• ثبت نام
    • ورود به سامانه
    مشاهده مورد 
    •   صفحهٔ اصلی
    • نشریات انگلیسی
    • Iranian Journal of Basic Medical Sciences
    • Volume 22, Issue 8
    • مشاهده مورد
    •   صفحهٔ اصلی
    • نشریات انگلیسی
    • Iranian Journal of Basic Medical Sciences
    • Volume 22, Issue 8
    • مشاهده مورد
    JavaScript is disabled for your browser. Some features of this site may not work without it.

    Effect of let-7a overexpression on the differentiation of conjunctiva mesenchymal stem cells into photoreceptor-like cells

    (ندگان)پدیدآور
    Ranjbarnejad, FatemehNadri, SamadBiglari, AlirezaMohammadi Yeganeh, SamiraParyan, Mahdi
    Thumbnail
    دریافت مدرک مشاهده
    FullText
    اندازه فایل: 
    615.0کیلوبایت
    نوع فايل (MIME): 
    PDF
    نوع مدرک
    Text
    Original Article
    زبان مدرک
    English
    نمایش کامل رکورد
    چکیده
    Objective(s): MicroRNAs (miRNAs) could regulate many cellular processes such as proliferation and differentiation. let-7a miRNA is one of the key regulators in the developmental transition of retinal progenitor cells into differentiated cells. Current evidence suggests that mesenchymal stem cells (MSCs) can isolate from various tissues such as bone marrow and conjunctiva. In this study, we investigated the effect of let-7a overexpression on induced differentiation of conjunctiva mesenchymal stem cells (CJMSCs) into photoreceptor-like cells.Materials and Methods: After isolation and characterization, CJMSCs were transduced with lentiviruses containing let-7a or empty vector. The effect of let-7a overexpression on expression of photoreceptor-specific markers was evaluated by quantitative real-time PCR (RT-qPCR) after 28 and 42 days of transduction.Results: The relative expression of rhodopsin and recoverin genes was evaluated by RT-qPCR in let-7a overexpressing cells, control vector transduced cells and untransduced CJMSCs (control cells). Our results indicated that following overexpression of let-7a, after 28 and 42 days of transduction, significant up-regulation in the expression of recoverin (574.7 and 43.9 folds) and rhodopsin (3334.7 and 53.1 folds) were observed, respectively.Conclusion: Our findings indicate that overexpression of let-7a microRNA can increase the expression of photoreceptor-specific genes in CJMSCs. Moreover, it is prospective that let-7a overexpression can use as an alternative protocol for the differentiation of mesenchymal stem cells into photoreceptors. It seems that the effect of let-7a on the differentiation of CJMSCs into photoreceptors is also time-dependent.
    کلید واژگان
    Conjunctiva Let
    7a Mesenchymal stem cells MiRNAs Photoreceptor differentiation
    Genetics

    شماره نشریه
    8
    تاریخ نشر
    2019-08-01
    1398-05-10
    ناشر
    Mashhad University of Medical Sciences
    سازمان پدید آورنده
    Department of Genetics and Molecular Medicine, Zanjan University of Medical Sciences, End of Mahdavi Blvd, Shahrak-e Karmandan, 4513956111, Zanjan, Iran
    Department of Medical Nanotechnology, Zanjan University of Medical Sciences, End of Mahdavi Blvd, Shahrak-e Karmandan, 4513956111, Zanjan, Iran
    Department of Genetics and Molecular Medicine, Zanjan University of Medical Sciences, End of Mahdavi Blvd, Shahrak-e Karmandan, 4513956111, Zanjan, Iran
    Department of Biotechnology, Shahid Beheshti University of Medical Sciences, Velenjak, 7th Floor, Bldg No 2 SBUMS, Arabi Ave, 19839-63113, Tehran, Iran
    Department of Research and Development, Production and Research Complex, Pasteur Institute, No 69, Pasteur Ave, 1316943551, Tehran, Iran

    شاپا
    2008-3866
    2008-3874
    URI
    https://dx.doi.org/10.22038/ijbms.2019.32736.7859
    http://ijbms.mums.ac.ir/article_13237.html
    https://iranjournals.nlai.ir/handle/123456789/340726

    مرور

    همه جای سامانهپایگاه‌ها و مجموعه‌ها بر اساس تاریخ انتشارپدیدآورانعناوینموضوع‌‌هااین مجموعه بر اساس تاریخ انتشارپدیدآورانعناوینموضوع‌‌ها

    حساب من

    ورود به سامانهثبت نام

    آمار

    مشاهده آمار استفاده

    تازه ترین ها

    تازه ترین مدارک
    © کليه حقوق اين سامانه برای سازمان اسناد و کتابخانه ملی ایران محفوظ است
    تماس با ما | ارسال بازخورد
    قدرت یافته توسطسیناوب