Amyloid plaques and tau tangles are common pathological hallmarks for Alzheimer’s disease (AD); however, reducing Aβ production failed to relieve the symptoms of AD patients. Here we report a high GABA (γ-aminobutyric acid) content in reactive astrocytes in the dentate gyrus (DG) of a mouse model for AD (5xFAD) that results in increased tonic inhibition and memory deficit. We also confirm in human AD patient brains that dentate astrocytes have a high GABA content, suggesting that high astrocytic GABA level may be a novel biomarker and a potential diagnostic tool for AD. The excessive GABA in 5xFAD astrocytes is released through an astrocyte-specific GABA transporter GAT3/4, and significantly enhances tonic GABA inhibition in dentate granule cells. Importantly, reducing tonic inhibition in 5xFAD mice rescues the impairment of long-term potentiation (LTP) and memory deficit. Thus, reducing tonic GABA inhibition in the DG may lead to a novel therapy for AD.
Alzheimer’s disease (AD) is a progressive neurodegenerative disorder with increasing morbidity among aging populations worldwide. Amyloid β peptide (Aβ) deposits and tau tangles have been recognized as two prominent pathological markers for AD1,2,3,4,5. One emerging consensus is that Aβ oligomers may be the initial trigger for a cascade of responses leading to eventual neurodegeneration2,3,6,7. However, clinical trials using γ-secretase inhibitors to reduce Aβ production unexpectedly worsened the symptoms in AD patients8,9,10, prompting a search for new drugs to treat the disorder.
γ-aminobutyric acid (GABA) is the major inhibitory neurotransmitter in the adult brain, activating both GABAA and GABAB receptors. GABAA receptors (GABAA-Rs) localize at both synaptic and extrasynaptic sites, mediating phasic and tonic inhibition, respectively11,12,13,14. Altered GABAergic function has been reported in AD patients as well as transgenic AD mouse models. For example, recent immunohistochemistry studies revealed a significant reduction in GABAergic nerve terminals in human AD brains15. In the hAPP J20 mouse model for AD, a sodium channel Nav1.1 was found depleted in parvalbumin interneurons, leading to reduced activity-dependent GABAergic input and increased network hyperactivity16. However, how GABAergic alterations lead to cognitive deficits in AD brains is largely understudied.
We investigated GABA function in the dentate gyrus (DG), the gateway for information input to the hippocampus, a critical brain region involved in learning and memory. We discovered unusually high GABA content in the reactive astrocytes of DG in a transgenic mouse model for AD (5xFAD17) as well as in brain samples from human AD patients. Reactive astrocytes are hypertrophic glial cells with elevated level of glial fibrillary acidic protein (GFAP) that are typically activated by injury or diseases18. The high GABA content in reactive astrocytes was released by astrocyte-specific GABA transporter GAT3/4 (human GAT3/mouse GAT4) and led to enhanced tonic inhibition in dentate granule cells. Interestingly, the α5-subunit-containing GABAA-Rs (α5-GABAA-Rs) were upregulated in the dentate granule cells of 5xFAD mice, further increasing tonic inhibition therein. As expected, the 5xFAD mice showed impairment in long-term potentiation (LTP) and memory deficit; reducing tonic inhibition in 5xFAD animals rescued the LTP impairment and memory deficit. Our results suggest that increased tonic GABA inhibition in the DG may contribute to functional deficit in AD brains, and astrocytic GABA transporters may serve as a novel drug target for therapeutic intervention.
Increased GABA content in dentate astrocytes of 5xFAD mice
To investigate the functional role of GABA in AD, we employed a rapid onset mouse model for AD, the 5xFAD mice (APPSwFlLon, PSEN1*M146L*L286V)17. Previous studies demonstrated that 5xFAD mice manifest symptoms similar to those of human AD patients, such as Aβ plaques, decreased synaptic proteins, increased reactive astrocytes and memory deficit in the Y-maze17. Examination of the Aβ1-42 level in the hippocampus of 5xFAD animals revealed substantially more Aβ1-42 deposits (Fig. 1a, left panels, red) as well as many more GFAP-labelled reactive astrocytes (Fig. 1a, green) in the DG than in the CA1 region. Quantitatively, the total areas covered by Aβ1-42 or GFAP immunostaining were significantly larger in the DG than in the CA1 region of 5xFAD brain (Fig. 1b). Thus, DG in 5xFAD brain is loaded with heavy Aβ1-42 deposits and massive numbers of reactive astrocytes. This led us to investigate potential GABA functional deficits in the DG of 5xFAD brain.
The imbalance of glutamate excitation and GABA inhibition has been associated with many neurological disorders including AD16,19. We performed immunostaining of glutamate and GABA in the DG and found no significant difference between wild type (WT) and 5xFAD brains in 3- to 4-month-old animals (Fig. 2a). Likewise at this young adult stage, no significant Aβ plaques were detected when examined with thioflavin-s staining in the 5xFAD animals (Fig. 2a, merged image). However, 6- to 8-month-old 5xFAD animals displayed a remarkable increase in both GABA and glutamate levels in the GFAP-labelled hypertrophic reactive astrocytes in the DG (Fig. 2b). These reactive astrocytes were intermingled with Aβ plaques labelled by thioflavin-s staining (Fig. 2b, merged image, blue). Since GABA is typically converted from glutamate by glutamic acid decarboxylase (GAD), we examined GAD67, a major GABA synthesis enzyme in the nervous system, and found that it increased significantly in the reactive astrocytes in the DG of 5xFAD mice (Fig. 2c). Quantitative analysis showed a clear increase in GABA, glutamate and GAD67 in dentate astrocytes in 5xFAD as compared with WT animals (Fig. 2d).
