Network Reconstruction Reveals that Valproic Acid Activates Neurogenic Transcriptional Programs in Adult Brain Following Traumatic Injury
To determine the mechanism of action of valproic acid (VPA) in the adult central nervous system (CNS) following traumatic brain injury (TBI) and hemorrhagic shock (HS).
Data were analyzed from different sources, including experiments in a porcine model, data from postmortem human brain, published studies, public and commercial databases.
The transcriptional program in the CNS following TBI, HS, and VPA treatment includes activation of regulatory pathways that enhance neurogenesis and suppress gliogenesis. Genes which encode the transcription factors (TFs) that specify neuronal cell fate, including MEF2D, MYT1L, NEUROD1, PAX6 and TBR1, and their target genes, are induced by VPA. VPA represses genes responsible for oligodendrogenesis, maintenance of white matter, T-cell activation, angiogenesis, and endothelial cell proliferation, adhesion and chemotaxis. NEUROD1 has regulatory interactions with 38% of the genes regulated by VPA in a swine model of TBI and HS in adult brain. Hi-C spatial mapping of a VPA pharmacogenomic SNP in the GRIN2B gene shows it is part of a transcriptional hub that contacts 12 genes that mediate chromatin-mediated neurogenesis and neuroplasticity.
Following TBI and HS, this study shows that VPA administration acts in the adult brain through differential activation of TFs responsible for neurogenesis, genes responsible for neuroplasticity, and repression of TFs that specify oligodendrocyte cell fate, endothelial cell chemotaxis and angiogenesis.
Short title: Mechanism of action of valproic acid in traumatic brain injury
KEY WORDSbioinformatics network modeling pharmacoepigenomics
ChIP-sequencing is a method used to analyze protein interactions with DNA
Expression quantitative trait loci
Genomewide association studies
Histone quantitative trait locus
Histone 3, one of the 5 main histone proteins involved in the structure of the nucleosome in the chromatin of eukaryotic cells
Histone H3 di- or tri-methylated at residue lysine 9. histone marks that are found in facultatively repressed genes
Histone H3 acetylated at residue lysine 27. H3K27ac is associated with the higher activation of transcription and therefore defined as an active mark of both enhancers and promoters
Histone H3 di- or tri-methylated at residue lysine 27. histone marks that are found in facultatively repressed genes
Histone 4, one of the 5 main histone proteins involved in the structure of the nucleosome in the chromatin of eukaryotic cells
High occupancy by transcription factors. indicative of enhancers and promoters, especially in developmentally important genes
Concentration of an inhibitor where the response (or binding) is reduced by half
Topologically-associating domain, the basic spatial unit of transcription in the human genome
Traumatic brain injury
SK human caucasian neuroblastoma, an immortalized human neuronal cell line
AT-rich interaction domain 1A
Achaete-Scute family BHLH transcription factor 1
Activating transcription factor 7 interacting protein
B-Cell CLL/Lymphoma 11A
BCL2 like 11
Bone morphogenetic protein 2
BTG family member 2
Coiled-coil domain containing 117
Chemokine C-C Motif Ligand 2
Chromatin assembly factor 1 subunit B
Cysteine rich angiogenic inducer
ELK1 ETS transcription factor
EPH receptor B2
EWS RNA binding protein 1
Fibroblast growth factor 7
Fibroblast growth factor 9
GRP1 (General receptor for phosphoinositides 1)-associated scaffold protein
Glutamate ionotropic receptor NMDA type subunit 2B
Interleukin 1 receptor antagonist
Kringle Containing Transmembrane Protein 1
Myocyte enhancer factor 2C
Myocyte enhancer factor 2D
Myelin transcription factor 1 Like
Neuronal differentiation 1
Nuclear receptor subfamily 1 group D member 1
Nuclear receptor subfamily 4 group A member 1
Nuclear receptor subfamily 6 group A member 1
Oligodendrocytic Myelin Paranodal and Inner Loop Protein
Paired box 6
Peripheral Myelin Protein 2
Peroxisome proliferator activated receptor delta
Prospero homeobox 1
Paired related homeobox 1
SET domain bifurcated 1
SWI/SNF related matrix associated, actin dependent regulator of chromatin, subfamily B, member 1
Suppression of Tumorigenicity 18 zinc finger
T-box brain 1
X-box binding protein 1
Zinc and ring finger 3
