Mediators of Inflammation

Mediators of Inflammation / 2019 / Article

Research Article | Open Access

Volume 2019 |Article ID 7634761 |

Min Shi, Yilin Deng, Heguo Yu, Ling Xu, Cuicui Shi, Jiong Chen, Guangming Li, Yiqi Du, Yu-gang Wang, "Protective Effects of Oridonin on Acute Liver Injury via Impeding Posttranslational Modifications of Interleukin-1 Receptor-Associated Kinase 4 (IRAK4) in the Toll-Like Receptor 4 (TLR4) Signaling Pathway", Mediators of Inflammation, vol. 2019, Article ID 7634761, 11 pages, 2019.

Protective Effects of Oridonin on Acute Liver Injury via Impeding Posttranslational Modifications of Interleukin-1 Receptor-Associated Kinase 4 (IRAK4) in the Toll-Like Receptor 4 (TLR4) Signaling Pathway

Academic Editor: Oleh Andrukhov
Received01 Jun 2019
Accepted09 Aug 2019
Published12 Sep 2019


Objective. Recent researches have demonstrated that inflammation-related diseases are effectively regulated by posttranslational modifications (PTMs) including phosphorylation and acetylation. Our previous study found a new acetyltransferase inhibitor, oridonin, which had a protective effect on acute liver injury (ALI). In the present study, we further investigated its protective mechanism against D-galactosamine (D-Gal) combined with lipopolysaccharide- (LPS-) induced ALI in mice. Methods. Intraperitoneal injections of LPS (40 μg/mouse)/D-Gal (5 mg/mouse) were given to the mice, and the experimental group was pretreated with intraperitoneal injection of oridonin (0.2 mg/mouse). To elucidate the protective mechanism of oridonin, we collected liver specimens and used RNA-sequencing (RNA-Seq) analysis. We focused on the genes that were upregulated by LPS/D-Gal and downregulated after pretreatment with oridonin. The downregulated genes examined by Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis were further verified by real-time polymerase chain reaction (PCR) and western blot. Results. GO analysis showed that genes that were downregulated after pretreatment with oridonin were extremely concentrated in immune response, chemotaxis, and inflammatory response. Real-time PCR confirmed that the expression of these genes was upregulated by LPS/D-Gal induction and reduced after treatment with oridonin, which was consistent with RNA-Seq results. KEGG pathway analysis showed a significantly enriched downregulated gene that was present in the Toll-like receptor (TLR) 4 signaling cascade. Our results manifested that phosphorylation levels of upstream signaling molecules in the TLR4 signaling cascade, including extracellular signal-regulated kinase (ERK), P38, and IκB, were significantly inhibited by oridonin. Furthermore, LPS/D-Gal stimulation triggered posttranslational modifications of related gene loci in the TLR4 signaling pathway, including phosphorylation of IL-1 receptor-associated kinase 4 (IRAK4 T345/S346) and acetylation of IRAK4 (K34). However, after treatment with oridonin, the modification pattern of IRAK4 expression stimulated by LPS/D-Gal was suggestively attenuated. Conclusion. Our study revealed that the protective effects of oridonin on LPS/D-Gal-induced ALI mediated by inhibition of the PTMs of IRAK4, including phosphorylation of T345/S346 and acetylation of K34.

1. Introduction

Severe acute liver injury (ALI) is a rapid pathological process that can be life-threatening [1]. Hepatitis virus, adverse drug effects, alcohol abuse, metabolic syndrome, and other factors can lead to ALI. ALI is a common starting point in a series of liver diseases that can result in acute or chronic liver failure, cirrhosis, and hepatocellular carcinoma [2]. Because these liver diseases account for around 2 million deaths per year globally, the global burden of liver disease is anticipated to rise; therefore, therapies for ALI are urgently needed [3, 4].

More and more studies have found that posttranslational modifications (PTMs), for example, acetylation, methylation, phosphorylation, ubiquitination, and SUMOylation, can control protein activity, facilitate protein interactions, and change protein subcellular localization, leading to regulation of important signaling pathways [57]. PTMs have a critical role in the duration and extent of the inflammatory response in liver injury through targeting the signaling molecules [3, 8, 9]. Interpretation of the correlation between various protein modifications is, to some extent, one of the keys to elucidate the mechanisms of liver injury [4, 10]. Regulation of PTMs might act as a significant therapeutic target during the liver injury treatment [11, 12]. Furthermore, related efficient inhibitors are now being explored as novel directions in drug research [13, 14].

Oridonin is a well-known diterpenoid acquired from the Chinese medicinal herb Rabdosia rubescens, also recognized as Dong Ling Cao [15]. Over the last few decades, oridonin has gained widespread attention because of its complex role in cancer treatment, such as leukemia [16, 17], lymphogenous malignancy [18], hepatocellular carcinoma [19], and colorectal cancer [20]. However, it has been documented that oridonin has many other therapeutic effects, comprising anti-inflammation [21, 22], neuroprotection [23], and antihepatic fibrosis [24]. Our previous study demonstrated that oridonin had protective effects on ALI stimulated by LPS/D-Gal, manifested as an improved survival rate, ameliorated histological abnormalities, and impaired liver function [25]. Additionally, we discovered that oridonin acted as an inhibitor of several acetyltransferases, such as pCAF, P300, Tip60, and GCN5 [26]. Therefore, in the current study, we intended to demonstrate whether the underlying protection mechanism of oridonin in ALI was related to the regulation of PTMs.

