their proposed role as positive modulators of PI(4,5)P(2) raft function, GAP43-like proteins confer competence for regulated morphogenetic activity on cells that express them. Their function has been investigated extensively in the nervous system, where their expression promotes neurite outgrowth, anatomical plasticity and nerve regeneration. Extrinsic signals and intrinsic factors may thus converge to modulate PI(4,5)P(2) rafts, upstream of regulated activity at the cell surface.


Asunto(s)
Actinas/metabolismo , Citoesqueleto/metabolismo , Microdominios de Membrana/metabolismo , Fosfatidilinositoles/metabolismo , Animales , Proteína GAP-43/metabolismo
5.
J Cell Biol ; 153(4): 763-72, 2001 May 14.
Artículo en Inglés | MEDLINE | ID: mdl-11352937

RESUMEN

In this study, we investigated cardiomyocyte cytoarchitecture in a mouse model for dilated cardiomyopathy (DCM), the muscle LIM protein (MLP) knockout mouse and substantiated several observations in a second DCM model, the tropomodulin-overexpressing transgenic (TOT) mouse. Freshly isolated cardiomyocytes from both strains are characterized by a more irregular shape compared with wild-type cells. Alterations are observed at the intercalated disks, the specialized areas of mechanical coupling between cardiomyocytes, whereas the subcellular organization of contractile proteins in the sarcomeres of MLP knockout mice appears unchanged. Distinct parts of the intercalated disks are affected differently. Components from the adherens junctions are upregulated, desmosomal proteins are unchanged, and gap junction proteins are downregulated. In addition, the expression of N-RAP, a LIM domain- containing protein located at the intercalated disks, is upregulated in MLP knockout as well as in TOT mice. Detailed analysis of intercalated disk composition during postnatal development reveals that an upregulation of N-RAP expression might serve as an early marker for the development of DCM. Altered expression levels of cytoskeletal proteins (either the lack of MLP or an increased expression of tropomodulin) apparently lead to impaired function of the myofibrillar apparatus and to physiological stress that ultimately results in DCM and is accompanied by an altered appearance and composition of the intercalated disks.


Asunto(s)
Proteínas de Microfilamentos , Fibras Musculares Esqueléticas/metabolismo , Fibras Musculares Esqueléticas/ultraestructura , Proteínas Musculares/genética , Proteínas Musculares/metabolismo , Animales , Cardiomiopatía Dilatada/metabolismo , Cardiomiopatía Dilatada/patología , Proteínas Portadoras/genética , Proteínas Portadoras/metabolismo , Uniones Comunicantes/metabolismo , Expresión Génica/fisiología , Proteínas con Dominio LIM , Ratones , Ratones Noqueados , Microscopía Electrónica , Fibras Musculares Esqueléticas/patología , Sarcómeros/metabolismo , Tropomodulina
6.
Eur J Neurosci ; 13(5): 857-70, 2001 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-11264659

RESUMEN

To determine whether the competence for axonal sprouting and/or regeneration in the cerebellar system correlates with GAP-43 expression, we have studied GAP-43 mRNA and protein expression in the postlesioned cerebellum and inferior olive. Purkinje cells transiently express GAP-43 during their developmental phase (from E15 to P5 in the rat) which consists of fast axonal growth and the formation of the corticonuclear projection. Adult Purkinje cells, which in control adult rats do not express GAP-43, are extremely resistant to the effects of axotomy but cannot regenerate axons. However, a late and protracted sprouting of axotomized Purkinje cells occurs spontaneously and correlates with a mild expression of GAP-43 mRNA. In contrast, inferior olivary neurons, despite their high constitutive expression of GAP-43, do not sprout but retract their axons and die after axotomy. Furthermore, mature Purkinje cells in cerebellar explants of transgenic mice that overexpress GAP-43 do not regenerate after axotomy, even in the presence of a permissive substrate (cerebellar embryonic tissue) and, contrary to the case in wild-type mice, they do not survive in the in vitro conditions and undergo massive cell death. These results show that the expression of GAP-43 is not only associated with axonal growth, but also with neuronal death.


