RESUMO
Facilitation and inactivation of P/Q-type Ca2+ currents mediated by Ca2+/calmodulin binding to Ca(V)2.1 channels contribute to facilitation and rapid depression of synaptic transmission, respectively. Other calcium sensor proteins displace calmodulin from its binding site and differentially modulate P/Q-type Ca2 + currents, resulting in diverse patterns of short-term synaptic plasticity. Neuronal calcium sensor-1 (NCS-1, frequenin) has been shown to enhance synaptic facilitation, but the underlying mechanism is unclear. We report here that NCS-1 directly interacts with IQ-like motif and calmodulin-binding domain in the C-terminal domain of Ca(V)2.1 channel. NCS-1 reduces Ca2 +-dependent inactivation of P/Q-type Ca2+ current through interaction with the IQ-like motif and calmodulin-binding domain without affecting peak current or activation kinetics. Expression of NCS-1 in presynaptic superior cervical ganglion neurons has no effect on synaptic transmission, eliminating effects of this calcium sensor protein on endogenous N-type Ca2+ currents and the endogenous neurotransmitter release machinery. However, in superior cervical ganglion neurons expressing wild-type Ca(V)2.1 channels, co-expression of NCS-1 induces facilitation of synaptic transmission in response to paired pulses and trains of depolarizing stimuli, and this effect is lost in Ca(V)2.1 channels with mutations in the IQ-like motif and calmodulin-binding domain. These results reveal that NCS-1 directly modulates Ca(V)2.1 channels to induce short-term synaptic facilitation and further demonstrate that CaS proteins are crucial in fine-tuning short-term synaptic plasticity.
Assuntos
Canais de Cálcio Tipo N/metabolismo , Proteínas Sensoras de Cálcio Neuronal/metabolismo , Neuropeptídeos/metabolismo , Sinapses/metabolismo , Transmissão Sináptica , Motivos de Aminoácidos , Animais , Sítios de Ligação , Canais de Cálcio Tipo N/química , Células Cultivadas , Células HEK293 , Humanos , Camundongos , Proteínas Sensoras de Cálcio Neuronal/genética , Neuropeptídeos/genética , Ligação Proteica , Ratos , Gânglio Cervical Superior/citologia , Gânglio Cervical Superior/metabolismo , Gânglio Cervical Superior/fisiologia , Sinapses/fisiologiaRESUMO
Modulation of P/Q-type Ca(2+) currents through presynaptic voltage-gated calcium channels (Ca(V)2.1) by binding of Ca(2+)/calmodulin contributes to short-term synaptic plasticity. Ca(2+)-binding protein-1 (CaBP1) and Visinin-like protein-2 (VILIP-2) are neurospecific calmodulin-like Ca(2+) sensor proteins that differentially modulate Ca(V)2.1 channels, but how they contribute to short-term synaptic plasticity is unknown. Here, we show that activity-dependent modulation of presynaptic Ca(V)2.1 channels by CaBP1 and VILIP-2 has opposing effects on short-term synaptic plasticity in superior cervical ganglion neurons. Expression of CaBP1, which blocks Ca(2+)-dependent facilitation of P/Q-type Ca(2+) current, markedly reduced facilitation of synaptic transmission. VILIP-2, which blocks Ca(2+)-dependent inactivation of P/Q-type Ca(2+) current, reduced synaptic depression and increased facilitation under conditions of high release probability. These results demonstrate that activity-dependent regulation of presynaptic Ca(V)2.1 channels by differentially expressed Ca(2+) sensor proteins can fine-tune synaptic responses to trains of action potentials and thereby contribute to the diversity of short-term synaptic plasticity.
Assuntos
Canais de Cálcio Tipo N/metabolismo , Calmodulina/metabolismo , Plasticidade Neuronal/fisiologia , Sinapses/fisiologia , Transmissão Sináptica/fisiologia , Análise de Variância , Humanos , Técnicas de Patch-Clamp , Terminações Pré-Sinápticas/metabolismoRESUMO
Voltage-gated Ca(2+) channels in presynaptic nerve terminals initiate neurotransmitter release in response to depolarization by action potentials from the nerve axon. The strength of synaptic transmission is dependent on the third to fourth power of Ca(2+) entry, placing the Ca(2+) channels in a unique position for regulation of synaptic strength. Short-term synaptic plasticity regulates the strength of neurotransmission through facilitation and depression on the millisecond time scale and plays a key role in encoding information in the nervous system. Ca(V)2.1 channels are the major source of Ca(2+) entry for neurotransmission in the central nervous system. They are tightly regulated by Ca(2+), calmodulin, and related Ca(2+) sensor proteins, which cause facilitation and inactivation of channel activity. Emerging evidence reviewed here points to this mode of regulation of Ca(V)2.1 channels as a major contributor to short-term synaptic plasticity of neurotransmission and its diversity among synapses.
