Renewal of extinguished fear memory in an altered context is widely believed to be a major limiting issue for exposure therapy in treating various psychiatric diseases. Effective prevention of fear renewal will significantly improve the efficacy of exposure therapy. DNA methyltransferase (DNMTs) mediated epigenetic processes play critical roles in long term memory, but little is known about their functions in fear memory extinction or renewal. Here we investigated whether DNMTs regulate fear renewal after extinction. We found that elevated Dnmt3a level in the dorsal dentate gyrus (dDG) of hippocampus was associated with the absence of fear renewal in an altered context after extinction training. Overexpression and knockdown of Dnmt3a in the dDG regulated the occurrence of fear renewal in a bi-directional manner. In addition, Dnmt3a overexpression was associated with elevated expression of c-Fos in the dDG during extinction training. Furthermore, we found that renewal of remote fear memory can be prevented, and the absence of renewal was concurrent with an elevated Dnmt3a level. Our results indicate that Dnmt3a in the dDG is a key regulator of fear renewal after extinction, and Dnmt3a may play a critical role in controlling fear memory return and thus has therapeutic values.
Exposure therapy has widely been used and is effective in treating various psychiatric disorders, especially phobia and PTSD. Clinical literature shows that fear may return with the passage of time or in a context distinct from the treatment context, after therapy1,2. The return of fear in an altered context is termed fear renewal. One possible cause of fear return is change of the post-treatment context, and this notion is supported by clinical demonstrations that entering a new context promotes fear return3,4,5,6. Therefore, preventing the return of fear in the post-exposure contexts, especially those distinct from the treatment/therapy context, is a critical obstacle to higher efficacy of exposure therapy.
Pavlovian fear conditioning and extinction is a widely used experimental model to study the biological mechanisms underlying exposure therapy. Most studies have shown fear extinction in the adult rodents to be context-dependent, using a standard extinction protocol (usually continuous presentation of conditioned stimulus (CS))7,8. Recent studies showed that a brief memory retrieval followed by extinction training led to an extinction that is insensitive to renewal, spontaneous recovery and reinstatement in both rodents9,10,11 and human12. However, the reproducibility of these findings has been questioned by recent studies13,14,15. More importantly, the mechanism of preventing fear renewal is not well understood.
Persistent and long-term changes in neuronal structure and function, such as those occurring during memory formation, generally require epigenetic modifications. Numerous studies have demonstrated that alterations in histone acetylation and DNA methylation are involved in the formation and extinction of long-term memory16,17,18,19. DNMTs (Dnmt1, Dnmt3a, Dnmt3b and Dnmt3l) catalyze the cytosine methylation and are required to establish and maintain genomic methylation. Dnmt3a and Dnmt3b are de novo DNA methyltransferases, Dnmt1 is the maintenance DNA methyltransferase, while Dnmt3l has no DNA methyltransferases activity20. Knockout restricted to the forebrain excitatory neurons in mice demonstrated learning deficits in several associative and episodic memory tasks in Dnmt3a knockout but not Dnmt1 knock out21. Knockdown of Dnmt3a but not Dnmt3b in hippocampus resulted in dysfunction of object-in-place memory22. Knocking down Dnmt3a in the medial prefrontal cortex increased anxiety while overexpression reduced anxiety23. Dnmt3a has also been shown to regulate emotional behavior and dendritic spine plasticity in the nucleus accumbens24. Thus, Dnmt3a plays important functions in neural plasticity, long-term modifications and emotional functions.
In this study, by using fear renewal in an altered context as readout, we found that Dnmt3a expression was elevated in the dorsal dentate gyrus (dDG) after extinction training followed by a brief memory retrieval (Rec+Ext), which was associated with the absence of fear renewal when tested in an altered context. Increasing Dnmt3a expression in the dDG using AAV expression led to the prevention of fear renewal following a standard extinction training protocol. Knockdown of Dnmt3a in the dDG using CRISPR/Cas9 resulted in fear renewal following Rec+Ext protocol. Furthermore, we found that renewal of remote fear memory can be prevented using the Rec+Ext protocol, and the absence of renewal was concurrent with an elevated Dnmt3a level.
