Concise Review: Ex Vivo Expansion of Cord Blood‐Derived Hematopoietic Stem and Progenitor Cells: Basic Principles, Experimental Approaches, and Impact in Regenerative Medicine. (7th October 2013)

• Record Type: Journal Article
• Authors: Flores-Guzmán, Patricia; Fernández-Sánchez, Verónica; Mayani, Hector
• Is Part Of: Stem cells translational medicine. Volume 2:Number 11(2013)
• Page Start: 830
• Page End: 838
• Publication Date: 2013-10-07
• Subjects: Hematopoietic stem cells -- Hematopoietic progenitors -- Stem cell expansion -- Umbilical cord blood; Stem cells -- Periodicals; Regenerative medicine -- Periodicals; Periodicals; 616.0277405
• DOI: 10.5966/sctm.2013-0071
• Languages: English
• ISSNs: 2157-6564

Abstract

Abstract : This review surveys current progress toward the ex vivo expansion of human umbilical cord blood‐derived hematopoietic stem cells (HSCs) and hematopoietic progenitor cells. Recent studies suggest that HSCs may also give rise to nonhematopoietic cells; this plasticity and the possibility of producing nonhematopoietic cells at the clinical scale could bring new alternatives for the treatment of neural, metabolic, orthopedic, cardiac, and neoplastic disorders. Abstract : Hematopoietic stem cells (HSCs) and hematopoietic progenitor cells (HPCs) play key roles in the production of mature blood cells and in the biology and clinical outcomes of hematopoietic transplants. The numbers of these cells, however, are extremely low, particularly in umbilical cord blood (UCB); thus, ex vivo expansion of human UCB‐derived HSCs and HPCs has become a priority in the biomedical field. Expansion of progenitor cells can be achieved by culturing such cells in the presence of different combinations of recombinant stimulatory cytokines; in contrast, expansion of actual HSCs has proved to be more difficult because, in addition to needing recombinant cytokines, HSCs seem to deeply depend on the presence of stromal cells and/or elements that promote the activation of particular self‐renewal signaling pathways. Hence, there is still controversy regarding the optimal culture conditions that should be used to achieve this. To date, UCB transplants using ex vivo‐expanded cells have already been performed for the treatment of different hematological disorders, and although results are still far from being optimal, the advances are encouraging. Recent studies suggest that HSCs may also give rise to nonhematopoietic cells, such as neural, cardiac, mesenchymal, and muscle cells. Such plasticity and the possibility of producing nonhematopoietic cells at the clinical scale could bring new alternatives for the treatment of neural, metabolic, orthopedic, cardiac, and neoplastic disorders. Once standardized, ex vivo expansion of human HSCs/HPCs will surely have a positive impact in regenerative medicine.