2016
DOI: 10.3109/08923973.2016.1138968
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Up-regulation of TDAG51 is a dependent factor of LPS-induced RAW264.7 macrophages proliferation and cell cycle progression

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Cited by 11 publications
(12 citation statements)
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“…However, the PTEN inhibitor SF1670 completely abrogated the effect of coelonin (Figure 8). We noticed that LPS treatment also induced RAW264.7 cells G1 phase arrest (Figure 8B), which contradicts a previous report [20], but is consistent with report [49]. The exact molecular mechanism underlying these contradictory results need to be further studied, but it is clear that LPS-induced G1 phase arrest in RAW264.7 cells did not occur through the up-regulation of p27 Kip1 .…”
Section: Discussionsupporting
confidence: 77%
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“…However, the PTEN inhibitor SF1670 completely abrogated the effect of coelonin (Figure 8). We noticed that LPS treatment also induced RAW264.7 cells G1 phase arrest (Figure 8B), which contradicts a previous report [20], but is consistent with report [49]. The exact molecular mechanism underlying these contradictory results need to be further studied, but it is clear that LPS-induced G1 phase arrest in RAW264.7 cells did not occur through the up-regulation of p27 Kip1 .…”
Section: Discussionsupporting
confidence: 77%
“…In addition, we performed a protein network analysis using REACTOME () to identify major interactions, three major cellular processes were significantly enriched ( p value < 0.05) as follows: (1) Immune system, (2) signal transduction, and (3) cell cycle. LPS is the component of the outer membrane of Gram-negative bacteria, and is one of the most well characterized pathogen-associated molecular patterns (PAMPs), which can be recognized by Toll-like receptor 4 (TLR4), and trigger innate responses [19], such as enhancing the secretion of cytokines and chemokines, and promoting macrophages migration and proliferation [20]. Therefore, it is evident that the protein network analysis results imply coelonin may block LPS induced RAW264.7 cell signal transduction, immune response, and proliferation.…”
Section: Resultsmentioning
confidence: 99%
“…The statistical significance of differences between mean values for the various experimental groups and controls was determined as previously described (Jiao et al, 2016). Values of P <0.05 were considered significantly different (*), and P<0.01 indicated high statistical differences (**).…”
Section: Discussionmentioning
confidence: 99%
“…PAM cells were seeded into 12-well culture plates (8×10 5 cells/well) at 0 h, stimulated by B.suis LPS at the concentrations of 0.1, 1, 10, 100, 1000 μg/mL after 24 h, harvested at 48 h. And then, the concentration of 100 ng/mL B. suis LPS was used for stimulation of the time points of 3, 6, 12, 24, 48 and 96 h. siRNAs transfection: PAM cells were seeded into 12-well culture plates (8×10 5 cells/well) at 0 h, to optimize siRNA transfection efficiency, we used X-tremeGENE siRNA Transfection Reagent (Roche, Basel, Switzerland) to transfect with the FITC-siRNA (Santa Cruz Biotechnology, CA, USA) at 12 h post-seeding, optimizing the ratio of X-tremeGENE siRNA Transfection Reagent and FITC-siRNA obtained a more than 90% transfection efficiency measured by flow cytometry. Caspase-11 siRNA targeting caspase-11 (Santa Cruz Biotechnology) siRNAs or Control siRNA-A (scramble siRNA, Santa Cruz Biotechnology) were introduced into PAM cells as described previously (Jiao et al, 2016), and according to the instructions of X-tremeGENE siRNA Transfection Reagent (Roche, Basel, Switzerland) .…”
Section: Bsuis Lps Extraction and Cell Stimulationmentioning
confidence: 99%
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