Asunto(s)
Vías Aferentes/embriología , Vías Aferentes/crecimiento & desarrollo , Axotomía/efectos adversos , Cerebelo/embriología , Cerebelo/crecimiento & desarrollo , Proteína GAP-43/metabolismo , Regeneración Nerviosa/fisiología , Neuronas/metabolismo , Vías Aferentes/metabolismo , Animales , Muerte Celular/fisiología , Cerebelo/metabolismo , Femenino , Ratones , Ratones Transgénicos/anatomía & histología , Ratones Transgénicos/crecimiento & desarrollo , Ratones Transgénicos/metabolismo , Neuronas/citología , Núcleo Olivar/embriología , Núcleo Olivar/crecimiento & desarrollo , Núcleo Olivar/metabolismo , Células de Purkinje/citología , Células de Purkinje/metabolismo , Ratas , Ratas Wistar , Regulación hacia Arriba/fisiología
7.
Nat Neurosci ; 4(1): 38-43, 2001 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-11135643

RESUMEN

In contrast to peripheral nerves, damaged axons in the mammalian brain and spinal cord rarely regenerate. Peripheral nerve injury stimulates neuronal expression of many genes that are not generally induced by CNS lesions, but it is not known which of these genes are required for regeneration. Here we show that co-expressing two major growth cone proteins, GAP-43 and CAP-23, can elicit long axon extension by adult dorsal root ganglion (DRG) neurons in vitro. Moreover, this expression triggers a 60-fold increase in regeneration of DRG axons in adult mice after spinal cord injury in vivo. Replacing key growth cone components, therefore, could be an effective way to stimulate regeneration of CNS axons.


Asunto(s)
Axones/metabolismo , Proteínas de Unión a Calmodulina , Conos de Crecimiento/metabolismo , Regeneración Nerviosa/fisiología , Proteínas del Tejido Nervioso , Neuronas/metabolismo , Médula Espinal/metabolismo , Animales , Axones/efectos de los fármacos , Axotomía , Separación Celular , Proteínas del Citoesqueleto/genética , Proteínas del Citoesqueleto/metabolismo , Proteínas del Citoesqueleto/farmacología , Proteína GAP-43/genética , Proteína GAP-43/metabolismo , Proteína GAP-43/farmacología , Ganglios Espinales/citología , Ganglios Espinales/efectos de los fármacos , Ganglios Espinales/metabolismo , Expresión Génica , Conos de Crecimiento/efectos de los fármacos , Técnicas In Vitro , Ratones , Ratones Transgénicos , Factores de Crecimiento Nervioso/biosíntesis , Factores de Crecimiento Nervioso/genética , Factores de Crecimiento Nervioso/farmacología , Regeneración Nerviosa/efectos de los fármacos , Neuronas/efectos de los fármacos , Médula Espinal/citología , Médula Espinal/efectos de los fármacos
8.
J Neurosci ; 20(16): 6021-9, 2000 Aug 15.
Artículo en Inglés | MEDLINE | ID: mdl-10934251

RESUMEN

The presynaptic protein alpha-synuclein is a prime suspect for contributing to Lewy pathology and clinical aspects of diseases, including Parkinson's disease, dementia with Lewy bodies, and a Lewy body variant of Alzheimer's disease. alpha-Synuclein accumulates in Lewy bodies and Lewy neurites, and two missense mutations (A53T and A30P) in the alpha-synuclein gene are genetically linked to rare familial forms of Parkinson's disease. Under control of mouse Thy1 regulatory sequences, expression of A53T mutant human alpha-synuclein in the nervous system of transgenic mice generated animals with neuronal alpha-synucleinopathy, features strikingly similar to those observed in human brains with Lewy pathology, neuronal degeneration, and motor defects, despite a lack of transgene expression in dopaminergic neurons of the substantia nigra pars compacta. Neurons in brainstem and motor neurons appeared particularly vulnerable. Motor neuron pathology included axonal damage and denervation of neuromuscular junctions in several muscles examined, suggesting that alpha-synuclein interfered with a universal mechanism of synapse maintenance. Thy1 transgene expression of wild-type human alpha-synuclein resulted in similar pathological changes, thus supporting a central role for mutant and wild-type alpha-synuclein in familial and idiotypic forms of diseases with neuronal alpha-synucleinopathy and Lewy pathology. These mouse models provide a means to address fundamental aspects of alpha-synucleinopathy and test therapeutic strategies.