2. Materials and Methods

2.1. Reagents

Oridonin (>98% purity; C20H28O6; M.W. 360.42), obtained from Selleck (USA), was suspended in dimethyl sulfoxide, stored at −20°C, and thawed prior to use. Lipopolysaccharide (LPS) (Escherichia coli, 0111:B4), D-Gal, and thiol-specific antioxidant (TSA) were purchased from Sigma (USA). A myeloperoxidase (MPO) assay kit was from Nanjing Jiancheng Bioengineering Institute (China). A ReverTra Ace qPCR RT Kit was purchased from Toyobo (Japan). A SYBR Green Real-time PCR Master Mix was acquired from ExCell Bio (China). RIPA lysis buffer was purchased from KeyGen Biotech (China). Antibodies against ERK, P-ERK, P38, P-P38, IκB, P-IκB, interleukin-1 receptor-associated kinase 4 (IRAK4), P-IRAK4 (T345/S346), histone 3 (H3), H4, α-tubulin, acetyl-α-tubulin (K40), and GAPDH were obtained from Cell Signaling Technology (USA). Pan-anti-acetyl-lysine monoclonal antibodies were generated by our own laboratory, as described previously [27]. Horseradish peroxidase- (HRP-) conjugated goat anti-mouse and goat anti-rabbit antibodies were from Beyotime (China).

2.2. Generation of Peptides and Anti-Acetyl-IRAK4 (K34) Monoclonal Antibodies

Synthesized peptide sequence of acetyl-IRAK4 was PQEGWKK (ac) LAVAIK. Peptides and anti-acetyl-lysine-IRAK4 (K34) monoclonal antibodies were manufactured by GL Biochem (Shanghai, China).

2.3. Cell Culture and Assay of Acetyltransferase Inhibitory Activity of Oridonin

The mouse immortalized stellate cell line JS1 was acquired from Cell Resource Center (Shanghai Institutes for Biological Sciences, China). These cells were grown in Dulbecco’s modified Eagle’s medium with 10% fetal bovine serum and 1% penicillin/streptomycin at a 37°C incubator with 5% CO2. JS1 cells were seeded in 10 cm dishes and incubated in culture medium for 24 h. The cells were pretreated with oridonin (5, 10, and 15 μm) for 3 h before adding TSA (1 mM). The cells were harvested after 4 h of TSA treatment. We performed western blot to detect the level of H3, H4, acetylated histone H3, acetylated histone H4, α-tubulin, and acetylated α-tubulin and compared with GAPDH as a control.

2.4. Animals

Animals were handled as per the institutional animal care policies of the Shanghai Institute of Planned Parenthood Research. Female C57BL/6 mice (specific pathogen-free, 20-22 g, wild type) were obtained from SIPPR-BK Animal Co. Ltd. (Shanghai, China). The mice were given with a regular chow diet and water. They were accommodated under standard laboratory environments (, 12 h light/dark cycle) and were adapted for a minimum of 2 weeks before beginning any experiment.

2.5. Experimental Design

ALI was prompted in mice with intraperitoneal injection of LPS (40 μg/0.5 mL) combined with D-Gal (5 mg/0.5 mL). Animals were randomly separated into five groups ( each): control group (a), ALI group (b), two oridonin treatment groups (c and d), and oridonin control group (e). In group c, oridonin (0.2 mg/0.5 mL) was given 1 h prior to LPS/D-Gal challenge, and in group d, oridonin (0.2 mg/0.5 mL) was given every 4 d for a total of three doses, where the final dose was given 1 h before LPS/D-Gal challenge. All animals were killed by amputation at 6 h following LPS/D-Gal challenge. The liver tissues were acquired and preserved at −80°C for future use.

2.6. Transcriptome Analysis of Gene Expression Profiles of ALI upon Oridonin Treatment and Validation of the Differentially Expressed Genes (DEGs) by Real-Time Quantitative Polymerase Chain Reaction (qPCR)

The total mRNAs of five groups were isolated and analyzed using next-generation RNA-sequencing (RNA-Seq) technology on an Illumina HiSeq 2000 platform (Genenergy Bio, Shanghai, China) to outline their global gene expression patterns. For qPCR verification, total RNA was collected from five groups with or without oridonin treatment. Fluorescent qPCR was carried out on an ABI 7500 Fast Real-Time PCR detective system (Applied Biosystems, CA, USA) for chemokines and inflammatory cytokines. The SYBR Green qPCR system was 20 μL in total, which consisted of 10 mL SYBR Premix Ex Taq, 1.6 mL of the forward and reverse primers, 7 mL of double-distilled water, and 1.4 mL cDNA template. The reaction conditions were performed according to the supplier’s instructions. GAPDH served as a control. All samples were run in triplicate. The relative expression was calculated by the 2ΔΔCt method. Table 1 shows the list of primers.