Assuntos
Canais de Cálcio Tipo N/metabolismo , Cálcio/metabolismo , Proteínas do Tecido Nervoso/metabolismo , Plasticidade Neuronal/fisiologia , Sinapses/genética , Transmissão Sináptica/fisiologia , Animais , Canais de Cálcio Tipo N/genética , Calmodulina/metabolismo , HumanosRESUMO
Alzheimer's disease (AD) drug discovery has focused on a set of highly studied therapeutic hypotheses, with limited success. The heterogeneous nature of AD processes suggests that a more diverse, systems-integrated strategy may identify new therapeutic hypotheses. Although many target hypotheses have arisen from systems-level modeling of human disease, in practice and for many reasons, it has proven challenging to translate them into drug discovery pipelines. First, many hypotheses implicate protein targets and/or biological mechanisms that are under-studied, meaning there is a paucity of evidence to inform experimental strategies as well as high-quality reagents to perform them. Second, systems-level targets are predicted to act in concert, requiring adaptations in how we characterize new drug targets. Here we posit that the development and open distribution of high-quality experimental reagents and informatic outputs-termed target enabling packages (TEPs)-will catalyze rapid evaluation of emerging systems-integrated targets in AD by enabling parallel, independent, and unencumbered research.
RESUMO
Regulation of synaptic transmission by modulation of the calcium influx that triggers transmitter release underlies different forms of synaptic plasticity, and thus could contribute to learning. In the mollusk Aplysia, the neuromodulator serotonin (5-HT) increases evoked transmitter release from sensory neurons and thereby contributes to dishabituation and sensitization of defensive reflexes. We combined electrophysiological recording with fluorescence measurements of intracellular calcium in sensory neuron synapses in culture to test whether direct up-modulation by 5-HT of calcium influx triggered by single action potentials contributes to facilitation of transmitter release. We observe increases in a previously undescribed calcium influx that are strongly correlated with increases in the amplitude of the evoked postsynaptic potentials and which cannot be accounted for by action potential prolongation. Our results suggest that direct modulation of a presynaptic calcium conductance that controls neurotransmitter release contributes to the presynaptic facilitation that underlies a simple form of learning.
Assuntos
Aplysia/fisiologia , Cálcio/metabolismo , Células Receptoras Sensoriais/fisiologia , Sinapses/metabolismo , Transmissão Sináptica/fisiologia , Potenciais de Ação/fisiologia , Animais , Bloqueadores dos Canais de Cálcio/metabolismo , Células Cultivadas , Eletrofisiologia , Nitrendipino/metabolismo , Células Receptoras Sensoriais/citologia , Serotonina/metabolismo , Potenciais Sinápticos/fisiologiaRESUMO
Protein kinase Cs (PKCs) are important effectors of synaptic plasticity. In Aplysia, there are two major phorbol ester-activated PKCs, Ca2+-activated PKC Apl I and Ca2+-independent PKC Apl II. Functional Apl II, but not Apl I, in sensory neurons is required for a form of short-term facilitation induced at sensorimotor synapses by the facilitatory transmitter serotonin (5-HT). Because PKCs are activated by translocating from the cytoplasm to the membrane, we used fluorescently tagged PKCs to determine the isoform and cell-type specificity of translocation in living Aplysia neurons. In Sf9 cells, low levels of diacylglycerol translocate Apl II, but not Apl I, which requires calcium for translocation at low concentrations of diacylglycerol. Accordingly, application of 5-HT to Aplysia sensory neurons in the absence of neuronal firing translocates Apl II, but not Apl I, consistent with the role of Apl II in short-term facilitation. This translocation is observed in sensory neurons, but not in motor neurons. Apl I translocates only if 5-HT is coupled to firing in the sensory neuron; firing alone is ineffective. Because combined 5-HT and firing are required for the induction of one type of intermediate-term facilitation at these synapses, we asked whether this form of synaptic plasticity involves activation of Apl I. We report here that dominant-negative Apl I, but not Apl II, blocks intermediate-term facilitation. Thus, different isoforms of PKC translocate under different conditions to mediate distinct types of synaptic plasticity: Ca2+-independent Apl II is involved in short-term facilitation, and Ca2+-dependent Apl I contributes to intermediate-term facilitation.