The mechanism of action of VPA as an anticonvulsant, mood stabilizer and analgesic in the human central nervous system (CNS) has not been adequately characterized. VPA and its derivatives exhibit a variety of effects which are cell- and tissue-specific, differ based on disease state, age, gender and ethnicity, and may be effective or deleterious. VPA is a weak blocker of sodium and calcium ion channels, and may inhibit key enzymes in the catabolism of gamma-aminobutyric acid (GABA), including ABAT (4-aminobutyrate aminotransferase) at physiologically relevant concentrations (1). There is also evidence that VPA exerts its antiepileptic action through differential regulation of the GRIN2B (Glutamate Ionotropic Receptor NMDA Type Subunit 2B) gene (2). VPA is an effective inhibitor of histone deacetylases (HDACs), with an IC50 (0.4 mM) well within the therapeutic range of VPA (0.35–0.7 mM in serum). VPA causes robust chromatin decondensation, with potent acetylation of core histones such as H3 and H4 that leads to activation of development gene expression (3,4). VPA has been shown to be neuroprotective in animal models of traumatic brain injury (TBI) (5,6), spinal cord injury (7), and in neurodegenerative disease (8). In a swine model of TBI and hemorrhagic shock (HS) VPA decreases brain lesion size, improves neurologic recovery, and down-regulates genes associated with necrosis, apoptosis, and inflammation (9). The HDAC inhibitor, sodium butyrate, with a mechanism of action like that of VPA, has been shown to activate neurogenesis in rodent brain following ischemic injury (10). These results suggest different ways in which VPA may act in parallel to provide benefit in epilepsy, mood disorders, migraine, as well as recovery following trauma.
It appears that VPA-induced histone acetylation is not sufficient for chromatin decondensation, but rather a downstream effect of HDAC inhibition, suggesting that the drug suppresses the expression of proteins involved in maintenance of heterochromatin and/or uses chromatin remodeling proteins as intermediaries (11, 12, 13). It is also routinely used to remove histone methylation in cellular domains such as the lamina-associating domain (LAD) located just interior of the nuclear membrane, a region containing heterochromatin, in which exposure to VPA abolishes H3K27 and H3K9 methylation (14).
Recent studies of the epigenomic control of gene expression that has identified distinct mechanisms through which chromatin interactions mediate transcriptional programs involving topologically-associating domains (TADs), enhancer-promoter loops and actively transcribed regions of the human genome characterized by the histone mark H3K27ac (15, 16, 17). It has been shown that SNPs which disrupt the boundaries of TADs cause serious health problems (18).; and causal SNPs exhibit significant allele bias in open chromatin (19). In addition, the greater the number of spatial connections a given enhancer or promoter maintains genomewide indicates both the potency of the regulatory element and its validity (20), especially for CNS genes that are involved in coordinated transcriptional programs of neurogenesis and neuroplasticity (20).
Our hypothesis is that VPA acts through transcriptional activation and repression of specific genes resulting in chromatin-mediated neurogenesis and neuroplasticity in the adult CNS and inhibition of glial scarring. To determine the validity of this premise, we analyzed experimental and public data. We then reconstructed a gene regulatory network that mediates VPA’s mechanism of action in human brain, and found that the drug exerts widespread effects in adult brain including a transcriptional program of neurogenesis and neuroplasticity, involving TFs that have been shown to program neuronal cell fate commitment and suppress oligodendrocyte cell fate.
Experimental data from an animal model of TBI and HS
Examination of gene expression data from a swine model of TBI and Hemorrhagic Shock exhibited functional recovery following VPA therapy showed remarkable enrichment of transcription factors (TFs) that were regulated in a significant manner by the drug. In the animal model, swine were subjected to controlled TBI and hemorrhage (40% blood volume), kept in shock for 2 h, and resuscitated with vehicle or vehicle + VPA (n = 3 per group). The vehicle was Hextend (Hospira Inc. Lake Forest, IL) at 50 mL/min versus (2) Hextend at 50 mL/min plus VPA at 300 mg/kg (EMD Biosciences Inc., La Jolla, CA). In the Hextend + VPA group, VPA treatment was started 1 h after hemorrhage at an infusion rate of 100 mg/kg per hour intravenously. The vehicle and treatment groups received identical volumes of fluid, which matched the volume of shed blood. After 6 h, brain RNA was isolated, and gene expression profiles were measured using a Porcine Gene ST 1.1 microarray (Affymetrix, Santa Clara, CA).