Asunto(s)
Sistema Nervioso Central/patología , Regulación de la Expresión Génica/fisiología , Cuerpos de Lewy/metabolismo , Mutación/fisiología , Degeneración Nerviosa/fisiopatología , Proteínas del Tejido Nervioso/metabolismo , Enfermedades Neurodegenerativas/fisiopatología , Animales , Sistema Nervioso Central/metabolismo , Sistema Nervioso Central/fisiopatología , Humanos , Cuerpos de Lewy/genética , Ratones , Ratones Transgénicos , Actividad Motora/fisiología , Neuronas Motoras/metabolismo , Neuronas Motoras/patología , Neuronas Motoras/ultraestructura , Trastornos del Movimiento/genética , Trastornos del Movimiento/patología , Trastornos del Movimiento/fisiopatología , Degeneración Nerviosa/genética , Degeneración Nerviosa/patología , Proteínas del Tejido Nervioso/genética , Enfermedades Neurodegenerativas/genética , Enfermedades Neurodegenerativas/patología , Desempeño Psicomotor/fisiología , Sinucleínas , alfa-Sinucleína
9.
Exp Neurol ; 165(1): 143-52, 2000 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-10964493

RESUMEN

It is well established that some populations of neurons of the adult rat central nervous system (CNS) will regenerate axons into a peripheral nerve implant, but others, including most thalamocortical projection neurons, will not. The ability to regenerate axons may depend on whether neurons can express growth-related genes such as GAP-43, whose expression correlates with axon growth during development and with competence to regenerate. Thalamic projection neurons which fail to regenerate into a graft also fail to upregulate GAP-43. We have tested the hypothesis that the absence of strong GAP-43 expression by the thalamic projection neurons prevents them from regenerating their axons, using transgenic mice which overexpress GAP-43. Transgene expression was mapped by in situ hybridization with a digoxigenin-labeled RNA probe and by immunohistochemistry with a monoclonal antibody against the GAP-43 protein produced by the transgene. Many CNS neurons were found to express the mRNA and protein, including neurons of the mediodorsal and ventromedial thalamic nuclei, which rarely regenerate axons into peripheral nerve grafts. Grafts were implanted into the region of these nuclei in the brains of transgenic animals. Although these neurons strongly expressed the transgene mRNA and protein and transported the protein to their axon terminals, they did not regenerate axons into the graft, suggesting that lack of GAP-43 expression is not the only factor preventing thalamocortical neurons regenerating their axons.


Asunto(s)
Axones/fisiología , Proteína GAP-43/metabolismo , Regeneración Nerviosa/fisiología , Tálamo/fisiología , Tálamo/cirugía , Nervio Tibial/trasplante , Animales , Aves/genética , Aves/metabolismo , Proteína GAP-43/genética , Expresión Génica , Inmunohistoquímica , Hibridación in Situ , Ratones , Ratones Transgénicos/genética , Neuronas/metabolismo , Neuronas/fisiología , Transmisión Sináptica/fisiología , Tálamo/citología , Tálamo/metabolismo , Nervio Tibial/fisiología , Transgenes/fisiología
10.
J Cell Biol ; 149(7): 1443-54, 2000 Jun 26.
Artículo en Inglés | MEDLINE | ID: mdl-10871284

RESUMEN

CAP23 is a major cortical cytoskeleton-associated and calmodulin binding protein that is widely and abundantly expressed during development, maintained in selected brain structures in the adult, and reinduced during nerve regeneration. Overexpression of CAP23 in adult neurons of transgenic mice promotes nerve sprouting, but the role of this protein in process outgrowth was not clear. Here, we show that CAP23 is functionally related to GAP43, and plays a critical role to regulate nerve sprouting and the actin cytoskeleton. Knockout mice lacking CAP23 exhibited a pronounced and complex phenotype, including a defect to produce stimulus-induced nerve sprouting at the adult neuromuscular junction. This sprouting deficit was rescued by transgenic overexpression of either CAP23 or GAP43 in adult motoneurons. Knockin mice expressing GAP43 instead of CAP23 were essentially normal, indicating that, although these proteins do not share homologous sequences, GAP43 can functionally substitute for CAP23 in vivo. Cultured sensory neurons lacking CAP23 exhibited striking alterations in neurite outgrowth that were phenocopied by low doses of cytochalasin D. A detailed analysis of such cultures revealed common and unique functions of CAP23 and GAP43 on the actin cytoskeleton and neurite outgrowth. The results provide compelling experimental evidence for the notion that CAP23 and GAP43 are functionally related intrinsic determinants of anatomical plasticity, and suggest that these proteins function by locally promoting subplasmalemmal actin cytoskeleton accumulation.