Elevated Dnmt3a expression associated with the absence of fear renewal after extinction
We modified the protocol from Monfils (2009)9, which consisted of a brief fear memory recall followed (in 1–2 hours) by 20 cycles of CS (termed Rec+Ext) (Fig. 1a). It has been shown that if extinction context is very distinct from the conditioning context, the Rec+Ext protocol did not prevent renewal of fear memory14. Thus, we used a Context B’ modified from the original fear conditioning chambers (see Methods) (Fig. 1b). A standard protocol with continuous 20-cycle CS presentation (termed Ext; Fig. 1a) was used in context B (see Methods) (Fig. 1b) which has been shown by many previous studies to lead to fear renewal after extinction. After fear conditioning (Day 1), mice were divided into three groups with similar freezing levels: no extinction training (termed No Ext), Ext or Rec+Ext. Day 2, the No Ext group did not receive any extinction training, while the Ext group received 20 cycles CS training in context B and the Rec+Ext group first received 4 cycles CS training in context B’ followed in 1~2 hours with 20 cycles CS training in context B’. All mice were tested in the extinction context (B/B’; after 24 hours, or on Day 3) and novel context (C; after 48 hours, or on Day 4) (Fig. 1a). The Ext and Rec+Ext groups exhibited similar freezing levels after fear conditioning and showed significant reduction in freezing during extinction training (Fig. 1c). The Rec+Ext group showed higher freezing level compared to the Ext group during extinction training (Fig. 1c), and this higher freezing level could be caused by the similarity between context B’ and conditioning context A. Although recall in the extinction context revealed no difference between these two groups, Ext group showed significantly higher freezing than the Rec+Ext group in novel context (C) (F1,29 = 12.7, P < 0.01, Fig. 1c). The Ext group showed higher freezing level in context C as compared to context B (T16 = 3.20, P < 0.01, Fig. 1d left), while the Rec+Ext group showed similar freezing level in these two contexts (Fig. 1d right).
Previous studies have shown that Dnmt3a is intimately involved in regulating the stable expression of fear memory21, thus we examined whether Dnmt3a level is altered using immunostaining in brain sections. Mouse brains were collected 3 hours after extinction training (Ext or Rec+Ext) on Day 2, or 3 hours after 4 cycles CS recall in context C on Day 4. Higher density of Dnmt3a-positive cells was observed in the dDG in Rec+Ext group (which showed an absence of renewal) compared to the Ext group, using brains collected either after extinction training (F2,9 = 9.95, P < 0.01, Fig. 1e left) or after recall in context C (F2,12 = 11.74, P < 0.05, Fig. 1e right, Fig. 1f). These results suggest an association between Dnmt3a expression and fear memory renewal in that elevated Dnmt3a level may prevent fear renewal.
Overexpression of Dnmt3a in the dDG prevented fear renewal after extinction
To determine whether Dnmt3a regulates fear renewal, we need to target the cells that show changes in Dnmt3a. We found that a large percentage of the Dnmt3a-positive cells were co-localized with NeuN, a neuronal marker (Fig. 2a–d), but not co-localized with GAD67 (a GABA-synthesizing enzyme and a marker of inhibitory neurons) (Fig. 2b–d), or GFAP (a marker of astrocytes) (Fig. 2c,d). Based on this finding, we generated recombinant adeno-associated virus (rAAV) containing eGFP-tagged Dnmt3a under the CaMKIIα promoter to selectively target excitatory neurons (Fig. 3a). Expression of AAV for 14 days led to over-expression of Dnmt3a in the excitatory neurons in the dDG (T10 = 3.84, P < 0.01, Fig. 3b,c).
After fear conditioning, mice were divided into two groups with comparable freezing levels. Seventy-two hours after conditioning, mice were injected with either AAV-GFP or AAV-Dnmt3a in the dDG. Behavioral testing was conducted after rAAV expression for 14 days, with mouse brains collected 90 min after recall in context B/C (Fig. 3d). We first measured freezing levels, twice in context B and once in context A (Fig. 3e Test I). There was no difference in freezing level between two groups (Fig. 3f). Since Morris et al.21, found that Dnmt3a CKO mice showed a deficit in the reduction of cued fear memory upon repeated testing; we wanted to test whether Dnmt3a over-expression in the dDG might lead to faster fear memory decay/reduction with repeated recall. We found no difference in freezing levels in context B on day 19 (both were not significant from the freezing levels after fear conditioning), or on day 20 (both were significantly different; AAV-Dnmt3a, T20 = 2.660, P < 0.05; AAV-GFP, T22 = 2.766, P < 0.05; Fig. 3g). In contrast, AAV-Dnmt3a group showed significantly lower freezing level in context A compared to that after fear conditioning on day 21 (T20 = 3.779, P < 0.001, Fig. 3g), but no such difference was found in the AAV-GFP group (Fig. 3g). These results suggest that overexpression of Dnmt3a appears to mask the effect of context on memory recall.
