Early Life Stress Effects on Glucocorticoid—BDNF Interplay in the Hippocampus
Nikolaos P. Daskalakis1,2* 
Edo Ronald De Kloet3,4 
Rachel Yehuda1,2,5 
Dolores Malaspina6 
Thorsten M. Kranz7*- 1Traumatic Stress Studies Division and Laboratory of Molecular Neuropsychiatry, Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA
- 2Mental Health Patient Care Center, James J. Peters Veterans Affairs Medical Center, Bronx, NY, USA
- 3Department of Medical Pharmacology, Leiden Academic Centre for Drug Research, Leiden, Netherlands
- 4Department of Endocrinology and Metabolism, Leiden University Medical Center, Leiden University, Leiden, Netherlands
- 5Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, USA
- 6Department of Psychiatry, New York University School of Medicine, New York, NY, USA
- 7Departments of Cell Biology, Physiology and Neuroscience, and Psychiatry, Skirball Institute of Biomolecular Medicine, New York University, New York, NY, USA
Early life stress (ELS) is implicated in the etiology of multiple psychiatric disorders. Important biological effects of ELS are manifested in stress-susceptible regions of the hippocampus and are partially mediated by long-term effects on glucocorticoid (GC) and/or neurotrophin signaling pathways. GC-signaling mediates the regulation of stress response to maintain homeostasis, while neurotrophin signaling plays a key role in neuronal outgrowth and is crucial for axonal guidance and synaptic integrity. The neurotrophin and GC-signaling pathways co-exist throughout the central nervous system (CNS), particularly in the hippocampus, which has high expression levels of glucocorticoid-receptors (GR) and mineralocorticoid-receptors (MR) as well as brain-derived neurotrophic factor (BDNF) and its receptor, tropomyosin-related kinase receptor B (TrkB). This review addresses the effects of ELS paradigms on GC- and BDNF-dependent mechanisms and their crosstalk in the hippocampus, including potential implications for the pathogenesis of common stress-related disorders.
Introduction
Glucocorticoids are steroid hormones and the end product of the hypothalamus-pituitary-adrenal (HPA) axis, which regulates the stress response. GC effects are mediated by MR and GR (De Kloet et al., 1998; McEwen, 1998; de Kloet et al., 2005a);. MR and GR are abundantly expressed in hippocampus and hippocampal function is implicated in both appraisal processes and stress adaptation. Through MR, GCs influence the brain's appraisal of novel information and memory retrieval, and thereby influence behavioral coping responses (de Kloet et al., 2005a). As GC concentrations increase in response to stressors, GR are activated to promote stress adaptation, reallocation of energy resources in preparation for future events and recovery of the system (de Kloet, 2003; de Kloet et al., 2005a).
One important target of GCs is BDNF-signaling, which is a crucial contributor to the modulation of axonal guidance, synaptic plasticity and neurite outgrowth (Jeanneteau and Chao, 2013). MR, GR and the BDNF receptor, TrkB, are co-expressed in hippocampal neurons, supporting this region as the primary site of immediate interactions between the GC- and BDNF-signaling pathways (Jeanneteau et al., 2012).
In this mini-review we present the effects of ELS on GC- and BDNF-dependent mechanisms in the hippocampus using primarily evidence from ELS animal models. The most commonly used rodent and non-human primate model in this context is the maternal separation (MS) paradigms with each displaying variations in developmental age, repetition and duration (Table 1). GC- and BDNF-signaling pathways influence each other and here we propose that ELS provokes a change in their equilibrium that contributes to heightened risk for stress-related psychopathology.
Table 1. Overview of rodent studies on BDNF signaling and Maternal Separation.
