How genetic differences shape the process of turning adult cells into stem cells

Leveraging genetic variation to dissect gene regulatory networks of reprogramming to pluripotency

NIH-funded research University of California Los Angeles · NIH-11136562

This project is looking at how natural genetic differences change the steps cells go through when they are reset into pluripotent stem cells, to help guide better stem-cell methods.

Quick facts

Grant typeU01 cooperative agreement
Study typeNIH-funded research
Funding institutionUniversity of California Los Angeles NIH-funded
Lab location1 site (Los Angeles, United States)
Project IDNIH-11136562 on NIH RePORTER

What this research studies

Researchers will take adult human cells and reprogram them back into induced pluripotent stem cells using the four classic factors (Oct4, Sox2, Klf4, cMyc). They will collect single-cell multi-omic data—including chromatin accessibility (ATAC-seq) and gene expression—at key time points during the reprogramming process. By comparing cells from different donors, the team will use natural genetic differences as a way to see which regulatory connections drive successful or stalled reprogramming. Computational models of gene regulatory networks will be built to map how transcription factors and chromatin changes coordinate the cell-fate switch.

Who could benefit from this research

Good fit: People who are able and willing to donate tissue or blood samples (healthy volunteers or patients with diverse genetic backgrounds) could be candidates for providing the cells used in this research.

Not a fit: Patients looking for immediate clinical treatment are unlikely to benefit directly because this is laboratory research into basic cell biology, not a therapeutic trial.

Why it matters

Potential benefit: If successful, this work could make generation of patient-specific stem cells more reliable and inform personalized approaches to regenerative therapies.

How similar studies have performed: Making iPSCs with the OSKM factors is well established, but combining donor genetic variation with single-cell multi-omics to map the regulatory steps of reprogramming is a newer and less-tested approach.

Where this research is happening

Los Angeles, United States

Researchers

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page below.
Last reviewed 2026-06-13 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.