Assuntos
Aplysia/fisiologia , Cálcio/metabolismo , Neurônios Aferentes/fisiologia , Proteína Quinase C/metabolismo , Proteína Quinase C/fisiologia , Transmissão Sináptica/fisiologia , Potenciais de Ação/fisiologia , Animais , Transporte Biológico/efeitos dos fármacos , Membrana Celular/metabolismo , Citoplasma/metabolismo , Diglicerídeos/farmacologia , Genes Dominantes , Membranas Intracelulares/metabolismo , Isoenzimas/metabolismo , Isoenzimas/fisiologia , Plasticidade Neuronal/fisiologia , Neurônios Aferentes/enzimologia , Proteína Quinase C/genética , Serotonina/farmacologia , Sinapses/fisiologiaRESUMO
Many factors influence the long-term functional and esthetic success of implant-supported restorations. This article reviews recent findings related to several of these factors, including the implant-abutment junction, bacterial adhesion to implant surfaces, and the esthetic and functional consequences of implant and abutment material choices, particularly titanium-nitride-coated abutments. Restoration of a failed maxillary central incisor using a platformswitched implant and titanium-nitride-coated abutment is presented.
Assuntos
Dente Suporte , Implantes Dentários , Maxila/cirurgia , Estética Dentária , HumanosRESUMO
Modulation of voltage-gated Ca(2+) channels controls activities of excitable cells. We show that high-voltage activated Ca(2+) channels are regulated by membrane phosphatidylinositol 4,5-bisphosphate (PIP(2)) with different sensitivities. Plasma membrane PIP(2) depletion by rapamycin-induced translocation of an inositol lipid 5-phosphatase or by a voltage-sensitive 5-phosphatase (VSP) suppresses Ca(V)1.2 and Ca(V)1.3 channel currents by approximately 35% and Ca(V)2.1 and Ca(V)2.2 currents by 29% and 55%, respectively. Other Ca(V) channels are less sensitive. Inhibition is not relieved by strong depolarizing prepulses. It changes the voltage dependence of channel gating little. Recovery of currents from inhibition needs intracellular hydrolysable ATP, presumably for PIP(2) resynthesis. When PIP(2) is increased by overexpressing PIP 5-kinase, activation and inactivation of Ca(V)2.2 current slow and voltage-dependent gating shifts to slightly higher voltages. Thus, endogenous membrane PIP(2) supports high-voltage activated L-, N-, and P/Q-type Ca(2+) channels, and stimuli that activate phospholipase C deplete PIP(2) and reduce those Ca(2+) channel currents.
Assuntos
Canais de Cálcio Tipo L/fisiologia , Ativação do Canal Iônico/fisiologia , Fosfatidilinositol 4,5-Difosfato/metabolismo , Trifosfato de Adenosina/análogos & derivados , Trifosfato de Adenosina/metabolismo , Trifosfato de Adenosina/farmacologia , Bário/farmacologia , Biofísica , Cálcio/metabolismo , Canais de Cálcio Tipo L/genética , Linhagem Celular Transformada , Quelantes/farmacologia , Ácido Egtázico/análogos & derivados , Ácido Egtázico/farmacologia , Estimulação Elétrica/métodos , Transferência Ressonante de Energia de Fluorescência/métodos , Proteínas de Fluorescência Verde/genética , Humanos , Imunossupressores/farmacologia , Ativação do Canal Iônico/efeitos dos fármacos , Ativação do Canal Iônico/genética , Potenciais da Membrana/efeitos dos fármacos , Potenciais da Membrana/genética , Agonistas Muscarínicos/farmacologia , Oxotremorina/farmacologia , Técnicas de Patch-Clamp/métodos , Monoéster Fosfórico Hidrolases/genética , Monoéster Fosfórico Hidrolases/farmacologia , Sirolimo/farmacologia , Fatores de Tempo , TransfecçãoRESUMO
En los estudios sobre el trabajo de reproducción social se ha enfatizado su carácter de trabajo invisible. No obstante, las trabajadoras del hogar y del cuidado asalariadas en Cataluña han decidido conformar un sindicato para promover su visibilidad y defender sus derechos. En este artículo me propongo una aproximación a la construcción de subjetividad de las trabajadoras del hogar inmigrantes sindicalizadas, a través de cuatro narrativas realizadas en la ciudad de Barcelona. En la coproducción de estos textos discuto sobre la valoración y significados del trabajo del hogar, la participación de las activistas en el sindicato y las posibles transformaciones que puede implicar estar organizadas. Con ello, se establece una comprensión situada de las trayectorias y los procesos subjetivos de las trabajadoras del hogar y el cuidado articuladas en una acción colectiva como es el sindicato.
In studies of the work for social reproduction has been emphasized its character of invisible work. However, domestic and care workers employed in Catalonia have decided to form a union to promote their visibility and defend their rights. In this article I propose an approach to the construction of subjectivity of migrant household workers unionized, through four narratives held in the city of Barcelona. Through the co-production of the setexts I discussi on the assessment and meanings of domestic work, the participation of activists in the union and possible changes that may involve being organized. Thus, is established a situated understanding of trajectories and subjective processes of domestic and care workers, articulated in collective action as is the union.