Gene expression data from postmortem human brain
Results of microarray expression analysis from postmortem human brain were obtained from different sources (21,22). In a patient cohort with epilepsy, patients on VPA therapy were compared to controls at time of death (TOD) for relative levels of several TFs, nuclear receptors, and other mRNAs (23). Sample sizes for each group were N = 6 for epileptic patients on VPA therapy at TOD, N = 6 for epileptic patients on a different anti-convulsant drug at TOD.
Experimental data from the human SK-N-SH cell line
Publicly available date from SK-N-SH cells were used for two applications: (1) For determination of DNAse I hypersensivity and allele bias, as they are included as examples in the deltaSVM machine learning algorithm (19), and (2) Evaluation of spatial interactions in the human genome using data from a high resolution Hi-C dataset (19). To discover how the VPA pharmacogenomic SNPs we selected produced robust pharmacogenomic stratification, evaluation of the chromatin interactions of regulatory elements they were located in was used to preliminarily map the putative VPA pharmacodynamic pathway in human brain.
SK-N-SH cells are a human neuroblastoma cell line which > contains a mixture of at least 2 cell types.
Published literature on pharmacogenomic associations and VPA targets and pathways
Two hundred and fifty-four peer-reviewed published articles were retrieved between January 1 and October 1 2016, including gene association studies, as well as basic and clinical pharmacology reports. An automated Boolean search string was used in PubMed (24), Google Scholar (23) and clinicaltrials.gov (25), consisting of “valproate OR valproic acid OR sodium valproate OR divalproex sodium AND pharmacodynamics OR mechanism of action OR brain OR pathways AND pharmacogenomic AND bipolar disorder AND epilepsy AND migraine headache AND gene OR SNP AND association AND human.” There are no published genomewide association studies (GWAS) that are focused on medication response or adverse events related to only valproic acid therapy in epilepsy, bipolar disorder or migraine. There are however, several GWAS that have investigated SNPs associated with human populations that have treatment-resistant or refractory epilepsy. These studies are made up primarily of patients who do not respond to a combination of anticonvulsant drugs or worsen on therapeutic regimens. Due to confounding related to polypharmacy these studies were excluded. For this study, we avoided anything but primary research studies in which we re-tested all the parameters and statistical tests that were employed. This dramatically reduced the number of studies from 254 to 52 that could be included in this analysis.
VPA pharmacogenomic SNPs
To better understand human CNS pathways that are involved in the mechanism of action of valproic acid, we combined SNP imputation with bioinformatics analysis as performed in a previous study (22). SNPs included in the analysis were those likely to be associated with known biological targets of VPA, could be functionally annotated, and were derived from primary research studies. For this analysis of potential pharmacodynamic pathways, we excluded pharmacokinetic genes and their variants such as the UGT and CYP super-families. To select VPA pharmacogenomic SNPs we combined SNP imputation from VPA pharmacogenomic association studies, and performed computational and bioinformatics analysis as described in detail (22). DrugBank (25) and the pharmacogenomic mutation database (PGMD®; Qiagen) lists pharmacodynamic targets that have been associated with VPA (26), and these were also interrogated to gather additional information.
In Fig. 1.1, bioinformatics analysis was used to identify the most probable causal SNP from the association regardless of the lead SNP(s) that were reported, and included the following bioinformatics analysis to determine the functionality of the variant (22): (1) Location in open chromatin as indicated by peaks of DNAse I hypersensitivity, (2) Low to moderate methylation of any cytosine residues, (3) The presence of histone marks that indicate regulatory function (H3K27ac + H3K4me1 = enhancer; H3K27ac + H3K4me3 = promoter), (3) The location of the variant within the context of the gene or in an intergenic domain, (4) Whether the regulatory element has yet to be annotated as a molecular quantitative trait locus (eQTL, hQTL, etcetera), (4) Proteins, including transcription factors, bound to the regulatory element as determined by ChIP-Seq indicating its regulatory function, (5) Disruption by the pharmacogenomic SNP of transcription factor binding sites as indicated by alterations in the position weight matrix, (6) Association of the regulatory element with the requisite RNA species (e.g., bi-directional enhancer RNA = enhancer; mRNA = promoter), (7) Connectivity of the regulatory element with other elements in the genome as indicated by the Hi-C chromatin conformation capture method limited to SK-N-SH cells, which are the ENCODE Tier 2.5 neural surrogate cell line, (8) Transcriptional programming by factors which are responsible for determination of neuronal cell fate, (9) Determination of the allele bias of the allelic variant using the deltaSVM algorithm (19), (10) examination of the neuroanatomical distribution of target gene expression data in postmortem human brain using both microarray and in situ hybridization data from the Human Brain Atlas of the Allen Brain Science Institute (21).