Asunto(s)
Actinas/metabolismo , Encéfalo/metabolismo , Encéfalo/fisiología , Proteínas de Unión a Calmodulina , Proteínas del Citoesqueleto/metabolismo , Proteína GAP-43/metabolismo , Proteínas del Tejido Nervioso , Neuritas/metabolismo , Neuritas/fisiología , Plasticidad Neuronal/fisiología , Factores de Edad , Animales , Toxinas Botulínicas Tipo A/farmacología , Encéfalo/citología , Células Cultivadas , Citocalasina D/farmacología , Citoesqueleto/metabolismo , Ganglios Espinales/citología , Ganglios Espinales/metabolismo , Conos de Crecimiento/metabolismo , Conos de Crecimiento/ultraestructura , Ratones , Ratones Noqueados , Neuronas Motoras/citología , Neuronas Motoras/metabolismo , Fibras Nerviosas/metabolismo , Fibras Nerviosas/ultraestructura , Fármacos Neuromusculares/farmacología , Unión Neuromuscular/metabolismo , Unión Neuromuscular/ultraestructura , Inhibidores de la Síntesis del Ácido Nucleico/farmacología , Fenotipo , Polímeros/metabolismo
11.
J Cell Biol ; 149(7): 1455-72, 2000 Jun 26.
Artículo en Inglés | MEDLINE | ID: mdl-10871285

RESUMEN

The dynamic properties of the cell cortex and its actin cytoskeleton determine important aspects of cell behavior and are a major target of cell regulation. GAP43, myristoylated alanine-rich C kinase substrate (MARCKS), and CAP23 (GMC) are locally abundant, plasmalemma-associated PKC substrates that affect actin cytoskeleton. Their expression correlates with morphogenic processes and cell motility, but their role in cortex regulation has been difficult to define mechanistically. We now show that the three proteins accumulate at rafts, where they codistribute with PI(4,5)P(2), and promote its retention and clustering. Binding and modulation of PI(4, 5)P(2) depended on the basic effector domain (ED) of these proteins, and constructs lacking the ED functioned as dominant inhibitors of plasmalemmal PI(4,5)P(2) modulation. In the neuron-like cell line, PC12, NGF- and substrate-induced peripheral actin structures, and neurite outgrowth were greatly augmented by any of the three proteins, and suppressed by DeltaED mutants. Agents that globally mask PI(4,5)P(2) mimicked the effects of GMC on peripheral actin recruitment and cell spreading, but interfered with polarization and process formation. Dominant negative GAP43(DeltaED) also interfered with peripheral nerve regeneration, stimulus-induced nerve sprouting and control of anatomical plasticity at the neuromuscular junction of transgenic mice. These results suggest that GMC are functionally and mechanistically related PI(4,5)P(2) modulating proteins, upstream of actin and cell cortex dynamics regulation.


Asunto(s)
Actinas/metabolismo , Proteínas de Unión a Calmodulina , Membrana Celular/metabolismo , Proteínas del Citoesqueleto/metabolismo , Citoesqueleto/metabolismo , Proteína GAP-43/metabolismo , Péptidos y Proteínas de Señalización Intracelular , Proteínas de la Membrana , Proteínas del Tejido Nervioso , Fosfatidilinositol 4,5-Difosfato/metabolismo , Proteínas/metabolismo , Animales , Bradiquinina/metabolismo , Bradiquinina/farmacología , Membrana Celular/ultraestructura , Proteínas del Citoesqueleto/genética , Citoesqueleto/ultraestructura , Proteína GAP-43/genética , Hipocampo/metabolismo , Hipocampo/ultraestructura , Ratones , Mutación/fisiología , Sustrato de la Proteína Quinasa C Rico en Alanina Miristoilada , Regeneración Nerviosa/efectos de los fármacos , Regeneración Nerviosa/fisiología , Neuritas/metabolismo , Neuritas/ultraestructura , Unión Neuromuscular/efectos de los fármacos , Unión Neuromuscular/metabolismo , Unión Neuromuscular/ultraestructura , Neuronas/metabolismo , Neuronas/ultraestructura , Células PC12 , Nervios Periféricos/efectos de los fármacos , Nervios Periféricos/metabolismo , Nervios Periféricos/ultraestructura , Fosfatidilinositoles/metabolismo , Estructura Terciaria de Proteína/fisiología , Proteínas/genética , Ratas , Fracciones Subcelulares
12.
Circulation ; 101(23): 2674-7, 2000 Jun 13.
Artículo en Inglés | MEDLINE | ID: mdl-10851202

