Hamuti Azeguli, Li Jinyu, Zhou Fangfang, Aipire Adila, Ma Ji, Yang Jianhua, Li Jinyao
Xinjiang Key Laboratory of Biological Resources and Genetic Engineering, College of Life Science and Technology, Xinjiang University, 666 Shengli Road, Urumqi 830046, China.
Texas Children's Cancer Center, Department of Pediatrics, Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, TX 77030, USA.
Molecules. 2017 Jan 7;22(1):97. doi: 10.3390/molecules22010097.
L. () has been used as food and traditional medicine and shows anti-inflammatory and anti-oxidant activities. Here, we prepared the fruit ethanol extracts (CSEs) using different procedures and investigated the effects of CSE on the maturation of mouse bone marrow-derived dendritic cells (DCs) in the absence or presence of lipopolysaccharide (LPS). DC maturation and cytokine production were detected by flow cytometry and ELISA, respectively. We obtained three different CSEs and dissolved in water or DMSO, named CSE2W, CSEMW, CSE3W, CSE2D, CSEMD, and CSE3D, respectively. These CSEs showed different effects on DC maturation. CSEMW and CSEMD significantly increased the expressions of CD40, CD80, and CD86, in a dose-dependent manner. CSE2W and CSE2D also showed a modest effect on DC maturation, which enhanced the expression of CD40. CSE3W and CSE3D did not change DC maturation but suppressed LPS-induced DC maturation characterized by the decreased levels of CD40 and CD80. CSE3W and CSE3D also significantly inhibited the secretions of IL-12p40, IL-6, IL-1β, and TNF-α induced by LPS. CSE3W further increased the level of IL-10 induced by LPS. Moreover, CSE3D suppressed LPS-induced DC maturation in vivo, which decreased the expressions of CD40 and CD80. These results suggested that CSE3W and CSE3D might be used to treat inflammatory diseases.
L.()已被用作食物和传统药物,并具有抗炎和抗氧化活性。在此,我们采用不同方法制备了果实乙醇提取物(CSEs),并研究了CSE在无脂多糖(LPS)或有LPS存在的情况下对小鼠骨髓来源树突状细胞(DCs)成熟的影响。分别通过流式细胞术和酶联免疫吸附测定法检测DC成熟和细胞因子产生情况。我们获得了三种不同的CSEs,并分别溶于水或二甲基亚砜(DMSO),命名为CSE2W、CSEMW、CSE3W、CSE2D、CSEMD和CSE3D。这些CSEs对DC成熟表现出不同影响。CSEMW和CSEMD以剂量依赖方式显著增加CD40、CD80和CD86的表达。CSE2W和CSE2D对DC成熟也有一定作用,增强了CD40的表达。CSE3W和CSE3D未改变DC成熟,但抑制了以CD40和CD80水平降低为特征的LPS诱导的DC成熟。CSE3W和CSE3D还显著抑制了LPS诱导的IL-12p40、IL-6、IL-1β和TNF-α的分泌。CSE3W进一步增加了LPS诱导的IL-10水平。此外,CSE3D在体内抑制了LPS诱导的DC成熟,降低了CD40和CD80的表达。这些结果表明CSE3W和CSE3D可能用于治疗炎症性疾病。