Evidence map›Paper›PMID 39386476›Full record

ArticlebioRxiv : the preprint server for biology2024

The Human Neural Cell Atlas of Zika Infection in developing human brain tissue: viral pathogenesis, innate immunity, and lineage reprogramming.

Caleb Stokes, Leanne S Whitmore, Dante Moreno, Karan Malhotra, Jennifer Tisoncik-Go, Emily Tran, Nick Wren, Ian Glass, Birth Defects Research Laboratory (BDRL), Jessica E Young and 1 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Caleb StokesDepartment of Pediatrics, University of Washington, Seattle WA.ORCID 0000-0003-3741-0057
Leanne S WhitmoreCenter for Innate Immunity and Immune Disease, Department of Immunology, University of Washington, Seattle WA.ORCID 0000-0002-8721-8701
Dante MorenoCenter for Innate Immunity and Immune Disease, Department of Immunology, University of Washington, Seattle WA.
Karan MalhotraUniversity of California, Berkeley, Berkeley CA.
Jennifer Tisoncik-GoCenter for Innate Immunity and Immune Disease, Department of Immunology, University of Washington, Seattle WA.ORCID 0000-0003-1381-265X
Emily TranCenter for Innate Immunity and Immune Disease, Department of Immunology, University of Washington, Seattle WA.
Nick WrenSchool of Medicine, University of Washington, Seattle WA.
Ian GlassDepartment of Pediatrics, University of Washington, Seattle WA.
Birth Defects Research Laboratory (BDRL)
Jessica E YoungInstitute for Stem Cell and Regenerative Medicine, University of Washington, Seattle WA.ORCID 0000-0003-2106-0339
Michael GaleCenter for Innate Immunity and Immune Disease, Department of Immunology, University of Washington, Seattle WA.ORCID 0000-0002-6332-7436

Funding

LABORATORY OF DEVELOPMENTAL BIOLOGYR24HD000836 · NICHD · UNIVERSITY OF WASHINGTON · PI Ian Amos Glass · 1995 to 2026
$16.9M
JAK-STAT Control of Zika Virus-Induced Fetal InjuryR01AI143265 · NIAID · UNIVERSITY OF WASHINGTON · PI ADAMS WALDORF, KRISTINA M., GALE, MICHAEL · 2019 to 2023
$4.6M
Characterization of AD-related endolysosomal dysfunction in human neural cellsR01AG080585 · NIA · UNIVERSITY OF WASHINGTON · PI SUMAN JAYADEV, Jessica E Young · 2024 to 2026
$2.5M
Innate Immunity of Zika Virus Infection In Human Neural ProgenitorsK08AI150996 · NIAID · UNIVERSITY OF WASHINGTON · PI STOKES, CALEB · 2020 to 2024
$975k
Role of HDAC2 as a modulator of aging and Alzheimer's disease phenotypes in stem-cell derived neuronsK01AG059841 · NIA · UNIVERSITY OF WASHINGTON · PI YOUNG, JESSICA ELAINE · 2019 to 2023
$612k
NIAID NIH HHS K08 AI150996NIAID NIH HHS R01 AI143265NIA NIH HHS K01 AG059841NIA NIH HHS R01 AG080585NICHD NIH HHS R24 HD000836
6 · The paper itself

Abstract

Zika virus (ZIKV) infection during pregnancy can lead to fetal brain infection and developmental anomalies collectively known as congenital Zika syndrome (CZS). To define the molecular features underlying CZS in a relevant human cell model, we evaluated ZIKV infection and neurodevelopment in primary fetal brain explants and induced pluripotent stem cell-derived mixed neural cultures at single cell resolution. We identified astrocytes as key innate immune sentinel cells detecting ZIKV and producing IFN-β. In contrast, neural progenitor cells displayed impaired innate immunity and supported high levels of viral replication. ZIKV infection of neurons suppressed differentiation and synaptic signaling networks and programmed a molecular switch from neurogenesis to astrogliogenesis. We identified a universal ZIKV-driven cellular stress response linked to intrinsic apoptosis and regulated by IFN-β. These findings reveal how innate immune signaling intersects with ZIKV-driven perturbations in cellular function to influence CZS outcomes including neuron developmental dysfunction and apoptotic cell death.

Identifiers

PMID39386476
PMCPMC11463344

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.