2-methylquinazoline derivative F7 as a potent and selective HDAC6 inhibitor protected against rhabdomyolysis-induced acute kidney injury


Authors: Jing Liu aff001;  Xue Cui aff002;  Fan Guo aff001;  Xinrui Li aff001;  Lingzhi Li aff001;  Jing Pan aff001;  Sibei Tao aff001;  Rongshuang Huang aff001;  Yanhuan Feng aff001;  Liang Ma aff001;  Ping Fu aff001
Authors place of work: Division of Nephrology and National Clinical Research Center for Geriatrics, Kidney Research Institute, West China Hospital of Sichuan University, Chengdu, China aff001;  State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University and Collaborative Innovation Center of Biotherapy, Chengdu, China aff002
Published in the journal: PLoS ONE 14(10)
Category: Research Article
doi: 10.1371/journal.pone.0224158

Summary

Histone deacetylases 6 (HDAC6) has been reported to be involved in the pathogenesis of rhabdomyolysis-induced acute kidney injury (AKI). Selective inhibition of HDAC6 activity might be a potential treatment for AKI. In our lab, N-hydroxy-6-(4-(methyl(2-methylquinazolin-4-yl)amino)phenoxy)nicotinamide (F7) has been synthesized and inhibited HDAC6 activity with the IC50 of 5.8 nM. However, whether F7 possessed favorable renoprotection against rhabdomyolysis-induced AKI and the involved mechanisms remained unclear. In the study, glycerol-injected mice developed severe AKI symptoms as indicated by acute renal dysfunction and pathological changes, accompanied by the overexpression of HDAC6 in tubular epithelial cells. Pretreatment with F7 at a dose of 40 mg/kg/d for 3 days significantly attenuated serum creatinine, serum urea, renal tubular damage and suppressed renal inflammatory responses. Mechanistically, F7 enhanced the acetylation of histone H3 and α-tubulin to reduce HDAC6 activity. Glycerol-induced AKI triggered multiple signal mediators of NF-κB pathway as well as the elevation of ERK1/2 protein and p38 phosphorylation. Glycerol also induced the high expression of proinflammatory cytokine IL-1β and IL-6 in kidney and human renal proximal tubule HK-2 cells. Treatment of F7 notably improved above-mentioned inflammatory responses in the injured kidney tissue and HK-2 cell. Overall, these data highlighted that 2-methylquinazoline derivative F7 inhibited renal HDAC6 activity and inflammatory responses to protect against rhabdomyolysis-induced AKI.

Keywords:

Apoptosis – Cytokines – Glycerol – Histones – Inflammation – Kidneys – Phosphorylation – Urea

Introduction

Acute kidney injury (AKI) consists of a series of heterogeneous conditions characterized by a sudden decline in glomerular filtration and oliguria [1], associated with high risk of chronic kidney disease (CKD) and high mortality [2]. Rhabdomyolysis, mainly induced by trauma, exertion, muscle hypoxia, infections, drugs and toxins, etc, is one of important causes leading to AKI[3]. Rhabdomyolysis-induced AKI is common but life-threatening, accounting for 5–15% of all community-acquired AKI cases [4, 5]. However, the detailed mechanism of rhabdomyolysis-AKI is poorly elucidated and treatment strategies remain limited.

Considerable evidences suggested that direct and ischemic tubular injury played a key role in myoglobin-induced AKI [6], and cellular damage is considered as main triggers initiating inflammatory response in acute tissue injury[7]. Multiple inflammatory genes and signaling pathways were activated in rhabdomyolysis-induced AKI [8]. A number of studies demonstrated that nuclear factor-kappa B (NF-κB) played crucial roles in modulating inflammation and cell proliferation in renal diseases [912]. NF-κB normally existed in cytoplasm in inactive form binding to its inhibitor, immuno-globulin (Ig) κ light chain gene of B lymphocytes (IκB) [13]. Stimuli could elicit the activation of IκB, thus inducing NF-κB released from IκB, and translocated into nucleus to promote transcriptional activity.

HDACs are a group of enzymes acting as removing acetyl group from lysine residues in histone or nonhistone proteins. HDACs are categorized into 4 classes based on homology: class I (HDAC 1, 2, 3, and 8), class II (HDAC 4, 5, 6, 7, 9 and 10), class III (SIRT 1–7) and class IV (HDAC 11)[14]. HDAC6 stands out because of its almost exclusive deacetylation in cytoplasm and the involvement of both dependent and independent of its catalytic activity, which opened the way for the identification of its substrates and development of highly selective inhibitor of its enzyme action [15]. Meanwhile, the elevated expression of histone deacetylase 6 (HDAC6) have been confirmed to be involved in renal diseases including AKI [1618], autosomal dominant polycystic kidney disease [19], and hypertensive nephropathy [20] for the contribution to inflammation, apoptosis and fibrosis.

We previously reported that a selective HDAC6 inhibitor 23BB possessed renoprotective effects by improving tubular cell apoptosis and down-regulating endoplasmic reticulum stress [16]. Recently, N-hydroxy-6-(4-(methyl(2-methylquinazolin-4-yl)amino)phenoxy)nicotinamide (F7) has been designed, synthesized in our lab and inhibited HDAC6 activity with the IC50 of 5.8 nM. However, whether novel HDAC6 inhibitor F7 possessed favorable renoprotection against rhabdomyolysis-induced AKI and the involved mechanisms remained unclear.