Harmonization of nomenclature: pig, human and rodent genes and their regulatory elements
This study involves cross-species comparisons from pig (Sus scrofa), rat (Rattus norvegicus) and human (Homo sapiens). To ensure that we could reliably use inter-species nomenclature in the context of the human CNS, we compared gene, promoter and enhancer data using 3 resources: (1) comparative assessment of pig, rodent and human transcriptomes for identity (27), (2) thorough analysis of human accelerated regions in human brain that are not present in other mammalian brains for exclusion (28), (3) cross-species assessment of histone modifications, open chromatin and deep learning methods applied to pigs, mice, rats and humans to ensure concordance of identifiable enhancers, promoters, super-enhancers and master TFs (29), and (4) enhancer-promoter loop conservation across species using context‐dependent conservation (30). All gene symbols and homologous regulatory elements were found to be the same, at least in regards to nomenclature, chromatin state annotation, and relative position within the genome. We then harmonized our nomenclature with the results of the roadmap epigenome mapping consortium. Thus, gene and protein symbols and definitions were consistent with HGNC nomenclature, except as indicated by citation in the text. Gene symbols are from GENCODE except where indicated, and genomic location coordinates are from build 38 of the Human Genome.
For annotation, we focused on active enhancers, promoters and transcription start sites, so other chromatin states were not used in the present study, including flanking and poised regulatory elements, transcribed domains or repressed elements. Although potential regulatory variants may be repressed in one tissue or brain region but not another, we could directly assess function in any biological system in this study, so we relied on the data provided by the association studies.
VPA-regulated transcription factors (TFs)
Selected Pharmacogenomic Variants Selected for Allelic Variation in VPA Dose, Response and Pharmacodynamics in Human Populations. Noncoding SNPs that Identified Regulatory Elements, Including Enhancers and Promoters
Response in children
Chromatin remodeling proteins and complexes
Several and chromatin remodelers, including ARID1A, BCL11A, CHAF1B, were among genes regulated by VPA. We determined the regulatory targets of these genomewide, and determined and to what degree they overlapped the VPA-responsive promoters as part of the reconstruction of the network. We also examined pioneer factors such as PAX6, which appears to act in concert with chromatin remodeling complexes during neurogenesis, including published data on TFs that are pioneer factors and chromatin state regulators (Supplementary Table 1).
Reconstruction of VPA gene regulatory networks in the human CNS
Figure 1.2 shows the method by which we reconstructed the central VPA pathway in the human CNS. It involved: Identification of databases relevant to modeling the VPA regulatory circuit, Data aggregation from public databases and in-house data, manual curation of the data in the context of a VPA central mechanism of action, preparation of curated data for model integration, iterative gene set enrichment analysis (GSEA) using different public and commercial software, and pathway analysis using IPA® and the STRING database of protein-protein interactions (40), as well as network analysis using weighted gene co-expression network analysis (WGCNA) in R (41) and node-edge modeling systems modeling using Python (42). In addition to applying redundant software analysis tools, we also used different open source and commercial databases, including IPA® (43), Pathway Commons (44) and Reactome (45) databases as well as manual curation of the scientific literature, to determine network interactions.
For reconstruction of VPA’s gene CNS regulatory pathway, we used a hybrid model development method that combines GSEA and pathway analysis/network modeling software used in bioinformatics with a technique for constructing core regulatory circuitry which includes super-enhancers, TFs and auto-regulation, based on defined biological attributes of transcriptional regulation in the human CNS (Supplementary Table 1). During the project, we discovered several other TFs that are regulated by VPA that directs cell fate, in addition to many genes whose was expression was regulated by ASCL1 (Achaete-Scute Family BHLH Transcription Factor 1), NEUROD1 (Neuronal Differentiation 1), MEF2C (Myocyte Enhancer Factor 2C), MEF2D (Myocyte Enhancer Factor 2D), MYT1L (Myelin Transcription Factor 1 Like), and TBR1 (T-Box, Brain 1). Many TFs were tightly coupled in terms of target promoters, many of which were also involved in neurogenesis and neuroplasticity. As such, this convoluted super-program was investigated in greater detailed.
