酪氨酸激酶Src在白色念珠菌感染中的机制研究  被引量:1

Effects of tyrosine kinase Src during C.albicans infection in murine macrophage

在线阅读下载全文

作  者:崔树娜[1] 钱静[1] 卜平[1] 

机构地区:[1]扬州大学医学院中西医结合学系,225001

出  处:《实用医学杂志》2014年第11期1702-1704,共3页The Journal of Practical Medicine

基  金:江苏省高校自然科学研究项目(编号:13KJB310022);中国博士后基金项目(编号:2013M541741);江苏省中医药局科技项目(编号:LZ13248);扬州大学高层次人才科研启动基金项目(2012)(编号:13KJB310022)

摘  要:目的:探讨酪氨酸激酶Src在白色念珠菌感染中的作用及其机制。方法:通过Alarmarblue法检测不同浓度Src抑制剂PP2作用巨噬细胞不同时间点对细胞增殖的影响,通过荧光定量法检测巨噬细胞对FITC标记的白色念珠菌感染吞噬作用的影响.采用ELISA法检测PP2对巨噬细胞感染白色念珠菌产生细胞因子TNF-α和IL-10的影响。结果:0~33.3μmol/L的PP2作用细胞2h后对细胞生长无明显影响。11.1、33.3μmol/L的PP2作用细胞24h后细胞增殖率分别为78%、9%,48h后增殖率分别为54%、13%。11.1μmol/L的PP2仅在作用巨噬细胞48h后,抑制巨噬细胞对白色念珠菌的吞噬,此作用可能与抑制增殖相关.然而,PP2能显著抑制白色念珠菌对巨噬细胞的免疫应答,表现为显著抑制细胞因子TNF—α和IL-10的产生.有效浓度为11.1~33.3μmol/L(P〈0.01)。结论:酪氨酸激酶Src在巨噬细胞识别白色念珠菌感染中起着重要作用,尤其在细胞因子免疫应答中作用更加显著。Objective To investigate the role of tyrosine kinase Src in a murine C.a!bicans infection model. Methods Observed cell proliferation by alarmarblue assay at 2, 24 and 48 h after Src inhibitor PP2 treatment. Phagocytosis was determined by a fluorometric assay. Cytokine TNF-α and IL-10 production was detected by ELISA. Results The 0 ~ 33.3 μmol/L PP2 had no effect on cell proliferation after PP2 treatment for 2 h. When the PP2 treatment extended to 24 or 48 h, PP2 (11.1, 33.3 μmol/L) showed significant inhibition on cell proliferation with 78%, 9%, and 54%, 13%, respectively. At 48 h after 11.1 μmol/L PP2 treatment, the internalization of C.albicans in macrophage is significantly inhibited, contributing to the inhibition of cell proliferation. However, the 11.1 and 33.3 μmol/L PP2 significantly inhibited the cytokine TNF-α and IL-10 production during C.albicons infection (P 〈 0.01 ). Conclusion Src kinase played an important role during C.albicans infection, especially for the cytokine TNF-α and IL- 10 production.

关 键 词:念珠菌病 SRC激酶 白色念珠菌 巨噬细胞 

分 类 号:R379.4[医药卫生—病原生物学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象