We then asked whether fear renewal could be blocked or prevented with the Ext protocol. Mice received Ext training in context B on day 22, and freezing levels were measured in the extinction context (B) on day 23, in conditioning context (A) on day 24 and in novel context (C) on day 25 (Fig. 3h, Test II). There was no difference in freezing levels between the AAV-Dnmt3a group and AAV-GFP group during extinction training, recall in the extinction context (B) and conditioning context (A), but there was a significant difference in recall in novel context (C). (F1,42 = 5.15, P < 0.05; Fig. 3i). In the AAV-Dnmt3a group, freezing levels in the above three contexts did not differ significantly from each (Fig. 3j). In contrast, AAV-GFP group showed significantly higher freezing in conditioning context (A) (T22 = 2.397, P < 0.05, Fig. 3j) and novel context (C) (T22 = 4.064, P < 0.001, Fig. 3j) than in the extinction context (B). Thus, fear renewal was absent with elevated Dnmt3a level in the dDG excitatory neurons. Dnmt3a has been reported to affect anxiety-like behavior23, and thus the effects on fear extinction and renewal we observed may be caused by altered innate anxiety level in the mice25,26. To address this possibility, we tested the performance of mice in the open field test and elevated plus maze. No significant difference in these two tests (such as percentage center time, open arm time) was found between the AAV-Dnmt3a and AAV-GFP group, with a trend towards increased total distance in the open field test (Fig. S1)
Dnmt3a overexpression affected neuronal activity
As the first step to understand the mechanism underlying the prevention of fear renewal in mice with overexpression of Dnmt3a in the dDG, we measured c-Fos expression in key brain regions involved in fear memory renewal. Numerous brain structures, including hippocampus, prefrontal cortex and amygdala participate in fear memory renewal27. We collected mouse brains 90 min after recall in context B or C on day 28 (Fig. 3d, behavioral results before c-Fos staining were shown in Fig. S2). AAV-Dnmt3a group showed similar density of c-Fos-positive cells in context B and C in vCA1, prelimbic PFC (PrL), infralimbic PFC (IL) and BLA (Fig. 4a), consistent with similar fear state in these mice. In contrast, AAV-GFP group showed elevated density of c-Fos cells in context C in PrL (T20 = 2.35, P < 0.05), IL (T20 = 2.82, P < 0.05), vDG (T20 = 4.32, P < 0.001), vCA1 (T20 = 3.27, P < 0.01), and BLA (T20 = 3.13, P < 0.01) (Fig. 4a), consistent with high fear state under this condition. AAV-GFP and AAV-Dnmt3a groups showed no difference in dHPC or vCA3 (Fig. S3). These results indicate that over-expression of Dnmt3a removes the context difference on neuronal activity level in key brain regions that regulate fear renewal28,29.
Since we had observed elevated Dnmt3a expression with Rec+Ext protocol which prevented fear renewal, we asked whether the activity level in the dDG might be altered during extinction training. To do so, we analyzed c-Fos expression in mouse brains collected 90 min after Ext training on day 22 (behavioral results shown in Fig. S4). The AAV-Dnmt3a group had higher density of c-Fos-positive cells than AAV-GFP group in the dDG (Fig. 4b; T19 = 2.97, P < 0.01, Fig. 4c), and there was a significant correlation between the density of c-Fos-positive and Dnmt3a-positive cells in the AAV-Dnmt3a group (Fig. S4). Due to technical reasons, we were unable to perform the same analysis for the AAV-GFP group. Furthermore, we examined the density of c-Fos-positive cells in mice received Rec+Ext protocol (which showed high Dnmt3a level in Fig. 1e left), and found higher density in the dDG compared to mice received the Ext protocol (Fig. S5). Put together, these results suggest that Dnmt3a overexpression in the dDG is associated with elevated neural activity in the dDG during extinction training which may serve to prevent fear renewal.
