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Regeneration of insulin- producing cells from wharton{u2019}s jelly mesenchymal stem cells for the treatment of type Ї diabetes mellitus / Nancy Mohamed Saad Elhossary ; Supervised Amr Saad Elsayed , Hamdy Mahmoud Hassanein , Abdelwahab AbouBakr Elghareeb

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Nancy Mohamed Saad Elhossary , 2015Description: 77 P. : charts , facsimiles ; 25cmOther title:
  • تجدد الخلايا المىتجة للإنسولين من الخلايا الجذعية الوسيطة لهلام وارتون لعلاج مرض البول السكرى من النوع الاول [Added title page title]
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  • Issued also as CD
Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Science - Department of Biochemistry Summary: Regenerative medicine represents one of the main concerns of medicine. The aim of this study is to investigate an alternative technique for islet transplantation to treat type Ї diabetes mellitus (T1DM) by efficiently inducing easily obtained and processed Wharton{u2019}s jelly {u2013} derived mesenchymal stem cells of human umbilical cord (huMSCs) to differentiate into islet-like cells (ILCs). HuMSCs were isolated, cultured and induced chemically by fibronectin to differentiate in vitro into ILCs). The response of huMSCs was observed under an inverted microscope and evaluated by flow cytometry, H&E staining and immunocytochemistry. Twenty five male albino rats were divided into five groups, one of which was used as a control. Four groups were injected with 30 mg/kg of streptozotocin (STZ) on 3 consecutive days to induce T1DM. 5{u00D7}10⁶ of the differentiated huMSCs into functional insulin-producing cells were transplanted into two STZ-induced diabetic groups via two various ways , one via the tail vein and the other was intraperitoneally .While, 5{u00D7}10⁶ of the undifferentiated huMSCs were transplanted into the third group via the tail vein. Random blood glucose level (RBGL) and body weight (B.wt) were monitored weekly. After eight weeks, all rats were sacrificed and the pancreatic tissue was harvested in order to examine the change of pancreatic islets{u2019} structure, area and diameter by histomorphologic and histomorphometric analysis.
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Item type Current library Home library Call number Copy number Status Barcode
Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.12.25.M.Sc.2015.Na.R (Browse shelf(Opens below)) Not for loan 01010110067062000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.12.25.M.Sc.2015.Na.R (Browse shelf(Opens below)) 67062.CD Not for loan 01020110067062000

Thesis (M.Sc.) - Cairo University - Faculty of Science - Department of Biochemistry

Regenerative medicine represents one of the main concerns of medicine. The aim of this study is to investigate an alternative technique for islet transplantation to treat type Ї diabetes mellitus (T1DM) by efficiently inducing easily obtained and processed Wharton{u2019}s jelly {u2013} derived mesenchymal stem cells of human umbilical cord (huMSCs) to differentiate into islet-like cells (ILCs). HuMSCs were isolated, cultured and induced chemically by fibronectin to differentiate in vitro into ILCs). The response of huMSCs was observed under an inverted microscope and evaluated by flow cytometry, H&E staining and immunocytochemistry. Twenty five male albino rats were divided into five groups, one of which was used as a control. Four groups were injected with 30 mg/kg of streptozotocin (STZ) on 3 consecutive days to induce T1DM. 5{u00D7}10⁶ of the differentiated huMSCs into functional insulin-producing cells were transplanted into two STZ-induced diabetic groups via two various ways , one via the tail vein and the other was intraperitoneally .While, 5{u00D7}10⁶ of the undifferentiated huMSCs were transplanted into the third group via the tail vein. Random blood glucose level (RBGL) and body weight (B.wt) were monitored weekly. After eight weeks, all rats were sacrificed and the pancreatic tissue was harvested in order to examine the change of pancreatic islets{u2019} structure, area and diameter by histomorphologic and histomorphometric analysis.

Issued also as CD

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