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Ultrasound-guided platelet-rich plasma injection and multimodality ultrasound examination of peripheral nerve crush injury

机译:超声引导血小板富含血浆注射和外周神经挤压损伤的多模超声检查

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摘要

a Immunostaining of harvested SCs. b SCs exposed to various PRP concentrations during 5 days of culture. c, d displayed the SCs count during 3 days and 5 days of culture (*P < 0.05, **P < 0.01). e CCK-8 colorimetric assay was performed to evaluate the effect of PRP in various concentration on the proliferation of SCs (**P < 0.01 vs. control group; ††P < 0.01 vs. PRP-6.5× group; ‡‡P < 0.05 vs. other five groups). f The NGF-β, VEGF and GDNF secreted by SCs that cultured with PRP at different concentrations were measured by ELISA at 5 days of culture (*P < 0.05 **P < 0.01 vs. control group; ††P < 0.01 vs. PRP-6.5× group; ‡‡P < 0.05 vs. other five groups). Error bars = SD, n = 3. SCs Schwann cells, PRP platelet-rich plasma, CCK-8 Cell Counting Kit-8.
机译:收获的SCS的免疫染色。在5天的培养期间暴露于各种PRP浓度的B SC。 C,D在3天和5天培养期间显示SCS计数(* P <0.05,** P <0.01)。进行CCK-8比色测定进行评价PRP在各种浓度上对SCs的增殖的影响(** P <0.01对照组;††P<0.01对照组;‡‡P < 0.05与其他五组)。 f通过以不同浓度培养的SCS分泌的NGF-β,VEGF和GDNF以ELISA在培养的5天中测量(* P <0.05 ** P <0.01对照组;††P <0.01 Vs. PRP-6.5×组;‡‡P <0.05与其他五组)。误差棒= SD,n = 3.SCS施万细胞,PRP富含血小板的等离子体,CCK-8 Cell计数套件-8。

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