Macrophage-activating lipopeptide-2 requires Mal and PI3K for efficient induction of heme oxygenase-1

• Published in: PloS one 2014-07, Vol.9 (7), p.e103433-e103433
• Main Authors: You, Xiaoxing, Liu, Liangzhuan, Zeng, Yanhua, Li, Ranhui, He, Jun, Ma, Xiaohua, Jiang, Chuanhao, Zhu, Cuiming, Chen, Liesong, Yu, Minjun, Ou, Guangli, Wu, Yimou
• Format: Article
• Language: English
• Subjects: 1-Phosphatidylinositol 3-kinase; Activation; Adapter proteins; Adapters; Antibodies; Biology; Biology and Life Sciences; Bruton's tyrosine kinase; Cell Line; Chemiluminescence; Confocal microscopy; Cytokines; Cytosol; Densitometers; Electrophoretic mobility; Enzyme Induction; Gel electrophoresis; Heme; Heme oxygenase (decyclizing); Heme Oxygenase-1 - biosynthesis; Homeostasis; Humans; Immunofluorescence; Immunoprecipitation; Incubation; Infection; Infections; Inflammation; Inhibition; Kinases; Laboratories; Lipopeptides - physiology; Localization; Luciferase; Macrophages; MALP2 protein; Membranes; Microscopy; Monocytes; Mutation; Mycoplasma; MyD88 protein; Oxygenase; Phosphatidylinositol 3-Kinases - metabolism; Plasmids; Pretreatment; Proteins; Rodents; Signal transduction; siRNA; Sodium lauryl sulfate; Src protein; TLR2 protein; Toll-like receptors; Toll-Like Receptors - physiology; Transfection; Translocation; Tumor necrosis factor-TNF; Western blotting
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0103433

This study is to investigate the mechanisms by which macrophage-activating lipopeptide-2 (MALP-2) induces heme oxygenase (HO)-1, a cytoprotective enzyme that catalyzes the degradation of heme, in human monocytes. Human monocytic THP-1 cells were cultured for transient transfection with plasmids and stimulation with MALP-2 for indicative time intervals. After incubation with MALP-2, cells were collected and disrupted, before being tested for promoter activity using luciferase assay. For analysis of proteins, immunoreactive bands were detected using an enhanced chemiluminescence Western blotting system, and the band intensity was measured by densitometryic analysis. For the detection of co-immunoprecipitation, SDS-PAGE was performed and the membranes were probed using respective antibodies. To investigate the cellular localization of NF-E2-related factor 2 (Nrf2), cells underwent immunofluorescence staining and confocal microscopy, and were analyzed using electrophoretic mobility shift assay. MALP-2-induced HO-1 expression and promoter activity were abrogated by transfection with dominant negative (DN) plasmids of TLR2 and TLR6, or their neutralizing antibodies. However, inhibition of MyD88 or transfection with the DN-MyD88 was insufficient to attenuate HO-1 expression. In contrast, mutation or silencing of MyD88 adapter-like (Mal) by DN-Mal or siRNA almost completely blocked HO-1 induction. Btk, c-Src and PI3K were also involved in MALP-2-induced HO-1 expression, as revealed by specific inhibitors LFM-A13, PP1 and LY294002, or by transfection with siRNA of c-Src. MALP-2-induced activation of PI3K was attenuated by transfection with DN mutant of Mal, and by pretreatment with LFM-A13 or PP1. Furthermore, MALP-2 stimulated the translocation of Nrf2 from the cytosol to the nucleus and Nrf2 binding to the ARE site in the HO-1 promoter, which could also be inhibited by pretreatment with a PI3K inhibitor, LY294002. These results indicated that MALP-2 required TLR2/6, Btk, Mal and c-Src to activate PI3K, which in turn initiated the activation of Nrf2 for efficient HO-1 induction.