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Human Cd34+ Hematopoietic Stem Cells Culture in Humanized Culture Medium for Cell Therapy Publisher



Yaghoubi Y1, 2 ; Zamani M3 ; Naimi A4 ; Hassanzadeh A5 ; Gharibeh N1 ; Madani J1 ; Motevali R1 ; Nikshad A1 ; Aghlmandi A1 ; Parhizkar F1 ; Mehdizadeh A7 ; Nazari M8 ; Yousefi M1, 6 ; Movassaghpour AA1, 9
Authors
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Authors Affiliations
  1. 1. Stem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
  2. 2. Student Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran
  3. 3. Department of Medical Laboratory Sciences, Faculty of Allied Medicine, Gonabad University of Medical Sciences, Gonabad, Iran
  4. 4. Cellular and Molecular Research Center, Sabzevar University of Medical Sciences, Sabzevar, Iran
  5. 5. Department of Tissue Engineering and Applied Cell Sciences, Tehran University of Medical Sciences, Tehran, Iran
  6. 6. Department of Immunology, Tabriz University of Medical Sciences, Tabriz, Iran
  7. 7. Endocrine Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
  8. 8. Department of Anesthesiology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
  9. 9. Hematology and Oncology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran

Source: Gene Reports Published:2020


Abstract

Introduction: Hematopoietic stem cell transplantation (HSCT) is a proper treatment for many cancers, including malignant and non-malignant hematologic and immune disorders. However, due to the small quantity of HSCTs, their number should be increased ex vivo. Cell proliferation increase by animal serum can transmit certain diseases and immune problems to the recipient; therefore, replacement of culture media with media of human origin seems to be crucial. Acellular Wharton's jelly (AWJ) can be considered as an alternative medium in this regard. This study aimed to investigate the effect of AWJ substitution for fetal bovine serum (FBS) on the expression of myeloid and lymphoid specific markers and CD34+ cells proliferation pattern following co-culture with mesenchymal stem cells. Materials and methods: In this study, CD34+ umbilical cord blood HSCs were co-cultured with MSCs in the presence of 10% FBS or AWJ, stem cell factor (SCF), thrombopoietin (TPO), and FLT3-L and the proliferation pattern and expression of myeloid as well as lymphoid lineage markers were then evaluated. Results: The expression of myeloid and lymphoid specific markers was increased and decreased in AWJ and FBS containing culture medium, respectively. Conclusion: This study provided evidence for the differentiation of UCB-derived CD34+ cells toward myeloid lineage and lack of their differentiation toward lymphoid lineage in AWJ containing culture medium. © 2020