RESUMEN

BACKGROUND: The cardiac LIM domain protein MLP, a member of the cysteine-rich protein family, is an essential regulator of cardiac muscle development. Mice with a disruption of the MLP gene resemble the morphological and clinical picture of dilated cardiomyopathy and heart failure in humans. We investigated whether altered MLP expression is significant for the pathogenesis of human heart failure. METHODS AND RESULTS: Immunohistochemistry and in situ hybridization confirmed the expression of MLP protein and mRNA in human cardiomyocytes. Western blot analysis revealed that the MLP peptide was present in the contractile protein fraction but not in the cytosolic or membrane fraction and that the binding of MLP to myofibrils required functional zinc finger domains. MLP immunoreactivity was decreased approximately 50% (P<0.05) in the left ventricular myocardium of patients with chronic heart failure due to dilated or ischemic cardiomyopathy compared with non-failing donor hearts. MLP mRNA expression, as assessed by Northern blot experiments, was not significantly different between failing and non-failing control hearts, which suggests that decreased MLP synthesis or increased MLP protein turnover, rather than a decreased number of RNA transcripts, may play a role. CONCLUSIONS: Because MLP may promote myofibril assembly, the down-regulation of this adapter protein might play an essential role in myofibril derangement or impaired myofibril rearrangement in the failing human myocardium.


Asunto(s)
Insuficiencia Cardíaca/metabolismo , Insuficiencia Cardíaca/fisiopatología , Proteínas Musculares/genética , Proteínas Musculares/metabolismo , Miocardio/metabolismo , Adulto , Cardiomiopatía Dilatada/metabolismo , Cardiomiopatía Dilatada/fisiopatología , Enfermedad Crónica , Regulación hacia Abajo/fisiología , Expresión Génica/fisiología , Humanos , Proteínas con Dominio LIM , Persona de Mediana Edad , Proteínas Musculares/química , Isquemia Miocárdica/metabolismo , Isquemia Miocárdica/fisiopatología , Miofibrillas/metabolismo , Unión Proteica/fisiología , Estructura Terciaria de Proteína , ARN Mensajero/análisis , Fracciones Subcelulares/metabolismo , Dedos de Zinc/fisiología
13.
J Neurosci ; 20(7): 2534-42, 2000 Apr 01.
Artículo en Inglés | MEDLINE | ID: mdl-10729333

RESUMEN

The addition or loss of synapses in response to changes in activity, disease, or aging is a major aspect of nervous system plasticity in the adult. The mechanisms that affect the turnover and maintenance of synapses in the adult are poorly understood and are difficult to investigate in the brain. Here, we exploited a unique anatomical arrangement in the neuromuscular system to determine whether subtypes of synapses can differ in anatomical plasticity and vulnerability. In three genetic mouse models of motoneuron disease of diverse origin and severity, we observed a gradual and selective loss of synaptic connections that begun long before the onset of clinical deficits and correlated with the timing of disease progression. A subgroup of fast-type (fast-fatiguable) neuromuscular synapses was highly vulnerable and was lost very early on. In contrast, slow-type synapses resisted up to the terminal phase of the disease. Muscle-specific differences were also evident. Similar selective losses were detected in aged mice. These selective vulnerability properties of synapses coincided with hitherto unrecognized major differences in stimulus-induced anatomical plasticity that could also be revealed in healthy mice. Using paralysis and/or growth-associated protein 43 overexpression to induce synaptic sprouting, we found that slow-type, disease-resistant synapses were particularly plastic. In contrast, fast-type synapses with the highest vulnerability failed to exhibit any stimulus-induced change. The results reveal pronounced subtype specificity in the anatomical plasticity and susceptibility to loss of neuromuscular synapses and suggest that degenerative motoneuron diseases involve a common early pathway of selective and progressive synaptic weakening also associated with aging.