Material and methods

Ethical statement

All applicable international, national, and/or institutional guidelines for the care and use of animals were followed. All procedures performed in studies involving animals were in accordance with the ethical standards of animal ethics committee of Sichuan University (IACUC number: 2017080A).

Animals

Male C57BL/6 mice (8 weeks; 25-28g) were purchased from the Animal Laboratory Center of Sichuan University (Chengdu, China). These mice were housed in the controlled environment with constant temperature at 23 ± 2°C, humidity at 50–60%, and 12-hour light/dark cycle, and had free access to water and food. All the experiment procedures were in accordance with The Guide for Care and Use of Laboratory Animals, and the study protocol was approved by the Animal Care and Use Committee of Sichuan University (IACUC number: 2017080A).

Rhabdomyolysis-induced AKI model and pretreatment

The synthesis of F7 was in six synthetic steps with moderate yield according to the previous procedures of selective HDAC6 inhibitor 23bb[21]. HDACs inhibition assay of F7 was performed utilizing 4-amino-7-methylcoumarin (AMC) labeled Ac-peptide (Ac-peptide-AMC) substrates, a service provided by Chempartner Company (Shanghai, China). Results of IC50 and selectivity of F7 against HDAC1-11 enzymes were all listed in S1 Fig.

After one week of adoption to the housing conditions, the mice were randomly divided into three groups (n = 8): control, glycerol, and glycerol+HDAC6 inhibitor (F7). For the latter two groups, a single intramuscular injection of 50% glycerol dissolved in 0.9% normal saline (10 μl/g) was divided between bilateral back limbs to induce rhabdomyolysis-induced AKI model. The mice in control group received the same dose of saline injection at the place of glycerol. Before glycerol injection, mice in pretreatment group were orally administrated with F7 (dissolved in DEG and diluted with 0.9% saline) at a dose of 40mg/kg/d (200 μl solution for 28g) for 3 days. For control and glycerol groups, mice were treated with the same dose of saline.

All the mice were euthanized via pentobarbital sodium injection (50 mg/kg, i.p.). Terminal blood samples were collected and serum samples were stored at -80°C. Kidney tissues were divided and respectively removed into 10% phosphate buffered formalin for histological staining, and into liquid nitrogen follows by storage at -80°C for further quantitative analysis and immunofluorescence staining.

Biochemical evaluation of blood sample

The serum level of creatinine kinase (CK), blood urea (UREA) and serum creatinine (sCr) were tested using high performance liquid chromatography (HPLC) by Institute of Drug Clinical Trial and the GCP center of West China Hospital of Sichuan University.

Histological examination

Paraffin-embedded kidney tissue samples were cut into 4-um sections and stained with haematoxylin and erosin (H&E) and periodic acid-Schiff (PAS) staining. These sections were viewed using light microscopy at magnifications of ⊆200 and ⊆400 respectively, and semiquantitative estimation of renal tubular damage was performed on a scale from 0 to 4 to grade the percentage of injured/damaged renal tubules: 0 for 0%, 0.5% for <10%, 1 for 10–25%, 2 for 26–50%, 3 for 51–75% and 4 for 76–100%[22]. At least 10 areas were randomly selected in the cortex per slide.

Immunofluorescence staining

Kidney tissue samples were mounted in O.C.T. compound medium (Tissue-Tek) for cryosectioning (4 μm). Sections were immediately fixed in 10% buffered formalin, washed, dehydrated and stored at -20°C. Before immunofluorescence staining, the tissue sections were rehydrated and blocked with 10% horse medium (diluted with PBS solution) for 1 hour at room temperature and incubated at 4°C overnight with indicated primary antibodies. Then sections were exposed to second antibodies labeled with Cy5 red or FITC green (Jackson ImmunoResearch Inc., West Grove, PA, United States). The nuclei were counterstained with DAPI (1:500, Life Technologies Corporation, OR, United States). The images were captured with AxioCam HRc digital camera (Carl Zeiss).