Knockdown of Dnmt3a in the dDG promoted fear renewal
To test whether Dnmt3a can regulate fear renewal in a bi-directional manner, we used CRISPR/Cas9 method to reduce Dnmt3a expression in the dDG30. We tested three guide RNA sequence (Supplementary Table) for constructing lenti-CRISPRv2 guide RNA vector, the efficiency of guide RNA was tested by transfecting HEK293T cells (Fig. 5a, Fig. S6). We packaged lentivirus using pLenti-CRISPRv2-gRNA2. Lenti-CRISPRv2-gRNA2 was able to significantly decrease Dnmt3a level in the dDG 10 days after infection (Fig. 5c; T10 = 2.27, P < 0.05, Fig. 5d). After fear conditioning on day 1, mice were divided into two groups with comparable freezing levels. On day 4, one group was injected with lenti-CRISPRv2-gRNA2, while the other group was injected with a control virus (lenti-CRIAPRv2-puro). Both groups received Rec+Ext training on day 15 and 16 (to ensure an effective extinction), followed by memory recall in context B’ on day 17 and in context C on day 18 (Fig. 5b). There was no difference in the freezing levels between the lenti-CRISPRv2-gRNA2 group and control group in all behavioral tests (Fig. 5e). When we analyzed renewal after extinction in these two groups, we found that control group showed no difference in freezing levels between context B’ and context C (Fig. 5f left), while the lenti-CRISPRv2-gRNA2 group showed higher freezing level in context C than in context B’ (T10 = 4.04, P < 0.01, Fig. 5f right). Thus knocking down Dnmt3a in the dDG promoted fear renewal with an extinction protocol that normally blocks fear renewal. Together with the Dnmt3a over-expression results, these results indicate that Dnmt3a regulates fear renewal in a bi-directional manner.
Extinction training with Rec+Ext protocol prevented renewal of remote fear memory
In our experiments using over-expression of Dnmt3a, we tested fear memory that was about 3 weeks old which can be regarded as remote memory. Remote memory is generally regarded as more resistant to extinction than recent memory31,32. The fact that renewal of this remote memory was absent with elevated Dnmt3a level suggests that Rec+Ext protocol may also be effective on remote memory. Alternatively, since Dnmt3a level was elevated for a sustained period of time in AAV-Dnmt3a over-expression (Fig. 3), this high level of Dnmt3a in the dDG might in some way “keep” the remote memory in a “recent” state (i.e., allowing this remote memory to be updated or modified as recent memory)33. To distinguish between these two possibilities, we fear conditioned mice on day 1, divided them into two groups based on their freezing levels, and subjected them to either Ext protocol or Rec+Ext protocol for 2 days on day 19 and 20 (Fig. 6a). Then, we tested memory recall in extinction context (B’ or B; day 21) and novel context (C; day 22) (Fig. 6a). As shown in Fig. 6b, freezing levels in both groups were significantly reduced with extinction training. When the freezing levels of each mouse was compared between extinction and novel context, we found a significant difference for the Ext group (T9 = 2.714, P < 0.05; Fig. 6c left) but not Rec+Ext group (T10 = 0.743, P = 0.47; Fig. 6c right), suggesting an absence of renewal in the Rec+Ext group. In addition, we also found a significant increase in the Dnmt3a level in the dDG in Rec+Ext group, compared to the Ext group after extinction training (T10 = 2.769, P < 0.05; Fig. 6d left, 6e) but only a trend towards increase after extinction training (T8 = 2.215, P = 0.058; Fig. 6d right). These results are consistent with the notion that Rec+Ext training is effective in preventing fear renewal, likely mediated by increasing the Dnmt3a level. However, this effect is less robust than we have found on recent memory (a few days old) using the same extinction procedure, in that: (1) we needed to give 2-day rather than 1-day extinction training (as used on recent memory) to significantly reduce freezing level; (2) although there was significant difference within group, there was no significant difference across groups (as there was for recent memory); (3) increase in Dnmt3a level was also less robust than that after extinction training for recent memory. Put together, our results suggest that an increase in Dnmt3a level might be effective in preventing fear renewal after extinction for both recent and remote memory.
In this study, we found: (1) Dnmt3a level was elevated in the dDG of mice underwent extinction training that resulted in the absence of fear renewal; (2) Over-expression of Dnmt3a in the dDG prevented while knockdown of Dnmt3a in the dDG promoted fear renewal; (3) renewal of both recent and remote memory can be prevented using an appropriate extinction protocol with concurrent increase in Dnmt3a level in the dDG. These findings strongly indicate that Dnmt3a regulates fear renewal after extinction. Further exploration of the underlying biological mechanism and therapeutic potential of these findings will deepen our understating of the nature of emotion-related psychiatric disorders (such as phobia, PTSD) and may also improve their treatment.
