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A Simple and Cost-Effective Method for Isolation and Expansion of Human Fetal Pancreas Derived Mesenchymal Stem Cells Pubmed



Larijani B1 ; Arjmand B1 ; Ahmadbeigi N2 ; Falahzadeh K3 ; Soleimani M4 ; Sayahpour FA5 ; Aghayan HR1
Authors
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Authors Affiliations
  1. 1. Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Research Institute, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Digestive Disease Research Institute, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Chronic Diseases Research Center, Endocrinology and Metabolism Research Institute, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Department of Hematology, School of Medical Sciences, Tarbiat Modares University, Tehran, Iran
  5. 5. Department of Stem Cells and Developmental Biology, Royan Institute for Stem Cell Biology and Technology, Tehran, Iran

Source: Archives of Iranian Medicine Published:2015


Abstract

Background: Previous studies have suggested mesenchymal stem cells (MSCs) as a suitable source for cell replacement therapy in diabetes. MSCs have successfully isolated from different adult and fetal tissues, including the pancreas. In vitro studies have shown that human fetal pancreatic stem cells could be extensively expanded and differentiated into islet-like structures. Here, we introduce a simple and cost-effective method for the generation of MSCs from the human fetal pancreas (FPMSCs). Methods: To isolate FPMSCs, pancreata from four aborted fetuses (second trimester) were processed with short collagenase digestion. The resulting tissue fragments were transferred to a basic media (DMEM+15%FBS) without adding any growth factor. Results: After 10 to14 days, fibroblast-like cells were harvested and passaged six times for further evaluations. Flow cytometry analysis and three-lineage differentiation capacity have demonstrated that these cells have MSC-like properties. We also continuously passaged samples of FPMSCs and found no evidence for chromosomal instability and morphological changes until 10th subculture. Moreover, our cell culture protocol can be easily modified and translated into a GMP-compliant one. Conclusion: In conclusion, the results of current study demonstrated that our simple and inexpensive method could yield a pure population of FPMSCs that might be suitable for transplantation. © 2015, Academy of Medical Sciences of the I.R. Iran. All rights reserved.
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