شماره ركورد :
411300
عنوان مقاله :
مطالعه تاثير بايو [ROMOINDIRUBIN-3 - OXIM BIO] بر تكثير و تمايز به استخوان سلول هاي بنيادي مزانشيمي مشتق از مغز استخوان موش صحرايي
عنوان به زبان ديگر :
Study ofBIO (6-Bromoindirubin-3ʹ-Oxim) Effect on Growth and Bone Differentiation of Rat Marrow-Derived Mesenchymal Stem Cells
پديد آورندگان :
آبنوسي، محمدحسين نويسنده Abnoosi, M.H. , باغبان اسلامي نژاد، محمدرضا نويسنده گروه سلولهاي بنيادي،پژوهشكده رويان-مركز تحقيقات علوم سلولي جهاد دانشگاهي، پژوهشكده رويان تهران-گروه جنين شناسي-مركز تحقيقات پزشكي توليد مثل-پژوهشكده رويان جهاد دانشگاهي تهران Baghban Eslami Nejhad, M.R. , سليماني مهرنجاني، ملك نويسنده گروه زيست شناسي، دانشكده علوم پايه، دانشگاه اراك Mehranjani, M.S , سلامي، فريماه نويسنده گروه زيست شناسي، دانشكده علوم پايه، دانشگاه اراك Salami, F
اطلاعات موجودي :
فصلنامه سال 1387 شماره 50
رتبه نشريه :
علمي پژوهشي
تعداد صفحه :
9
از صفحه :
5
تا صفحه :
13
كليدواژه :
Adipogenesis , mesenchymal stem cells , osteogenesis , Wnt Signaling Pathway , مسير سيگنال دهي WNT , چربي , تمايز به استخوان , سلولهاي بنيادي مزانشيمي
چكيده لاتين :
Introduction & Objective: According to some study, wnt signaling pathway is among those molecular pathways that involve in cellular proliferation and bone differentiation. On the other hand, investigations have indicated that 6-bromoindirubin-3ʹ-oxim (BIO) is able to activate this pathway. In the present study, effect of BIO on in vitro proliferation and bone differentiation of mesenchymal stem cell (MSC) was considered. Materials & Metbods: In this experimental study, rat marrow-derived MSCs was used. Initially, a range of BIO concentration was examined in terms of their effect on MSC viability using MTT assay. The concentrations with no toxic effect on cell viability including 0.01, 0.1, I and 1.5 flM were then selected and added into either MSC proliferation or bone differentiation culture medium. To determine the BIO effect on MSC proliferation, population doubling number (PDN) was calculated and to quantify the BIO effect on MSC bone differentiation, expression level of the bone specific genes and the amount of culture mineralization was measured. In these experiments, culture without BIO was considered as control. Results: PDN results indicated that the cell population at cultures with 0.1 and 1 flM BIO was doubled in number significantly more than the other cultures (P<0.05). Differentiation experiment indicated the negative effect of BIO on MSC bone differentiation. At all BI0treated cultures, the expression level of osteocalcin and alkaline phosphatase genes as well as the amount of culture mineralization appeared to be significantly lower than those in control cultures (P<0.05). Conclusion: It seems that BI0 enhances MSC proliferation in culture while inhibits the in vitro bone differentiation.
سال انتشار :
1387
عنوان نشريه :
مجله علمي دانشگاه علوم پزشكي و خدمات درماني همدان
عنوان نشريه :
مجله علمي دانشگاه علوم پزشكي و خدمات درماني همدان
اطلاعات موجودي :
فصلنامه با شماره پیاپی 50 سال 1387
كلمات كليدي :
#تست#آزمون###امتحان
لينک به اين مدرک :
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