Target genesForward primersReverse primers


2.7. Hepatic Myeloperoxidase (MPO) Activity Assay

Activity of MPO was measured via spectrophotometry using the MPO assay kit.

2.8. Protein Isolation and Immunoblot

RIPA lysis buffer with protease inhibitor cocktail was used to extract the total protein. Protein concentrations were measured via the BCA method. Equivalent quantities of protein were utilized to examine ERK, P-ERK, P38, P-P38, IRAK4, P-IRAK4 (S345/T346) and acetyl-IRAK4 (K34), IκB, P-IκB, H3, H4, α-tubulin, acetyl-α-tubulin (K40), and pan-acetylation in comparison with GAPDH as a control. Goat anti-rabbit or goat anti-mouse IgG–HRP antibody was the secondary antibody. An enhanced chemiluminescence (ECL) detection kit was utilized to visualize the protein bands.

2.9. Statistical Analysis

All results are showed as the and from a minimum of three different independent experiments. Student’s -test was utilized to determine the difference between two groups. A 2 test was utilized to the evaluation of sample rates among multiple samples. All analyses were accomplished with GraphPad Prism 6. and signified statistical significance.

3. Results

3.1. Oridonin Decreased Acetylation of H3, H4, and α-Tubulin in JS1 Cells and LPS/D-Gal-Induced ALI

To assess the acetyltransferase inhibitory activity of oridonin in vitro and in vivo, we studied manifestation of acetyl-α-tubulin (K40), acetyl-H3, and acetyl-H4. The results indicated that the acetylation level of tubulin (K40), H3, and H4 decreased suggestively when the final concentration of oridonin was 15 μm (Figure 1(a)). There was a noteworthy rise in the overall pan-acetylation level, especially the expression of acetyl-H3, acetyl-H4, and acetyl-α-tubulin in LPS/D-Gal-induced ALI. However, the overall pan-acetylation level reduced in a concentration-dependent way upon oridonin treatment (Figure 1(b)). Our study established that oridonin harbors the activity of acetyltransferase inhibitor in vitro and in vivo.

3.2. Bioinformatics Revealed the GOs and Signaling Pathways Regulated by Oridonin

We focused on the genes that were induced by LPS/D-Gal compared with the control group and then downregulated by oridonin treatment. Screening analysis indicated that LPS/D-Gal stimulated expression of 581 genes. In the oridonin-treated group c, 121 genes with were downregulated by oridonin (Supplementary Table S1). GO analysis suggested that the downregulated genes were extremely enriched in chemotaxis, locomotor activity, inflammatory response, and immune response. KEGG pathway analysis presented abundance of downregulated genes in several cascades, comprising the NOD-like receptor signaling pathway, mitogen-activated protein kinase (MAPK) signaling pathway, and TLR signaling pathway (Supplementary Figure S1). In the oridonin-treated group d, 278 genes with were downregulated by three doses of oridonin (Supplementary Table S2). GO analysis showed that the downregulated genes were greatly enriched in immune response, chemotaxis, and inflammatory response. KEGG pathway analysis indicated enhancement of downregulated genes in several cascades such as TLR and NOD-like receptor signaling pathways. Our previous research revealed that the prophylactic effects of oridonin were more obvious in group d, so we used the bioinformatics interpretation of group d, which better suggested the target of oridonin (Figure 2).

3.3. Significantly Enriched GO Term-Related Genes Verified by Real-Time PCR

To verify the outcomes of RNA-Seq, the genes involved in chemotaxis, immune, and inflammatory responses were subjected to real-time PCR. Hepatic expression of 11 chemotaxis and immune and inflammatory response-related genes (IL-1α, IL-1β, IL-6, TNF-α, CCL2, CCL3, CCL4, CCL5, CCL7, CXCL1, and CXCL10) was analyzed among the five groups. Coherent with RNA-Seq outcomes, expression of these 11 genes was elevated in the LPS/D-Gal group and reduced due to oridonin treatment. Oridonin suppressed chemotaxis, immune, and inflammatory response-related genes in a concentration-dependent way. These outcomes provide more evidence for the reliability of bioinformatics analysis, indicating that oridonin suppressed the production of cytokines involved in the immune and inflammatory processes, which might protect the liver from injury (Figure 3).

3.4. Oridonin Suppressed MPO Activity Prompted by LPS/D-Gal

Inflammatory response, including excessive inflammation-related cell activation and infiltration into liver tissues, contributes to LPS/D-Gal-induced liver injury [28]. A large amount of neutrophil infiltration was observed in an ALI model, characterized by high levels of MPO activity. Pretreatment with oridonin inhibited neutrophil infiltration into liver tissues as demonstrated by reduced MPO activity (Figure 4).