Relationship between VPA-regulated TFs and other TFs in human brain and cell types
To understand the relationship between genes whose expression is highly regulated by VPA following brain injury in the CNS, we first examined sets of TFs which were known to be differentially regulated by VPA in brain and whose function was linked to neurogenesis and suppression of gliogenesis in human brain. Comparisons were made between VPA-responsive master TFs and their targets and other TFs in the human telencephalon, and the different sets are represented on a coronal section of the human telencephalon (Fig. 4). Adult human brain regions, examined in the roadmap epigenome mapping consortium (15), included the angular gyrus, anterior caudate, cingulate gyrus, hippocampal formation, inferior temporal lobe and mid-frontal lobe. Cell types included astrocytes and HUVEC, the latter a lymphoblastoid cell line derived from human vascular endothelial cells.
TFs were assigned using a subset of ENCODE brain regions and in astrocytes based on annotation of super-enhancer status using histone marks such as H3K27ac and other characteristics (15,17). From this analysis, only 8 of the TFs and nuclear receptors regulated by VPA exhibit enhancer-like attributes in various brain regions. Other enriched TFs include NFIX, regulated by CHAF1B and SOX2. The correlation between VPA-TFs and TFs which function with superenhancer status in different human brain regions is obvious, with this small subset accounting for 31–48% of all TFs across the telencephalon. In astrocytes, as shown in Fig. 4, although only MEF2D is represented as a VPA-TF, 17% of all TFs in this cell type are regulated by VPA-TFs. HUVEC cells were used as a surrogate for CNS endothelial cells, and MEF2C, MEF2D and NR1D1 are VPA-TFs, with these TFs and their targets accounting for 18% of the TFs in this lymphoblastoid cell line
VPA regulation of gene expression following injury to the brain in a swine model
Most the genes differentially-regulated by VPA were several master TFs that are highly expressed during development of the CNS, and are also found in the developing adult human telencephalon. TFs that target the greatest number of differentially expressed genes were NEUROD1, ASCL1, MEF2C, MEF2D, BCL2L11 (BCL2 Like 11), ELK1 (ELK1, ETS Transcription Factor), MYT1L, PPARD (Peroxisome Proliferator Activated Receptor Delta), SIRT1 (Sirtuin 1), SMARCB1 (SWI/SNF Related, Matrix Associated, Actin Dependent Regulator Of Chromatin, Subfamily B, Member 1), and TF (Transferrin). All of these genes except for SMARCB1, which is induced by VPA, were found in the VPA-regulated set.
TFs that program oligodendrocytic cell fate, endothelial cell fate and angiogenesis were significantly down-regulated compared to other TFs in this dataset (p = 2.78E-04; Fisher’s exact test). These included FGF7 (Fibroblast Growth Factor 7; −3.2 log2-fold), PROX1 (Prospero Homeobox 1; −1.81 log2-fold), SOX10 (SRY-Box 10; −1.81 log2-fold), PRRX1 (Paired Related Homeobox 1; BMP2 (Bone Morphogenetic Protein 2; −1.73 log2-fold) and ST18 (Suppression Of Tumorigenicity 18, Zinc Finger; −1.22 log2-fold). Other significantly down-regulated genes included CYR61 (Cysteine Rich Angiogenic Inducer), OPALIN (Oligodendrocytic Myelin Paranodal And Inner Loop Protein), PMP2 (Peripheral Myelin Protein 2) and THBS1 (Thrombospondin 1).
Supplementary Figure 3 shows the significant functions of the 50 most up-regulated and most down-regulated genes following VPA therapy in a swine model of TBI and hemorrhage. These results show that in an animal model of TBI and hemorrhage, VPA therapy induces genes associated with neurogenesis and neuroplasticity, and represses those associated with cell loss, endothelial cell invasion, and angiogenesis.