Western blotting

Kidney tissue or cultured cell samples were sufficiently lysed in the mixture of RIPA buffer (50 mM Tris (pH7.4), 150 mM NaCl, 1% TritonX-100, 1% sodium deoxycholate, 0.1% SDS) containing 4% cocktail proteinase inhibitor (Roche, Switzerland) on ice. After centrifuged at 13,000 rpm for 15 min at 4°C, supernate of the homogenate were collected for protein quantification. Protein equivalent to 50 ug were loaded into 10–12% SDS-PAGE gels for electrophoretic separation, and then transferred to polyvinylidene difluoride (PVDF) membranes (0.2 μm, Bio-Rad Laboratories, Inc.). After protein blotting, membranes were blocks using 5% non-fat dried milk for 1h at room temperature, then probed with primary antibodies at 4°C overnight, and incubated with secondary antibodies for 1h at room temperature. Primary antibodies included: mouse anti-GAPDH (1:2000, 200306-7E4, Zen BioScience Inc., Research Triangle Park, NC, USA), mouse anti-IL-6 (1:1000, EM170414, HuaAn Biotechnology Co., Ltd, Hangzhou, China), mouse anti-HDAC6 (1:200, sc-28386, Santa Cruz Biotechnology Inc., Dallas, TX, United States)), rabbit anti-acetyl-H3 (1:1000, #9649), rabbit anti-IκBα (1:1000, #4812), rabbit anti-phospho-IκBα (1:1000, #2859), rabbit anti-NF-κB p65 (1:1000, #8242s), rabbit anti-phospho-NF-κB p65 (1:1000, #3031), rabbit anti-ERK1/2 (1:1000, #9102), and rabbit anti-phospho-ERK1/2 (1:1000, #8544) (all the seven were purchased from Cell Signaling Technology, Danvers, MA, USA), rabbit anti-alpha-tubulin (1:500, ab179484), rabbit anti-IL-1β (1:1000, ab9722) (both were obtained from Abcam, Cambridge, MA, USA) and rabbit anti-acetyl-alpha-tubulin (1:1000, DF2982, Affinity BioScience, Cincinnati, OH, United States). Secondary antibodies included goat anti-mouse and goat anti-rabbit IgG (1:2000, Biosynthesis Biotechnology Co., Ltd., Beijing, China). Immunoblots were visualized with the Immobilon Western Chemiluminescent HRP Substrate (Millipore Corporation, Billerica, MA, United States) and measured with Bio-Rad Chemi Doc MP.

Quantitative real-time PCR analysis

Total RNA was obtained from frozen kidney tissue using the total RNA extraction Kit (BioTek, Winooski, VT, United States), and reverse transcription was performed using PrimeScript RT Reagent Kit (Takara Bio, Inc., Otsu, Japan) according to protocols. Reactions of PCR amplification were quantified using the iTaq Universal SYBR Green Supermix (Bio-Rad Laboratories, Inc.) in a PCR system (CFX Connect; Bio-Rad, Hercules, CA, United States). All results were presented with relative expression levels normalized to GAPDH. Primer sequences: IL-6 (Mouse): Forward: 5'-ACAACCACGGCCTTCCCTACTT-3', Reverse: 5'-CACGATTTCCCAGAGAACATGTG-3'; TNF-α (Mouse): Forward: 5'-ACCCTCACACTCAGATCATCTTC-3', Reverse: 5'-TGGTGGTTTGCTACGACGT-3'; NGAL(Mouse): Forward: 5'-GCAGGTGGTACGTTGTGGG-3', Reverse: 5'-CTCTTGTAGCTCATAGATGGTGC-3'.

HK-2 Cells, myoglobin administration and F7 treatment

Human renal proximal tubule cell line (HK-2) cells were purchased from Shanghai Institute of Biochemistry and Cell Biology, Shanghai, China and maintained in DMEM/F12 (Hyclone, Beijing, China) supplemented with 10% fetal bovine serum (FBS, Hyclone, Australia) and 1% penicillin and streptomycin at 37°C under humidified atmosphere of 5% carbon dioxide. Then cells were seeded on six-well plates (Shanghai Sunub Bio-Tech Development Inc., Shanghai, China) at a density of 200,000 cells per well, divided into four groups at exponential phase: the control group (cells incubated with DMEM/F12+10%FBS), the model group (cells incubated with 200 μM ferrous myoglobin (M0630, Sigma-Aldrich, St. Louis, MO, USA)), the F7-1.25 nM group (cells incubated with ferrous myoglobin+F7 at 1.25nM) and the F7-10 nM group (cells incubated with ferrous myoglobin+F7 at 10 nM).

Annexin V and PI staining

Cell apoptosis was evaluated by flow cytometry using an Annexin V-FITC apoptosis analysis kit (AO-2001-02P-H, Tianjin Sungene Biotech Co., Ltd, Tianjin, China). After the four group of cells were cultured under the condition as described above for 24 hours, they were digested by trypsin, collected, and washed three times with PBS diluted 1×binding buffer (1ml per tube). For each sample with 100 μL cell suspension, 5 μL (2.5 μg/mL) of Annexin-V-FITC were added, and after gentle vortex the samples were incubated for 10 min at room temperature in the dark. Then 5 μL of PI solution were added and incubated at the same condition. After being supplemented to 500 μL using cold PBS followed by gentle vortex, samples were ready to be testes. Apoptosis signals were detected using a CytoFLEX by Beckman & Coulter.

Statistical analysis

Description data were presented as means ± standard deviation. A Student two-tailed unpaired t test was used for pairwise comparison. One-way ANOVA and further Turkey test were used for multiple comparisons. A two-sided p value less than 0.05 was considered statistically significant.

Results

Selective HDAC6 inhibitor F7 improved acute renal function and alleviated kidney damage in rhabdomyolysis-induced AKI

We firstly examined whether the mice model of glycerol-induced AKI was successfully established, and tested the protective effect of F7 at a dose of 40 mg/kg/d for 3 days on renal function and pathological changes. Serum creatine kinase (CK) in glycerol group and glycerol+F7 group was markedly elevated compared to that of control at 24 hours after glycerol injection (Fig 1A). The values of serum urea (UREA) and serum creatinine (sCr) in glycerol group were approximately five and three-fold more than that of control (Fig 1B and 1C), while the value of glycerol+F7 group was remarkably decreased compared to that of glycerol group. Consistent findings were obtained from histological changes in H&E and PAS-staining sections: serious tubular damages (tubular dilatation, swelling, necrosis and cast formation) were observed in glycerol group while pathological injuries were effectively alleviated by the pretreatment of F7 (Fig 1D and 1E). We also evaluated the liver, kidney, spleen, heart and lung tissues of mice with oral administration of F7 at the same dose as that in F7+glycerol group for 3 days, but without glycerol injections. Histological sections confirmed the F7 did not exhibited organ damage (S2 Fig).

