Evidence map›Paper›PMID 38866017›Full record

ArticleCell2024

TNF-NF-κB-p53 axis restricts in vivo survival of hPSC-derived dopamine neurons.

Tae Wan Kim, So Yeon Koo, Markus Riessland, Fayzan Chaudhry, Benjamin Kolisnyk, Hyein S Cho, Marco Vincenzo Russo, Nathalie Saurat, Sanjoy Mehta, Ralph Garippa and 2 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 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing 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

40 citing papers in PubMed.

  1. Review
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  8. Review
  9. Selective CaStem cell reports · 2026
    Article
  10. Review
  11. Article
  12. Article
  13. Current issues in molecular biology · 2026
    Article
  14. Article
  15. Article
  16. Frontiers in aging neuroscience · 2026
    Review
  17. Review
  18. Article
  19. Review
  20. Nervonic Acid fromBiomaterials research · 2026
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Tae Wan KimThe Center for Stem Cell Biology, Sloan-Kettering Institute for Cancer Research, New York, NY 10065, USA; Developmental Biology Program, Sloan-Kettering Institute for Cancer Research, New York, NY 10065, USA; Department of Interdisciplinary Engineering, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu 42988, Republic of Korea; Aligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD 20815, USA. Electronic address: taewan79@dgist.ac.kr.
So Yeon KooThe Center for Stem Cell Biology, Sloan-Kettering Institute for Cancer Research, New York, NY 10065, USA; Developmental Biology Program, Sloan-Kettering Institute for Cancer Research, New York, NY 10065, USA; Weill Cornell Neuroscience PhD Program, New York, NY, USA.
Markus RiesslandDepartment of Neurobiology and Behavior, Center for Nervous System Disorders, Stony Brook University, Stony Brook, NY 11794, USA.
Fayzan ChaudhryTri-Institutional PhD program in Computational Biology, New York, NY, USA.
Benjamin KolisnykLaboratory of Molecular and Cellular Neuroscience, The Rockefeller University, 1230 York Avenue, New York, NY 10065, USA.
Hyein S ChoThe Center for Stem Cell Biology, Sloan-Kettering Institute for Cancer Research, New York, NY 10065, USA; Developmental Biology Program, Sloan-Kettering Institute for Cancer Research, New York, NY 10065, USA.
Marco Vincenzo RussoGene Editing and Screening Core Facility, Memorial Sloan Kettering Cancer Center, New York, NY, USA; Sylvester Comprehensive Cancer Center, Miller School of Medicine, University of Miami, Miami, FL 33136, USA.
Nathalie SauratThe Center for Stem Cell Biology, Sloan-Kettering Institute for Cancer Research, New York, NY 10065, USA; Developmental Biology Program, Sloan-Kettering Institute for Cancer Research, New York, NY 10065, USA; Aligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD 20815, USA.
Sanjoy MehtaGene Editing and Screening Core Facility, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Ralph GarippaGene Editing and Screening Core Facility, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Doron BetelDivision of Hematology & Oncology, Department of Medicine, Weill Cornell Medicine, New York, NY, USA; Institute for Computational Biomedicine, Weill Cornell Medicine, New York, NY, USA.
Lorenz StuderThe Center for Stem Cell Biology, Sloan-Kettering Institute for Cancer Research, New York, NY 10065, USA; Developmental Biology Program, Sloan-Kettering Institute for Cancer Research, New York, NY 10065, USA; Aligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD 20815, USA. Electronic address: studerl@mskcc.org.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Directing Fate, Subtype Identity and Survival in Human Pluripotent-Derived Midbrain Dopamine NeuronsR01NS118067 · NINDS · SLOAN-KETTERING INST CAN RESEARCH · PI BETEL, DORON, STUDER, LORENZ P. · 2021 to 2025
$3.2M
Molecular Assessment of Cause and Consequence of Cellular Senescence in Diverse Midbrain Cell Types in Parkinson's DiseaseR01NS124735 · NINDS · STATE UNIVERSITY NEW YORK STONY BROOK · PI Markus Riessland · 2022 to 2026
$2.0M
NCI NIH HHS P30 CA008748NINDS NIH HHS R01 NS118067NINDS NIH HHS R01 NS124735
6 · The paper itself

Abstract

Ongoing, early-stage clinical trials illustrate the translational potential of human pluripotent stem cell (hPSC)-based cell therapies in Parkinson's disease (PD). However, an unresolved challenge is the extensive cell death following transplantation. Here, we performed a pooled CRISPR-Cas9 screen to enhance postmitotic dopamine neuron survival in vivo. We identified p53-mediated apoptotic cell death as a major contributor to dopamine neuron loss and uncovered a causal link of tumor necrosis factor alpha (TNF-α)-nuclear factor κB (NF-κB) signaling in limiting cell survival. As a translationally relevant strategy to purify postmitotic dopamine neurons, we identified cell surface markers that enable purification without the need for genetic reporters. Combining cell sorting and treatment with adalimumab, a clinically approved TNF-α inhibitor, enabled efficient engraftment of postmitotic dopamine neurons with extensive reinnervation and functional recovery in a preclinical PD mouse model. Thus, transient TNF-α inhibition presents a clinically relevant strategy to enhance survival and enable engraftment of postmitotic hPSC-derived dopamine neurons in PD.

Indexed as

Cell SurvivalDopaminergic NeuronsNF-kappa BTumor Necrosis Factor-alphaTumor Suppressor Protein p53AnimalsApoptosisCRISPR-Cas SystemsDisease Models, AnimalHumansMiceParkinson DiseasePluripotent Stem CellsSignal TransductionNF-kappa BTumor Necrosis Factor-alphaTumor Suppressor Protein p53apoptosiscell purificationcell survivalcell therapydopamine neuronsgenetic screenParkinson’s diseaseTNF-α inhibitionTP53transplantation

Identifiers

PMID38866017
PMCPMC11641762

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.