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

Output Details

Preprint May 30, 2023

Published July 11, 2024

Ongoing, first-in-human clinical trials illustrate the feasibility and translational potential of human pluripotent stem cell (hPSC)-based cell therapies in Parkinson’s disease (PD). However, a major unresolved challenge in the field is the extensive cell death following transplantation with <10% of grafted dopamine neurons surviving. Here, we performed a pooled CRISPR/Cas9 screen to enhance survival of postmitotic dopamine neurons in vivo. We identified p53-mediated apoptotic cell death as major contributor to dopamine neuron loss and uncovered a causal link of TNFa-NFκB signaling in limiting cell survival. As a translationally applicable strategy to purify postmitotic dopamine neurons, we performed a cell surface marker screen that enabled purification without the need for genetic reporters. Combining cell sorting with adalimumab pretreatment, a clinically approved and widely used TNFa inhibitor, enabled efficient engraftment of postmitotic dopamine neurons leading to extensive re-innervation and functional recovery in a preclinical PD mouse model. Thus, transient TNFa inhibition presents a clinically relevant strategy to enhance survival and enable engraftment of postmitotic human PSC-derived dopamine neurons in PD.
Tags
  • Cell therapy
  • Dopaminergic neurons
  • hiPSCs (Human induced pluripotent stem cells)
  • Human embryonic stem cells (hESC)
  • Original Research
  • Purification

Meet the Authors

  • Tae Wan Kim, PhD

    Key Personnel: Team Studer

    Memorial Sloan Kettering Cancer Center

  • So Yeon Koo, BSc

    Key Personnel: Team Studer

    Memorial Sloan Kettering Cancer Center

  • Lorenz Studer, MD

    Lead PI (Core Leadership): Team Studer

    Memorial Sloan Kettering Cancer Center

  • Nathalie Saurat, PhD

    Key Personnel: Team Studer

    Memorial Sloan Kettering Cancer Center