Human Platelet-Rich Plasma-Derived Exosomes Promote the Proliferation of Schwann Cells Cultured in Vitro.
10.3881/j.issn.1000-503X.15332
- Author:
Dan YI
1
;
Yong-Yi ZHANG
1
;
Wen-Li JIANG
2
;
Mo-Lin LI
1
;
Xiang-Hui CHEN
1
;
Jiang YU
1
;
Hong-Yu YI
1
;
Ya-Qiong ZHU
2
;
Yue-Xiang WANG
2
Author Information
1. Medical School of Chinese PLA,Beijing 100853,China.
2. Department of Ultrasound,the First Medical Centre,Chinese PLA General Hospital,Beijing 100853,China.
- Publication Type:Journal Article
- Keywords:
Schwann cell;
exosomes;
nerve regeneration;
platelet-rich plasma;
proliferation
- MeSH:
Humans;
Rats;
Animals;
Exosomes/metabolism*;
Platelet-Rich Plasma;
Schwann Cells;
Coculture Techniques;
Cell Proliferation;
Cells, Cultured
- From:
Acta Academiae Medicinae Sinicae
2023;45(3):374-381
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the effect of human platelet-rich plasma-derived exosomes(PRP-exos)on the proliferation of Schwann cell(SC)cultured in vitro. Methods PRP-exos were extracted by polymerization-precipitation combined with ultracentrifugation.The morphology of PRP-exos was observed by transmission electron microscopy,and the concentration and particle size distribution of PRP-exos were determined by nanoparticle tracking analysis.Western blotting was employed to determine the expression of the marker proteins CD63,CD81,and CD9 on exosome surface and the platelet membrane glycoprotein CD41.The SCs of rats were isolated and cultured,and the expression of the SC marker S100β was detected by immunofluorescence staining.The fluorescently labeled PRP-exos were co-cultured with SCs in vitro for observation of their interaction.EdU assay was employed to detect the effect of PRP-exos on SC proliferation,and CCK-8 assay to detect the effects of PRP-exos at different concentrations(0,10,20,40,80,and 160 μg/ml)on SC proliferation. Results The extracted PRP-exos appeared as uniform saucer-shaped vesicles with the average particle size of(122.8±38.7)nm and the concentration of 3.5×1012 particles/ml.CD63,CD81,CD9,and CD41 were highly expressed on PRP-exos surface(P<0.001,P=0.025,P=0.004,and P=0.032).The isolated SCs expressed S100β,and PRP-exos could be taken up by SCs.PRP-exos of 40,80,and 160 μg/ml promoted the proliferation of SCs,and that of 40 μg/ml showed the best performance(all P<0.01). Conclusions High concentrations of PRP-exos can be extracted from PRP.PRP-exos can be taken up by SCs and promote the proliferation of SCs cultured in vitro.
