Evidence map›Paper›PMID 21292765›Full record

ArticleThe Journal of biological chemistry2011

P2X7 receptors trigger ATP exocytosis and modify secretory vesicle dynamics in neuroblastoma cells.

Yolanda Gutiérrez-Martín, Diego Bustillo, Rosa Gómez-Villafuertes, Jesús Sánchez-Nogueiro, Cristina Torregrosa-Hetland, Thomas Binz, Luis Miguel Gutiérrez, María Teresa Miras-Portugal, Antonio R Artalejo

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.3field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
  2. Article
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  4. Alpha synuclein modulates mitochondrial CaNPJ Parkinson's disease · 2023
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  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. NeuroinflammatoryFrontiers in pharmacology · 2021
    Review
  14. Review
  15. Review
  16. Article
  17. Inflammation-induced upregulation of P2XAmerican journal of physiology. Lung cellular and molecular physiology · 2019
    Article
  18. Article
  19. Article
  20. Neuronal P2X7 Receptor: Involvement in Neuronal Physiology and Pathology.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 3 countries.

Yolanda Gutiérrez-MartínDepartamento de Toxicología y Farmacología, Universidad Complutense de Madrid, Madrid, Spain.
Diego Bustillo
Rosa Gómez-Villafuertes
Jesús Sánchez-Nogueiro
Cristina Torregrosa-Hetland
Thomas Binz
Luis Miguel Gutiérrez
María Teresa Miras-Portugal
Antonio R Artalejo
Universidad Complutense de Madrid · ESConsejo Superior de Investigaciones Científicas · ESIstituto di Farmacologia Traslazionale · ITMedizinische Hochschule Hannover · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previously, we reported that purinergic ionotropic P2X7 receptors negatively regulate neurite formation in Neuro-2a (N2a) mouse neuroblastoma cells through a Ca(2+)/calmodulin-dependent kinase II-related mechanism. In the present study we used this cell line to investigate a parallel though faster P2X7 receptor-mediated signaling pathway, namely Ca(2+)-regulated exocytosis. Selective activation of P2X7 receptors evoked exocytosis as assayed by high resolution membrane capacitance measurements. Using dual-wavelength total internal reflection microscopy, we have observed both the increase in near-membrane Ca(2+) concentration and the exocytosis of fluorescently labeled vesicles in response to P2X7 receptor stimulation. Moreover, activation of P2X7 receptors also affects vesicle motion in the vertical and horizontal directions, thus, involving this receptor type in the control of early steps (docking and priming) of the secretory pathway. Immunocytochemical and RT-PCR experiments evidenced that N2a cells express the three neuronal SNAREs as well as vesicular nucleotide and monoamine (VMAT-1 and VMAT-2) transporters. Biochemical measurements indicated that ionomycin induced a significant release of ATP from N2a cells. Finally, P2X7 receptor stimulation and ionomycin increased the incidence of small transient inward currents, reminiscent of postsynaptic quantal events observed at synapses. Small transient inward currents were dependent on extracellular Ca(2+) and were abolished by Brilliant Blue G, suggesting they were mediated by P2X7 receptors. Altogether, these results suggest the existence of a positive feedback mechanism mediated by P2X7 receptor-stimulated exocytotic release of ATP that would act on P2X7 receptors on the same or neighbor cells to further stimulate its own release and negatively control N2a cell differentiation.

Indexed as

Calcium SignalingExocytosisAdenosine TriphosphateAnimalsAutocrine CommunicationCalciumCell DifferentiationCell Line, TumorIonomycinIonophoresMiceNeoplasm ProteinsNeuroblastomaParacrine CommunicationReceptors, Purinergic P2X7Secretory VesiclesAdenosine TriphosphateCalciumIonomycinIonophoresNeoplasm ProteinsReceptors, Purinergic P2X7Slc18a1 protein, mouseSlc18a2 protein, mouseSNARE ProteinsVesicular Monoamine Transport Proteins

Identifiers

PMID21292765
PMCPMC3064193
OpenAlexW2027757316

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.