HPA-axis and ELS
There is a distinct pattern of HPA-axis activity during early development first described in rodents, which maintains stable and low circulating GC levels during the stress hyporesponsive period [SHRP; postnatal days (pnd) 1–10 in mice and pnd 3–14 in rats] (Sapolsky and Meaney, 1986; de Kloet et al., 2005b). Early life experiences can disrupt the SHRP by elevating basal GC secretion and turning the HPA-axis responsive to subsequent stressors. Thus, ELS not only exerts acute effects but also impacts long-term developmental trajectories in the brain (de Kloet et al., 2005b). In humans, the SHRP occurs during the postnatal months 6–12 and adverse experiences during this period can have a long-lasting impact on the HPA-axis (Gunnar and Quevedo, 2007).
MS is an established procedure of inducing acute stress effects during early life that yields long-term effects. MS results in heightened HPA-axis responsiveness in the early postnatal period and triggers a variety of stress-related behavioral phenotypes in later life (Daskalakis et al., 2014). However, MS effects are dependent on many factors, including the duration and frequency of the separations, age of the pups, and context under which the pups experienced the separation from the dam (Rosenfeld et al., 1992; van Oers et al., 1998; Enthoven et al., 2010; Daskalakis et al., 2011). Furthermore, the long-term effects of MS depend on match or mismatch with later life context (Daskalakis et al., 2012). Studies using other ELS paradigms (variations of maternal care, limited nesting) demonstrate similar long-term effects that are mediated through GC-dependent mechanisms (Liu et al., 1997; Champagne et al., 2008; Ivy et al., 2008).
Long-lasting alterations in the HPA-axis induced by ELS in rodents have been linked to experience-dependent epigenetic modifications in regulatory regions of stress-related genes (Weaver et al., 2004; Murgatroyd et al., 2009). In humans, where early adversity is associated with adult stress-related disorders and HPA-axis dysregulation, similar epigenetic changes were reported as observed in the above-mentioned rodent studies (McGowan et al., 2009; Daskalakis and Yehuda, 2014; Ruby et al., 2015). Interestingly, epigenetic changes caused by ELS might depend on genetic predisposition (Klengel et al., 2013). Therefore, the interplay of genetic background (hit-1) with early experiences (hit-2), might create a vulnerable or resilient neuroendocrine profile which, upon adult stress exposure (hit-3), can produce an adaptive healthy or a maladaptive pathologic response (Daskalakis et al., 2013).
BDNF Signaling and ELS
ELS has consequences for structural and physiological properties of stress-sensitive brain regions and behavior. For instance, rats with a history of low maternal care displayed decreased hippocampal synaptogenesis, BDNF, long-term potentiation and memory at baseline (Liu et al., 2000). Neurotrophins are crucial mediators in the facilitation of brain connectivity, neuronal plasticity, synaptic integrity and the promotion of basal neurogenesis (Ghosh and Greenberg, 1995; Lee et al., 2002). The most abundant neurotrophin in the mammalian CNS is BDNF. It is synthesized in the endoplasmic reticulum as a pre-pro-molecule and undergoes two cleavage steps from pre-pro via pro-BDNF to its mature form, which is packaged in secretory vesicles (Pang et al., 2004; Revest et al., 2014). Upon neuronal activity, BDNF is released from the synapse and diffuses to its receptor TrkB. Upon BDNF-binding, TrkB undergoes homodimerization and autophosphorylation and thus, the activation of downstream signaling cascades involved in neuronal integrity and survival (Chao, 2003). Genetic modifications of BDNF have a crucial effect on synaptic plasticity as shown in an animal study using BDNF heterozygous (+/Met) for the Val66Met polymorphism. After 7 days of restraint stress with BDNF het and wild-type (WT) mice, BDNF het mice displayed reduced apical dendrite density in the prefrontal cortex (PFC) and in addition, impaired working memory in comparison to WT littermates (Yu et al., 2012). Moreover, BDNF influences synaptic transmission and its efficacy is influenced by this single nucleotide polymorphism (SNP) in its prodomain. In the same mouse model, the amount of NMDA receptor mediated currents in the hippocampus and the infralimbic medial PFC of BDNF Met/Met mice was significantly lower than in BDNF Val/Val mice (Ninan et al., 2010; Pattwell et al., 2012). The human BDNF gene seems to be under high selection pressure against genetic variability, since in a whole exome sequencing study of 14 schizophrenia trios and a subsequent study performing targeted exome capture in 48 sporadic schizophrenia cases, both cohorts displaying a high number of cases with childhood trauma, no novel genetic variants in the BDNF gene were observed (Kranz et al., 2015a,b).
