Endothelial-Derived Exteracellular Vesicles Promote In Vitro Human Embryonic Stem Cell-Derived Retinal Pig-ment Epithelium Proliferation
سال انتشار: 1398
نوع سند: مقاله کنفرانسی
زبان: انگلیسی
مشاهده: 412
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شناسه ملی سند علمی:
RROYAN20_077
تاریخ نمایه سازی: 29 مهر 1398
چکیده مقاله:
Background: Human embryonic stem cell-derived retinal pig-mented epithelium (hESC-RPE) transplantation inspires some hopes for the treatment of retinal degenerative diseases. There are some studies that confirmed the powerful role of endothelial cells conditioned medium (ECs-CM) on RPE cells expansion. A current study aimed to investigate the effect of ECs extracel-lular vesicles (EVs), as an important part of paracrine factors on hESC-RPE Proliferation.Materials and Methods: The EVs were isolated from HU-VECs conditioned, then characterized by BCA protein assay, Dynamic light scattering, and western blot. 24 h post 50,000 cells/cm2 hESC-RPE cells seeding, the 75 µg/ml EVs were add-ed every two each day. At 9th days, both groups including PBS and EVs were considered for further experiments. To evaluate the effect of EVs on hESC-RPE proliferation, we conducted Ki-67 immunostaining and evaluate the monolayer organization by ZO1 staining.Results: The isolated EVs passed all criteria, the mean parti-cle diameter was 88.6 nm, and the expression of EVs marker was approved by CD81 western blot. At the 9th day, Ki-67 posi-tive cells in EVs treated hESC-RPE were 143.41 ± 9.72 which is significantly higher compared to the control group 41.00 ± 10.39 (P<0.0001). The result of ZO1 staining also indicates that EVs could accelerate the hESC-RPE monolayer formation.Conclusion: These results confirmed that the EVs secreted by HUVECs promoted expansion and monolayer formation that could be beneficial for obtaining higher numbers of hESC-RPE cells. Also, it is plausible that EVs could potentially stimulate RPE proliferation and regeneration at the early stages of retinal degenerative diseases. Further investigations on the effects of HUVECs- EVs are needed.
کلیدواژه ها:
نویسندگان
FS Hosseini Mazinani
۱. Department of Medical Genetics, National Institute of Genetic Engineering and Biotechnology, Tehran, Iran. Department of Brain and Cognitive Science, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran
MH Sanati
Department of Medical Genetics, National Institute of Genetic Engineering and Biotechnology, Tehran, Iran
H Baharvand
Department of Stem Cells and Developmental Biology, Royan In-stitute for Stem Cell Biology and Technology, ACECR, Tehran, Iran
L Satarian
Department of Brain and Cognitive Science, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran