Contact:jerry.he@wecistanche.com

Hongbing Liu1

Received: 17 November 2019 / Accepted: 10 November 2020 / Published online: 4 January 2021

©The Author(s) 2020

Cistanche can improve kidney function

Abstract

Histone deacetylases (HDACs) are important epigenetic regulators that mediate the deacetylation of both histone and non-histone proteins. HDACs, especially class I HDACs, are highly expressed in developing kidneys and subject to developmental control. HDACs play an important role in kidney formation, especially nephron progenitor maintenance and differentiation. Several lines of evidence support the critical role of HDACs in the development and progression of various kidney diseases. HDAC inhibitors (HDACis) are very effective in the prevention and treatment of kidney diseases (including kidney cancer). A better understanding of the molecular mechanisms underlying the role(s) of HDACs in the pathogenesis and progression of renal disease are likely to be of great help in developing more effective and less toxic selective HDAC inhibitors and combinatorial therapeutics.

Keywords: Histone deacetylases · Histone deacetylase inhibitors · Kidney disease · Kidney cancer

Introduction

Epigenetics refers to the study of heritable changes in gene expression and regulation independently of DNA sequence. Recent years have witnessed an emerging awareness of the critical role of epigenetic mechanisms in health and disease [1]. During development, epigenetic modifcations, such as DNA methylation, histone acetylation, and histone meth- ylation, are set in the chromatin to determine the genome programming in a particular cell by alteration of chromatin structure and thus DNA accessibility to the transcriptional machinery. Disruptions of these epigenetic modifcations resulting from environmental exposures (e.g., diet, toxins, drugs, viral infections) can lead to dysregulation of gene function, without altering the DNA sequence itself [1–3]. As epigenetic abnormalities depend on the interplay between genes and the environment, they are often phenotypically variable, which fts well with the broad phenotypic spec- trum of congenital anomalies of the kidney and urinary tract (CAKUT) and another kidney disease [4–9]. Therefore,

* Hongbing Liu

hliu8@tulane.edu

Department of Pediatrics and The Tulane Hypertension and Renal Center of Excellence, Tulane University School of Medicine, SL-37, 1430 Tulane Avenue, New Orleans,

LA 70112, USA

understanding the epigenetic basis of kidney development might provide new insights into the pathological mecha- nisms of kidney and, hopefully, open new avenues to treat- ment or prevention of CAKUT, through pharmaceutical agents that target epigenetic modifers. Such epigenetic drugs are already in clinical use or under investigation for the treatment of cancer as well as other diseases [10].

Histone acetylation leads to the covalent addition of an acetyl group to a lysine. Such an addition results in local open chromatin, a mark of active transcription, by neutral- izing the net positive charge of histone tail and reducing its binding to negatively charged DNA. In contrast, deacety- lated histones interact strongly with DNA and result in local close chromatin, a mark of inactive transcription. Diferen- tial acetylation of promoter and enhancer histones plays a very important regulatory role in developmental processes, cellular proliferation and diferentiation. Aberrant acetyla- tion or deacetylation leads to diverse disorders such as leuke- mia, epithelial cancers, fragile X syndrome and Rubinstein- Taybi syndrome [11]. Histone deacetylases (HDACs) are a large family of evolutionarily conserved enzymes which catalyze the removal of acetyl groups from histone tails. The action of HDACs is counteracted by histone acetyltrans- ferases (HATs), which acetylate histone tails. To date, 18 mammalian HDACs have been identifed. According to phy- logenetic analysis and their functions, HDACs are divided into four classes: class1 (Hdac1-3, and 8), class II (Hdac4-7,9–10), class III (Sir2/Sirt 1–7), and class IV (Hdac11). Class I, II and IV require zinc for their catalyze activity, while class III members rely on NAD for activity. Among them, class I HDACs have been extensively studied and character- ized. Given that histone acetylation is commonly associated with active transcription, HDACs were originally regarded as general transcriptional co-repressors. However, later on, it has become clear that HDACs regulate gene expression in a highly selective way and exhibit both repressive and acti- vating efects [12]. Due to a lack of intrinsic DNA binding activities, HDACs cannot operate alone for their functions in various fundamental biological processes [12].