3.5. Participation of NF-κB and MAPK Signaling Pathways in the Anti-Inflammatory Impact of Oridonin on LPS/D-Gal-Induced ALI

KEGG analysis specified that the TLR4 signaling pathway was significantly enriched (Figure 2(c)). NF-κB and MAPK are two critical downstream cascades participating in LPS-stimulated TLR4 signal transduction [29]. Stimulation of the MAPK pathway causes initiation of transcription factor AP-1, which plays a critical role in the regulation of proinflammatory cytokines [30]. We established that the elevated levels of P-ERK and P-P38 prompted by LPS/D-Gal were abolished by pretreatment of mice with oridonin. NF-κB also has a vital role in controlling downstream signaling events that mediate proinflammatory gene transcription. In resting cells, NF-κB is preserved in the cytoplasm by IκB inhibitors, which are phosphorylated and then quickly degraded due to stimuli, resulting in NF-κB nuclear activation [31]. It means that we could use the phosphorylation of IκB to indicate the activation of NF-κB. Thus, we analyzed the phosphorylation of IκB to further elucidate the anti-inflammatory mechanism of oridonin. As expected, phosphorylation of IκB was depressed by oridonin in a concentration-dependent way (Figure 5).

3.6. Modification (Phosphorylation and Acetylation) of IRAK4 Was Inhibited in LPS/D-Gal-Induced ALI by Oridonin

Protein PTMs have a deep impact on protein activity and stability along with binding capacity [32]. IRAK4 is indispensable for the MyD88-dependent TLR4 signaling pathway, including the activation of MAPK and NF-κB signaling cascades [33]. Initial studies revealed that the kinase activity of IRAK4 is required for the proper activation of MAPK and NF-κB [34]. Furthermore, another study using LC-MS/MS analysis recognized three phosphorylation sites (T342, T345, and S346) within the stimulation loop, which are critical to the kinase activity of IRAK4 [35]. Our results indicated that oridonin inhibited expression of P-IRAK4 (T345/S346) induced by LPS/D-Gal. IRAK4 is presumed to interact with MyD88 through the death domain, and the downstream signaling pathway is blocked without their interaction [36]. UniProt database indicated that the K34 site that resides in the death domain could be acetylated. The acetylation status of IRAK4 (K34) may influence the interaction between IRAK4 and MyD88, resulting in the blockade of signal transduction. Thus, we further identified that oridonin inhibited the acetylation level of IRAK4 (K34) stimulated by LPS/D-Gal. All the results suggested that LPS/D-Gal-induced PTMs of IRAK4 and oridonin pretreatment reversed the changes. The impediment of PTMs of IRAK4 may be one of the reasons of the anti-inflammatory mechanisms of oridonin (Figure 6).

4. Discussion

An established model for studying ALI in mice involves coadministration of LPS plus D-Gal, which results in a pathological progression parallel to clinical ALI and is also an imperative platform for screening novel medications for the treatment of ALI [37]. Our previous researches have shown that oridonin improves the survival rate of mice and liver histopathology and reduces plasma alanine and aspartate aminotransferase levels, indicating that oridonin has significant protective effects on ALI [25].

We further explored the possible mechanisms underlying oridonin-mediated hepatoprotection. Transcriptome analysis indicated that the protective mechanism of oridonin might be correlated with suppression of TLR4-mediated immune and inflammatory responses. The MPO activity of the liver, which is believed to be a key step in the initiation of the inflammatory response, was markedly reduced by oridonin treatment. The parallel inhibition of chemotaxis and immune as well as inflammatory response-related genes’ mRNA expression implies that obstruction of transcription might have a crucial role in the protective impact of oridonin. The production of inflammatory mediators is known to depend mainly on activation of transcription factor NF-κB [38]. The crucial step in NF-κB stimulation is IκB phosphorylation by IKK, and then, NF-κB enters the nucleus and controls manifestation of inflammatory cytokines [38]. Activation of the MAPK family has a crucial function in a large number of cellular processes, including proliferation, differentiation, and expression of proinflammatory factors [39]. Our results revealed that oridonin inhibited the stimulation of NF-κB. The inhibitory effect was demonstrated by the reduction of IκB phosphorylation. At the same time, activation of the MAPK family members was inhibited by oridonin treatment. These results presented that the anti-inflammatory impact of oridonin is partly dependent on the MAPK and NF-κB signaling pathways, which indicates that the target of oridonin might be stimulated earlier due to LPS/D-Gal challenge.