Asunto(s)
Enfermedad de la Neurona Motora/patología , Unión Neuromuscular/patología , Sinapsis/patología , Envejecimiento/patología , Animales , Inmunidad Innata , Ratones , Ratones Endogámicos C57BL , Ratones Mutantes Neurológicos , Fibras Musculares Esqueléticas/clasificación , Fibras Musculares Esqueléticas/patología , Plasticidad Neuronal , Superóxido Dismutasa/genética , Sinapsis/clasificación
14.
Genes Dev ; 13(19): 2538-48, 1999 Oct 01.
Artículo en Inglés | MEDLINE | ID: mdl-10521398

RESUMEN

The ErbB2 tyrosine kinase functions as coreceptor for the neuregulin receptors ErbB3 and ErbB4 and can participate in signaling of EGF receptor (ErbB1), interleukin receptor gp130, and G-protein coupled receptors. ErbB2(-/-) mice die at midgestation because of heart malformation. Here, we report a genetic rescue of their heart development by myocardial expression of erbB2 cDNA that allows survival of the mutants to birth. In rescued erbB2 mutants, Schwann cells are lacking. Motoneurons form and can project to muscle, but nerves are poorly fasciculated and disorganized. Neuromuscular junctions form, as reflected in clustering of AChR and postsynaptic expression of the genes encoding the alpha-AChR, AChE, epsilon-AChR, and the RI subunit of the cAMP protein kinase. However, a severe loss of motoneurons on cervical and lumbar, but not on thoracic levels occurs. Our results define the roles of Schwann cells during motoneuron and synapse development, and reveal different survival requirements for distinct motoneuron populations.


Asunto(s)
Corazón/embriología , Sistema Nervioso Periférico/embriología , Receptor ErbB-2/fisiología , Factores de Transcripción , Proteínas de Xenopus , Alelos , Animales , Proteína Homeótica Nkx-2.5 , Proteínas de Homeodominio/genética , Ratones , Ratones Mutantes , Neuronas Motoras , Mutación , Cresta Neural , Unión Neuromuscular , Sistema Nervioso Periférico/anomalías , Receptor ErbB-2/genética , Células de Schwann , Sinapsis
15.
J Neurobiol ; 36(3): 379-94, 1998 Sep 05.
Artículo en Inglés | MEDLINE | ID: mdl-9733073

RESUMEN

During development of the avian neuromuscular system, lumbar spinal motoneurons (MNs) innervate their muscle targets in the hindlimb coincident with the onset and progression of MN programmed cell death (PCD). Paralysis (activity blockade) of embryos during this period rescues large numbers of MNs from PCD. Because activity blockade also results in enhanced axonal branching and increased numbers of neuromuscular synapses, it has been postulated that following activity blockade, increased numbers of MNs can gain access to muscle-derived trophic agents that prevent PCD. An assumption of the access hypothesis of MN PCD is the presence of an activity-dependent, muscle-derived sprouting or branching agent. Several previous studies of sprouting in the rodent neuromuscular system indicate that insulin-like growth factors (IGFs) are candidates for such a sprouting factor. Accordingly, in the present study we have begun to test whether the IGFs may play a similar role in the developing avian neuromuscular system. Evidence in support of this idea includes the following: (a) IGFs promote MN survival in vivo but not in vitro; (b) neutralizing antibodies against IGFs reduce MN survival in vivo; (c) both in vitro and in vivo, IGFs increase neurite growth, branching, and synapse formation; (d) activity blockade increases the expression of IGF-1 and IGF-2 mRNA in skeletal muscles in vivo; (e) in vivo treatment of paralyzed embryos with IGF binding proteins (IGF-BPs) that interfere with the actions of endogenous IGFs reduce MN survival, axon branching, and synapse formation; (f) treatment of control embryos in vivo with IGF-BPs also reduces synapse formation; and (g) treatment with IGF-1 prior to the major period of cell death (i.e., on embryonic day 6) increases subsequent synapse formation and MN survival and potentiates the survival-promoting actions of brain-derived neurotrophic factor (BDNF) and glial cell line-derived neurotrophic factor (GDNF) administered during the subsequent 4- to 5-day period of PCD. Collectively, these data provide new evidence consistent with the role of the IGFs as activity-dependent, muscle-derived agents that play a role in regulating MN survival in the avian embryo.


