Do the human umbilical cord blood CD34+ progenitor cells home in the pancreas and kidney of diabetic mice?
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  • 作者:Dalia M. Abd-Elhalim ; Yasser M. El-Wazir
  • 关键词:Homing of CD34 cells ; Human umbilical cord blood ; Streptozotocin ; induced diabetic mice
  • 刊名:International Journal of Diabetes in Developing Countries
  • 出版年:2016
  • 出版时间:March 2016
  • 年:2016
  • 卷:36
  • 期:1
  • 页码:70-74
  • 全文大小:348 KB
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  • 作者单位:Dalia M. Abd-Elhalim (1)
    Yasser M. El-Wazir (1)

    1. Physiology Department, Faculty of Medicine, Suez Canal University, Ismailia, Egypt
  • 刊物主题:Medicine/Public Health, general; General Practice / Family Medicine; Health Administration; Diabetes;
  • 出版者:Springer India
  • ISSN:1998-3832
文摘
Type 1 diabetes is a chronic metabolic disorder in which pancreatic islet β cells are irreversibly destroyed by autoimmunity. Many studies suggest great promise for the utility of human umbilical cord blood (HUCB) stem cells as a cure for diabetes; however, the mechanism for their effect requires further elucidation. This study investigated the presence of human DNA in the pancreas and kidney of diabetic mice treated with HUCB CD34+ cells. Eighteen albino male mice were equally and randomly divided into three groups: normal control group, diabetic untreated streptozotocin (STZ) group, and diabetic STZ-treated group. Diabetes was induced by intraperitoneal (IP) injection of STZ (180 mg/kg). CD34+ progenitor cells were separated from HUCB and injected intravenously in dose of 106 cells/mouse. Blood glucose was measured every 2 days for 3 weeks. Mice were sacrificed after 3 weeks, and real-time PCR analysis was conducted for the presence of human-specific ALU sequence in the pancreata and kidneys from all animals. Injection of CD34+ cells caused significant improvement in blood glucose level (230 ± 50 mg/dl in treated group vs. 590 ± 24 mg/dl in untreated group, p = 0.001). Real-time PCR analysis showed negative results in the control and untreated groups, while in the treated group, engraftment of the HUCB CD34 cells was positive in 100 % of the kidneys with a mean transplanted cell percentage 1.8 ± 0.98 % and 66 % of the pancreata with a mean 0.41 ± 0.42 %. A significant negative correlation was found between the concentration of the ALU sequence in the pancreata and the change of glucose level in the treated group (p value =0.03 and r = −0.6). HUCB CD34 cells engraft in the pancreas of the diabetic mice and improve hyperglycemia. Based on our results, HUCB CD34 cell transplantation may provide a potential therapy for human diabetes mellitus.

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