TLR4 signaling originally causes congregation of the LPS/TLR4 recognition complex, which prompts a cascade of PTMs of proteins, for example, IRAK4. The crucial involvement of IRAK4 in TLR4-mediated inflammatory responses has been documented in knockout (KO) studies [35]. Be in composition to IRAK1 KO mice, IRAK4 KO mice were absolutely unaffected to LPS-induced septic shock and did not have a cytokine response when challenged with numerous TLR ligands. Additionally, IL-1-stimulated NF-κB, JNK, and p38 expressions were rigorously faulty in cells deficient in IRAK4. LPS-induced stimulation of JNK was also repressed, and LPS-induced NF-κB stimulation was postponed [33]. Furthermore, some studies documented that the kinase activity of IRAK4 was vital for its action. Using IRAK4-deficient murine embryonic fibroblasts that were reconstructed with an IRAK4 kinase inactive mutant, researchers indicated that the kinase activity of IRAK4 was necessary for the best stimulation of IL-1-induced NF-κB, JNK activation, and proinflammatory cytokines [34]. What is more, studies on IRAK4 kinase inactive knock-in mice showed that the kinase activity of IRAK4 is necessary for its action [40, 41]. One study reported there are three phosphorylation sites (T342, T345, and S346) that are responsible for IRAK4 kinase activity [35]. As expected, our results indicated that LPS/D-Gal-stimulated IRAK4 activation demonstrated by upregulation of P-IRAK4 (T345/S346), which was inhibited by oridonin treatment. However, macrophages from IRAK4 kinase inactive knock-in mice indicated that the kinase activity of IRAK4 was necessary for the stimulation of IL-1/TLR4-induced NF-κB [40, 41]. Moreover, there was obvious diminishing of IL-1/TLR-induced cytokine as well as chemokine generation in IRAK4 kinase inactive knock-in mice [4143]. Why are there two opposite conclusions? At present, different cell types are the causes of different results, and the specific mechanism has yet to be further studied. However, at least it is certain that IRAK4 kinase activity is necessary for the optimal inflammatory signaling pathway mediated by IL-1/TLR4.

All IRAK family members share analogous domain structures, comprising a conserved N-terminal death domain plus a central kinase domain [44]. IRAK4 binds to the adaptor protein MyD88 via its death domain. The downstream signaling pathway fails to activate without combination of the two proteins [45]. Thus, we infer that the death domain of IRAK4 has a crucial role in molecular recognition and activation of the downstream signaling pathway. Protein acetylation and the reverse process, named deacetylation, are PTMs. Histone acetyltransferases (HATs) as well as histone deacetylases (HDACs) could control gene expression by modifying histone proteins [46]. Nonetheless, HAT and HDAC can modulate precise signaling cascades and have additional targets apart from histones, comprising NF-κB, signal transducer, and activator of transcription 3 (STAT3) as well as p53 [4750]. Scientists have identified 3600 lysine acetylation sites on 1750 proteins, and the modification preferentially targets large macromolecular complexes [51]. Their findings support the concept that acetylation might control innate immune response-related proteins, for example, DDX58, IRAK4 (K34), OAS2, and TRIM25 [51]. K34, the acetylation modification target of IRAK4, is located in the death domain of IRAK4. Our results suggested that LPS/D-Gal can upregulate the level of acetyl-IRAK4 (K34), and we speculated that the acetylation of IRAK4 (K34) may promote the binding of IRAK4 to MyD88, thus enabling activation of downstream MyD88-dependent signaling pathways. Our results showed that oridonin pretreatment with LPS/D-Gal-induced ALI inhibits acetylation of IRAK4, resulting in blockade of the TLR4 signaling pathway.

However, our study had certain limitations, which require further studies. First of all, our results that could not provide direct and sufficient evidence to support the acetylation status of IRAK4 (K34) may influence the combination of MyD88 and IRAK4. We need to construct the wild type, site-modified type, and mutant type of IRAK4 to further clarify the different binding capacities with MyD88. Second, we should further identify whether these two PTMs are cross-linked.

5. Conclusions

In conclusion, our study revealed that the protective effects of oridonin on LPS/D-Gal-induced ALI are mediated by inhibition of the PTMs of IRAK4, including phosphorylation of T345/S346 and acetylation of K34.

Data Availability

The data used to support the findings of this study are available from the corresponding author upon request.


Part of the study has been presented as conference abstract in Abstracts of the 26th Annual Conference of APASL [52].

Conflicts of Interest

The authors of this manuscript have no conflicts of interest to disclose.

Authors’ Contributions

Min Shi and Yilin Deng contributed equally to this work and share first authorship.


This work was performed at the NPFPC Key Laboratory of Contraceptives and Devices, Shanghai Institute of Planned Parenthood Research (SIPPR), Institutes of Reproduction and Development, Fudan University, Shanghai, China. This work was supported/funded by the National Natural Science Foundation of China (Nos. 81570549, 81871912, and 81472242).