F7 alleviated kidney injury in rhabdomyolysis-induced AKI.
Fig. 1. F7 alleviated kidney injury in rhabdomyolysis-induced AKI.
(A) Serum creatine kinase (CK); (B) serum urea (UREA); (C)serum creatinine (sCr). (D) Photomicrographs (×200 and ×400) illustrated PAS staining of the kidney tissues, and the histogram presented a semiquantitative assessment of tubular injury. (E) Photomicrographs (×200 and ×400) illustrated H&E staining of the kidney tissues, and the histogram presented a semiquantitative assessment of tubular injury. N = 6, ****P<0.0001, ***P<0.001, **P<0.01, *P<0.05. Images (Fig 1D and 1E) are representative of more than 10 area views from each group (N = 6).

F7 inhibited HDAC6 activity in the kidney of rhabdomyolysis-induced AKI

Results of western blot and immunofluorescence demonstrated that HDAC6 minimally expressed in normal kidneys of control group, while HDAC6 level in the glycerol group was markedly increased. Pretreatment of F7 significantly inhibited the expression of HDAC6 in the damaged kidney. Since HDAC6 deacetylated both histone (i.e. histone H3[23]) and non-histone (i.e. α-tubulin[15, 24]), thus the inhibition of HDAC6 could be reflected by enhancing the acetylation of HDAC6 substrates. Protein expression and immunoblot analysis results were shown in Fig 2A. The high overlapping level of lectin and HDAC6 from merged immunofluorescence results also indicated HDAC6 mainly overexpressed in tubular cells (Fig 2B), which was consistent with the finding that HDAC6 actively maintained in the cytoplasm[25].

F7 inhibited HDAC6 expression and enhanced the deacetylation of α-tubulin and histone H3 in the kidney of rhabdomyolysis-induced AKI.
Fig. 2. F7 inhibited HDAC6 expression and enhanced the deacetylation of α-tubulin and histone H3 in the kidney of rhabdomyolysis-induced AKI.
(A) Protein expression level of HDAC6, α-tubulin, acetyl-α-tubulin and acetyl-H3. Immunoblot analysis of HDAC6 and its substrates. The densitometry values of acetyl-α-tubulin was normalized to α-tubulin. The densitometry values of HDAC6 and acetyl-H3 were normalized to GAPDH. N = 5, **P<0.01, *P<0.05. The data are representative of 2–3 independent experiments. (B) F7 inhibited expression of HDAC6 as measured by Double immunofluorescence staining of HDAC6 and lectin using kidney tissue frozen sections. Lectin was the marker of tubular epithelial cells. Images are representative of more than 10 area views from each group (N = 3).

F7 attenuated tubular damage of rhabdomyolysis-induced AKI

Neutrophil gelatinase-associated lipocalin (NGAL) is a main biomarker of kidney tubular injuries, and the increase in NGAL production and release from tubular cells could be found after kidney receiving harmful stimuli [26]. We firstly found that the NGAL expression significantly increased and was mainly located in tubules of glycerol group by immunofluorescence staining, while the expression level was largely diminished by F7 treatment (Fig 3A). Renal protection by HDAC6 inhibition was further tested by real-time PCR and immunoblot analysis. NGAL mRNA expression and protein expression were both obviously elevated in glycerol group while pre-treatment of F7 markedly reduced expressions (Fig 3B).

F7 alleviated tubular damages, suppressed NF-κB and MAPK signaling pathway, and effectively attenuated inflammatory responses in rhabdomyolysis-induced AKI.
Fig. 3. F7 alleviated tubular damages, suppressed NF-κB and MAPK signaling pathway, and effectively attenuated inflammatory responses in rhabdomyolysis-induced AKI.
(A) Double immunofluorescence staining of gelatinase-associated lipocalin (NGAL) and lectin in kidney tissues (×200). Lectin was the marker of tubular epithelial cells. (B) Effect of F7 on tubular damages quantified by real-time PCR. (C) Expression level of key proteins of NF-κB signaling pathway in control, glycerol and glycerol+F7 group. (D) Protein expression level of p38 and ERK1/2 in control, glycerol and glycerol+F7 group. (E) Protein expression level of IL-1β and IL-6; Immunoblot of IL-1β and IL-6 normalized to GAPDH; (F) Real-time PCR analysis of TNF-α and IL-6. (G) ELISA analysis of serum proinflammatory cytokines (TNF-α and IL-β). (H) ELISA analysis of proinflammatory cytokines in kidney lysates (TNF-α, IL-1β and IL-6). ****P<0.0001, ***P<0.001, **P<0.01, *P<0.05. Images are representative of more than 10 area views from each group (N = 3). Data are representative of 2–3 independent experiments.

