Impact of Mummy Substance on Proliferation and Migration of Human Wharton’s Jelly-Derived Stem Cells and Fibroblasts in an In Vitro Culture System

Impact of Mummy Substance on Proliferation and Migration of Human Wharton’s Jelly-Derived Stem Cells and Fibroblasts in an In Vitro Culture System


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نویسندگان: سپیده حسن پور خدایی , مسعود ملکی , لیلا روشنگر , جعفر سلیمانی راد

کلمات کلیدی: Cell migration and proliferation, HFFF-2, Mummy Substance, WJSCs, Wound healing

نشریه: 0 , 3 , 5 , 2018

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نویسنده ثبت کننده مقاله لیلا روشنگر
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه مرکز سلولهای بنیادی
کد مقاله 67901
عنوان فارسی مقاله Impact of Mummy Substance on Proliferation and Migration of Human Wharton’s Jelly-Derived Stem Cells and Fibroblasts in an In Vitro Culture System
عنوان لاتین مقاله Impact of Mummy Substance on Proliferation and Migration of Human Wharton’s Jelly-Derived Stem Cells and Fibroblasts in an In Vitro Culture System
ناشر 5
آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ بلی
عنوان نشریه (خارج از لیست فوق) Crescent Journal of Medical and Biological Sciences
نوع مقاله Original Article
نحوه ایندکس شدن مقاله ایندکس شده سطح چهار – Embase
آدرس لینک مقاله/ همایش در شبکه اینترنت

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Objectives: Because of the high prevalence of chronic wounds, wound repair has become one of the health challenges. Numerous therapeutic strategies have been proposed for repairing wounds and recently, the use of herbal medicines has been considered because of lower costs and complications. The use of mummy is recommended in traditional medicine for treating bone fractures, bleeding control, poisoning treatment, headache relief and wound repair. Therefore, the purpose of the present study was to provide a scientific assessment of the effect of mummy on wound healing. Materials and Methods: Human fetal foreskin fibroblast cells (HFFF-2) were purchased from Pasteur Institute (Tehran, Iran). The fibroblast cell lines and stem cells derived from Wharton’s jelly (WJSCs) were isolated by means of explant culture. MTT assay was used to determine the effective concentration of mummy. Scratch assay method was used to examine the effect of mummy on cell migration rate and flow cytometry was used to assess the rate of cell proliferation using Ki-67 antibody. WJSCs and HFFF-2, each under mono-culture and two-cell co-culture condition with 50-50 and 30/70 ratio respectively, were in an experimental group including culture medium and mummy and in a control group including culture medium only. Results: Scratch assay results for HFFF-2 cell migration showed a significant increase (P≤0.0001), but the mummy had no significant impact on WJSCs and a significant increase was observed in 50/50 and 30/70 co-culture conditions with P≤0.001 and P≤0.0001, respectively. The proliferation rate of WJSCs increased significantly while no significant increase was found in fibroblast groups in mono-culture and co-culture conditions. Conclusions: Results showed that by stimulating fibroblast cell migration both in mono-culture and co-culture conditions with stem cells and by increasing WJSCs proliferation, the mummy can be used as a treatment to accelerate wound repair procedure.

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نویسنده نفر چندم مقاله
سپیده حسن پور خداییسوم
مسعود ملکیچهارم
لیلا روشنگرپنجم
جعفر سلیمانی راددوم

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