Supplementary Materials

See Supplementary Tables S1-S2 in the Supplementary Materials for comprehensive image analysis. Figure S1: A. GO analysis of target genes for biological processes revealed that the downregulated genes were highly concentrated in chemotaxis, locomotory behavior, and inflammatory response biological processes. B. KEGG pathway analysis of target genes showed that the downregulated genes are enriched in several pathways including the NOD-like receptor signaling pathway and chemokine signaling pathway. (Supplementary Materials)


  1. N. Kaplowitz, “Liver biology and pathobiology,” Hepatology, vol. 43, no. S1, pp. S235–S238, 2006. View at: Publisher Site | Google Scholar
  2. W. Tian and Y. Xu, “Decoding liver injury: a regulatory role for histone modifications,” The International Journal of Biochemistry & Cell Biology, vol. 67, pp. 188–193, 2015. View at: Publisher Site | Google Scholar
  3. S. K. Asrani, H. Devarbhavi, J. Eaton, and P. S. Kamath, “Burden of liver diseases in the world,” Journal of Hepatology, vol. 70, no. 1, pp. 151–171, 2019. View at: Publisher Site | Google Scholar
  4. R. Ferriero, E. Nusco, R. de Cegli, A. Carissimo, G. Manco, and N. Brunetti-Pierri, “Pyruvate dehydrogenase complex and lactate dehydrogenase are targets for therapy of acute liver failure,” Journal of Hepatology, vol. 69, no. 2, pp. 325–335, 2018. View at: Publisher Site | Google Scholar
  5. S. L. Planey, R. Kumar, and J. A. Arnott, “Post-translational modification of transcription factors: mechanisms and potential therapeutic interventions,” Current Molecular Pharmacology, vol. 6, no. 3, pp. 173–182, 2013. View at: Publisher Site | Google Scholar
  6. A. S. Venne, L. Kollipara, and R. P. Zahedi, “The next level of complexity: crosstalk of posttranslational modifications,” Proteomics, vol. 14, no. 4-5, pp. 513–524, 2014. View at: Publisher Site | Google Scholar
  7. K. Helin and D. Dhanak, “Chromatin proteins and modifications as drug targets,” Nature, vol. 502, no. 7472, pp. 480–488, 2013. View at: Publisher Site | Google Scholar
  8. W. Yao, T. Wang, and F. Huang, “p300/CBP as a key nutritional sensor for hepatic energy homeostasis and liver fibrosis,” BioMed Research International, vol. 2018, Article ID 8168791, 14 pages, 2018. View at: Publisher Site | Google Scholar
  9. N. A. Osna, W. G. Carter, M. Ganesan et al., “Aberrant post-translational protein modifications in the pathogenesis of alcohol-induced liver injury,” World Journal of Gastroenterology, vol. 22, no. 27, pp. 6192–6200, 2016. View at: Publisher Site | Google Scholar
  10. C. Ji, “Advances and new concepts in alcohol-induced organelle stress, unfolded protein responses and organ damage,” Biomolecules, vol. 5, no. 2, pp. 1099–1121, 2015. View at: Publisher Site | Google Scholar
  11. K. Murata, M. Hamada, K. Sugimoto, and T. Nakano, “A novel mechanism for drug-induced liver failure: inhibition of histone acetylation by hydralazine derivatives,” Journal of Hepatology, vol. 46, no. 2, pp. 322–329, 2007. View at: Publisher Site | Google Scholar
  12. T. Hitosugi and J. Chen, “Post-translational modifications and the Warburg effect,” Oncogene, vol. 33, no. 34, pp. 4279–4285, 2014. View at: Publisher Site | Google Scholar
  13. H. Ü. Kaniskan, M. L. Martini, and J. Jin, “Inhibitors of protein methyltransferases and demethylases,” Chemical Reviews, vol. 118, no. 3, pp. 989–1068, 2018. View at: Publisher Site | Google Scholar
  14. T. Lanyon-Hogg, M. Faronato, R. A. Serwa, and E. W. Tate, “Dynamic protein acylation: new substrates, mechanisms, and drug targets,” Trends in Biochemical Sciences, vol. 42, no. 7, pp. 566–581, 2017. View at: Publisher Site | Google Scholar
  15. C. Y. Li, E. Q. Wang, Y. Cheng, and J. K. Bao, “Oridonin: an active diterpenoid targeting cell cycle arrest, apoptotic and autophagic pathways for cancer therapeutics,” The International Journal of Biochemistry & Cell Biology, vol. 43, no. 5, pp. 701–704, 2011. View at: Publisher Site | Google Scholar
  16. T. Zhen, C. F. Wu, P. Liu et al., “Targeting of AML1-ETO in t(8;21) leukemia by oridonin generates a tumor suppressor-like protein,” Science Translational Medicine, vol. 4, no. 127, article 127ra38, 2012. View at: Publisher Site | Google Scholar