BDNF-signaling is also influenced by ELS (Alleva and Francia, 2009). In humans, ELS can evoke significant memory impairments in adulthood (Bremner et al., 2003) in association with reduced BDNF levels (Grassi-Oliveira et al., 2008). Moreover, these associations depend on the Val66Met polymorphism (Chen et al., 2006; Elzinga et al., 2011; Molendijk et al., 2012). A similar pattern was observed for peripheral BDNF expression in young rhesus macaques. Carriers of the Met allele of the functionally ortholog polymorphism at codon 46 displayed decreased BDNF levels after maternal deprivation (Cirulli et al., 2011). Besides the combined effects of genetics and MS on BDNF expression, there are epigenetic effects associated with ELS. The relationship of MS and epigenetic regulation of BDNF has been studied extensively in rodent models (Table 1).
Effects of ELS on BDNF mRNA and Protein Expression
There are too few studies to conclude on the direction of changes in BDNF expression levels in the hippocampus or other brain regions (<24 h after first maternal separation onset). One possibility is that BDNF expression decreases acutely after MS. However, pups exposed to MS also experience dietary restriction due to the absence of the mother. It has been demonstrated that dietary restriction increases BDNF expression in the hippocampus, striatum and the PFC in rats (Duan et al., 2001).
In the postweaning period and depending on the characteristics of the MS protocol, increased BDNF expression is reported more consistently. In the period between adulthood and senescence, BDNF expression is reduced, but the time of the switch depends on experimental characteristics (ELS paradigm, stress context in adulthood), sex, rodent strain and brain region of interest.
Effects of ELS on Epigenetic Regulation of BDNF
ELS influences the methylation status of the activity-dependent BDNF exon IV expression. One study has shown in rats that repeated maternal separation (RMS) leads to a biphasic effect of the exon IV promoter methylation status. At P21, RMS results in lower H3K9 dimethylation of the exon IV promoter but from adolescence (2 months) into adulthood (15 months), the initially decreased dimethylation after RMS reverses into a significantly increased dimethylation. Low dimethylation status at P21 yields a high BDNF exon IV transcription and vice versa during adolescence and adulthood (Suri et al., 2013). In another study where the exon IV promoter methylation change was not confirmed, increased exon IX promoter methylation was reported in hippocampus in maternally separated pups (Kundakovic et al., 2013). In a different ELS paradigm, rat dams with restricted availability of nesting material resulted in reduced maternal licking and grooming behaviors toward their pups and reduced physical interaction between the dams and their offspring (Ivy et al., 2008). This paradigm mimics infant neglect as well, which entails increased basal corticosterone levels in the offspring (Rice et al., 2008). Interestingly, maltreated offspring display hypermethylation of the activity-dependent BDNF exon IV promoter region in the PFC, which leads to decreased exon IV expression (Roth et al., 2009). A follow-up study demonstrated additional methylation changes in the hippocampus and amygdala upon exposure to this stress paradigm. These effects were sex and brain region specific (hypermethylation of exon I in males in ventral hippocampus and of exon I in basolateral amygdala (BLA) in females) (Roth et al., 2014). These results were obtained using adult rats and highlight the robust methylation alterations in BDNF that occur through ELS. Finally, another study showed that communal nesting of the pups increased histone acetylation at the BDNF exon IV promoter (Branchi et al., 2011).
