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Translocation of mixed lineage kinase domain-like protein to plasma membrane leads to necrotic cell death
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Translocation of mixed lineage kinase domain-like protein to plasma membrane leads to necrotic cell death
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Journal Article
Translocation of mixed lineage kinase domain-like protein to plasma membrane leads to necrotic cell death
2014
Overview
Mixed lineage kinase domain-like protein （MLKL） was identified to function downstream of receptor interacting protein 3 （RIP3） in tumor necrosis factor-α （TNF）-induced necrosis （also called necroptosis）. However, how MLKL functions to mediate necroptosis is unknown. By reconstitution of MLKL function in MLKL-knockout cells, we showed that the N-terminus of MLKL is required for its function in necroptosis. The oligomerization of MLKL in TNF-treated cells is essential for necroptosis, as artificially forcing MLKL together by using the hormone-binding domain （HBD＊） triggers necroptosis. Notably, forcing together the N-terminal domain （ND） but not the C-terminal kinase domain of MLKL causes necroptosis. Further deletion analysis showed that the four-α-helix bundle of MLKL （1-130 amino acids） is sufficient to trigger necroptosis. Both the HBD＊-mediated and TNF-induced complexes of MLKL（ND） or MLKL are tetramers, and translocation of these complexes to lipid rafts of the plasma membrane precedes cell death. The homo-oligomerization is required for MLKL translocation and the signal sequence for plas- ma membrane location is located in the junction of the first and second a-helices of MLKL. The plasma membrane translocation of MLKL or MLKL（ND） leads to sodium influx, and depletion of sodium from the cell culture medium inhibits necroptosis. All of the above phenomena were not seen in apoptosis. Thus, the MLKL oligomerization leads to translocation of MLKL to lipid rafts of plasma membrane, and the plasma membrane MLKL complex acts either by itself or via other proteins to increase the sodium influx, which increases osmotic pressure, eventually leading to membrane rupture.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
/ Animals
/ Biomedical and Life Sciences
/ Humans
/ Membrane Microdomains - metabolism
/ Mice
/ Original
/ Osmotic Pressure - physiology
/ Protein Kinases - metabolism
/ Protein Transport - physiology
/ Receptor-Interacting Protein Serine-Threonine Kinases - genetics
/ Signal Transduction - genetics
/ Sodium
/ Tumor Necrosis Factor-alpha - metabolism
/ 坏死性
/ 易位
/ 激酶
/ 细胞死亡
/ 结构域
/ 蛋白
/ 谱系
/ 质膜