  17. Y. Guo, Q. Shan, Y. Gong, J. Lin, X. Yang, and R. Zhou, “Oridonin in combination with imatinib exerts synergetic anti-leukemia effect in Ph+ acute lymphoblastic leukemia cells in vitro by inhibiting activation of LYN/mTOR signaling pathway,” Cancer Biology & Therapy, vol. 13, no. 13, pp. 1244–1254, 2012. View at: Publisher Site | Google Scholar
  18. T. Ikezoe, Y. Yang, K. Bandobashi et al., “Oridonin, a diterpenoid purified from Rabdosia rubescens, inhibits the proliferation of cells from lymphoid malignancies in association with blockade of the NF-κB signal pathways,” Molecular Cancer Therapeutics, vol. 4, no. 4, pp. 578–586, 2005. View at: Publisher Site | Google Scholar
  19. G. Chen, K. Wang, B. Y. Yang, B. Tang, J.-X. Chen, and Z.-C. Hua, “Synergistic antitumor activity of oridonin and arsenic trioxide on hepatocellular carcinoma cells,” International Journal of Oncology, vol. 40, no. 1, pp. 139–147, 2012. View at: Publisher Site | Google Scholar
  20. F. H. Gao, X. H. Hu, W. Li et al., “Oridonin induces apoptosis and senescence in colorectal cancer cells by increasing histone hyperacetylation and regulation of p16, p21, p27 and c-myc,” BMC Cancer, vol. 10, no. 1, article 610, 2010. View at: Publisher Site | Google Scholar
  21. W. Guo, P. Zheng, J. Zhang, L. Ming, C. Zhou, and S. Zhang, “Oridonin suppresses transplant rejection by depleting T cells from the periphery,” International Immunopharmacology, vol. 17, no. 4, pp. 1148–1154, 2013. View at: Publisher Site | Google Scholar
  22. S. Wang, H. Yang, L. Yu et al., “Oridonin attenuates Aβ1-42-induced neuroinflammation and inhibits NF-κB pathway,” PLoS One, vol. 9, no. 8, article e104745, 2014. View at: Publisher Site | Google Scholar
  23. Z. Y. Zhang, R. Daniels, and H. J. Schluesener, “Oridonin ameliorates neuropathological changes and behavioural deficits in a mouse model of cerebral amyloidosis,” Journal of Cellular and Molecular Medicine, vol. 17, no. 12, pp. 1566–1576, 2013. View at: Publisher Site | Google Scholar
  24. F. J. Bohanon, X. Wang, B. M. Graham et al., “Enhanced effects of novel oridonin analog CYD0682 for hepatic fibrosis,” The Journal of Surgical Research, vol. 199, no. 2, pp. 441–449, 2015. View at: Publisher Site | Google Scholar
  25. Y. Deng, C. Chen, H. Yu et al., “Oridonin ameliorates lipopolysaccharide/D-galactosamine-induced acute liver injury in mice via inhibition of apoptosis,” American Journal of Translational Research, vol. 9, no. 9, pp. 4271–4279, 2017. View at: Google Scholar
  26. M. Shi, X. J. Lu, J. Zhang et al., “Oridonin, a novel lysine acetyltransferases inhibitor, inhibits proliferation and induces apoptosis in gastric cancer cells through p53- and caspase-3-mediated mechanisms,” Oncotarget, vol. 7, no. 16, pp. 22623–22631, 2016. View at: Publisher Site | Google Scholar
  27. H. Yu, H. Diao, C. Wang et al., “Acetylproteomic analysis reveals functional implications of lysine acetylation in human spermatozoa (sperm),” Molecular & Cellular Proteomics, vol. 14, no. 4, pp. 1009–1023, 2015. View at: Publisher Site | Google Scholar
  28. G. L. Su, “Lipopolysaccharides in liver injury: molecular mechanisms of Kupffer cell activation,” American Journal of Physiology. Gastrointestinal and Liver Physiology, vol. 283, no. 2, pp. G256–G265, 2002. View at: Publisher Site | Google Scholar
  29. Y. C. Lu, W. C. Yeh, and P. S. Ohashi, “LPS/TLR4 signal transduction pathway,” Cytokine, vol. 42, no. 2, pp. 145–151, 2008. View at: Publisher Site | Google Scholar
  30. L. Chang and M. Karin, “Mammalian MAP kinase signalling cascades,” Nature, vol. 410, no. 6824, pp. 37–40, 2001. View at: Publisher Site | Google Scholar
  31. M. S. Hayden and S. Ghosh, “Shared principles in NF-κB signaling,” Cell, vol. 132, no. 3, pp. 344–362, 2008. View at: Publisher Site | Google Scholar
  32. J. Liu, C. Qian, and X. Cao, “Post-translational modification control of innate immunity,” Immunity, vol. 45, no. 1, pp. 15–30, 2016. View at: Publisher Site | Google Scholar
  33. N. Suzuki, S. Suzuki, G. S. Duncan et al., “Severe impairment of interleukin-1 and Toll-like receptor signalling in mice lacking IRAK-4,” Nature, vol. 416, no. 6882, pp. 750–754, 2002. View at: Publisher Site | Google Scholar
  34. E. Lye, C. Mirtsos, N. Suzuki, S. Suzuki, and W. C. Yeh, “The role of interleukin 1 receptor-associated kinase-4 (IRAK-4) kinase activity in IRAK-4-mediated signaling,” Journal of Biological Chemistry, vol. 279, no. 39, pp. 40653–40658, 2004. View at: Publisher Site | Google Scholar
