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Institución detectada Período Navegá Descargá Solicitá
No detectada desde mar. 1997 / hasta dic. 2023 Science Journals

Información

Tipo de recurso:

revistas

ISSN impreso

0036-8075

ISSN electrónico

1095-9203

Editor responsable

American Association for the Advancement of Science (AAAS)

País de edición

Estados Unidos

Fecha de publicación

Cobertura temática

Tabla de contenidos

The digital citizen Dignity in a Digital Age Ro Khanna Simon & Schuster, 2022. 368 pp. The Digital Republic Jamie Susskind Pegasus, 2022. 304 pp.

Michael Neblo; Avery White

<jats:p>Two new books advocate for technological agency</jats:p>

Palabras clave: Multidisciplinary.

Pp. 38-38

Bringing inanimate matter to life Transformer: The Deep Chemistry of Life and Death Nick Lane Norton, 2022. 400 pp.

Joseph Moran

<jats:p>A biochemist probes the origins and vital nature of the Krebs cycle</jats:p>

Palabras clave: Multidisciplinary.

Pp. 39-39

In Science Journals

Michael Funk (eds.)

<jats:p> Highlights from the <jats:italic>Science</jats:italic> family of journals </jats:p>

Palabras clave: Multidisciplinary.

Pp. 41-43

In Other Journals

Caroline Ash; Jesse Smith (eds.)

<jats:p>Editors’ selections from the current scientific literature</jats:p>

Palabras clave: Multidisciplinary.

Pp. 42-43

Zonated leucine sensing by Sestrin-mTORC1 in the liver controls the response to dietary leucine

Andrew L. CangelosiORCID; Anna M. PuszynskaORCID; Justin M. RobertsORCID; Andrea Armani; Thao P. Nguyen; Jessica B. SpinelliORCID; Tenzin KunchokORCID; Brianna WangORCID; Sze Ham ChanORCID; Caroline A. LewisORCID; William C. Comb; George W. BellORCID; Aharon HelmanORCID; David M. SabatiniORCID

<jats:p>The mechanistic target of rapamycin complex 1 (mTORC1) kinase controls growth in response to nutrients, including the amino acid leucine. In cultured cells, mTORC1 senses leucine through the leucine-binding Sestrin proteins, but the physiological functions and distribution of Sestrin-mediated leucine sensing in mammals are unknown. We find that mice lacking Sestrin1 and Sestrin2 cannot inhibit mTORC1 upon dietary leucine deprivation and suffer a rapid loss of white adipose tissue (WAT) and muscle. The WAT loss is driven by aberrant mTORC1 activity and fibroblast growth factor 21 (FGF21) production in the liver. Sestrin expression in the liver lobule is zonated, accounting for zone-specific regulation of mTORC1 activity and FGF21 induction by leucine. These results establish the mammalian Sestrins as physiological leucine sensors and reveal a spatial organization to nutrient sensing by the mTORC1 pathway.</jats:p>

Palabras clave: Multidisciplinary.

Pp. 47-56

Conservation and divergence of cortical cell organization in human and mouse revealed by MERFISH

Rongxin FangORCID; Chenglong XiaORCID; Jennie L. Close; Meng ZhangORCID; Jiang He; Zhengkai HuangORCID; Aaron R. HalpernORCID; Brian LongORCID; Jeremy A. MillerORCID; Ed S. LeinORCID; Xiaowei ZhuangORCID

<jats:p>The human cerebral cortex has tremendous cellular diversity. How different cell types are organized in the human cortex and how cellular organization varies across species remain unclear. In this study, we performed spatially resolved single-cell profiling of 4000 genes using multiplexed error-robust fluorescence in situ hybridization (MERFISH), identified more than 100 transcriptionally distinct cell populations, and generated a molecularly defined and spatially resolved cell atlas of the human middle and superior temporal gyrus. We further explored cell-cell interactions arising from soma contact or proximity in a cell type–specific manner. Comparison of the human and mouse cortices showed conservation in the laminar organization of cells and differences in somatic interactions across species. Our data revealed human-specific cell-cell proximity patterns and a markedly increased enrichment for interactions between neurons and non-neuronal cells in the human cortex.</jats:p>

Palabras clave: Multidisciplinary.

Pp. 56-62

A specific circuit in the midbrain detects stress and induces restorative sleep

Xiao YuORCID; Guangchao ZhaoORCID; Dan WangORCID; Sa Wang; Rui Li; Ao LiORCID; Huan Wang; Mathieu NolletORCID; You Young Chun; Tianyuan Zhao; Raquel Yustos; Huiming Li; Jianshuai Zhao; Jiannan LiORCID; Min CaiORCID; Alexei L. VyssotskiORCID; Yulong LiORCID; Hailong DongORCID; Nicholas P. FranksORCID; William WisdenORCID

<jats:p> In mice, social defeat stress (SDS), an ethological model for psychosocial stress, induces sleep. Such sleep could enable resilience, but how stress promotes sleep is unclear. Activity-dependent tagging revealed a subset of ventral tegmental area γ-aminobutyric acid (GABA)–somatostatin (VTA <jats:italic> <jats:sup>Vgat-Sst</jats:sup> </jats:italic> ) cells that sense stress and drive non–rapid eye movement (NREM) and REM sleep through the lateral hypothalamus and also inhibit corticotropin-releasing factor (CRF) release in the paraventricular hypothalamus. Transient stress enhances the activity of VTA <jats:italic> <jats:sup>Vgat-Sst</jats:sup> </jats:italic> cells for several hours, allowing them to exert their sleep effects persistently. Lesioning of VTA <jats:italic> <jats:sup>Vgat-Sst</jats:sup> </jats:italic> cells abolished SDS-induced sleep; without it, anxiety and corticosterone concentrations remained increased after stress. Thus, a specific circuit allows animals to restore mental and body functions by sleeping, potentially providing a refined route for treating anxiety disorders. </jats:p>

Palabras clave: Multidisciplinary.