Current exposure therapy, although effective in many patients, suffers from the inability to generalize its efficacy over time, or is limited by the potential return of adverse memory in the new/novel contexts5,34. These limitations are caused by the context-dependent nature of extinction which is widely viewed as the biological basis of exposure therapy5,6,27. Thus, achieving a context-independent extinction may significantly reduce fear renewal to improve the efficacy of exposure therapy. Reduced renewal has been reported to occur after brief memory retrieval followed by extinction training9,35, or after extinction training in multiple contexts36,37,38. The effectiveness and consistency of these approaches are still in debate13,14,35,39. Our current study suggests that the effectiveness of these approaches, and ultimately the occurrence of fear renewal, is determined by the level of Dnmt3a after extinction training, especially in the dDG. This conclusion is based on our findings of bi-directional regulation of fear renewal by the Dnmt3a level.
What are the potential mechanisms underlying this Dnmt3a-depedent prevention of fear renewal? There are two potential mechanisms underlying extinction, one is erasure or updating of the formed memory16,40,41, and the other is the formation of a new extinction memory which suppresses or competes with the existing memory in a context-dependent manner39. While most studies favor the suppression mechanism in the adult, limited studies do suggest that erasure occurs in the immature animals42,43,44. Erasure of fear memory is consistent with the absence of spontaneous recovery, renewal or reinstatement observed with the Rec+Ext protocol9. Currently, there is no direct evidence as whether fear memory is erased after Rec+Ext protocol, and such evidence may involve direct examination of memory engram45. Our results showed that elevated Dnmt3a in the dDG led to a rapid and continuous reduction in freezing level with daily memory recall, regardless of the contexts where this recall took place (Fig. 3g). In contrast, in the GFP-expressing (control) mice, a continuous reduction in freezing level was seen with recall in the same contexts but recovery of freezing occurred in the novel/different text (Fig. 3g). Cued fear memory was resistant to decay after repetitive recall in the Dnmt3a KO mice and LTP was reduced in the hippocampal CA1 region21. Based on the above results, we propose that high Dnmt3a level makes memory more susceptible to modification, such as decay with recall and alteration in its properties (for example, its association with cue/context). On the other hand, with Dnmt3a level unaltered or reduced, memory is more resistant to modification. More specifically, we propose that if Dnmt3a level is elevated with extinction training (such as with Rec+Ext protocol), modification to the existing memory occurs and as a consequence extinction does not act as a separate mechanism or form a new memory; but if Dnmt3a level is unaltered with extinction training, a separate extinction memory is formed which acts to suppress or compete with the existing memory. This model is also consistent with findings from studies in infant/juvenile rodents that: (1) fear extinction is resistant to renewal, spontaneous recovery or reinstatement, and hence suggestive of erasure in nature43; (2) Dnmt3a level is high in these young rodents46,47. Thus, high Dnmt3a level may keep the formed memory in a dynamic, modifiable state. In this context, it is interesting to note that we were able to prevent renewal of remote fear memory with Rec+Ext protocol and this absence of fear renewal was associated with elevated Dnmt3a level in the dDG. Thus, it is worthy of further exploration of whether Dnmta3a level is a dynamic control of memory stability and modifiability which may play a critical role in the transition between recent and remote memory. It is important to note that the efficacy of extinction of remote memory is less robust than that for recent memory, which is consistent with the general findings that remote memory is more stable and less subjective to modification33,48. An alternative possibility is related to the epigenetic nature of DNMTs’ regulation of memory17,49,50. High Dnmt3a level may enhance extinction memory sufficiently to suppress/out-compete the existing fear memory in a persistent manner that is indistinguishable from erasure when measured using behavioral readout.
