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Andrea Volterra

Researcher at University of Lausanne

Publications -  106
Citations -  17081

Andrea Volterra is an academic researcher from University of Lausanne. The author has contributed to research in topics: Glutamate receptor & Astrocyte. The author has an hindex of 50, co-authored 105 publications receiving 15050 citations. Previous affiliations of Andrea Volterra include Columbia University & University of Milan.

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Astrocytes, from brain glue to communication elements: the revolution continues.

TL;DR: The recent recognition that astrocytes are organized in separate territories and possess active properties — notably a competence for the regulated release of 'gliotransmitters', including glutamate — has enabled us to develop an understanding of previously unknown functions for astroCytes.
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Prostaglandins stimulate calcium-dependent glutamate release in astrocytes.

TL;DR: It is shown that coactivation of the AMPA/kainate and metabotropic glutamate receptors (mGluRs) on astrocytes stimulates these cells to release glutamate through a Ca2+-dependent process mediated by prostaglandins, revealing a new pathway of regulated transmitter release from astroCytes and outlining the existence of an integrated glutamatergic cross-talk between neurons and astroicytes in situ.
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CXCR4-activated astrocyte glutamate release via TNFalpha: amplification by microglia triggers neurotoxicity.

TL;DR: It is demonstrated that altered glial communication has direct neuropathological consequences and that agents interfering with CXCR4-dependent astrocyte–microglia signaling prevent neuronal apoptosis induced by the HIV-1 coat glycoprotein, gp120IIIB.
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Gliotransmitters Travel in Time and Space

TL;DR: It is proposed that astrocytes mainly signal through high-affinity slowly desensitizing receptors to modulate neurons and perform integration in spatiotemporal domains complementary to those of neurons.
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Reactive astrocyte nomenclature, definitions, and future directions

Carole Escartin, +88 more
- 15 Feb 2021 - 
TL;DR: In this article, the authors point out the shortcomings of binary divisions of reactive astrocytes into good-vs-bad, neurotoxic vs-neuroprotective or A1-vs.A2.