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E-ISSN : 2148-9696
Crescent Journal of
Medical and Biological Sciences
Jul 2018, Vol 5, Issue 3
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Original Article
Impact of Mummy Substance on Proliferation and Migration of Human Wharton's Jelly-Derived Stem Cells and Fibroblasts in vitro culture system
Shahnaz Sabetkam1, Jafar Soleimani Rad1, Sepideh Hassan Pour Khodaie1, Leila Roshangar1
1Stem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
2Department of Anatomical Sciences, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran

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Keywords : Cell migration and proliferation, HFFF-2, Mummy Substance, WJSCs, Wound healing
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Objective: Because of the 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 substance 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 substance on wound healing.

Materials and Methods: Human fetal skin fibroblast cells (HFFF-2) were purchased from cell line and stem cells derived from Wharton"s jelly (WJSCs) were isolated by means of explant culture. MTT assay method 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 mummyhad 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.

Conclusion: 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 mummycan be used as a treatment to accelerate wound repair procedure.


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Aras Part Medical International Press Editors in Chief
Arash Khaki
Zafer Akan Deputy Editor
Javadi, Leila
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