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Nature

Resumen/Descripción – provisto por la editorial en inglés
Nature is a weekly international journal publishing the finest peer-reviewed research in all fields of science and technology on the basis of its originality, importance, interdisciplinary interest, timeliness, accessibility, elegance and surprising conclusions. Nature also provides rapid, authoritative, insightful and arresting news and interpretation of topical and coming trends affecting science, scientists and the wider public.
Palabras clave – provistas por la editorial

No disponibles.

Disponibilidad
Institución detectada Período Navegá Descargá Solicitá
No detectada desde jul. 2012 / hasta dic. 2023 Nature.com
No detectada desde jul. 2006 / hasta ago. 2012 Ovid

Información

Tipo de recurso:

revistas

ISSN impreso

0028-0836

ISSN electrónico

1476-4687

Editor responsable

Springer Nature

País de edición

Reino Unido

Fecha de publicación

Tabla de contenidos

Concern at Cochrane: evidence giant battles funding cuts and closures

Helen Pearson

Palabras clave: Multidisciplinary.

Pp. No disponible

How would room-temperature superconductors change science?

Davide Castelvecchi

Palabras clave: Multidisciplinary.

Pp. No disponible

Author Correction: Women are credited less in science than men

Matthew B. Ross; Britta M. GlennonORCID; Raviv Murciano-GoroffORCID; Enrico G. BerkesORCID; Bruce A. WeinbergORCID; Julia I. LaneORCID

Palabras clave: Multidisciplinary.

Pp. No disponible

Surprising reaction pathway observed in lithium–sulfur batteries

Palabras clave: Multidisciplinary.

Pp. No disponible

An ‘alien meteorite’ probably didn’t slam into Earth — how will we know if one does?

Alexandra Witze

Palabras clave: Multidisciplinary.

Pp. No disponible

How to supercharge T cells against cancer

Nick Petrić Howe

Palabras clave: Multidisciplinary.

Pp. No disponible

Specialized astrocytes mediate glutamatergic gliotransmission in the CNS

Roberta de CegliaORCID; Ada Ledonne; David Gregory LitvinORCID; Barbara Lykke Lind; Giovanni Carriero; Emanuele Claudio Latagliata; Erika Bindocci; Maria Amalia Di Castro; Iaroslav Savtchouk; Ilaria VitaliORCID; Anurag Ranjak; Mauro CongiuORCID; Tara Canonica; William WisdenORCID; Kenneth HarrisORCID; Manuel MameliORCID; Nicola MercuriORCID; Ludovic TelleyORCID; Andrea VolterraORCID

<jats:title>Abstract</jats:title><jats:p>Multimodal astrocyte–neuron communications govern brain circuitry assembly and function<jats:sup>1</jats:sup>. For example, through rapid glutamate release, astrocytes can control excitability, plasticity and synchronous activity<jats:sup>2,3</jats:sup> of synaptic networks, while also contributing to their dysregulation in neuropsychiatric conditions<jats:sup>4–7</jats:sup>. For astrocytes to communicate through fast focal glutamate release, they should possess an apparatus for Ca<jats:sup>2+</jats:sup>-dependent exocytosis similar to neurons<jats:sup>8–10</jats:sup>. However, the existence of this mechanism has been questioned<jats:sup>11–13</jats:sup> owing to inconsistent data<jats:sup>14–17</jats:sup> and a lack of direct supporting evidence. Here we revisited the astrocyte glutamate exocytosis hypothesis by considering the emerging molecular heterogeneity of astrocytes<jats:sup>18–21</jats:sup> and using molecular, bioinformatic and imaging approaches, together with cell-specific genetic tools that interfere with glutamate exocytosis in vivo. By analysing existing single-cell RNA-sequencing databases and our patch-seq data, we identified nine molecularly distinct clusters of hippocampal astrocytes, among which we found a notable subpopulation that selectively expressed synaptic-like glutamate-release machinery and localized to discrete hippocampal sites. Using GluSnFR-based glutamate imaging<jats:sup>22</jats:sup> in situ and in vivo, we identified a corresponding astrocyte subgroup that responds reliably to astrocyte-selective stimulations with subsecond glutamate release events at spatially precise hotspots, which were suppressed by astrocyte-targeted deletion of vesicular glutamate transporter 1 (VGLUT1). Furthermore, deletion of this transporter or its isoform VGLUT2 revealed specific contributions of glutamatergic astrocytes in cortico-hippocampal and nigrostriatal circuits during normal behaviour and pathological processes. By uncovering this atypical subpopulation of specialized astrocytes in the adult brain, we provide insights into the complex roles of astrocytes in central nervous system (CNS) physiology and diseases, and identify a potential therapeutic target.</jats:p>

Palabras clave: Multidisciplinary.

Pp. No disponible

Hydrogen-bond-acceptor ligands enable distal C(sp3)–H arylation of free alcohols

Daniel A. StrassfeldORCID; Chia-Yu ChenORCID; Han Seul Park; D. Quang PhanORCID; Jin-Quan YuORCID

Palabras clave: Multidisciplinary.

Pp. No disponible

Dynamic regulation of messenger RNA structure controls translation

Yizhu LinORCID; Stephen N. FloorORCID

Palabras clave: Multidisciplinary.

Pp. No disponible

Thymic mimetic cells function beyond self-tolerance

Tal Givony; Dena LeshkowitzORCID; Diana Del CastilloORCID; Shir Nevo; Noam KadouriORCID; Bareket Dassa; Yael Gruper; Razi Khalaila; Osher Ben-Nun; Tom GomeORCID; Jan DobešORCID; Shifra Ben-DorORCID; Merav Kedmi; Hadas Keren-Shaul; Rebecca Heffner-Krausz; Ziv PoratORCID; Ofra GolaniORCID; Yoseph AddadiORCID; Ori Brenner; David D. LoORCID; Yael Goldfarb; Jakub AbramsonORCID

Palabras clave: Multidisciplinary.

Pp. No disponible