It has become clear that HDACs can act on numerous substrates in addition to histones. It is difcult to determine the histone substrate specifcity of diferent HDACs. The main reason is that many purifed HDACs possess very low deacetylation activity and functional redundancy of difer- ent HDACs [13]. The loss or knockdown of one member of HDACs may not be enough to change the overall histone acetylation. In addition, HDACs are recruited to target genes via association with transcriptional complexes (e.g. Sin3 complex, NuRD complex, and Co-REST complex) [14]. Thus, the specifcity of HDACs in gene regulation depends on the partner proteins they associate within diferent cell types. Although three members of class I HDACs (HDAC1, HDAC2 and HDAC3) generally share similar sequence fea- tures, some studies showed that HDAC3 (and perhaps all class I HDACs) has distinct substrate specifcity [15, 16]. Very likely, each HDAC has its specifc target profle in cer- tain substrates, which requires a more comprehensive inves- tigation. Like almost all enzymes, HDACs are functionally regulated for their activities. Among numerous regulation mechanisms at diferent levels, protein–protein interaction and post-translation modifcations (PTMs) are the two well- fned mechanisms. Many HDACs do not function alone but act as a component in a multiprotein complex, which help individual HDAC to exert its catalytic activity in a more efective and specifc manner [17]. It is very common for HDACs to function through the formation of large protein complexes. Extensive biochemical analyses showed that HDAC1 and HDAC2 co-exist in three major multiprotein co-repressor complexes: Sin3, NuRD (nucleosome remod- eling and deacetylation) and CoREST (co-repressor for element-1-silencing transcription factor) [14]. HDACs are not only protein modifers, they can also be the subject to various PTMs. Phosphorylation is the most extensively stud- ies modifcation. HDAC1 can be phosphorylated by casein kinase (CK2) and cAMP-dependent kinase PKA [18]. Phos- phorylation at both Serine (S) 421 and S423 is essential for the enzymatic activity of HDAC1, and mutations of these two sites signifcantly decrease its activity and complex for- mation. CK2 can also phosphorylate HDAC2 on sites 422 and 424 (homologues to S421 and S423 ofHDAC1), and on S394, the main phosphorylation site of HDAC2 [19]. Con- sistently, we also found the presence of S394 phosphoryl- ated Hdac2 in the developing kidneys via mass spectrometry analysis (Liu et al., unpublished). In addition, phosphoryla- tion of HDAC1 and HDAC2 is reversibly regulated by the protein phosphatase PP1 [20]. Studies also revealed that PP2A regulates the hypertrophic response by dephospho- rylating S394 of HDAC2 in the human heart [21]. Collec- tively, HDACs are important epigenetic modulators and play roles in a multitude of biological processes. Their activities are tightly controlled by multiple mechanisms, such as pro- tein–protein interaction, and PTMs. The formation of a mul- tiprotein complex determines not only the activity of HDACs but also their substrate specifcity. The molecular changes by HDACs are likely to exert a signifcant impact on human health and disease. In this review, we would like to descript the roles of HDACs in kidney development and disease.

The roles of HDACs in the kidney development

The ubiquitous expression and high deacetylase activity of class I HDAC are consistent with their functional signifcance. HDAC1 conventional knock-out mice is embryonic lethal, resulting in severe proliferation defects and growth retardation [22]. Surprisingly, the conditional knock out of HDAC1 is well tolerated in multiple tissues and the mice are viable, very likely due to the functional redundancy of HDAC1 and HDAC2 in later development and postnatal life [22]. Co-deletion of HDAC 1 and HDAC2 is detrimental in all tissues examined [22]. Moreover, HDAC2-null mice die after birth within 24 h due to heart dysfunction [22]. In the kidney, HDACs are ubiquitously and highly expressed. RT-PCR analysis indicates that HDAC1, 2, 3, 4, 7, 9 are subject to developmental control and decline signifcantly during the maturation from embryonic to neonatal and adult life [23]. Western blot analysis of kidney nuclear lysates further confirms that Hdac1–3 proteins are highly abundant in the embryonic kidney and are down-regulated postnatally [23]. Immunostaining reveals that Hdac 1 and 2 are highly expressed in diferent populations of the developing kidney at kidneys of newborn (P0) mice, including the undiferen- tiated metanephric mesenchyme, branching ureteric buds, and the stroma (Fig. 1). Hdac1 and 2 are overlappingly and exclusively in nuclear expressed in developing and P21 kidneys (Fig. 1). High expression of Hdac3 was also detected in developing kidney, including podocytes. By contrast, Hdac 5, 6, and 8 are constitutively expressed. The renal microvasculature expresses Hdac 7, 8, and 9 [24]. Collectively, class I and class II HDAC genes are differentially regulated during kidney development. The expression of all the HDACs in the kidney was well documented by a recent review [25].