Selection of VPA pharmacogenomic SNPs for further examination
The intronic SNP rs2857654_A located within the CCL2 gene, which encodes the Chemokine C-C Motif Ligand 2, and is most significantly associated with cell movement and migration of cells and this enhancer interacts with VPA (31);
- 2.The 5′ SNP rs3764028_G located in the distal GRIN2B promoter (32). Spatial mapping in SK-N-SH cells shows that it forms an inter-chromosomal transcriptional hub (Fig. 3a), contacting genes in cis- and trans- in SK-N-SH cells that are enriched for genes involved in neuronal differentiation and development of the CNS (Fig. 3a);
The 5′ SNP rs2269577_G located in the promoter of the XBP1 (X-Box Binding Protein 1) gene (33), which functions as a transcription factor during endoplasmic reticulum (ER) stress by regulating the unfolded protein response. Required for cardiac myogenesis and hepatogenesis during embryonic development, and the development of secretory tissues such as exocrine pancreas and salivary gland. An enhancer co-regulates XBP1, EWSR1 (EWS RNA Binding Protein 1), CCDCC117 (Coiled-Coil Domain Containing 117), KREMEN1 (Kringle Containing Transmembrane Protein 1) and ZNRF3 (Zinc And Ring Finger 3) genes, which are co-localized within a TAD located on chromosome 22 (46). The location of this SNP 5′ to the XBP1 gene is shown in Fig. 3b.
VPA modulates a transcriptional hub consisting of 12 genes in spatial contact with the GRIN2B promoter
The 5′ SNP rs3764028_G located in the distal GRIN2B promoter is in a region associated with massive chromatin reorganization in brain (48,49) in rodents and human cell lines. This SNP detects a promoter that maintains spatial contact, as determined by Hi-C maps of SK-N-SH cells. SK-N-SH cells are a lymphoblastoid cell line which contains a mixture of 2 cell types. This regulatory community also contains 3 known enhancers including 2 super enhancers as well as a promoter with spatial contacts to genes associated with neuronal survival and plasticity. This replicates a result from a study in mouse brain in which researchers combined genome-wide analysis of data sets for chromatin accessibility (FAIRE-Seq) and the enhancer mark H3K27ac, in which they found a subset of genes associated with neuroprotection and plasticity that increased transcription in adult mouse brain following activation of the glutamate receptor (49). In our study, both gene set enrichment using Gene Ontology, as well as manual inspection of genes that maintain spatial contacts with the promoters and enhancers detected by our putative causal SNPs demonstrate selectivity for neuroplasticity and chromatin reorganization. In agreement with their findings, genes whose abundance increased included NR4A1, which regulates dendritic spindle density and organization in human brain following neuronal excitation, BTG2, a transcription factor that inhibits neural precursor cell proliferation and stimulates neuron cell differentiation and acts in histone arginine methylation, ILRN, which is also in contact with an enhancer associated with SNP rs2857654_A, and NF1, which differentially controls neural stem cell proliferation. In addition, we identified contacts with GRASP, part of a receptor complex scaffold that regulates G protein-coupled glutamate receptor signaling, MEF2D, which is regulated by NEUROD1, and EPHB2 (EPH Receptor B2), a developmentally-regulated receptor tyrosine kinase that functions in axonal guidance during development. This promoter also maintains long distance spatial contact with SETDB1, an H3-K9 histone methyltransferase that regulates epigenetic gene silencing to maintain stem cell pluripotency, a result that has been experimentally shown in rodent brain and cell lines by other researchers (48,49).
The distal GRIN2B promoter maintains spatial interactions with genes that program neuronal cell fate in humans, and are highly responsive to VPA. These are TBR1 (T-Box, Brain 1), which is up-regulated by VPA following TBI in our animal model. TBR1 is a TF that acts as a potent programmer of neurogenesis (50), controls the differentiation of pyramidal cells in neocortex, and controls expression of the GRIN2B gene in developing cerebral cortex (51). The other is FGF9 (Fibroblast Growth Factor 9), which is produced by developing neurons to maintain homeostasis within the surrounding milieu. It plays an important role in the regulation of embryonic development, cell proliferation, cell differentiation and cell migration, regulation of gliosis during repair and regeneration of brain tissue after damage and the differentiation and survival of neuronal cells (52). Several of these genes that exhibit spatial proximity to the GRIN2B promoter in human SK-N-SH cells are also up-regulated by VPA in the swine model of TBI and hemorrhage. These include FGF9, NR6A1, TBR1 and MEF2D.
Relationship between VPA-regulated TFs and other TFs in human brain and cell types
To understand the relationship between genes whose expression is highly regulated by VPA following brain injury in the CNS, we first examined sets of TFs which were known to be differentially regulated by VPA in brain and whose function was linked to neurogenesis and suppression of gliogenesis in human brain. Comparisons were made between VPA-responsive master TFs and their targets and other TFs in the human telencephalon, and the different sets are represented on a coronal section of the human telencephalon (Fig. 6). Adult human brain regions included the angular gyrus, anterior caudate, cingulate gyrus, hippocampal formation, inferior temporal lobe and mid-frontal lobe. Cell types included astrocytes and HUVEC, the latter a lymphoblastoid cell line derived from human vascular endothelial cells.
