RESUMEN
Phosphatidylinositol 4-kinase IIα (PI4KIIα) generates essential phospholipids and is a cargo for endosomal adaptor proteins. Activity-dependent bulk endocytosis (ADBE) is the dominant synaptic vesicle endocytosis mode during high neuronal activity and is sustained by glycogen synthase kinase 3ß (GSK3ß) activity. We reveal the GSK3ß substrate PI4KIIα is essential for ADBE via its depletion in primary neuronal cultures. Kinase-dead PI4KIIα rescues ADBE in these neurons but not a phosphomimetic form mutated at the GSK3ß site, Ser-47. Ser-47 phosphomimetic peptides inhibit ADBE in a dominant-negative manner, confirming that Ser-47 phosphorylation is essential for ADBE. Phosphomimetic PI4KIIα interacts with a specific cohort of presynaptic molecules, two of which, AGAP2 and CAMKV, are also essential for ADBE when depleted in neurons. Thus, PI4KIIα is a GSK3ß-dependent interaction hub that silos essential ADBE molecules for liberation during neuronal activity.
Asunto(s)
1-Fosfatidilinositol 4-Quinasa , Glucógeno Sintasa Quinasa 3 , Ratas , Animales , Humanos , 1-Fosfatidilinositol 4-Quinasa/metabolismo , Glucógeno Sintasa Quinasa 3 beta/metabolismo , Glucógeno Sintasa Quinasa 3/metabolismo , Ratas Sprague-Dawley , Vesículas Sinápticas/metabolismo , Endocitosis/fisiología , FosforilaciónRESUMEN
BACKGROUND: Activity-dependent bulk endocytosis (ADBE) is the dominant mode of synaptic vesicle (SV) endocytosis during intense neuronal activity, implicating it as a major contributor to presynaptic plasticity under these stimulation conditions. However methods to monitor this endocytosis mode have been limited to either morphological or optical observation of the uptake of large fluid phase markers. NEW METHOD: We present here a method to monitor ADBE using the genetically-encoded reporter VAMP4-pHluorin in primary neuronal cultures. RESULTS: Individual nerve terminals expressing VAMP4-pHluorin display either an increase or decrease in fluorescence after stimulation terminates. The decrease in fluorescence reflects the slow acidification of large bulk endosomes to which VAMP4-pHluorin is selectively recruited. Use of VAMP4-pHluorin during sequential high frequency stimuli revealed that all nerve terminals perform ADBE, but not all do so in response to a single stimulus. VAMP4-pHluorin also displays a rapid activity-dependent decrease in fluorescence during high frequency stimulation, a response which is particularly prominent when expressed in hippocampal neurons. The molecular mechanism responsible for this decrease is still unclear, but is not due to loss of VAMP4-pHluorin from the nerve terminal. COMPARISON WITH EXISTING METHODS: This method allows the selective reporting of ADBE for the first time, when compared to previous approaches using markers of fluid phase uptake. CONCLUSIONS: The development of VAMP4-pHluorin as a selective genetically-encoded reporter of ADBE increases the palette of approaches used to monitor this endocytosis mode both in vitro and in vivo.
Asunto(s)
Endocitosis/fisiología , Proteínas Fluorescentes Verdes/metabolismo , Microscopía Fluorescente , Proteínas R-SNARE/metabolismo , Vesículas Sinápticas/fisiología , Animales , Células Cultivadas , Cerebelo/citología , Cerebelo/fisiología , Femenino , Proteínas Fluorescentes Verdes/genética , Hipocampo/citología , Hipocampo/fisiología , Masculino , Ratones Endogámicos C57BL , Microscopía Fluorescente/métodos , Neuronas/citología , Neuronas/fisiología , Proteínas R-SNARE/genética , Ratas Sprague-Dawley , Transmisión Sináptica/fisiología , Sinaptofisina/genética , Sinaptofisina/metabolismo , TransfecciónRESUMEN
The efficient retrieval of synaptic vesicle membrane and cargo in central nerve terminals is dependent on the efficient recruitment of a series of endocytosis modes by different patterns of neuronal activity. During intense neuronal activity the dominant endocytosis mode is activity-dependent endocytosis (ADBE). Triggering of ADBE is linked to calcineurin-mediated dynamin I dephosphorylation since the same stimulation intensities trigger both. Dynamin I dephosphorylation is maximised by a simultaneous inhibition of its kinase glycogen synthase kinase 3 (GSK3) by the protein kinase Akt, however it is unknown how increased neuronal activity is transduced into Akt activation. To address this question we determined how the activity-dependent increases in intracellular free calcium ([Ca(2+)]i) control activation of Akt. This was achieved using either trains of high frequency action potentials to evoke localised [Ca(2+)]i increases at active zones, or a calcium ionophore to raise [Ca(2+)]i uniformly across the nerve terminal. Through the use of either non-specific calcium channel antagonists or intracellular calcium chelators we found that Akt phosphorylation (and subsequent GSK3 phosphorylation) was dependent on localised [Ca(2+)]i increases at the active zone. In an attempt to determine mechanism, we antagonised either phosphatidylinositol 3-kinase (PI3K) or calmodulin. Activity-dependent phosphorylation of both Akt and GSK3 was arrested on inhibition of PI3K, but not calmodulin. Thus localised calcium influx in central nerve terminals activates PI3K via an unknown calcium sensor to trigger the activity-dependent phosphorylation of Akt and GSK3.
Asunto(s)
Calcio/metabolismo , Neuronas/metabolismo , Fosfatidilinositol 3-Quinasa/metabolismo , Terminales Presinápticos/metabolismo , Proteínas Proto-Oncogénicas c-akt/metabolismo , Potenciales de Acción , Animales , Bloqueadores de los Canales de Calcio/farmacología , Quelantes del Calcio/farmacología , Ionóforos de Calcio/farmacología , Calmodulina/antagonistas & inhibidores , Células Cultivadas , Cerebelo/citología , Activación Enzimática , Femenino , Glucógeno Sintasa Quinasa 3/metabolismo , Masculino , Inhibidores de las Quinasa Fosfoinosítidos-3 , Fosforilación , Ratas Sprague-DawleyRESUMEN
The accurate formation of synaptic vesicles (SVs) and incorporation of their protein cargo during endocytosis is critical for the maintenance of neurotransmission. During intense neuronal activity, a transient and acute accumulation of SV cargo occurs at the plasma membrane. Activity-dependent bulk endocytosis (ADBE) is the dominant SV endocytosis mode under these conditions; however, it is currently unknown how ADBE mediates cargo retrieval. We examined the retrieval of different SV cargo molecules during intense stimulation using a series of genetically encoded pH-sensitive reporters in neuronal cultures. The retrieval of only one reporter, VAMP4-pHluorin, was perturbed by inhibiting ADBE. This selective recovery was confirmed by the enrichment of endogenous VAMP4 in purified bulk endosomes formed by ADBE. VAMP4 was also essential for ADBE, with a cytoplasmic di-leucine motif being critical for this role. Therefore, VAMP4 is the first identified ADBE cargo and is essential for this endocytosis mode to proceed.