Fig. 1 High expression and nuclear localization of Hdac1 and Hdac2 in the kidneys of new-born (P0) (a, b) and P21 (c, d) mice, respectively

However, the spatially and temporally restricted distribution of HDACs do not change the global acetylation levels of histones H3 and H4, suggesting a tight coupling of HAT and HDAC functions during normal development [23].

Among class I HDACs, HDAC1 and HDAC2 are evo- lutionarily related to each other and both are very abun- dantly expressed in many tissues. HDAC1 and HDAC2 can form homo- or heterodimers and are found together in almost all nuclear protein complexes, including three well-characterized co-repressor complexes: Sin3, NuRD and Co-REST [14, 26]. By conditional deletion of Hdac1 and Hdac2 in ureteric bud (UB) lineage with Hoxb7-Cre, studies revealed that mice with no more than three deleted alleles of Hdac1 and Hdac2 exhibit no signifcant abnor- malities in kidney development [27]. These mice can sur- vive to adulthood without any abnormalities in growth or development. By contrast, concurrent deletion of all four alleles of Hdac1 and Hdac2 results in early postnatal lethal- ity by 2–4 weeks of age [27]. The kidney tissue of knockout mice at P0 showed the absence of nephrogenic zone, lack of cortical-medullary patterning, and the formation of multi- ple epithelial cysts, suggesting a critical role and functional redundancy of Hdac1 and Hdac2 in kidney formation and function [27]. Studies also demonstrate that loss of Hdac1 and Hdac2 in the UB epithelium leads to marked hypera- cetylation of the tumor suppressor protein p53 to boost p53 stability and transcriptional activity [27]. While p53 is a very important tumor suppressor, unconstrained p53 activity is detrimental to kidney formation, most likely due to inap- propriate cellular death or proliferation defects [28].

The kidney contains multiple specialized cell types with district physiological functions. Kidney formation in mam- mals is initiated by reciprocal interactions between two tis- sues types, the ureteric bud and metanephric mesenchyme [5, 29–31]. The Six2 + cap mesenchyme is a multipotent self-renewing nephron progenitor cells (NPCs) that gives rise to the functional nephron epithelium [30]. To gain insights into the role of HDAC1/2 in NPC maintenance and diferentiation, we conditionally removed Hdac1 and Hdac2 with Six2eGFPCre (Six2TGC) mice [30]. Mice with NPC- specifc double deletion of HDAC1 and HDAC2 (all four alleles) were born in normal Mendelian ratios but died soon after birth [4]. The mutant kidneys at postnatal day (P) 0 showed small kidney size, absence of the nephrogenic zone,lack of nascent nephrons and glomeruli, and formation of multiple cysts [4]. Similar to the Hdac1 and Hdac2 deletion in UB lineage, one allele of either HDAC1 or HDAC2 is sufcient to ensure nephrogenesis [4]. Our results showed that histone deacetylases 1 and 2 (HDAC1/2) are essential to regulate the transcriptional programs of nephron progenitors and renal vesicles [4]. HDAC1/2 play dual roles to balance the self-renewal and diferentiation of NPC during nephro- genesis (Fig. 2): On the one hand, HDAC1/2 are required for the expression of all the marker genes (such as Six2, Sall1 and Osr1) in NPC and the self-renewal of these cells; on the other hand, they are also important to repress the expression of canonical Wnt target genes and prevent the NPCs from pre-mature diferentiation. Our biochemical and ChIP analyses also revealed that HDAC1 and HDAC2 inter- act with Six2, Osr1 and Sall1, a network of transcriptional regulators that maintain the balance of NPC proliferation and diferentiation [4]. Six2 is a master transcription factor in the developing kidney and plays a central role in maintain- ing a functional pool of self-renewing, by dually suppress- ing NPCs diferentiation and driving self-renewal. Six2 and HDAC1/2 are co-expressed in the undiferentiated NPCs and all are required for maintenance of the nephron progenitor cells and prevention of premature diferentiation [4]. We reason that HDAC1/2 are required for Six2′s dual function to precisely control the self-renewal and diferentiation of NPCs. HDACs can deacetylate not only histone proteins but also non-histone proteins [12]. The in silico prediction by the acetylation set enrichment based (ASEB) computer program [32] indicates several potential sites responsible for Six2 acetylation by p300 and deacetylation by Hdac1/2 (Table 1). Among them, Lysine (K) 46, K52, and K71 are located at Six domain (1–124) domain of Six2, and K138 is located at homeodomain of Six2 [33]. Studies showed that the Six domain has a much stronger tendency to nucleus

accumulation and a protein consisting of the Six domain and the homeodomain was found to be exclusively at the nucleus [33]. Therefore, the acetylation of these potential sites would be very likely associated with the nucleus localization of Six2 protein and/or transcriptional activity. Recently, our genome-wide analysis showed that Hdac1 and Six2 co- occupy the enhancer regions of NPC renewal genes and the binding of Hdac1 indicates the open chromatin at the pro- moter region of actively transcribed genes in NPC [34]. How HDAC1/2 regulates Six2 function for kidney development definitely warrants further investigation.