Examination of the interaction and correlation between diverse datasets led to a definitive set of master TFs and their target TFs that were involved in VPA-mediated neurogenesis. Forty-seven TF targets of the 18 master transcription factors regulated by VPA include are controlled by 18 master TFs (Supplementary Table 2), but not all the master TFs are expressed in the adult human telencephalon at high abundance (Fig. 4). These data show that VPA-regulated TFs responsible for neuronal cell fate are found in the adult human brain, and TFs that can program fibroblasts into oligodendrocytes including OLIG2 and ST18, are also present. For details concerning Fig. 4 see (53).
Next, we performed a GSEA on VPA-responsive versus non-VPA TFs found in these different adult brain regions and compared these results to those found in our animal model. Supplementary Figure 4 shows a comparison of gene set enrichment, including brain region subsets from the data used for Fig. 4, including (Supplementary Figure 4A), the set of VPA-regulated TFs and (Supplementary Figure 4B) the set of non VPA-responsive TFs. TFs found in human telencephalon that are not VPA-responsive are not enriched for neurogenesis, but are enriched for differentiation and development of other cell types.
Preliminary evidence from microarray expression data from postmortem human brain tissue
Supplementary Figure 1 only includes a fraction of the pathway, including direct targets such as master TFs and some of the genes they regulate, and represents a union of data from human and a swine model of TBI and hemorrhage. Green symbols show up-regulated genes following VPA treatment versus vehicle in the swine model of TBA, and red symbols are down-regulated genes following VPA treatment in the animal model of brain injury. Blue symbols are VPA pharmacogenomic genes (Table I). Symbols lacking colors are VPA-regulated genes that were predicted by IPA® using the “connect” function, as essential components of the same interconnected pathway expressed in human brain. We then compared overlap of pathway components to previously defined networks in the Reactome database (45), the IPA® database (43) and Gene Ontology (54). Previously defined biological networks across tissues and species exhibited significant overlap with the set of VPA pathway molecules. As might be expected from the widespread action of VPA-responsive TFs that direct neurogenesis, the 3 most significant overlaps were: (1) Neuronal cell fate determination in mammals (p-value < 1.30E-13; q-value < 4.39E-10), (2) Nuclear receptor transcription pathway in humans (p < 3.94E-13; q < 1.67E-10) and (3) Neurogenesis in humans (p < 5.17E-12; q < 7.18E-10). Supplementary Table 2 shows a summary of the overlap of TFs found in this reconstructed VPA gene regulatory network with a matrix of known TFs responsible for: (1) CNS developmental processes, (2) Specification of germinal layers of cerebral cortex, and (3) Reprogramming/trans differentiation of different cell types to neuroblasts, neural crest, neural progenitor cells and neurotransmitter-specific neurons.
Many TFs in the VPA regulatory network are located in HOT regions
It has been found that many master TFs regulated by super-enhancers are also sites of high TF occupancy (HOT regions) (39). HOT regions correlate with decreased nucleosome density and increased nucleosome turnover and are primarily associated with open chromatin. Collectively, these HOT regions span approximately 19% of the genome in other species (39,55). Since the reconstructed VPA gene regulatory pathway contains not only master TFs normally found in adult brain (Fig. 4), and the drug induces numerous master TFs in human brain that are expressed at high abundance during CNS development, we examined the overlap between HOT regions and genes in our pathway. Many genes in the reconstructed VPA pathway were in HOT regions.
The rapid action of VPA in the adult brain appears to reduce the impact of ensuing trauma following TBI and hemorrhage, and mitigates neuronal atrophy in bipolar disorder and epilepsy. This raises the question of whether newly differentiated neurons are absorbed into active neuronal regulatory networks to become part of functional neurophysiological pathways. The highly significant changes related to neuroplasticity that is observed in our animal model of TBI and hemorrhage suggest this may be true. However, it is most probable that VPA acts through different pathways following traumatic injury than that observed in healthy tissue. Previous studies in rodent models of ischemia followed by treatment with HDAC inhibitors including VPA and sodium butyrate have observed activation of neurogenesis in the adult brain (10,56), although repair mechanisms may depend on the post-injury timeframe (56).