F7 pretreatment inhibited the activation of NF-κB and MAPKs, and ameliorated the levels of inflammatory cytokines in rhabdomyolysis-induced AKI

Inflammatory response played an essential role in the pathogenesis of AKI[27], and the activation of NF-κB is the critical mechanism mediating the expression of key inflammatory molecules in the process of rhabdomyolysis[28]. Data from Fig 3C demonstrated that the phosphorylation of IκBα was the highest in glycerol group, and pretreatment with F7 decreased the IκBα phosphorylation. Consistently, the increased phosphorylated NF-κB (p65) was found in glycerol group, and F7 effectively down-regulated the p65 phosphorylation. Moreover, total extracellular signal-regulated kinases (ERK1/2) expression and ERK1/2 phosphorylation level was upregulated in the glycerol group, together with obvious p38 phosphorylation. F7 effectively inhibited total ERK1/2 expression and p38 phosphorylation (Fig 3D).

From analysis of western blot, a dramatic increase of proinflammatory cytokines (IL-6 and IL-β) could be observed in glycerol group, and F7 remarkably down-regulated the levels, as shown in Fig 3E. Similarly, the increased mRNA expression of IL-6 and TNF-α could be found in glycerol group compared to that of control, while F7 significantly decreased the mRNA level of these two cytokines (Fig 3F). Proinflammatory cytokines in kidney lysates and serum were also examined using ELISA. It could be found in both serum and kidney lysates that IL-β and TNF-α were obviously elevated in glycerol group while decreased in F7 treatment group. Additionally, similar change was observed in IL-6 from kidney lysates (Fig 3G and 3H).

F7 improved cell growth and inflammatory cytokines by inhibiting NF-κB activity in HK-2 cells

To further verify the in vitro renoprotection of F7, we examined the pharmacological toxicity and effectiveness of F7 at a respective concentration of 2.5 nM, 5 nM and 10 nM, to select the optimal F7-treated concentration. Apoptosis signals from flow cytometry revealed that F7 improved growth of HK-2 cells under stimulation of myoglobin (Mb) in a dose-dependent manner (Fig 4A), thus indicated that the optimal F7-treated concentration was 10 nM. Results of western blot analysis indicated that successful inhibition of HDAC6 in vitro suppressed the phosphorylation of NF-κB (p65) and reduced the degree of inflammatory response compared to those of Mb group as shown in Fig 4B and 4C.

F7 improved the cell growth and ameliorated myoglobin-induced inflammation in HK-2 cells.
Fig. 4. F7 improved the cell growth and ameliorated myoglobin-induced inflammation in HK-2 cells.
(A) HK-2 cells in myoglobin group and glycerol+F7 group were stimulated by ferrous myoglobin (200 μM) for 24 hrs. Apoptosis due to myoglobin and treatment effect of F7 on cell growth were detected using flow cytometry, thus to select optimal F7-treated concentration. (B) F7 effectively inhibited HDAC6 expression in vitro; (C) F7 ameliorated inflammation in HK-2 cells by inhibiting HDAC6 and suppressing the activation of NF-κB pathway in vitro. Data are representative of 2–3 independent experiments.

Discussion

In our previous studies, we have confirmed that HDAC6 contributed to the pathogenesis of rhabdomyolysis-induced AKI. Selective inhibition of HDAC6 activity by a small-molecule compound N-hydroxy- 4-(2-methoxy-5-(methyl(2-methylquinazolin-4-yl)-amino)phenoxy)butanamide (23bb) might be a promising strategy for the treatment of AKI. Recently, N-hydroxy-6-(4-(methyl(2-methylquinazolin-4-yl)amino)phenoxy)nicotinamide (F7) has been designed, synthesized in our lab and inhibited HDAC6 activity with the IC50 of 5.8 nM. HDAC enzyme inhibition assay indicated that HDAC6 inhibition efficacy of F7 was three times higher than that of 23BB, and inhibition selectivity ratio of F7 (inhibition activity of HDAC6 vs other HDACs) were all much higher than that of 23BB (details were listed in S1 Table). Base on the good performance on inhibition efficacy and selectivity, we further investigated the renoprotective effect of F7 and the involved mechanisms in rhabdomyolysis-induced AKI. The overexpression of HDAC6 was observed in the injured kidneys of rhabdomyolysis-induced AKI. Pretreatment of F7 effectively improved renal functions, alleviated kidney histopathological damages, decreased the expression of kidney injury biomarkers, and suppressed NF-κB signaling pathway. The consistent findings also could be observed in vitro in HK-2 cells. These results strongly indicated that HDAC6 contributed to the development of inflammation in AKI induced by rhabdomyolysis through activating NF-κB signaling pathways.

In rhabdomyolysis-induced AKI, myoglobin plays the key role in leading to renal toxicity through multiple deleterious effects including tubular obstruction by myoglobin-derived casts, oxidative stress, inflammation, apoptosis and vasoconstriction [4]. Inflammation in AKI is known to be a complex biological process that is crucial to repairing injured tissue. As a key modulator, HDAC6 is involved in multiple biological processes ranging from gene expression to protein activity, thus participating in the inflammation. Recently, several studies demonstrated the increased expression of HDAC6 in cytoplasm of tubular epithelial cells in AKI induced by cisplatin [29] and rhabdomyolysis [16, 17], among which the elevated production of pro-inflammatory cytokines [17, 29] and apoptosis-related biomarkers [16] were observed. Under the treatment of HDAC6 inhibitor, inflammatory response and apoptosis were ameliorated accompanied by the decreased HDAC6 activity. The mechanism of HDAC6 regulating apoptosis through endoplasmic reticulum stress was evidenced in our previous study [16].

