Evidence map›Paper›PMID 38670072›Full record

ArticleCell2024

Functional sensory circuits built from neurons of two species.

Benjamin T Throesch, Muhammad Khadeesh Bin Imtiaz, Rodrigo Muñoz-Castañeda, Masahiro Sakurai, Andrea L Hartzell, Kiely N James, Alberto R Rodriguez, Greg Martin, Giordano Lippi, Sergey Kupriyanov and 5 more

Abstract read
In one paragraph

Article in Cell, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Recent advances in interspecies chimeras and organogenesis.Current opinion in genetics & development · 2025
    Review
  4. Review
  5. Review
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  7. Article
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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

15 authors.

Benjamin T ThroeschDepartment of Neuroscience, The Scripps Research Institute, La Jolla, San Diego, CA, USA; Neuroscience Graduate Program, University of California, San Diego, La Jolla, San Diego, CA, USA.
Muhammad Khadeesh Bin ImtiazCecil H. and Ida Green Center for Reproductive Biology Sciences, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Rodrigo Muñoz-CastañedaCold Spring Harbor Laboratory, Cold Spring Harbor, NY, USA.
Masahiro SakuraiSalk Institute for Biological Studies, La Jolla, San Diego, CA, USA; Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Andrea L HartzellDepartment of Neuroscience, The Scripps Research Institute, La Jolla, San Diego, CA, USA.
Kiely N JamesDepartment of Neuroscience, The Scripps Research Institute, La Jolla, San Diego, CA, USA; Neuroscience Graduate Program, University of California, San Diego, La Jolla, San Diego, CA, USA.
Alberto R RodriguezMouse Genetics Core, The Scripps Research Institute, La Jolla, San Diego, CA, USA.
Greg MartinMouse Genetics Core, The Scripps Research Institute, La Jolla, San Diego, CA, USA.
Giordano LippiDepartment of Neuroscience, The Scripps Research Institute, La Jolla, San Diego, CA, USA.
Sergey KupriyanovMouse Genetics Core, The Scripps Research Institute, La Jolla, San Diego, CA, USA.
Zhuhao WuIcahn School of Medicine at Mount Sinai, New York, NY, USA.
Pavel OstenCold Spring Harbor Laboratory, Cold Spring Harbor, NY, USA.
Juan Carlos Izpisua BelmonteSalk Institute for Biological Studies, La Jolla, San Diego, CA, USA; Gene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, San Diego, CA, USA; Altos Labs, San Diego, CA, USA.
Jun WuSalk Institute for Biological Studies, La Jolla, San Diego, CA, USA; Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA; Hamon Center for Regenerative Science and Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA; Cecil H. and Ida Green Center for Reproductive Biology Sciences, University of Texas Southwestern Medical Center, Dallas, TX, USA. Electronic address: jun2.wu@utsouthwestern.edu.
Kristin K BaldwinDepartment of Neuroscience, The Scripps Research Institute, La Jolla, San Diego, CA, USA; Neuroscience Graduate Program, University of California, San Diego, La Jolla, San Diego, CA, USA; Department of Genetics and Development, Columbia Stem Cell Initiative, Columbia University Medical Center, New York, NY, USA. Electronic address: kb238@columbia.edu.

Funding

Defining a transcriptional periodic table of the human brain using reprogrammingDP1AG055944 · NIA · SCRIPPS RESEARCH INSTITUTE, THE · PI BALDWIN, KRISTIN KAY · 2016 to 2020
$7.2M
Generation of functional organs and tissues using organism interspecific blastocyst complementationDP1DK113616 · NIDDK · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI DUBBAKA VENU, PRADEEP REDDY · 2016 to 2020
$5.3M
Genome-wide investigation of somatic mutation in the developing and aging brainR01MH102698 · NIMH · SCRIPPS RESEARCH INSTITUTE, THE · PI BALDWIN, KRISTIN KAY, HALL, IRA M · 2014 to 2018
$3.4M
Contributions of cell type and exosome signaling to prodromal synaptic and circuit changes in Alzheimer's Disease modelsRF1AG079517 · NIA · SCRIPPS RESEARCH INSTITUTE, THE · PI BALDWIN, KRISTIN KAY, CLINE, HOLLIS T. · 2022 to 2022
$2.6M
Programs for generating inhibitory interneuron diversity and connectivityR01MH133381 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Edmund Au, Kristin Kay Baldwin · 2024 to 2026
$2.4M
The architecture and development of a sensory processing circuit for smellR01DC012592 · NIDCD · SCRIPPS RESEARCH INSTITUTE, THE · PI BALDWIN, KRISTIN KAY · 2012 to 2016
$2.3M
Dissect the mechanisms underlying interspecies pluripotent stem cell competitionR01HD103627 · NICHD · UT SOUTHWESTERN MEDICAL CENTER · PI Michael Buszczak, Ondine B Cleaver · 2022 to 2026
$1.8M
Cell type influence on exosome signaling and early pathologic signatures in Alzheimers diseaseR56AG062618 · NIA · SCRIPPS RESEARCH INSTITUTE, THE · PI BALDWIN, KRISTIN KAY, CLINE, HOLLIS T. · 2020 to 2020
$887k
Multilevel Analysis of Cortical Interneuron Dysfunction in Fragile X SyndromeR21MH131947 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI AU, EDMUND · 2023 to 2024
$442k
NIA NIH HHS DP1 AG055944NIA NIH HHS R56 AG062618NIA NIH HHS RF1 AG079517NICHD NIH HHS R01 HD103627NIDCD NIH HHS R01 DC012592NIDDK NIH HHS DP1 DK113616NIMH NIH HHS R01 MH102698NIMH NIH HHS R01 MH133381NIMH NIH HHS R21 MH131947
6 · The paper itself

Abstract

A central question for regenerative neuroscience is whether synthetic neural circuits, such as those built from two species, can function in an intact brain. Here, we apply blastocyst complementation to selectively build and test interspecies neural circuits. Despite approximately 10-20 million years of evolution, and prominent species differences in brain size, rat pluripotent stem cells injected into mouse blastocysts develop and persist throughout the mouse brain. Unexpectedly, the mouse niche reprograms the birth dates of rat neurons in the cortex and hippocampus, supporting rat-mouse synaptic activity. When mouse olfactory neurons are genetically silenced or killed, rat neurons restore information flow to odor processing circuits. Moreover, they rescue the primal behavior of food seeking, although less well than mouse neurons. By revealing that a mouse can sense the world using neurons from another species, we establish neural blastocyst complementation as a powerful tool to identify conserved mechanisms of brain development, plasticity, and repair.

Indexed as

NeuronsAnimalsBlastocystBrainFemaleHippocampusMaleMiceMice, Inbred C57BLPluripotent Stem CellsRatsSpecies Specificityblastocyst complementationbrain evolutionbrain regenerationdevelopmentdisease modelsinterspecies chimerasneural circuitsneuronsolfactionpluripotent stem cells

Identifiers

PMID38670072
PMCPMC11293795

What OpenQuestion holds

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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.