Itkin T, Houghton S, Schreiner R, Lin Y, Badwe CR, Voisin V, Murison A, Seyedhassantehrani N, Kaufmann KB, Garcia-Prat L, Booth GT, Geng F, Liu Y, Gomez-Salinero JM, Shieh JH, Redmond D, Xiang JZ, Josefowicz SZ, Trapnell C, Pietras EM, Spencer JA, Levine R, Xiao W, Zangi L, Hadland B, Dick JE, Xie SZ, Rafii S. (2025) Transcriptional activation of regenerative hematopoiesis via microenvironmental sensing. Nat Immunol 26(3):378-390. [article]
An international research team, led by scientists from Tel Aviv University and Sheba Medical Center, has unveiled an innovative method for activating adult stem cells from human bone marrow, enabling their expansion outside the body for use in bone marrow regeneration and the construction of a new blood and immune system.
The findings, published in the prestigious journal Nature Immunology, represent a breakthrough that could significantly improve transplant success rates for patients who have undergone intensive chemotherapy, suffer from genetic disorders, or require a bone marrow transplant but are unable to source a sufficient number of stem cells from a donor.
The study was led by Dr. Tomer Itkin from the Faculty of Medical and Health Sciences and the Sagol Center for Regenerative Medicine at Tel Aviv University, and the Neufeld Cardiac Research Institute at Sheba Medical Center, Tel Hashomer. The research also included contributions from leading medical institutions worldwide, including Weill Cornell Medical College and Hospital in New York, the Memorial Sloan Kettering Cancer Center (MSKCC), Mount Sinai Hospital, the University of Toronto Medical Center, and the Fred Hutchinson Cancer Research Center in Seattle.
Switching On Stem Cells
In the study, which is based on a comprehensive big data analysis of RNA sequencing and epigenetic DNA sequencing, the researchers identified a key protein—the Fli-1 transcription factor—that activates stem cells of the immune and blood system. These stem cells are highly active when sourced from umbilical cord blood but remain in a “dormant” and inactive state when obtained from adult bone marrow donors. Using modified mRNA technology—the same technology used to develop COVID-19 vaccines—the researchers successfully “awakened” the adult stem cells, allowing them to divide in a controlled manner without cancer risk. The activated cells were expanded on endothelial cells, which mimic the blood vessels that support stem cells in the bone marrow environment, demonstrating an enhanced ability to integrate and restore blood production under transplant conditions.
The key takeaway from the study is that activating stem cells through molecular programming, rather than arbitrary cell transplantation, substantially improves the success rates of regenerative treatments. The next stage of research involves testing the method in clinical trials to bring this groundbreaking technology into widespread therapeutic use. Furthermore, the researchers plan to apply the same therapeutic approach to regenerate additional tissues, including those without existing adult stem cells, such as the heart.
Source – Tel Aviv University
Itkin T, Houghton S, Schreiner R, Lin Y, Badwe CR, Voisin V, Murison A, Seyedhassantehrani N, Kaufmann KB, Garcia-Prat L, Booth GT, Geng F, Liu Y, Gomez-Salinero JM, Shieh JH, Redmond D, Xiang JZ, Josefowicz SZ, Trapnell C, Pietras EM, Spencer JA, Levine R, Xiao W, Zangi L, Hadland B, Dick JE, Xie SZ, Rafii S. (2025) Transcriptional activation of regenerative hematopoiesis via microenvironmental sensing. Nat Immunol 26(3):378-390. [article]
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An international research team, led by scientists from Tel Aviv University and Sheba Medical Center, has unveiled an innovative method for activating adult stem cells from human bone marrow, enabling their expansion outside the body for use in bone marrow regeneration and the construction of a new blood and immune system.
The findings, published in the prestigious journal Nature Immunology, represent a breakthrough that could significantly improve transplant success rates for patients who have undergone intensive chemotherapy, suffer from genetic disorders, or require a bone marrow transplant but are unable to source a sufficient number of stem cells from a donor.
The study was led by Dr. Tomer Itkin from the Faculty of Medical and Health Sciences and the Sagol Center for Regenerative Medicine at Tel Aviv University, and the Neufeld Cardiac Research Institute at Sheba Medical Center, Tel Hashomer. The research also included contributions from leading medical institutions worldwide, including Weill Cornell Medical College and Hospital in New York, the Memorial Sloan Kettering Cancer Center (MSKCC), Mount Sinai Hospital, the University of Toronto Medical Center, and the Fred Hutchinson Cancer Research Center in Seattle.
Switching On Stem Cells
In the study, which is based on a comprehensive big data analysis of RNA sequencing and epigenetic DNA sequencing, the researchers identified a key protein—the Fli-1 transcription factor—that activates stem cells of the immune and blood system. These stem cells are highly active when sourced from umbilical cord blood but remain in a “dormant” and inactive state when obtained from adult bone marrow donors. Using modified mRNA technology—the same technology used to develop COVID-19 vaccines—the researchers successfully “awakened” the adult stem cells, allowing them to divide in a controlled manner without cancer risk. The activated cells were expanded on endothelial cells, which mimic the blood vessels that support stem cells in the bone marrow environment, demonstrating an enhanced ability to integrate and restore blood production under transplant conditions.
The key takeaway from the study is that activating stem cells through molecular programming, rather than arbitrary cell transplantation, substantially improves the success rates of regenerative treatments. The next stage of research involves testing the method in clinical trials to bring this groundbreaking technology into widespread therapeutic use. Furthermore, the researchers plan to apply the same therapeutic approach to regenerate additional tissues, including those without existing adult stem cells, such as the heart.
Source – Tel Aviv University
Itkin T, Houghton S, Schreiner R, Lin Y, Badwe CR, Voisin V, Murison A, Seyedhassantehrani N, Kaufmann KB, Garcia-Prat L, Booth GT, Geng F, Liu Y, Gomez-Salinero JM, Shieh JH, Redmond D, Xiang JZ, Josefowicz SZ, Trapnell C, Pietras EM, Spencer JA, Levine R, Xiao W, Zangi L, Hadland B, Dick JE, Xie SZ, Rafii S. (2025) Transcriptional activation of regenerative hematopoiesis via microenvironmental sensing. Nat Immunol 26(3):378-390. [article]
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Novel biosensor uses DNA ‘barcodes’ to uncover disease signals in cells
CellART extracts single-cell information from high-resolution spatial transcriptomics
Cell2space restores spatial context to single-cell RNA sequencing data
Urine test may improve bladder cancer diagnosis and guide treatment decisions
DeCoRE – a computational method to resolve RNA structural heterogeneity from RNA structure probing data by direct RNA sequencing
Tracing 700 million years of cell evolution
How should biological replicates be handled in long-read RNA sequencing?
RNA-Seq reveals a new way the developing heart controls its growth
The Human RNome Project Consortium seeks to publish first-ever complete sequence of the body’s RNA
scFlowReport brings multiple single-cell RNA sequencing analyses into one workflow
Long-read RNA sequencing reveals how neurons choose alternative RNA endings
DeOPUS improves cell-type estimates from bulk RNA sequencing
ResolVI improves accuracy in spatial transcriptomics analysis
RNA sequencing reveals transcriptional allele differences in prostate cancer stem cells
Unmasking “zombie cells” in aging tissue with an AI-powered barcode
RNA variant imaging for cancer diagnosis
Autism-risk mutations reveal two opposing patterns of brain gene activity
A real-data approach to evaluating RNA transcript analysis methods
Detection and sequencing of Ap2N-capped RNAs in human cells
Single-cell RNA sequencing provides a closer look at the Aedes aegypti midgut
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