As a key transcription regulator of inflammation, NF-κB promotes the expression of pro-inflammatory cytokines and adhesion molecules. Both clinical and experimental data confirmed the elevation and activation of NF-κB in a variety of renal inflammatory disorders [12, 30, 31]. Meanwhile, it was found that NGAL could be induced to overexpress by NF-κB as a member of lipocalin superfamily and biomarker of AKI [32]. The close linking between HDAC6 and NF-κB was further strengthened by our study with the sharp elevation of NGAL in glycerol group and dramatic reduction in glycerol+F7 group. As for the mechanism of NF-κB activation, if receiving potent stimuli, IκBα could be rapidly degraded within minutes by phosphorylation, polyubiquitinylation and/or proteasome [33, 34]. Consequently, NF-κB was free and translocated into the nucleus where it bound and modulated the expression of target genes [35]. The signal is ultimately terminated by the new synthesis of IκB [12]. Our study demonstrated the increased phosphorylation of IκB and the elevated expression of p65 in the injured kidneys of rhabdomyolysis-induced AKI and in myoglobin-induced HK-2 cells. Additionally, total IκB expression was the least in glycerol group. After treatment of F7 both in vivo and in vitro, IκBα phosphorylation and activation of p65 were both obviously inhibited, accompanied by the markedly suppressed inflammation. All the findings highlighted that HDAC6 inhibitor regulated NF-κB pathway which participated in the rhabdomyolysis-induced AKI.

In the study, our data also revealed that F7 could alleviate inflammation through inhibiting the phosphorylation of IκBα and p65, but how HDAC6 interacted with IκBα, p65 and other NF-κB family factors was unclear. Previous study [11] found HDAC6 coimmunoprecipitated with NF-κB p50 and p65, and reported that p50 and p65 seemed to recruit HDAC6 from cytoplasm to nuclear DNA-protein complex. Although HDAC6 predominantly existed in cytoplasm, our results found that F7 induced the acetylation of α-tubulin and histone H3, which indicated that HDAC6 might be involved in multiple mechanisms and compartments to mediate activation of NF-κB pathway. Moreover, NF-κB was unlikely to be the sole pathway interacting with HDAC6 to induce inflammatory response. MAPK and PI3K/Akt signaling pathways were also upregulated in rhabdomyolysis-induced AKI [8]. In our study, the overexpression of ERK1/2 and the activation of p38 phosphorylation could be found in glycerol group where HDAC6 protein was elevated, while no significant change was observed about c-Jun NH2-terminal kinase (JNK). These findings could be supported by the previous reports that ERK1/2 bound and phosphorylated HDAC6 [36], and HDAC6 activated the phosphorylation of p38 by deacetylation [37]. It was reported that the overexpression of HDAC6 could activate JNK and increase the phosphorylation of JNK in liver cancer cells [38]. Specifically, JNK1 was associated the with sustaining HDAC6 level in several organ-derived cell lines [39]. Of notes, the association between JNK and HDAC6 were not previously reported in kidney which needed to be further investigated.

In summary, the most significant thing was that we confirmed novel HDAC6 inhibitor F7 alleviated acute renal function against rhabdomyolysis-induced AKI and selective inhibition of HDAC6 activity was a promising strategy for the treatment of AKI. These findings also indicated that F7 suppressed HDAC6 activity to reduce inflammatory responses via the inhibition of NF-κB pathway in rhabdomyolysis-induced AKI.

Supporting information

S1 Fig [tiff]
The IC and selectivity of F7 against HDAC1-11 enzymes.

S2 Fig [tif]
Histological examinations of different organs from the normal mice administrated with F7.

S1 Table [pdf]
Comparison of HDAC Inhibition Activity among HDAC6 inhibitors.


Zdroje

1. Lameire NH, Bagga A, Cruz D, De Maeseneer J, Endre Z, Kellum JA, et al. Acute kidney injury: an increasing global concern. Lancet. 2013;382(9887):170–9. doi: 10.1016/S0140-6736(13)60647-9 23727171

2. Venkatachalam MA, Weinberg JM, Kriz W, Bidani AK. Failed Tubule Recovery, AKI-CKD Transition, and Kidney Disease Progression. J Am Soc Nephrol. 2015;26(8):1765–76. doi: 10.1681/ASN.2015010006 25810494

3. Bosch X, Poch E, Grau JM. Rhabdomyolysis and acute kidney injury. N Engl J Med. 2009;361(1):62–72. doi: 10.1056/NEJMra0801327 19571284

4. Panizo N, Rubio-Navarro A, Amaro-Villalobos JM, Egido J, Moreno JA. Molecular Mechanisms and Novel Therapeutic Approaches to Rhabdomyolysis-Induced Acute Kidney Injury. Kidney Blood Press Res. 2015;40(5):520–32. doi: 10.1159/000368528 26512883

