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19 kDa结核分枝杆菌脂蛋白(LpqH)通过外源性和内源性途径诱导巨噬细胞凋亡:线粒体凋亡诱导因子的作用。

The 19 kDa Mycobacterium tuberculosis lipoprotein (LpqH) induces macrophage apoptosis through extrinsic and intrinsic pathways: a role for the mitochondrial apoptosis-inducing factor.

作者信息

Sánchez Alejandro, Espinosa Patricia, García Teresa, Mancilla Raúl

机构信息

Departamento de Inmunología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Circuito Escolar S/N, Ciudad Universitaria, 04510 México, DF, Mexico.

出版信息

Clin Dev Immunol. 2012;2012:950503. doi: 10.1155/2012/950503. Epub 2012 Dec 19.

Abstract

We describe the association of caspase-dependent and caspase-independent mechanisms in macrophage apoptosis induced by LpqH, a 19 kDa Mycobacterium tuberculosis lipoprotein. LpqH triggered TLR2 activation, with upregulation of death receptors and ligands, which was followed by a death receptor signaling cascade with activation of initiator caspase 8 and executioner caspase 3. In this caspase-mediated phase, mitochondrial factors were involved in loss of mitochondrial transmembrane potential (ΔΨm), release of cytochrome c, and caspase 9 activation. Interestingly, a caspase-independent pathway was also identified; by immunoblot, the mitochondrial apoptosis inducing factor (AIF) was demonstrated in nuclei and cytosol of LpqH-treated macrophages. Confocal microscopy revealed translocation of AIF to the nuclei of the majority of apoptotic cells. These findings emphasize the complex and redundant nature of the macrophage death response to mycobacteria.

摘要

我们描述了19 kDa结核分枝杆菌脂蛋白LpqH诱导巨噬细胞凋亡过程中,半胱天冬酶依赖性和非依赖性机制之间的关联。LpqH触发了Toll样受体2(TLR2)激活,导致死亡受体及其配体上调,随后是死亡受体信号级联反应,起始半胱天冬酶8和执行半胱天冬酶3被激活。在这个由半胱天冬酶介导的阶段,线粒体因子参与了线粒体跨膜电位(ΔΨm)的丧失、细胞色素c的释放以及半胱天冬酶9的激活。有趣的是,还发现了一条不依赖半胱天冬酶的途径;通过免疫印迹法,在LpqH处理的巨噬细胞核和细胞质中证实了线粒体凋亡诱导因子(AIF)的存在。共聚焦显微镜显示,AIF易位至大多数凋亡细胞的细胞核。这些发现强调了巨噬细胞对分枝杆菌死亡反应的复杂性和冗余性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b89/3536062/046fd73ca1a1/CDI2012-950503.001.jpg

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