ELS Effects on Synaptic Plasticity and Behavior
Irrespective of the MS paradigm, neurogenesis in the subventricular zone of the hippocampus appears to be consistently increased in the early postweaning phase and decreased during late adulthood. Moreover, synaptic plasticity related proteins such as neural cell adhesion molecule 1 (NCAM1) and synaptophysin are downregulated during adulthood after MS. Finally, a behavioral phenotype occurs in association with the temporal appearance of the above-mentioned changes, including memory impairment, learned helplessness, reduced social interaction, anhedonia and anxiety.
Synthesis
These studies indicate that ELS induced alterations of BDNF expression in a brain-region specific and age-dependent manner and provide evidence that BDNF upregulation potentially acts as a neuroprotective mechanism upon ELS exposure.
Interplay between BDNF and GC
Effects of BDNF and GC on GR Transcriptome
The GC- and BDNF-signaling pathways influenced by ELS are interlinked throughout life. A recent study confirmed that the GR-specific transcriptome is significantly altered by BDNF. Furthermore, simultaneous treatment of primary rat hippocampal neurons with a synthetic GC, dexamethasone (DEX), and BDNF induces the expression of a unique set of GC-BDNF responsive genes. The majority of these genes are involved in neurite outgrowth and differentiation (Lambert et al., 2013). In the same study, the authors established that BDNF leads to specific phosphorylation of the GR at serines 155 and 287 (Lambert et al., 2013). The latter serine (S287) is stress-hormone responsive, since DEX alone is sufficient to increase phosphorylation. In addition, increased S287 phosphorylation is observed in corticotropin-releasing hormone (CRH) expressing neurons in the parventricular nucleus (PVN) in mice that were exposed to 10 min of forced swim test.
Impact of BDNF and GCs on Brain Morphology
It is well established that chronic stress affects the morphology of brain structures such as the hippocampus and the amygdala (Watanabe et al., 1992; Magarinos et al., 1996; Vyas et al., 2002). However, questions remain as how stress load and duration affect these brain regions on a structural level. Interestingly, a single exposure to emotional stress has been shown to increase dendritic length and number in amygdala and vice versa in the hippocampus (Rao et al., 2012). However, a recent study suggests that these neuronal phenotypes exclusively occur in rats displaying a vulnerable phenotype, with the degree of cytoarchitectural change predicting the changes in behavioral patterns (Cohen et al., 2014). Based on these findings it is of interest to understand if these stress effects on brain morphology are mediated by GCs. Corticosterone injections over the course of 3 days led to increased spine formation and concomitant spine elimination. In contrast to these findings, administering daily corticosterone over 10 days caused higher spine elimination (12.1–22.7%), but no increase in spine formation (Liston and Gan, 2011). Interestingly, the developing brain (P30) was even more sensitive. This GC effect seems to be mediated in the CNS directly and preferentially through MR. In another study investigating pubertal rats revealed that a single corticosterone administration evokes differential spatio-temporal effects in the PFC and the BLA (Kim et al., 2014). In particular, 6 days after a moderate dose of corticosterone injection (10 mg/kg) in the medial PFC the dendritic branches and lengths were decreased in parallel with working memory performance. Those effects returned to baseline 1 week after these measurements (day 12). In the BLA the effects of an acute corticosterone injection were slower in onset (day 12 after injection) and were also normalized after a week (day 20). When stress and acute corticosterone administration coincide, they antagonize each other rather than acting in an additive manner (Rao et al., 2012; Cohen et al., 2014).
GC and neurotrophin systems both act in antagonistic as well as in synergistic manners. BDNF and GC are involved in dendritic arborization, whereas BDNF is generally more associated with spine formation and stabilization with GC rather playing an important role in spine turnover (Jeanneteau and Chao, 2013). Mice carrying the minor allele (Met) of the human BDNF Val66Met (rs6265) variant, which alters the structural conformation of the BDNF pro-domain, display less branching in the dentate gyrus (Chen et al., 2006). With regard to GC, one study showed that chronic GC application results in spine loss in the barrel cortex. Interestingly, transient increased GC levels mostly affected newly formed spines, whereas chronically increased GCs affected spines that have been developed early in life (Liston and Gan, 2011).