In cell lines, treatment with VPA causes rapid and extensive chromatin decondensation, suggesting that VPA broadly and directly acetylates histones for transformation of chromatin state from heterochromatin to euchromatin. Thus, it may be that VPA acts directly to inhibit histone deacetylases. Alternatively, rapid activation of chromatin remodeling proteins such as the ARID1A component of the neural progenitors-specific chromatin remodeling complexes npBAF and nBAF may mediate chromatin remodeling following administration of VPA. Ultimately, it may be that all of these mechanisms contribute to VPA’s mechanism of action in the human CNS.
Adequate data now exist to elucidate the transcriptional program that resolves all of the components that are necessary and sufficient to determine VPA’s mechanism in the human brain using knowledge-based discovery. This capability has been demonstrated in other domains, including modeling of the core regulatory circuits in different human tissues and cell lines, including super-enhancers, master TFs and TFs responsible for specifying cell fate (Supplementary Tables 1, 3). In this study, we identified important master TFs such as NEUROD1 and TBR1 that are induced by VPA following TBI in adult brain, but normally expressed at low levels in the mature human telencephalon.
Preliminary data from postmortem human brain must be considered preliminary, as complete medical histories are not available on either patients or controls, there is heterogeneity in the data, and this microarray expression reflects variability associated with a single time point in the analysis of postmortem human brain tissue lacking cause of death in most cases. In addition, although controls were selected based on lack of medication history, medical history was not well characterized.
Since VPA relieves symptoms in disorders such as bipolar disorder, which involves neuronal loss and neural atrophy (64), it is tempting to speculate that VPA may have a positive effect on a range of damaged brain tissue, from mild atrophy to the critical damage that is often observed following TBI. Conversely, VPA may generate aberrant hyperplasia of different cell types in human brain as has been suggested (65). This could account for rebound seizures and CNS impairment including encephalopathy after chronic treatment with VPA (66).
Further investigation is warranted to completely understand how VPA and other HDAC inhibitors can provide functional recovery after severe trauma to the human brain and spinal cord, and to a lesser extent, suppress epileptogenesis, alleviate mania in bipolar disorder, and act as an analgesic in migraine. Modeling using rich data resources as was performed in the current study generate testable hypotheses for more focused experiments in subsequent studies.
- 5.Halaweish I, Bambakidis T, Chang Z, et al. Addition of low-dose valproic acid to saline resuscitation provides neuroprotection and improves long-term outcomes in a large animal model of combined traumatic brain injury and hemorrhagic shock. J Trauma Acute Care Surg. 2015;79(6):911–9.PubMedCrossRefGoogle Scholar
- 24.Jessen WJ, Landschulz KT, Turi TG, Reams RY. Mining PubMed for biomarker-disease associations to guide discovery. PeerJ. 2015;3, e1802.Google Scholar
- 27.Dawson HD. A comparative assessment of the pig, mouse and human genomes. The minipig in biomedical research. 2011;323–42.Google Scholar
- 30.di Iulio J, Bartha I, Wong E, Yu HC, Hicks M, Shah N, et al. The human functional genome defined by genetic diversity. bioRxiv. 2016 :082362.Google Scholar
- 39.Li H, Liu F, Ren C, Bo X, Shu W. Genome-wide identification and characterization of HOT regions in the human genome. bioRxiv. 2016;036152.Google Scholar
- 40.Szklarczyk D, Franceschini A, Wyder S, Forslund K, Heller D, Huerta-Cepas J, et al. STRING v10: protein–protein interaction networks, integrated over the tree of life. Nucleic Acids Res. 2014;gku1003.Google Scholar
- 43.Krämer A, Green J, Pollard J, Tugendreich S. Causal analysis approaches in ingenuity pathway analysis (ipa). Bioinformatics. 2013;btt703.Google Scholar
- 50.Mihalas AB, Hevner RF. Control of neuronal development by T-Box genes in the brain. Curr Top Dev Biol. 2016;122(2017):279–312Google Scholar
- 53.Berto S, Perdomo-Sabogal A, Gerighausen D, Qin J, Nowick K. A consensus network of gene regulatory factors in the human frontal lobe. Front Genet. 2016;7.Google Scholar
- 63.Tesar, Paul J., Robert H. Miller, Fadi J. Najm. Cell fate conversion of differentiated somatic cells into glial cells. U.S. Patent Application 13/280,562, filed April 26, 2012.Google Scholar
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