• 中国科学论文统计源期刊
  • 中国科技核心期刊
  • 美国化学文摘(CA)来源期刊
  • 日本科学技术振兴机构数据库(JST)

临床输血与检验 ›› 2021, Vol. 23 ›› Issue (4): 442-445.DOI: 10.3969/j.issn.1671-2587.2021.04.007

• 基础研究 • 上一篇    下一篇

冰冻保存PRP对IL-1β诱导的软骨细胞炎症反应的影响

杨晓亚, 高裕华, 刘素蕊, 李烛   

  1. 050082 石家庄,联勤保障部队第九八〇医院输血医学科
  • 收稿日期:2021-03-04 发布日期:2021-08-18
  • 作者简介:杨晓亚(1979-),女,河北石家庄人,主管技师,博士,主要从事血液治疗方面研究,(Tel)0311-87978562(E-mail)hpyykyzy@163.com。

Effect of Frozen Storage Platelet-rich Plasma on Inflammatory Response of IL-1β-I Induced Chondrocyte

YANG Xiao-ya, GAO Yu-hua, LIU Su-rui, et al   

  1. Transfusion Department, The 980th Hospital of Joint Logistic Support Force,Shijiazhuang 050082
  • Received:2021-03-04 Published:2021-08-18

摘要: 目的 探讨冰冻保存对富血小板血浆(platelet-rich plasma,PRP)释放生长因子及体外抗软骨细胞炎症作用的影响,为合理利用自体PRP技术,保证临床治疗效果提供实验依据。方法 以机采血小板为原料,用4种不同方式冰冻保存,分别为-20 ℃、-80 ℃直接冻存及加5% DMSO -20 ℃、-80 ℃冻存,3个月后解冻制备PRP凝胶。ELISA法检测凝胶上清液中PDGF-AB、VEGF和IGF-1含量。制备体外软骨炎症细胞模型,CCK-8法检测冻存PRP对其增殖的影响,ELISA检测PRP对软骨炎症细胞分泌炎症因子IL-6的影响。结果 与新鲜PRP组相比,冷冻保存的PRP制备的凝胶上清液中PDGF-AB含量无显著变化,而VEGF、IGF-1含量明显下降。CCK-8结果表明,加5% DMSO -80 ℃冻存的PRP,对软骨炎症模型细胞增殖有显著促进作用,效果与新鲜制备的PRP相当,而-20 ℃、-80 ℃直接冻存以及加DMSO保护剂-20 ℃冻存的PRP对软骨炎症模型细胞增殖没有促进作用。检测软骨炎症模型细胞培养上清液中细胞因子IL-6的含量发现,PRP以四种冻存方式冻存3个月后,和新鲜PRP相比,在抑制软骨炎症细胞分泌炎症细胞因子IL-6方面无显著性差异。结论 冻存之后PRP凝胶上清液中部分细胞因子含量减少,但在体外针对IL-1β诱导的软骨细胞损伤,冻存PRP和新鲜PRP有相同的保护作用。

关键词: 富血小板血浆, PRP凝胶, 冰冻, 软骨细胞炎症

Abstract: Objective The aim of the present study is to investigate whether frozen could influence platelet-rich plasma (PRP) releases growth factors, and whether frozen PRP could protect chondrocyte from IL-1β-induced injury. Methods PRP concentrates were obtained from healthy subjects by apheresis and were divided into 4 groups, then were frozen for as long as 3 months. The storage condition was -20 ℃ without preservation agent, -80 ℃ without preservation agent, -20 ℃ in 5% DMSO and -80 ℃ in 5% DMSO. The growth factors (PDGF-AB, VEGF and IGF-1) in PRP releasates were quantified by ELISA. The effect of PRP on the proliferation of IL-1β induced chondrocytes’inflammation was detected by CCK-8. The levels of IL-6 in cells were detected by ELISA. Results No significant difference was observed in PDGF-AB levels among fresh PRP group and frozen PRP groups. VEGF and IGF-1 levels were significantly decreased in the PRP samples stored at frozen conditions. No obvious difference with CCK-8 assay was observed between the PRP stored in -80 ℃ in 5% DMSO group and fresh PRP group. They both can promote IL-1β-induced inflammatory chondrocyte' s proliferation. The other three experimental groups can’t promote IL-1β-induced chondrocyte proliferation. After PRP treatment, IL-6 production of inflammatory chondrocyte was decreased. No statistically significant differences were found in IL-6 production between fresh PRP and frozen PRPs. Conclusions ome growth factor levels of PRP were reduced after frozen storage. But the frozen PRP can protect IL-1β-induced chondrocyte injury by inhibiting inflammatory response.

Key words: Platelet-rich plasma, PRP gel, Frozen storage, Chondrocyte inflammation

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