Molecular Mechanisms of BDNF and GC Interplay
BDNF can directly influence the HPA-axis regulation through alterations of CRH expression levels. In primary hippocampal neurons, BDNF administration induced a three-fold increase in CRH expression. On the other hand, DEX administration led to repression of CRH, which could not be normalized by BDNF treatment (Jeanneteau et al., 2012). A chromatin immunoprecipitation experiment revealed that DEX treatment evoked increased GR-binding to the CRH promoter (Miller et al., 2011; Jeanneteau et al., 2012). In contrast to DEX, BDNF leads to an increase of cAMP response element-binding protein (CREB) -binding to its site on the CRH promoter, which is in proximity (22 bp) to the GR-binding site. The central mechanistic element in CRH regulation is the recruitment of CREB to the CRH promoter. For transcriptional activity, CREB requires the interaction with a coactivator protein named CREB-regulated transcription coactivator 2 (CRTC2). The increase of GC levels lead to the relocalization of the nuclear CRTC2 to the cytosol and thus decreased CREB transcriptional activity at the CRH promoter (Jeanneteau et al., 2012). In the same study, hypomorphic GR mice had increased BDNF expression and TrkB phosphorylation levels in the PVN in comparison to control littermates. This data is consistent with cross-talk between the neurotrophin and HPA-axis systems through the converging pathways, which are yet to be fully elucidated (Figure 1).
Figure 1. Interplay of TrkB and GR signaling pathways in the CNS. In the presence of BDNF, the TrkB receptor homodimerizes and initiates several signaling pathways promoting neuronal survival, growth and differentiation (Akt and MAPK). Activation of the PLCy pathway leads to CAMKII-mediated phosphorylation of the transcription factor CREB. In presence of a low amount of GC, the CREB-coactivator CRTC2 is dephosphorylated and translocates to the nucleus and binds to phospho-CREB. The phospho-CREB-CRTC2 complex binds at the CRH promoter and drives basal CRH expression in the PVN. Upon occurrence of ELS, the HPA axis signaling pathway is activated, yielding increasing GC levels. GC pass the plasma membrane and enter in to the cytosol and binds to GR, thereby inducing homodimerization (GR-GC complex). The GR-GC complex targets the BDNF promoter and drives basal BDNF production. Exceeding GC levels evoke a translocation of the CREB-coactivator CRTC2 to the cytosol and its phosphorylation, thereby inactivating CREB-dependent CRH production. Thus, the GR and TrkB pathways are calibrated and a specific balance of both GC and BDNF levels is necessary during neurodevelopment to keep homeostasis. Abbreviations: CNS, central nervous system; TrkB, tyrosine kinase receptor type 2; GR, glucocorticoid receptor; CAMKII, Calcium/Calmodulin-Dependent Protein Kinase II; CREB, cAMP Responsive Element Binding Protein; CRTC2, CREB Regulated Transcription Coactivator 2; ELS, early life stress; GC, glucocorticoids; BDNF, brain-derived neurotrophic factor; ACTH, adrenocorticotropic hormone; HPA axis, hypothalamus-pituitary-adrenal gland axis.
Another link between the GC- and BDNF-signaling pathways seems to involve the mitogen-activated protein kinase (MAPK) pathway. Chronic stress not only produces high levels of corticosterone and depressive-like behavior (de Kloet et al., 2005a), but also increases levels of a phosphatase in the MAPK pathway, (i.e., dual specificity phosphatase 1; MKP-1) in the brain. Chronic overexpression of MKP-1 induces detrimental effects by inhibiting axonal growth (Duric et al., 2010). Normalizing GC levels and consecutively MKP-1 expression levels leads to a restoration of stress-related depressive phenotypes through normalization of BDNF expression. Alternatively, constitutive knockdown of MPK-1 is associated with stress-resilience (Jeanneteau et al., 2010).