Asunto(s)
Apoptosis/fisiología , Neuronas Motoras/fisiología , Músculo Esquelético/embriología , Músculo Esquelético/inervación , Somatomedinas/fisiología , Animales , Recuento de Células , Células Cultivadas , Embrión de Pollo , Miembro Posterior/inervación , Inmunohistoquímica , Proteínas de Unión a Factor de Crecimiento Similar a la Insulina/farmacología , Factor I del Crecimiento Similar a la Insulina/genética , Factor II del Crecimiento Similar a la Insulina/genética , Oligonucleótidos/farmacología , Terminales Presinápticos/fisiología , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Somatomedinas/genética , Sinapsis/fisiología
17.
Nature ; 393(6687): 805-9, 1998 Jun 25.
Artículo en Inglés | MEDLINE | ID: mdl-9655397

RESUMEN

Cell division, cell motility and the formation and maintenance of specialized structures in differentiated cells depend directly on the regulated dynamics of the actin cytoskeleton. To understand the mechanisms of these basic cellular processes, the signalling pathways that link external signals to the regulation of the actin cytoskeleton need to be characterized. Here we identify a pathway for the regulation of cofilin, a ubiquitous actin-binding protein that is essential for effective depolymerization of actin filaments. LIM-kinase 1, also known as KIZ, is a protein kinase with two amino-terminal LIM motifs that induces stabilization of F-actin structures in transfected cells. Dominant-negative LIM-kinasel inhibits the accumulation of the F-actin. Phosphorylation experiments in vivo and in vitro provide evidence that cofilin is a physiological substrate of LIM-kinase 1. Phosphorylation by LIM-kinase 1 inactivates cofilin, leading to accumulation of actin filaments. Constitutively active Rac augmented cofilin phosphorylation and LIM-kinase 1 autophosphorylation whereas phorbol ester inhibited these processes. Our results define a mechanism for the regulation of cofilin and hence of actin dynamics in vivo. By modulating the stability of actin cytoskeletal structures, this pathway should play a central role in regulating cell motility and morphogenesis.


Asunto(s)
Actinas/metabolismo , Proteínas de Unión al ADN/metabolismo , Proteínas de Microfilamentos/metabolismo , Proteínas Serina-Treonina Quinasas/metabolismo , Células 3T3 , Factores Despolimerizantes de la Actina , Animales , Línea Celular , Movimiento Celular , Citoesqueleto/metabolismo , Proteínas de Unión al GTP/metabolismo , Quinasas Lim , Ratones , Proteínas de Microfilamentos/genética , Neuronas/metabolismo , Células PC12 , Fosforilación , Proteínas Quinasas , Ratas , Transducción de Señal , Acetato de Tetradecanoilforbol/farmacología , Transfección
18.
Essays Biochem ; 33: 53-64, 1998.
Artículo en Inglés | MEDLINE | ID: mdl-10488441

RESUMEN

Specificity of connectivity is essential to nervous system function. It is determined by intrinsic programmes of gene expression that define neuronal phenotypes, and by activity-dependent mechanisms. Neuro-regeneration in the adult may involve re-activation of growth programmes within the constraints of neuron-type specific phenotypes. Lesion-induced re-induction of an axonal growth mode in adult neurons correlates with a vigorous cell body reaction that can also lead to apoptotic cell death. Directing the cell body reaction towards regeneration is a major goal towards improving regeneration. Extrinsic factors that prevent axonal regeneration in the adult CNS of higher vertebrates include inhibitory components on the surface of oligodendrocytes and CNS myelin, and proteoglycans associated with scar material; grafts of certain glial cells can promote regeneration. Local nerve sprouting and synaptic plasticity can produce dramatic functional adaptation to lesions in the adult and greatly enhance the impact of the partial regeneration of lesioned axons; nerve sprouting is promoted by diffusible and contact-mediated extrinsic mechanisms, and by intrinsic neuronal components. As a result of recent discoveries, significant progress in promoting axonal regeneration and recovery of function in the adult can be anticipated.