Another possible mechanism underlying Dnmt3a effect is altered context encoding, by which over-expression of Dnmt3a in the dDG alters how context is encoded during extinction to influence fear renewal. It is widely accepted that the dDG is more involved in the encoding of contextual information which enables the hippocampus to link context to memory51,52. Inactivation of dHPC pharmacologically in rats before extinction training led to renewal of fear even when tested in the extinction context53. Inactivating DG using optogenetic method impaired fear extinction in contextual fear conditioning54. Thus, increased neural activity in the HPC and dDG more specifically may prevent renewal by altering context encoding during extinction training, but whether this elevated dDG activity is sufficient is unclear. We found significant elevation of c-Fos expression in the dDG during extinction training using Rec+Ext protocol, or in mice with Dnmt3a OE in the dDG. The fact that manipulating Dnmt3a level in the dDG led to similar changes in c-Fos patterns as with Rec+Ext protocol supports the notion that Dnmt3a may alter context encoding by affecting neural activity in the dDG and that local changes in the dDG activity might be sufficient to affect renewal. Neural circuits underlying fear renewal has been found to involve ventral hippocampus, prefrontal cortex and amygdala27,55. Ventral hippocampal neurons projecting to both amygdala and prefrontal cortex has been shown to be critical for fear renewal28,29. These results were consistent with our finding of elevated density of c-Fos neurons in the ventral hippocampus but not dorsal hippocampus during fear memory renewal in AAV-GFP-expressing mice (Fig. 4a). Our findings on the elevated c-Fos density in both PrL and IL, together with elevated c-Fos density in the vHPC, are consistent with the finding of Wang et al.56 who showed that renewal of extinguished fear activates ventral hippocampal neurons projecting to the PrL and IL. Wang et al. interpreted their findings as that vHPC activation leads to enhanced PrL activation to promote fear and enhanced activation of local inhibitory neurons in the IL. This interpretation is in agreement with the general view that PrL and IL play different and likely opposite roles in fear related functions especially fear extinction27. For our c-Fos results, we did not distinguish between excitatory and inhibitory neurons. Another possible explanation is that the involvement of IL in fear renewal is different between recent and remote memory. No prior study has examined the role of IL in the renewal of remote fear memory while our c-Fos results were conducted on the renewal of remote memory. This possibility of IL may play different roles in renewal of recent and remote memory is worthy of further exploration.
Over expression of Dnmt3a in mPFC led to reduced anxiety-like behavior23, which could affect freezing. However, anxiety level was not altered in Dnmt3a KO mice57, and we found no changes in open field and elevated plus maze, two tests of innate anxiety. Nonetheless, we cannot exclude the possibility of over-expressing Dnmt3a in the dDG decreases anxiety level after traumatic experience (such as fear).
What are the potential targets of Dnmt3a? Using the next generation sequencing, genes regulated by Dnmt3a has been found to include NMDA receptors, AMPA receptors, BDNF, Fos, egr1, which are involved plasticity58. At this time, we cannot exclude the non-epigenetic targets of Dnmt3a. In addition, we also do not know whether the benefit of Dnmt3a OE is caused by and hence can be mimicked with enhancing Dnmt3a activity, since there is no selective enhancer of Dnmt3a at this time. Alternatively, Dnmt3a may play a structural role, such as functioning as a scaffold.
In conclusion, we have identified a key molecule in regulating fear memory renewal after extinction. Since our current results showed that renewal can be prevented for both recent and remote fear memory, we suggest that modulating Dnmt3a level/activity may have the potential to treat various chronic psychiatric diseases involving disregulated fear and/or anxiety.
Materials and Methods
C57BL/6 J mice were purchased from Guangdong Medical Laboratory Animal Center (China). Mice were maintained in a pathogen-free temperature-controlled (22 ± 1 °C) mouse facility on a reversed 12 h light-dark cycle (8:00 am~ 20:00 pm), with a maximum of 6 mice per cage, in Peking University Shenzhen Graduate School. Mice of 8–12 week of age were used. Recent studies showed that Dnmt3a expression is regulated by sex59 and age46,47. To exclude the impact of sex and age, we used male mice for all experiments, with every group of mice for a given set of experiment from the same butch of mice with the same age. All behavioral experiments were completed between 9:00 am to 18:00 pm. All animal experiments were performed in accordance with the ARRIVE guidelines on the Care and Use of Experimental Animals, approved by the Peking University Shenzhen Graduate School Animal Care and Use Committee.
We have followed previously published protocols60, four contexts were used in fear conditioning and extinction (Fig. 1b): Context A (Coul-bourn conditioning chamber, cleaned/wiped with 70% alcohol between each animal, lighting from Coul-bourn), Context B (20 cm × 35 cm × 20 cm, rectangular box, made of Plexiglas plate, black with white floor, cleaned/wiped with the 1% acetic acid between each animal, lighting by a LED light covered with yellow shade), Context B’ (Coul-bourn conditioning chamber, switched the electric palisade to a plastic plate, cleaned/wiped with the 1% acetic acid between each animal, lighting by a LED light covered with yellow lampshade), Context C (white trihedral box, made by plexiglass plate, cleaned/wiped with 70% alcohol between each animal, lighting by a white LED light). Mice were placed in an empty cage and transferred to the training room and taken into the testing chamber. Mice that completed the tests were first transferred to a new cage and were then sent back to their home cages together after all mice were done with testing. Conditioning training took place in context A, with mice explored the chamber for 180 s before a 20 s tone (80 dB; 2700 Hz) was presented which was co-terminated with a 2 s foot shock (0.7 mA); a total of 4 pairing were given with an interval of 120 s. For recall, mice were placed into the test chamber (Context A/Context B/Context B’/Context C), allowed to explore the chamber for 180 s before a 20 s tone was delivered; tones were given for 4 times with an interval of 40 s. For extinction training, mice were allowed to explore the extinction chamber (Context B or B’) for 180 s before a 20 s tone; 20 CS was given with an interval of 20 s. Mice were kept in the chamber for 120 s after training was completed. Freezing levels were analyzed using Coul-bourn analyze system (USA) by computer, the threshold of freezing was set to as at least more than 1 s without any movement.