The mammalian kidney develops from reciprocal interactions between the metanephric mesenchyme and the ureteric bud. The stroma, the third lineage which fills up the interstitial space, is derived from distinct progenitors that express the transcription factor Foxd1 [35]. Studies demonstrate that the Foxd1 expressing cortical stroma is a multipotent self-renewing progenitor population, which will give rise to cortical and medullary interstitial cells, mesangial cells, and pericytes of the kidney [35]. HDAC1 and HDAC2 are also higher expressed in the stroma of developing kidneys [4, 23, 27]. To examine the role of the two HDACs in stroma lineage, we are employing a mouse model to conditionally remove HDAC1 and HDAC2 with Foxd1-Cre [36]. Our

Fig. 2 HDAC1/2 play dual roles to balance the self-renewal and diferentiation of NPC during nephrogenesis

preliminary results showed that specifc HDAC1/2 dele- tion in stromal progenitors leads to aberrant expansion of nephron progenitors (Fig. 3), the similar phenotype observed in Foxd1-Cre driven Sall1 deletion or ablation of the renal stroma [37, 38]. Further characterization on how stromal HDAC1/2 to restrict and regulate excessive nephron expan- sion would help advance our understanding toward the epi- genetic regulation of kidney formation and the cross talk between stromal and nephron.

HDACs and renal interstitial fibrosis

Chronic kidney disease (CKD) is an increasingly recog- nized public health issue and marked by a gradual and irreversible decline in kidney function. Renal interstitial fbrosis is a hallmark of CKD. Renal interstitial fbro- sis is characterized by renal tubular atrophy, abnormal deposition of extracellular matrix (ECM) and progres- sive expansion of fbroblasts. The underlying pathogenic mechanisms are complex and diverse. Accumulating evi- dence has shown that HDACs participate in the pathog- enies of renal interstitial fbrosis and HDAC inhibition exerts anti-fbrotic efects mainly via following mecha- nisms: (1) suppressing the pro-fbrotic TGF-β signaling, (2) preventing tubular epithelia cell apoptosis, and (3) increasing the expression of bone morphogenesis protein 7 (BMP7) [39]. Transforming growth factor beta (TGF-β) is a member of the transforming growth factor, which is essential in the regulation of various biological processes. In mammals, three isoforms of TGF-β have been identi- fed in the kidney: TGF-β1, TGF-β2, and TGF-β3. Among them, TGF-β1 exerts its biological activity through Smad and non-Smad pathways and its role in renal fbrosis is the best characterized (Yu et al. 2003; Meng et al. 2016). Aberrant activation of TGF-β1 in the kidney causes inter- stitial fbrosis by the promoting fbroblast proliferation and deposition of abnormal extracellular matrix [40]. Earlier studies demonstrated that treatment with trichostatin A (TSA), a pan HDAC inhibitor (HDACi) for both class I and class II HDACs, attenuates renal fbrosis in unilateral ureteral obstruction (UUO) mouse model [41]. TSA treat- ment also signifcantly inactivated fbroblasts. Moreover, silencing of HDAC1 or HDAC2 blocked renal fbroblast proliferation by reducing phosphorylation of STAT3 (sig- nal transducer and activator of transcription 3), a signaling molecule associated with the proliferation of renal fbro- blasts and the development of renal fbrosis [42]. Further studies demonstrated that TSA treatment also upregulates the expression of BMP-7 and attenuates the pathogen- esis of renal injury [43, 44]. As BMP-7 induces protec- tion against TGF-β-mediated renal fbrosis, restoration of BMP-7 expression represents another major mechanism by which HDAC inhibition prevents progressive CKD [44]. In addition, administration of MS-275 or Fk228 (selective inhibitors of class I HDACs) signifcantly attenuate the progression of kidney fbrosis by inhibiting renal fbroblast activation and proliferation, suggesting that class I HDACs play predominant roles in renal fbrosis [45, 46].