  35. H. Cheng, T. Addona, H. Keshishian et al., “Regulation of IRAK-4 kinase activity via autophosphorylation within its activation loop,” Biochemical and Biophysical Research Communications, vol. 352, no. 3, pp. 609–616, 2007. View at: Publisher Site | Google Scholar
  36. S. Flannery and A. G. Bowie, “The interleukin-1 receptor-associated kinases: critical regulators of innate immune signalling,” Biochemical Pharmacology, vol. 80, no. 12, pp. 1981–1991, 2010. View at: Publisher Site | Google Scholar
  37. R. Silverstein, “D-galactosamine lethality model: scope and limitations,” Journal of Endotoxin Research, vol. 10, no. 3, pp. 147–162, 2004. View at: Publisher Site | Google Scholar
  38. A. S. J. Baldwin Jr., “The NF-κB and IκB proteins: new discoveries and insights,” Annual Review of Immunology, vol. 14, no. 1, pp. 649–681, 1996. View at: Publisher Site | Google Scholar
  39. T. P. Garrington and G. L. Johnson, “Organization and regulation of mitogen-activated protein kinase signaling pathways,” Current Opinion in Cell Biology, vol. 11, no. 2, pp. 211–218, 1999. View at: Publisher Site | Google Scholar
  40. T. Kawagoe, S. Sato, A. Jung et al., “Essential role of IRAK-4 protein and its kinase activity in Toll-like receptor–mediated immune responses but not in TCR signaling,” Journal of Experimental Medicine, vol. 204, no. 5, pp. 1013–1024, 2007. View at: Publisher Site | Google Scholar
  41. T. W. Kim, K. Staschke, K. Bulek et al., “A critical role for IRAK4 kinase activity in Toll-like receptor-mediated innate immunity,” Journal of Experimental Medicine, vol. 204, no. 5, pp. 1025–1036, 2007. View at: Publisher Site | Google Scholar
  42. M. Koziczak-Holbro, C. Joyce, A. Glück et al., “IRAK-4 kinase activity is required for interleukin-1 (IL-1) receptor- and Toll-like receptor 7-mediated signaling and gene expression,” Journal of Biological Chemistry, vol. 282, no. 18, pp. 13552–13560, 2007. View at: Publisher Site | Google Scholar
  43. X. Li, “IRAK4 in TLR/IL-1R signaling: possible clinical applications,” European Journal of Immunology, vol. 38, no. 3, pp. 614–618, 2008. View at: Publisher Site | Google Scholar
  44. Z. Wang, J. Liu, A. Sudom et al., “Crystal structures of IRAK-4 kinase in complex with inhibitors: a serine/threonine kinase with tyrosine as a gatekeeper,” Structure, vol. 14, no. 12, pp. 1835–1844, 2006. View at: Publisher Site | Google Scholar
  45. A. Kuglstatter, A. G. Villaseñor, D. Shaw et al., “Cutting edge: IL-1 receptor-associated kinase 4 structures reveal novel features and multiple conformations,” The Journal of Immunology, vol. 178, no. 5, pp. 2641–2645, 2007. View at: Publisher Site | Google Scholar
  46. H. A. Doyle and M. J. Mamula, “Autoantigenesis: the evolution of protein modifications in autoimmune disease,” Current Opinion in Immunology, vol. 24, no. 1, pp. 112–118, 2012. View at: Publisher Site | Google Scholar
  47. J. Y. Lim, M. A. Oh, W. H. Kim, H. Y. Sohn, and S. I. Park, “AMP-activated protein kinase inhibits TGF-β-induced fibrogenic responses of hepatic stellate cells by targeting transcriptional coactivator p300,” Journal of Cellular Physiology, vol. 227, no. 3, pp. 1081–1089, 2012. View at: Publisher Site | Google Scholar
  48. M. Breaux, K. Lewis, L. Valanejad et al., “p300 regulates liver functions by controlling p53 and C/EBP family proteins through multiple signaling pathways,” Molecular and Cellular Biology, vol. 35, no. 17, pp. 3005–3016, 2015. View at: Publisher Site | Google Scholar
  49. Z. L. Yuan, Y. J. Guan, D. Chatterjee, and Y. E. Chin, “Stat3 dimerization regulated by reversible acetylation of a single lysine residue,” Science, vol. 307, no. 5707, pp. 269–273, 2005. View at: Publisher Site | Google Scholar
  50. L. Chen, W. Fischle, E. Verdin, and W. C. Greene, “Duration of nuclear NF-κB action regulated by reversible acetylation,” Science, vol. 293, no. 5535, pp. 1653–1657, 2001. View at: Publisher Site | Google Scholar
  51. C. Choudhary, C. Kumar, F. Gnad et al., “Lysine acetylation targets protein complexes and co-regulates major cellular functions,” Science, vol. 325, no. 5942, pp. 834–840, 2009. View at: Publisher Site | Google Scholar
  52. Y. Deng, G. Li, and C. Shi, “Abstracts of the 26th Annual Conference of APASL, February 15–19, 2017, Shanghai, China,” Hepatology International, vol. 11, Supplement 1, pp. 1–1093, 2017. View at: Publisher Site | Google Scholar

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