Hematopoietic stem cells (HSCs) have the capacity to both self-renew and differentiate into all mature blood cell types, making them promising treatments for a variety of diseases.
However, the mechanisms involved in engraftment-;when the cells start to grow and make healthy blood cells after being transplanted into a patient-;are poorly understood. A recent study led by researchers at Massachusetts General Hospital (MGH) and Boston University School of Medicine has revealed the unique signature of genes expressed by HSCs capable of undergoing this process.
The findings, which are published in Nature Communications, could enable scientists to expand these cells outside of the body or to convert other types of stem cells into cells that can repopulate the blood system.
In adults, HSCs are found in the bone marrow and bloodstream, but before birth, they can be found to a greater extent in the liver, where they multiply, or proliferate, into additional HSCs at a very high rate. Moreover, research in animals has shown that HSCs in the fetal liver are more capable of engraftment than HSCs from bone marrow.
To understand what allows fetal liver HSCs to have these superior proliferation and engraftment characteristics, investigators examined the gene expression patterns that are unique to these highly potent stem cells. They combined this examination with a variety of experimental methods to characterize the protein expression and functionality of those same cells.
"This in-depth analysis revealed that these stem cells express a protein on their surface called CD201 that correlates very closely with this engraftment potential and can be used to isolate functional stem cells away from other cell types," says co–senior author Alejandro B. Balazs, PhD, a principal investigator at the Ragon Institute of MGH, MIT and Harvard. "This will help us improve the process of bone marrow and stem cell transplantation by allowing us to purify these cells."
The enhanced understanding of the genes involved will also help scientists propagate HSCs with high engraftment potential in the lab and manipulate them to more efficiently fight blood cell–related diseases such as sickle cell anemia, HIV and certain types of cancer.
Altogether, this work has resulted in a detailed blueprint of the most potent blood stem cells and will lead to a better understanding of why these cells have such an extraordinary regenerative capacity. Such insights will allow us to create safer and more efficient therapies for patients suffering from blood disorders."
Kim Vanuytsel, PhD, Study Lead Author and Research Assistant Professor of Medicine, School of Medicine, Boston University
Massachusetts General Hospital
Vanuytsel, K., et al. (2022) Multi-modal profiling of human fetal liver hematopoietic stem cells reveals the molecular signature of engraftment. Nature Communications. doi.org/10.1038/s41467-022-28616-x
Posted in: Cell Biology
Tags: Amyloidosis, Anemia, Arthritis, Blood, Bone, Bone Marrow, Cancer, Cardiovascular Disease, Cell, Dermatology, Gene, Gene Expression, Genes, Healthcare, HIV, Hospital, Infectious Diseases, Liver, Medical School, Medicine, Proliferation, Protein, Protein Expression, Research, Sickle Cell Anemia, Stem Cells, students
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