Collectively, HDACs play important roles to renal fbro- blast activation and renal interstitial fbrosis, and the use of inhibitors of HDACs (especially class I HDACs) may therefore provide efective therapy to alleviate and treat renal fbrosis.

HDACs and diabetic kidney disease

Diabetes afects over 451 million people in the world and diabetic nephropathy (DN, kidney disease in diabetes) is the most common cause of CKD. End-stage kidney dis-ease (ESKD) is the last stage of CKD. This is when both kidneys can no longer support the body’s needs for day-to- day life. The most common causes of ESRD in the United States are diabetes and high blood pressure [47]. Progres- sive accumulation of ECM in glomerular mesangium and tubulointerstitium is the hallmark of DN. A number of preclinical studies have demonstrated the efcacy of HDAC inhibition in experimental models of diabetic kid- ney disease [48, 49]. The early studies reported an increase of HDAC2 activity in streptozotocin (STZ)-induced dia- betic kidneys and rat kidney proximal tubular epithelia cells (NRK-52E) exposed to TGF-β1 [50]. siRNA knock- down of HDAC2 reduced the expression of fibronectin and α-SMA in NRK-52E cells. TSA treatment decreased the expression of ECM components and prevented epithe- lial-mesenchymal-transition (EMT). Valproic acid (VPA) (another HDACI/II inhibitor) or SK704 (selective class I HDAC inhibitor) were observed to have similar efects on NRK-52E cells, which supports the essential role of class I HDACs in the development of diabetic kidney disease [50].

Endoplasmic reticulum (ER) stress caused by reactive oxygen species (ROS) is associated with DN development [51]. Epidermal growth factor receptor (EGFR) mediates oxidative stress and EGFR activation was implicated in diabetic mice. EGFR/AKT/ROS/ER stress signaling plays an essential role in DN progression and inhibiting EGFR may serve as a potential therapeutic strategy in DN [51]. Studies showed that treatment of diabetic rats with vori- nostat for 4 weeks signifcantly decreased EGFR level and repressed kidney growth and glomerular hypertrophy, indi- cating that HDACs may play role in early DN via EGFR activation [48].

The podocytes are terminally diferentiated epithelia cells and present an important component of the kidney fltration barrier [52]. Podocyte damage accelerates the progression of DN through the loss of kidney fltration barrier integrity, resulting in the escape of proteins to the urine (proteinuria) [52]. With database analysis, higher HDAC1 and HDAC2 activity were detected in microarray from glomeruli of proteinuric mice (Inoue et al. 2019). Recently studies demonstrated the important role of podo- cyte HDAC activity in the regulation of murine and human glomerular disease, and strongly suggest that inhibition of HDAC1 and HDAC2 activities may suppress the progres- sion of human proteinuric kidney disease. Administration of VPA (a class I HDAC inhibitor, FDA-approved drug) and suberanilohydroxamic acid (SAHA) alleviated pro- teinuria and reduced development to glomerulosclerosis in many rodent glomerular injury models. Podocye-spe- cifc HDAC1 and HDAC2 ablation mice were resistant to progressive glomerulosclerosis. In addition, longitudi- nal analysis of 120,000 participants in the Veteran aging Cohort Study demonstrated a strong protective efect of VPA treatment on the decline of estimated glomerular fl- tration rate [52].

In summary, kidney disease due to diabetes remains the most common cause of chronic kidney failure, and HDACi provides clinical beneft for the treatment of diabetic kidney disease.

HDACs and renal carcinoma

HDAC inhibitors have been extensively studied in various cancer types. Renal cell carcinoma (RCC) is the most common kidney cancer and accounts for 2–3% of adult can- cers in the United States [53]. Class I HDACs, especially HDAC1, 2, and 3 are highly expressed in RCC, making them interesting targets for therapy [54]. Recent studies showed that HDAC1 and HDAC2 are required for the growth and survival of renal carcinoma cells [55]. HDACis lead to a decrease of E-cadherin (the cell adhesion molecule) and platelet-derived growth factor receptor β (PDGFR, a key driver of RCC metastasis formation) [55]. Clear cell renal cell carcinoma (ccRCC) is the most common form of renal cell carcinoma. ccRCC is characterized by the inactivation of the tumor suppressor gene von Hippel Lindau (VHL) [56]. Studies showed that HDAC1 and 6 are highly expressed and modulate cell invasion and migration in ccRCC [56]. Recently, we also detected higher activity of HDAC1 and HDAC2 in Wilms Tumor, a solid cancerous tumor of the kidney that arises from immature kidney cells (Liu et al., unpublished). By targeting both histone and non-histone pro- teins, HDACs play a critical role in the growth and progres- sion of solid tumors [57]. HDACi has been demonstrated to efectively induce growth arrest, apoptosis, and diferentia- tion of cancer cells, and inhibition of tumor angiogenesis [57, 58].