Recombinant adeno-associated virus (AAV)
An AAV vector expressing eGFP under CaMKIIα promoter (pAAV-CaMKIIα-eGFP) was purchased from Addgene (#50469). Mouse Dnmt3a (GenBank: AF068625.2) was cloned from mouse brain cDNA, inserted into pAAV-CaMKIIα-eGFP using restriction enzyme EcoR I and Hind III, then sequenced by BGI (China). Viral particles were produced as described in the rAAV Production protocol of AAV- DJ/8 Helper Free Packaging System (Cell Biolabs, USA). pAAV-CaMKIIα-eGFP-Dnmt3a, pAAV-DJ/861 and pHelper (Cell Biolabs, VPK-400-DJ-8) were co-transfected (1.5:1:1) into HEK293T at 70% confluence using the lipofectin-mediated transfection method (Lipofectamine™ LTX, Invitrogen). Cells were incubated for 72 hours at 37 °C with 5% CO2. After 72 hours, cells were collected to purify virus using an AAV purification kit (Biomiga, USA). Purified AAV particles were titered for genome content using real-time qPCR (Promega, USA). Titers were 6 × 1012 GC (Genome Copy) per milliliter. Control virus, rAAV-CaMKIIα-GFP, was obtained from HANBIO company (China), with a titer of 1.3 × 1012 GC.
We used a lentivirus vector LentiCRISPRv2 from Addgene (#52961), inserted the guide RNA sequence as the lentiGuide oligo cloning protocol62. The Dnmt3a CRISPR Guide RNA sequences were designed by Feng Zhang’s laboratory at the Broad institute to selectively target Dnmt3a gene in the genome, and purchased from GENEWIZ (China). CRISPR/Cas9-Mediated Gene Knock-Down via Lentivirus has been used in neuron system63. The lentivirus was produced as described previously64. Lenti-CRISPRv2-gRNA, pMD2.G and psPAX2 was co-transfected (2: 1.5: 2) into HEK293T cells at 70% confluence using lipofectin-mediated transfection method (Lipofectamine™ LTX, Invitrogen, USA). Cells were incubated for 72 hours at 37 °C with 5% CO2. After 72 hours, culture medium was collected and lentivirus were purified using a lentivirus purification kit (Biomiga, USA). A control virus, Lenti-CRISPRv2-puro, was obtained from HANBIO (China).
All surgeries were performed under stereotaxic guidance. Mice were anaesthetized using isoflurane. Virus was injected using a 5 microliter microsyringe (Hamilton) through a 33 G needle, A microsyringe pump controller (KD Scientific) were used to control the speed of injection. rAAV sand lentivirus were injected into the dDG of hippocampus using the following coordinates, from Bregma: AP = −2.1 mm; ML = ±1.4 mm; DV = −1.9 mm. Injection speed was 150 nl/min (0.8~1.0 μl for AAV-Dnmt3a, 0.3 μl for AAV-GFP, 1.0~1.5 μl for lentivirus). The capacity of AAV was about 5k bp, while the insert DNA of pAAV-CaMKIIα-eGFP-Dnmt3a is 4.7k, hence very close to this limit. As a result, the infection efficiency of the AAV-Dnmt3a virus is lower than that of the control virus when similar titers were used. To ensure the efficacy of infection, we had used 3 times higher titer for the AAV-Dnmt3a virus than the control virus, and the control virus was diluted 5 times before use. The injection needle was kept in place for at least 180 s to allow sufficient diffusion.
