Article Summary
李晓燕,张 艳,李 辉,董春萍,吴贵福.富含血小板血浆和脐带干细胞联用对糖尿病足模型lncRNA表达谱的影响[J].现代生物医学进展英文版,2018,(22):4224-4228.
富含血小板血浆和脐带干细胞联用对糖尿病足模型lncRNA表达谱的影响
Effects of Platelet Rich Plasma and Umbilical Cord Stem Cells on the lncRNA Expression Profiles in Diabetic Foot Models
Received:April 09, 2018  Revised:May 06, 2018
DOI:10.13241/j.cnki.pmb.2018.22.005
中文关键词: 富含血小板血浆  脐带干细胞  糖尿病足  lncRNA表达谱
英文关键词: Platelet rich plasma  Umbilical cord stem cells  Diabetic foot  Expression profiles of lncRNA
基金项目:陕西省自然科学基础研究计划项目(2016JQ8055)
Author NameAffiliationE-mail
李晓燕 陕西省人民医院内分泌科 陕西 西安 710068 lkl2652@163.com 
张 艳 陕西省人民医院内分泌科 陕西 西安 710068  
李 辉 陕西省人民医院内分泌科 陕西 西安 710068  
董春萍 陕西省人民医院内分泌科 陕西 西安 710068  
吴贵福 陕西省人民医院内分泌科 陕西 西安 710068  
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中文摘要:
      摘要 目的:探讨富含血小板血浆(PRP)和脐带干细胞(UBC-MSCs)联用对糖尿病足(DF)模型lncRNA表达谱的影响。方法:采用SPF级SD大鼠(20只)建立糖尿病足模型,随机分为4组,每组5只大鼠。A组注射PBS于DF动物溃疡处,B组采用人PRP注射于DF动物溃疡处,C组采用人UBC-MSCs注射于DF动物溃疡处,D组采用人UBC-MSCs+PRP注射于DF动物溃疡处。治疗14d后,记录大鼠的血糖水平与血清CRP、TNF-α、VEGF相对表达,采用arraystar公司12×135K芯片测定lncRNA的表达谱。结果:治疗14d后,B、C、D组均较A组显著降低,D组显著低于B、C组,组间差异有统计学意义(P<0.05);D组大鼠的血清CRP、TNF-α相对表达较A、B、C组显著降低,血清VEGF相对表达较A、B、C组显著升高,差异都有统计学意义(P<0.05)。B组与A组比较存在1563个显著差异的IncRNA,C组与A组比较存在1982个显著差异的IncRNA,D组与A组比较存在2854个显著差异的IncRNA。将靶基因带入差异mRNA数据,筛选得到与DF相关的靶基因的lncRNA有6条,具体为CHI3L1、FA2H、CAMTA1、DOCK、STRADB和TNFRSF1A(P1101039、BF74369、Uc001aoh、N385370、AF116618和HMlincRNA1336)。结论:UBC-MSCs和PRP联合可能通过改变lncRNA的表达,影响炎症因子、血管生成因子等的表达,进而发挥降血糖和治疗DF的目的。
英文摘要:
      ABSTRACT Objective: To investigate the effect of platelet rich plasma (PRP) and umbilical cord stem cells (UBC-MSCs) on the expression profiles of lncRNA in diabetic foot (DF) models. Methods: The diabetic foot model of SPF SD rats (20 rats) were established and were divided into 4 groups randomly, 5 rats in each group. Group A were injected with PBS to DF animal ulcers, Group B were injected with PRP to DF animal ulcer, Group C were injected with UBC-MSCs to DF animal ulcer, Group D were injected with UBC-MSCs+PRP to DF animal ulcer, The expression level of lncRNA were detected by arraystar 12×135K chip. Results: After treatment for 14d, the blood glucose levels in group A, group B, group C and D group were 23.38±2.85 mmol/L, 13.88±3.19 mmol/L, 13.48±2.84 mmol/L and 7.22±3.18 mmol/L respectively, and compared the difference were statistically significant (P<0.05). The relative expression level of CRP and TNF-α in group Dwere decreased significantly, while VEGF were increased significantly, compared the difference were statistically significant (P<0.05). There were 1563 IncRNAs were significant differences compared between group B and group A, so that were 1982IncRNAs and 2854IncRNAs compared between the group C and group A, group D and group A; there were 6 lncRNAs of DF related target genes of common screened DF were changed in the difference mRNA data[CHI3L1, FA2H, CAMTA1, DOCK, STRADB and TNFRSF1A(P1101039, BF74369, Uc001aoh, N385370, AF116618 and HMlincRNA1336)]. Conclusion: The combination of UBC-MSCs and PRP could decrease the blood glucose and treat DF via may changing the expression of lncRNA and further mediating the expression of inflammatory factors, angiogenic factors, etc.
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