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
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
| 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) |
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| 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. |
| نام فایل |
تاریخ درج فایل |
اندازه فایل |
دانلود |
| nourazarian.pdf | 1398/05/03 | 4622263 | دانلود |