首页> 外文期刊>The Journal of protozoology research >Toxoplasma gondii modulates neutral lipid metabolism in macrophage J774 cells.
【24h】

Toxoplasma gondii modulates neutral lipid metabolism in macrophage J774 cells.

机译:弓形虫调节巨噬细胞J774细胞的中性脂质代谢。

获取原文
获取原文并翻译 | 示例
           

摘要

The intracellular protozoan Toxoplasma gondii scavenges cholesterol from host cells for its growth. Here, we demonstrated that T. gondii modified neutral lipid metabolism in macrophage cell line J774A.1 cells. Cell-surface expression of low-density lipoprotein receptor (LDLR) and the scavenger receptor SR-A were increased upon T. gondii infection at 40 hours post infection (hpi). In addition, RT-PCR analyses showed that the infection induced the upregulation of hydroxymethylglutaryl-CoA (HMG-CoA) reductase at 20 hpi and ATP-binding cassette, sub-family A (ABC1), member 1 (ABCA1) at 40 hpi. On the other hand, the downregulation of acyl-CoA: cholesterol acyltransferase 1 (ACAT1) and hormone sensitive lipase (HSL) was observed at 40 hpi. Acyl-CoA: diacylglycerol acyltransferase 1 (DGAT1) expression increased in both infected and uninfected cells at 40 hpi. Accumulation of lipid bodies and high levels of cellular cholesterol and triacylglycerols (TAG) were observed in J774A.1 cells following T. gondii infection. These results suggest that intracellular cholesterol may be used for T. gondii replication, not for lipid body formation. Our findings support the notion that modulation of the lipid metabolism in host cells is a potential strategy for the treatment and prevention of toxoplasmosis.
机译:细胞内的原生动物弓形虫会清除宿主细胞中的胆固醇以使其生长。在这里,我们证明了 T。刚地改良巨噬细胞J774A.1细胞中的中性脂质代谢。 T后,低密度脂蛋白受体(LDLR)和清道夫受体SR-A的细胞表面表达增加。感染后40小时(hpi)感染了刚地犬。此外,RT-PCR分析显示,感染在20 hpi时诱导了羟甲基戊二酰辅酶A(HMG-CoA)还原酶的上调,在40 hpi时诱导了ATP结合盒,亚家族A(ABC1),成员1(ABCA1)的上调。另一方面,在40 hpi时观察到了酰基辅酶A:胆固醇酰基转移酶1(ACAT1)和激素敏感性脂肪酶(HSL)的下调。酰基辅酶A:二酰基甘油酰基转移酶1(DGAT1)在感染后和未感染的细胞中均在40 hpi时表达增加。 T后,在J774A.1细胞中观察到脂质体的积累以及高水平的细胞胆固醇和三酰基甘油(TAG)。刚地感染。这些结果表明细胞内胆固醇可用于T。刚地复制,而不是用于脂质体的形成。我们的发现支持以下观点:调节宿主细胞中的脂质代谢是治疗和预防弓形虫病的潜在策略。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号