5. Komada T, Usui F, Kawashima A, Kimura H, Karasawa T, Inoue Y, et al. Role of NLRP3 Inflammasomes for Rhabdomyolysis-induced Acute Kidney Injury. Sci Rep. 2015;5:10901. doi: 10.1038/srep10901 26045078

6. Zager RA, Gamelin LM. Pathogenetic mechanisms in experimental hemoglobinuric acute renal failure. Am J Physiol. 1989;256(3 Pt 2):F446–55. doi: 10.1152/ajprenal.1989.256.3.F446 2923223

7. Chen GY, Nunez G. Sterile inflammation: sensing and reacting to damage. Nat Rev Immunol. 2010;10(12):826–37. doi: 10.1038/nri2873 21088683

8. Geng X, Wang Y, Hong Q, Yang J, Zheng W, Zhang G, et al. Differences in gene expression profiles and signaling pathways in rhabdomyolysis-induced acute kidney injury. Int J Clin Exp Pathol. 2015;8(11):14087–98. 26823722

9. Siddiqui RA, Simjee SU, Kabir N, Ateeq M, Shah MR, Hussain SS. N-(2-hydroxyphenyl)acetamide and its gold nanoparticle conjugation prevent glycerol-induced acute kidney injury by attenuating inflammation and oxidative injury in mice. Mol Cell Biochem. 2019;450(1–2):43–52. doi: 10.1007/s11010-018-3371-3 29790115

10. Zhang F, Lu S, Jin S, Chen K, Li J, Huang B, et al. Lidanpaidu prescription alleviates lipopolysaccharide-induced acute kidney injury by suppressing the NF-kappaB signaling pathway. Biomed Pharmacother. 2018;99:245–52. doi: 10.1016/j.biopha.2018.01.059 29334668

11. Zhang W, Kone BC. NF-kappaB inhibits transcription of the H(+)-K(+)-ATPase alpha(2)-subunit gene: role of histone deacetylases. Am J Physiol Renal Physiol. 2002;283(5):F904–11. doi: 10.1152/ajprenal.00156.2002 12372765

12. Guijarro C, Egido J. Transcription factor-kappa B (NF-kappa B) and renal disease. Kidney Int. 2001;59(2):415–24. doi: 10.1046/j.1523-1755.2001.059002415.x 11168923

13. Sen R, Baltimore D. Inducibility of kappa immunoglobulin enhancer-binding protein Nf-kappa B by a posttranslational mechanism. Cell. 1986;47(6):921–8. doi: 10.1016/0092-8674(86)90807-x 3096580

14. de Ruijter AJ, van Gennip AH, Caron HN, Kemp S, van Kuilenburg AB. Histone deacetylases (HDACs): characterization of the classical HDAC family. Biochem J. 2003;370(Pt 3):737–49. doi: 10.1042/BJ20021321 12429021

15. Boyault C, Sadoul K, Pabion M, Khochbin S. HDAC6, at the crossroads between cytoskeleton and cell signaling by acetylation and ubiquitination. Oncogene. 2007;26(37):5468–76. doi: 10.1038/sj.onc.1210614 17694087

16. Feng Y, Huang R, Guo F, Liang Y, Xiang J, Lei S, et al. Selective Histone Deacetylase 6 Inhibitor 23BB Alleviated Rhabdomyolysis-Induced Acute Kidney Injury by Regulating Endoplasmic Reticulum Stress and Apoptosis. Front Pharmacol. 2018;9:274. doi: 10.3389/fphar.2018.00274 29632491

17. Shi Y, Xu L, Tang J, Fang L, Ma S, Ma X, et al. Inhibition of HDAC6 protects against rhabdomyolysis-induced acute kidney injury. Am J Physiol Renal Physiol. 2017;312(3):F502–F15. doi: 10.1152/ajprenal.00546.2016 28052874

18. Tang J, Shi Y, Liu N, Xu L, Zang X, Li P, et al. Blockade of histone deacetylase 6 protects against cisplatin-induced acute kidney injury. Clin Sci (Lond). 2018;132(3):339–59. doi: 10.1042/cs20171417 29358506

19. Cebotaru L, Liu Q, Yanda MK, Boinot C, Outeda P, Huso DL, et al. Inhibition of histone deacetylase 6 activity reduces cyst growth in polycystic kidney disease. Kidney Int. 2016;90(1):90–9. doi: 10.1016/j.kint.2016.01.026 27165822

20. Choi SY, Ryu Y, Kee HJ, Cho SN, Kim GR, Cho JY, et al. Tubastatin A suppresses renal fibrosis via regulation of epigenetic histone modification and Smad3-dependent fibrotic genes. Vascul Pharmacol. 2015;72:130–40. doi: 10.1016/j.vph.2015.04.006 25921924

21. Yang Z, Wang T, Wang F, Niu T, Liu Z, Chen X, et al. Discovery of Selective Histone Deacetylase 6 Inhibitors Using the Quinazoline as the Cap for the Treatment of Cancer. J Med Chem. 2016;59(4):1455–70. doi: 10.1021/acs.jmedchem.5b01342 26443078

22. Kim JH, Lee SS, Jung MH, Yeo HD, Kim HJ, Yang JI, et al. N-acetylcysteine attenuates glycerol-induced acute kidney injury by regulating MAPKs and Bcl-2 family proteins. Nephrol Dial Transplant. 2010;25(5):1435–43. doi: 10.1093/ndt/gfp659 20037173