Mice were anesthetized with pentobarbital sodium, perfused with 4% paraformaldehyde and PBS through the heart. Brains were removed, post-fixed in the 4% PFA at 4 °C overnight and placed in PBS containing 30% sucrose. For quick-freeze by liquid nitrogen in OCT, slices were cut at 30 μm. Brain sections for immunofluorescence were treated with 0.5% Triton X-100, 10% goat serum and 0.2% skim milk powder in PBS for 1 hour at room temperature. Section were incubated with primary antibody (anti-DNMT3A (Rabbit), 1:1000, CST, #3598, USA) overnight at room temperature, washed with PBS three time (each for 10 min), incubated with secondary antibody (goat anti-Rabbit 488/546, 1:400, Invitrogen, A11008 or A-11035, USA) for 1 hour in the dark at room temperature, and washed three times in PBS (each for 10 min). Finally, sections were incubated with Hoechst for 5 min and mounted on glass slides. For c-Fos immunohistochemistry, sections were treated with 3% H2O2 in PBS for 30 min at room temperature, permeabilized with 0.5% TritonX-100 in PBS for 10 min at room temperature, treated using the protocol of Mouse on Mouse Basic Kit (VECTOR, BMK-2202, USA). c-Fos antibody (anti-c-Fos (mouse) 1:1000; Abcam ab208942, USA) was used. Cells were stained using the DAB method (VECTOR, SK-4105, USA) and mounted on glass slides.
For double immunostaining of Dnmt3a and NeuN, we used anti-DNMT3A (CST, #3598, 1:1000). anti-NeuN (mouse) (Milipore, MAB377, 1:5000) as primary antibodies, and secondary antibody from Invitrogen (goat anti-Rabbit 488, A11008, 1:400; goat anti-Mouse 546, A-11003, 1:400). For double immunostaining of Dnmt3a and GAD67 (using GAD67-GFP mouse), we used anti-DNMT3A (CST, #3598, 1:1000) with secondary antibody from Invitrogen (Goat anti-Rabbit IgG 546, A-11035, 1:400). For double immunostaining of Dnmt3a and GFAP, we used anti-DNMT3A (CST, #3598, 1:1000), anti-GFAP (mouse) (Millipore, MAB360, 1:500), with secondary antibody from Invitrogen (goat anti-Rabbit 488, A11008, 1:400; goat anti-Mouse 546, A11003, 1:400).
c-Fos IHC images (DAB method) were taken on inverted fluorescence microscope (IX73, Olympus, Japan) with a 4× objective was used, positive cells were counted by using Image J based on The Mouse Brain in Stereotaxic Coordinates65. More than three sections for every region were taken for each mouse. Every experiment on c-Fos IHC was repeated twice for one brain simple. For Ext and Rec+Ext group Dnmt3a immunofluorescence, images were taken on inverted fluorescence microscope with a 10× objective was used. Positive cells merged with Hoechst were counted by using Image J, and sample images were taken using confocal microscope (LSM510 META, ZEISS, Germany). For Dnmt3a double staining (NeuN, GAD67, GFAP) all images were taken using a confocal microscope with a 20× objective. Co-localization of Dnmt3a- and NeuN-positive cells was counted using Image J.
Open field test
Mice were habituated in the testing room (lighting 10 Lux) for 1–2 hours before behavioral testing. Each mouse was placed in the open field apparatus (50 cm × 50 cm × 50 cm). Total distance, distance in the center area and time in the center area during a period of 15 min were analyzed using ANY-maze software.
Elevated plus maze test
The apparatus consists of two open arms: two closed arms with a wall (30 cm × 5 cm × 15 cm) and a central area (5 cm × 5 cm). This apparatus was placed 35 cm above the floor. Mice were habituated in the testing room (the light is 50 Lux) for 1–2 hours before behavioral test. Each mouse was placed in the center platform and faced to the open arms. Time and distance in the open arms and closed arms for during a 5 min period was analyzed using ANY-maze software.
Mice used for OF and EPM were from different cohorts that those used in behavioral testing and did not undergo any extinction test, but only to test the potential effect of AAV expression.
Behavioral data were recorded and analyzed using softwares from Coul-bourn(USA), and ANY-maze Behavioural tracking software(USA). Mice without any virus expression in the dDG were excluded from data analysis and removed from data set. Statistical analysis was performed using paired/unpaired t-test and Two-way ANOVA (GraphPad Prism software), as noted. Results were expressed as mean ± SEM. P < 0.05 was considered as significant.
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This work was supported by Shenzhen Science and Technology Innovation Funds JCYJ20170306165021201, JCYJ20170412150845848, JCYJ20150629144658017 and JCYJ20150529153646078.