Treatment of human neuroblastoma cell line SH‐SY5Y with HSP27 siRNA tagged‐exosomes decreased differentiation rate into mature neurons

Treatment of human neuroblastoma cell line SH‐SY5Y with HSP27 siRNA tagged‐exosomes decreased differentiation rate into mature neurons


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نویسندگان: الهامه شکراللهی , علیرضا نورآذریان , رضا رهبرقاضی , لیلا سلیمی , سعیده کرباس فروش , مجید خاکسار , صادق سالاری نسب , علیرضا ابهری , مرتضی حیدرزاده

کلمات کلیدی: differentiation, exosome, HSP27, human neuroblastoma cell line

نشریه: 19614 , 11 , 234 , 2019

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نویسنده ثبت کننده مقاله علیرضا نورآذریان
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه دانشکده پزشکی
کد مقاله 66521
عنوان فارسی مقاله Treatment of human neuroblastoma cell line SH‐SY5Y with HSP27 siRNA tagged‐exosomes decreased differentiation rate into mature neurons
عنوان لاتین مقاله Treatment of human neuroblastoma cell line SH‐SY5Y with HSP27 siRNA tagged‐exosomes decreased differentiation rate into mature neurons
ناشر 9
آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ بلی
عنوان نشریه (خارج از لیست فوق)
نوع مقاله Original Article
نحوه ایندکس شدن مقاله ایندکس شده سطح یک – ISI - Web of Science
آدرس لینک مقاله/ همایش در شبکه اینترنت

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Heat shock proteins (HSPs) participate in the regulation of different cell activities in response to stimuli. By applying different strategies, the modulation of heat shock proteins is at the center of attention. Conventional delivery approaches are not fully encouraged due to cytotoxicity and immunogenicity issues. Exosomes are touted as bio‐shuttles for delivery of distinct biomolecules inside the cells. Here, we aimed to HSP27 small interfering RNA (siRNA)‐tagged exosomes for the inhibition of Hsp27 in human neuroblastoma cell line SH‐SY5Y and explored differentiation into neuron‐like cells. Exosomes were isolated, characterized by scanning electron microscope (SEM) and CD63 then enriched with siRNA against Hsp27. Neuroblastoma cells were incubated with exosomes carrying siRNA for 48 hr. Exosome uptake was monitored by immunofluorescence assay. The cell viability and proliferation were analyzed using 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide and bromodeoxyuridine/ 5‐bromo‐2′‐deoxyuridine incorporation assays. The ability of cells to form colonies was evaluated by clonogenic assay. The cell potential to express NeuN, a mature neuron factor, was studied by flow cytometry analysis. SEM showed the nanosized particles and a high level of CD63 after enrichment. Immunofluorescence imaging revealed an appropriate transfection rate in cell exposed to Hsp27 siRNA tagged exosomes. The cell viability and proliferation were reduced compared to cells received nude exosomes (p < 0.05). Clonogenic activity of cells was diminished by the inhibition of Hsp27. Flow cytometry analysis revealed that the inhibition of Hsp27 prohibited NeuN content, showing the maturation of SH‐SY5Y cells to mature cells compared to control. These data confirmed that exosomes could be used as appropriate bio‐shuttles for the inhibition of Hsp27‐aborted cell differentiation toward mature neuron.

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نویسنده نفر چندم مقاله
الهامه شکراللهیاول
علیرضا نورآذریاندوم
رضا رهبرقاضیسوم
لیلا سلیمیچهارم
سعیده کرباس فروشپنجم
مجید خاکسارششم
صادق سالاری نسبهفتم
علیرضا ابهریهشتم
مرتضی حیدرزادهنهم

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