Hematopoietic Stem Cells in Wound Healing Response.
Norifumi UraoJinghua LiuKentaro TakahashiGayathri GaneshPublished in: Advances in wound care (2021)
Significance: Emerging evidence has shown a link between the status of hematopoietic stem cells (HSCs) and wound healing responses. Thus, better understanding HSCs will contribute to further advances in wound healing research. Recent Advances: Myeloid cells such as neutrophils and monocyte-derived macrophages are critical players in the process of wound healing. HSCs actively respond to wound injury and other tissue insults, including infection and produce the effector myeloid cells, and a failing of the HSC response can result in impaired wound healing. Technological advances such as transcriptome at single-cell resolution, epigenetics, three-dimensional imaging, transgenic animals, and animal models, have provided novel concepts of myeloid generation (myelopoiesis) from HSCs, and have revealed cell-intrinsic and -extrinsic mechanisms that can impact HSC functions in the context of health conditions. Critical Issues: The newer concepts include-the programmed cellular fate at a differentiation stage that is used to be considered as the multilineage, the signaling pathways that can activate HSCs directly and indirectly, the mechanisms that can deteriorate HSCs, the roles and remodeling of the surrounding environment for HSCs and their progenitors (the niche). Future Directions: The researches on HSCs, which produce blood cells, should contribute to the development of blood biomarkers predicting a risk of chronic wounds, which may transform clinical practice of wound care with precision medicine for patients at high risk of poor healing.
Keyphrases
- wound healing
- induced apoptosis
- single cell
- cell cycle arrest
- stem cells
- dendritic cells
- signaling pathway
- bone marrow
- acute myeloid leukemia
- public health
- endoplasmic reticulum stress
- palliative care
- high resolution
- cell death
- risk assessment
- dna methylation
- high throughput
- epithelial mesenchymal transition
- chronic pain
- endothelial cells