摘要
目的:探讨酶修饰低密度脂蛋白(E-LDL)对外周血中树突状细胞(DC)分化成熟的影响以及地尔硫对其的影响作用。方法:梯度离心法分离人外周血单核细胞,用含重组人粒细胞-巨噬细胞集落刺激因子和重组人白介素4的Cellgro培养液培养5d,使其分化为DC。分别用E-LDL、地尔硫加E-LDL刺激DC48h后,镜下观察DC的形态,采用流式细胞术检测DC表型(CD1a、CD80、CD86、HLA-DR)的表达,并设磷酸缓冲盐对照组进行比较。结果:光镜下DC形态无明显变化,各组DC的CD1a、CD80、CD86和HLA-DR的表达有显著性差异(P<0.05),E-LDL处理后DC表面抗原的表达较对照组升高,地尔硫加E-LDL处理后DC表面抗原的表达较E-LDL组下调。结论:E-LDL可促进DC的分化成熟,地尔硫对E-LDL激活DC具有抑制作用。
OBJECTIVE: To investigate the effect of enzymatically modified low density lipoprotein (E - LDL) on differation and maturation of human dendritic cells(DC) in peripheral blood and the effect of diltiazem on it. METHODS: Human monoeytes were isolated by using gradient centrifugation method and cultured in DC Cellgro medium containing rhGM CSF and rhIL - 4 for 5 days, then DC was then obtained. DC were treated with E - LDL or E - LDL plus diltiazem for 48 hours,the morphological changes were observed under the microscope, and the FACS was used to investigate the expression of DC (CDla, CD80, CD86 and HLA - DR) .PBS group was set up for comparison. RESULTS: The morphological changes were nor observed. The expressions of CDla, CD80, CD86 and HLA DR in each groups were significant different(P〈0.05) . The immunophenotypic expression of DC in E - LDL group increased compared with the control group. The expression reduced significantly in diltiazem plus E- LDL group compared with E- LDL group. CONCLUSIONS: It suggests that E- LDL can promote the differation and maturation of DC which may be inhibited by diltiazem.
出处
《中国药房》
CAS
CSCD
北大核心
2009年第13期989-990,共2页
China Pharmacy
关键词
酶修饰低密度脂蛋白
树突状细胞
地尔硫[
]
表达
Enzymatically modified low density lipoprotein
Dendritic Cell
Diltiazem
Expression