23. Wang XX, Wan RZ, Liu ZP. Recent advances in the discovery of potent and selective HDAC6 inhibitors. Eur J Med Chem. 2018;143:1406–18. doi: 10.1016/j.ejmech.2017.10.040 29133060

24. Hubbert C, Guardiola A, Shao R, Kawaguchi Y, Ito A, Nixon A, et al. HDAC6 is a microtubule-associated deacetylase. Nature. 2002;417(6887):455–8. doi: 10.1038/417455a 12024216

25. Verdel A, Curtet S, Brocard MP, Rousseaux S, Lemercier C, Yoshida M, et al. Active maintenance of mHDA2/mHDAC6 histone-deacetylase in the cytoplasm. Curr Biol. 2000;10(12):747–9. doi: 10.1016/s0960-9822(00)00542-x 10873806

26. Bolignano D, Donato V, Coppolino G, Campo S, Buemi A, Lacquaniti A, et al. Neutrophil gelatinase-associated lipocalin (NGAL) as a marker of kidney damage. Am J Kidney Dis. 2008;52(3):595–605. doi: 10.1053/j.ajkd.2008.01.020 18725016

27. Rabb H, Griffin MD, McKay DB, Swaminathan S, Pickkers P, Rosner MH, et al. Inflammation in AKI: Current Understanding, Key Questions, and Knowledge Gaps. Journal of the American Society of Nephrology. 2016;27(2):371–9. doi: 10.1681/ASN.2015030261 26561643

28. de Jesus Soares T, Costa RS, Balbi AP, Coimbra TM. Inhibition of nuclear factor-kappa B activation reduces glycerol-induced renal injury. J Nephrol. 2006;19(4):439–48. 17048201

29. Tang J, Shi Y, Liu N, Xu L, Zang X, Li P, et al. Blockade of histone deacetylase 6 protects against cisplatin-induced acute kidney injury. Clinical Science. 2018;132(3):339–59. doi: 10.1042/CS20171417 29358506

30. Sharawy MH, Abdelrahman RS, El-Kashef DH. Agmatine attenuates rhabdomyolysis-induced acute kidney injury in rats in a dose dependent manner. Life Sciences. 2018;208:79–86. doi: 10.1016/j.lfs.2018.07.019 30009822

31. Niu X, Yao Q, Li W, Zang L, Li W, Zhao J, et al. Harmine mitigates LPS-induced acute kidney injury through inhibition of the TLR4-NF-kappaB/NLRP3 inflammasome signalling pathway in mice. Eur J Pharmacol. 2019;849:160–9. doi: 10.1016/j.ejphar.2019.01.062 30716318

32. Meldrum KK, Hile K, Meldrum DR, Crone JA, Gearhart JP, Burnett AL. Simulated ischemia induces renal tubular cell apoptosis through a nuclear factor-kappaB dependent mechanism. J Urol. 2002;168(1):248–52. 12050551

33. Baldwin AS Jr. The NF-kappa B and I kappa B proteins: new discoveries and insights. Annu Rev Immunol. 1996;14:649–83. doi: 10.1146/annurev.immunol.14.1.649 8717528

34. Ghosh S, May MJ, Kopp EB. NF-kappa B and Rel proteins: evolutionarily conserved mediators of immune responses. Annu Rev Immunol. 1998;16:225–60. doi: 10.1146/annurev.immunol.16.1.225 9597130

35. Grilli M, Chiu JJ, Lenardo MJ. NF-kappa B and Rel: participants in a multiform transcriptional regulatory system. Int Rev Cytol. 1993;143:1–62. doi: 10.1016/s0074-7696(08)61873-2 8449662

36. Williams KA, Zhang M, Xiang S, Hu C, Wu JY, Zhang S, et al. Extracellular signal-regulated kinase (ERK) phosphorylates histone deacetylase 6 (HDAC6) at serine 1035 to stimulate cell migration. J Biol Chem. 2013;288(46):33156–70. doi: 10.1074/jbc.M113.472506 24089523

37. Kästle M, Woschee E, Grune T. Histone deacetylase 6 (HDAC6) plays a crucial role in p38MAPK-dependent induction of heme oxygenase-1 (HO-1) in response to proteasome inhibition. Free Radical Biology and Medicine. 2012;53(11):2092–101. doi: 10.1016/j.freeradbiomed.2012.09.023 23010497

38. Jung KH, Noh JH, Kim JK, Eun JW, Bae HJ, Chang YG, et al. Histone deacetylase 6 functions as a tumor suppressor by activating c-Jun NH2-terminal kinase-mediated beclin 1-dependent autophagic cell death in liver cancer. Hepatology. 2012;56(2):644–57. doi: 10.1002/hep.25699 22392728

39. Zhang D, Li J, Costa M, Gao J, Huang C. JNK1 mediates degradation HIF-1alpha by a VHL-independent mechanism that involves the chaperones Hsp90/Hsp70. Cancer Res. 2010;70(2):813–23. doi: 10.1158/0008-5472.CAN-09-0448 20068160


Článek vyšel v časopise

PLOS One


2019 Číslo 10