Pp. 63-72

Ancient DNA reveals five streams of migration into Micronesia and matrilocality in early Pacific seafarers

Yue-Chen LiuORCID; Rosalind Hunter-AndersonORCID; Olivia CheronetORCID; Joanne Eakin; Frank CamachoORCID; Michael Pietrusewsky; Nadin Rohland; Alexander IoannidisORCID; J. Stephen AthensORCID; Michele Toomay DouglasORCID; Rona Michi Ikehara-Quebral; Rebecca BernardosORCID; Brendan J. CulletonORCID; Matthew MahORCID; Nicole AdamskiORCID; Nasreen BroomandkhoshbachtORCID; Kimberly CallanORCID; Ann Marie LawsonORCID; Kirsten MandlORCID; Megan MichelORCID; Jonas OppenheimerORCID; Kristin Stewardson; Fatma ZalzalaORCID; Kenneth Kidd; Judith Kidd; Theodore G. SchurrORCID; Kathryn AucklandORCID; Adrian V. S. HillORCID; Alexander J. MentzerORCID; Consuelo D. Quinto-CortésORCID; Kathryn RobsonORCID; Douglas J. KennettORCID; Nick PattersonORCID; Carlos D. BustamanteORCID; Andrés Moreno-EstradaORCID; Matthew SpriggsORCID; Miguel VilarORCID; Mark LipsonORCID; Ron PinhasiORCID; David ReichORCID

<jats:p>Micronesia began to be peopled earlier than other parts of Remote Oceania, but the origins of its inhabitants remain unclear. We generated genome-wide data from 164 ancient and 112 modern individuals. Analysis reveals five migratory streams into Micronesia. Three are East Asian related, one is Polynesian, and a fifth is a Papuan source related to mainland New Guineans that is different from the New Britain–related Papuan source for southwest Pacific populations but is similarly derived from male migrants ~2500 to 2000 years ago. People of the Mariana Archipelago may derive all of their precolonial ancestry from East Asian sources, making them the only Remote Oceanians without Papuan ancestry. Female-inherited mitochondrial DNA was highly differentiated across early Remote Oceanian communities but homogeneous within, implying matrilocal practices whereby women almost never raised their children in communities different from the ones in which they grew up.</jats:p>

Palabras clave: Multidisciplinary.

Pp. 72-79

Microglia-mediated degradation of perineuronal nets promotes pain

Shannon TansleyORCID; Ning GuORCID; Alba Ureña Guzmán; Weihua Cai; Calvin WongORCID; Kevin C. ListerORCID; Einer Muñoz-PinoORCID; Noosha YousefpourORCID; R. Brian Roome; Jordyn HealORCID; Neil WuORCID; Annie CastonguayORCID; Graham LeanORCID; Elizabeth M. Muir; Artur Kania; Masha Prager-KhoutorskyORCID; Ji ZhangORCID; Christos G. GkogkasORCID; James W. FawcettORCID; Luda DiatchenkoORCID; Alfredo Ribeiro-da-SilvaORCID; Yves De KoninckORCID; Jeffrey S. MogilORCID; Arkady KhoutorskyORCID

<jats:p>Activation of microglia in the spinal cord dorsal horn after peripheral nerve injury contributes to the development of pain hypersensitivity. How activated microglia selectively enhance the activity of spinal nociceptive circuits is not well understood. We discovered that after peripheral nerve injury, microglia degrade extracellular matrix structures, perineuronal nets (PNNs), in lamina I of the spinal cord dorsal horn. Lamina I PNNs selectively enwrap spinoparabrachial projection neurons, which integrate nociceptive information in the spinal cord and convey it to supraspinal brain regions to induce pain sensation. Degradation of PNNs by microglia enhances the activity of projection neurons and induces pain-related behaviors. Thus, nerve injury–induced degradation of PNNs is a mechanism by which microglia selectively augment the output of spinal nociceptive circuits and cause pain hypersensitivity.</jats:p>

Palabras clave: Multidisciplinary.

Pp. 80-86

Cenozoic evolution of deep ocean temperature from clumped isotope thermometry

A. N. MecklerORCID; P. F. SextonORCID; A. M. PiaseckiORCID; T. J. LeutertORCID; J. MarquardtORCID; M. ZieglerORCID; T. AgterhuisORCID; L. J. LourensORCID; J. W. B. RaeORCID; J. BarnetORCID; A. TripatiORCID; S. M. BernasconiORCID

<jats:p>Characterizing past climate states is crucial for understanding the future consequences of ongoing greenhouse gas emissions. Here, we revisit the benchmark time series for deep ocean temperature across the past 65 million years using clumped isotope thermometry. Our temperature estimates from the deep Atlantic Ocean are overall much warmer compared with oxygen isotope–based reconstructions, highlighting the likely influence of changes in deep ocean pH and/or seawater oxygen isotope composition on classical oxygen isotope records of the Cenozoic. In addition, our data reveal previously unrecognized large swings in deep ocean temperature during early Eocene acute greenhouse warmth. Our results call for a reassessment of the Cenozoic history of ocean temperatures to achieve a more accurate understanding of the nature of climatic responses to tectonic events and variable greenhouse forcing.</jats:p>

Palabras clave: Multidisciplinary.

Pp. 86-90