Accumulating evidence has shown that HDACi inhibit cancer cell proliferation and induce cell cycle arrest [57, 58]. VPA treatment of RCC cells led to G1 arrest by upregulation of p21 [59]. In addition, LBH589 (panobinostat; Farydak®, Novartis Pharms Corp.) induced G2/M arrest of RCC cells by the depletion of aurora A and B and downregulation of Survivin [60], which was specifcally mediated through HDAC3 and 6 [60]. Aurora A and B are highly conserved serine/threonine kinases that play important roles during mitosis and meiosis, especially in G2-M cell cycle progres- sion. Survivin is a member of the inhibitor of apoptosis (IAP) family, which function to inhibit apoptosis or pro- grammed cell death. G2/M arrest has also been induced by KBH-A145, a γ-lactam-based hydroxamic acid derivative that inhibits HDAC [61]. In human renal cancer cells, KBH- A145 upregulates p21 by inhibiting recruitment of HDAC1 to the p21 promoter [61]. Collectively, these fndings indi- cate that HDAC inhibitors cause cycle arrest in RCC by afecting cell cycle regulators, such as p21, aurora A, and aurora B.

Despite the FDA approval for the treatment of many can- cers, the single therapeutic use of HDAC inhibitor (HDACi) has limited therapeutic efcacy against solid tumors [62]. Numerous studies have demonstrated the benefts of combi- natorial use of HDACis with other cancer agents for treating RCC [58]. For examples, VPA in combination with low- dosed interferon α, or AEE788 (a receptor tyrosine kinase inhibitor), or RAD001 (an inhibitor ofmTOR), is much more efective in inhibiting HDAC activity and cell proliferation in RCC cell [63]. Results of a single-arm phase I/II study show that addition of class 1 HDAC inhibitor entinostat to high dose IL-2 treatment in patients with metastatic ccRCC might be benefcial [64]. The same group also reported that that the recombination of class II HDAC inhibitor vorinostat and the VEGF blocker bevacizumab is relatively well toler- ated in single-arm phase I/II clinical trial [65].

Collectively, these studies strongly suggest that HADC inhibition, especially when coupled with additional therapy agents, may provide an efective method for treating RCC.

Conclusion and outlook

HDACs, especially class I HDACs, have been demonstrated to play a critical role in kidney development [4, 23, 27, 9]. Aberrant expression level and activity of HDACs are closely associated with the pathogenesis and progression of various kidney diseases. Many HDACi have been shown to be very effective in treating kidney diseases. The comprehensive information on the therapeutic effect of histone deacetylase inhibitors on kidney disease was provided in a review paper (Chun, 2018). More studies are necessary to better understand the molecular mechanisms of HDACs in normal kidney formation and kidney diseases. HDACs and HDACi regulate (or alter) gene expression by changing protein acetylation. Currently, the profile of HDAC-modulated or HDCAi-mediated protein acetylation in the kidneys (at physiological or pathological conditions) is not well known. An extensive analysis of global protein lysine acetylation in response to HDAC knockout or HDAC inhibition using proteomic approaches will provide novel insights into the regulation mechanisms of HDACs in kidney development and open new therapeutic avenues for the prevention and treatment of kidney diseases and associated renal-cardiovascular diseases. Numerous studies successfully demonstrated the renoprotective effects of HDAC inhibitors, however, most of them are pan-HDAC inhibitors. Broad-spectrum HDAC inhibition is more likely to cause nephrotoxicity, and the development of specific HDAC inhibitors is required to improve the clinical outcome and reduce the toxicity. Combinatorial therapy by coupling HDAC inhibitor with additional agents will also be of benefit for the treatment. Furthermore, a comprehensive understanding of the roles of HDACs and HDAC inhibitors will be also of great help for the development of new tools to recapitulate nephrogenesis in regenerative medicine.

Acknowledgment Great thanks to Dr. El-Dahr for critically read- ing and editing this manuscript. Research reported in this publication was supported by the American Heart Association (17SDG33660072), the National Institutes of Health grants P50 DK096373-03 and P30GM103337.

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