Asunto(s)
Regeneración Nerviosa/fisiología , Adaptación Fisiológica , Adulto , Animales , Axones/fisiología , Axotomía , Humanos , Plasticidad Neuronal/fisiología
19.
Exp Cell Res ; 236(1): 103-16, 1997 Oct 10.
Artículo en Inglés | MEDLINE | ID: mdl-9344590

RESUMEN

Local regulation of the cortical cytoskeleton controls cell surface dynamics. GAP-43 and MARCKS are two abundant cytosolic protein kinase C substrates that are anchored to the cell membrane via acyl groups and interact with the cortical cytoskeleton. Each of them has been implicated in several forms of motility involving the cell surface. Although their primary sequences do not reveal significant homologies, GAP-43, MARCKS, and the cortical cytoskeleton-associated protein CAP-23 (in the following, the three proteins will be abbreviated as GMC) share a number of characteristic biochemical and biophysical properties and an unusual amino acid composition. In this study we determined whether GMC may be related functionally. In double-labeling immunocytochemistry experiments GMC accumulated at unique surface-associated structures, where they codistributed. In transfected cells GMC induced the same range of characteristic changes in cell morphology and cell surface activities, including prominent blebs and filopodia. These activities correlated with local accumulation of transgene and had characteristic features of locally elevated actin dynamics, including loss of stress fiber structures, accumulation of beta-(cytosolic) actin at cell surface protrusions, and dynamic blebbing activity. Analysis of appropriate deletion and fusion constructs revealed that the surface accumulation pattern and cell surface activities were correlated and that minimal structural requirements included acylation-mediated targeting to the cell membrane and the presence of a predominantly GMC-type sequence composition. Based on these experiments and on the results of previous studies on GAP-43, MARCKS, and CAP-23, we propose that GMC may define a class of functionally related proteins whose local accumulation promotes actin dynamics and the formation of dynamic structures at the cell periphery. Superimposed on these general properties, differences in the regulation of membrane association and binding properties of effector domains would confer individual properties to each of these proteins.


Asunto(s)
Antígenos de Superficie/metabolismo , Proteínas de Unión a Calmodulina , Proteínas del Citoesqueleto/metabolismo , Proteína GAP-43/metabolismo , Péptidos y Proteínas de Señalización Intracelular , Proteínas de la Membrana , Proteínas del Tejido Nervioso , Proteínas/metabolismo , Células 3T3/química , Células 3T3/enzimología , Células 3T3/ultraestructura , Actinas/metabolismo , Animales , Antígenos de Superficie/análisis , Antígenos de Superficie/genética , Células COS/química , Células COS/enzimología , Células COS/ultraestructura , Tamaño de la Célula , Embrión de Pollo , Proteínas del Citoesqueleto/análisis , Proteínas del Citoesqueleto/genética , Citoesqueleto/metabolismo , Proteína GAP-43/análisis , Proteína GAP-43/genética , Ganglios Espinales/citología , Dosificación de Gen , Ratones , Microscopía Electrónica , Sustrato de la Proteína Quinasa C Rico en Alanina Miristoilada , Proteína Quinasa C/análisis , Proteína Quinasa C/genética , Proteína Quinasa C/metabolismo , Proteínas/análisis , Proteínas/genética , Proteínas Recombinantes , Transfección
20.
Bioessays ; 19(9): 767-75, 1997 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-9297967

RESUMEN

Nerve processes elongate, branch and form synaptic contacts in a highly regulated and specific manner. Long-distance axon elongation is restricted to the main phase of axon formation during development, but can be reinduced upon lesions in the adult (regeneration). It correlates with the expression of defined genes, including proteins involved in signalling (e.g. src, NCAM, integrins), transcription factors (e.g. c-jun) and structural proteins (e.g. actin and tubulin isoforms). Activation of an exon elongation program may require bcl-2. The formation and growth of local branches (sprouting) is controlled by mechanisms in the target region. In addition, the expression of growth-associated proteins such as GAP-43 and CAP-23 in neurons lowers the threshold for nerve sprouting and potentiates its vigour. Recent studies suggest that nerve sprouting and long-distance elongation depend on the expression of different intrinsic components in neurons. One implication of these findings is that the differential expression of genes facilitating local branching may affect structural plasticity in the intact adult nervous system.


Asunto(s)
Axones , Moléculas de Adhesión Celular Neuronal , Proteínas del Tejido Nervioso/fisiología , Plasticidad Neuronal , Neuronas , Animales , Axones/fisiología , Axones/ultraestructura , Humanos , Neuronas/citología , Neuronas/fisiología , Transducción de Señal
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