High GR levels decrease the abundance of the activity-dependent BDNF exon IV transcript in the dentate gyrus, CA1 and CA3 regions of the hippocampus without influencing exon I and II transcripts (Smith et al., 1995; Hansson et al., 2006). This calibration effect is corroborated by observations from adrenalectomized mice, in which corticosterone production is abolished and BDNF expression is increased in the CA1, CA3 and dentate gyrus of the hippocampus (Chao et al., 1998). In a further study it was demonstrated that acute GC activity evokes transiently increased tissue-plasminogen activator (tPA) protein levels. The presence of higher levels of tPA yields an increased proteolytic cleavage of pro-BDNF to mature BDNF. The higher amount of mature BDNF itself binds TrkB and enhances downstream MAPK phosphorylation, which is necessary for the formation of enhanced contextual fear memory (Revest et al., 2014).
Conclusion
There is growing body of evidence that the GC–BDNF crosstalk is essential for the early-life programming of the HPA-axis and neurotrophin signaling. During early life, high BDNF and low GC levels are required for neuronal maintenance, synaptic integrity and dendritic spine stabilization in the hippocampus. BDNF-GC equilibrium is crucial throughout life as a major mechanism for stress response regulation. ELS can influence the set point of this equilibrium and thus cause long-term sensitizing effects on stress vulnerability. There is a body of evidence that ELS shifts BDNF as well as GR expression levels in the developing CNS. The long term effect of ELS exposure is a downregulation of BDNF expression (Table 1) and GR expression in the hippocampus (Sutanto et al., 1996; Aisa et al., 2007). The combination of both low BDNF and low GR expression favors the vulnerability to develop stress-related disorders during adolescence and adulthood, especially upon additional stress exposures. Phenotypes associated with the ELS-induced reductions of BDNF and GR expression in rodents (Table 1) have been additionally observed to be associated with the interaction of the BDNF Met risk allele (Val66Met) and childhood trauma in humans (Molendijk et al., 2012; Aas et al., 2013). Therefore, it is important to understand that genetic and epigenetic factors moderate the long term consequences of early adversity (Daskalakis and Binder, 2015). From a therapeutic point of view, preventing steep GC elevations induced by ELS has beneficial effects through constitutive BDNF expression with a concomitant stable, physiological calibration of the GC- and BDNF-signaling pathways.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
This work was supported by the Top Institute of Pharmaceutical Sciences T5#209 (NPD, ERdK), Royal Netherlands Academy of Arts and Sciences (ERdK), the National Institute of Health NS21072 (MVC) and RC1-MH88843 (DM).
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Keywords: early life stress, glucocorticoid, glucocorticoid receptor, BDNF, HPA-axis, TrkB, hippocampus
Citation: Daskalakis NP, De Kloet ER, Yehuda R, Malaspina D and Kranz TM (2015) Early Life Stress Effects on Glucocorticoid—BDNF Interplay in the Hippocampus. Front. Mol. Neurosci. 8:68. doi: 10.3389/fnmol.2015.00068
Received: 02 June 2015; Accepted: 27 October 2015;
Published: 16 November 2015.
Edited by:
Xiao-Dong Wang, Zhejiang University, ChinaReviewed by:
Mohiuddin Ahmad, University of Oklahoma Health Sciences Center, USAHyunsoo Shawn JE, Duke-NUS Graduate Medical School, Singapore
Copyright © 2015 Daskalakis, De Kloet, Yehuda, Malaspina and Kranz. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Nikolaos P. Daskalakis, nikolaos.daskalakis@mssm.edu;
Thorsten M. Kranz, thorsten.kranz@nyumc.org