High GABA concentration in 5xFAD hippocampal tissue
To independently verify that GABA content is indeed increased in the hippocampus of 5xFAD brain, we developed a novel method to assay GABA concentration in brain homogenate. We first transfected HEK293T cells with GABAA-R α2β3γ2 subunits for detecting GABA responses11,12. The hippocampal region was dissected out from WT or 5xFAD brain and made into homogenate by repeated freeze and thaw and sonication. The homogenate was then diluted 100-fold and puffed on HEK cells expressing GABAA-Rs (24–48 h after transfection) to assay GABA responses. To validate the method, which we named brain homogenate puff (BHP) assay, we carried out a series of control experiments. First, we puffed brain homogenate on non-transfected HEK cells and found no responses (Supplementary Fig. 1a). Second, we puffed bath solution on GABAA-R-expressing HEK cells and also observed no responses (Supplementary Fig. 1b). Third, we demonstrated that puffing GABA on GABAA-R-expressing HEK cells evoked large inward currents, which were blocked by GABAA-R antagonist bicuculline (BIC, 50 μM; Supplementary Fig. 1c). Similarly, puffing hippocampal homogenate on GABAA-R-expressing HEK cells also evoked a significant current, which was blocked by BIC as well (Supplementary Fig. 1d). Fourth, in order to compare WT and 5xFAD brain homogenate side by side, we filled a bundle of triple identical micropipettes with WT homogenate, GABA (10 μM, determined after pilot experiments; in the middle) and 5xFAD homogenate (Fig. 3a). When the three micropipettes were filled with the same concentration of GABA, they evoked the same size of GABA responses (Fig. 3b,c). Similarly, when they were filled with the same brain homogenate, either from WT or 5xFAD hippocampal tissue, they evoked the same size of GABA responses (Supplementary Fig. 1e–h). Alternatively, when the three micropipettes were filled with different concentrations of GABA (1, 3 and 10 μM), they evoked different sizes of GABA responses (Fig. 3d,f). After these rigorous control experiments, we tested GABA responses in the same HEK cells expressing GABAA-Rs by puffing WT and 5xFAD hippocampal homogenate, together with 10 μM GABA. We found that the 5xFAD hippocampal homogenate consistently evoked larger GABA responses than the WT counterpart (Fig. 3g–i). Quantitatively, the GABA current evoked by 5xFAD hippocampal homogenate was about twice as large as that evoked by WT hippocampal homogenate (Fig. 3j; WT, 363.7±99.2 pA; 5xFAD, 637.1±84.5 pA; n=3 sets, total 24 cells; P<0.03; paired Student’s t-test). After normalization, WT hippocampal homogenate-evoked GABA current was 39.1±8.7%, whereas the 5xFAD hippocampal homogenate-evoked GABA current was 72.7±2.1% of that evoked by 10 μM GABA (Fig. 3k). In addition to electrophysiology assay, we further performed GABA ELISA assay to quantitatively measure the GABA concentration in hippocampal tissue from WT or 5xFAD mice. Interestingly, young animals (3–4 months old) did not show any difference in GABA content (WT, 0.41±0.01 μg mg−1, n=6; 5xFAD, 0.42±0.02 μg mg−1, n=5; P>0.6) but old 5xFAD mice (7–8 months old) showed significantly increased GABA content in hippocampal homogenate (Fig. 3l; WT, 0.41±0.03 μg mg−1, n=5; 5xFAD, 0.55±0.04 μg mg−1, n=4; P<0.02). Therefore, the hippocampal tissue in 5xFAD mice has higher GABA content than that in WT mice, likely because of the accumulation of GABA in the reactive astrocytes in 5xFAD brains.
High GABA content in dentate astrocytes of human AD brains
Reactive astrocytes have been widely reported in neurodegenerative disorders including AD20,21. However, such high levels of GABA found in the reactive astrocytes of 5xFAD mouse brain are unexpected. To ensure that this is not an artifact only found in transgenic AD animal models, we examined human hippocampal tissue from post-mortem AD patients (Emory Brain Bank, sample information in Supplementary Table 1). Consistent with the finding in 5xFAD mice, we found a substantial accumulation of GABA in GFAP-labelled astrocytes in the DG (molecular layer) in AD patients but not healthy controls (Fig. 4a, quantified in Fig. 4c, P<0.001). Similarly, the level of GAD67 also significantly increased in the DG-reactive astrocytes of AD patients (Fig. 4b, quantified in Fig. 4c, P<0.001). These results suggest that the high GABA level in the reactive astrocytes of AD brains may serve as a novel biomarker for AD.
Increased astrocytic GABA transporter in AD brains
GABA is mainly synthesized from glutamate by GAD. Alternatively, GABA may also be uptaken through GABA transporters. Astrocytes have unique GABA transporters that are distinctly different from neuronal GABA transporters (GAT1)22. GAT4 is the major isoform of astroglial GABA transporter in mouse, while its orthologue in human and rat is GAT3, and GAT3/4 is often used when more than one species is studied together. We found a significant increase in GAT3/4 in the reactive astrocytes of DG in 5xFAD mice (Fig. 5a; WT, 15.7±3.6 a.u., n=6; AD, 66±14 a.u., n=6; P<0.01, Student’s t-test). Such elevated levels of GAT3/4 were further confirmed in the reactive astrocytes of DG in human AD brains (Fig. 5b; control, 16.0±1.5 a.u., n=6; AD patients, 44.2±1.7 a.u., n=6; P<0.001). Thus, the astrocytic GABA transporter GAT3/4 is significantly increased in both human and mouse AD brains.
Enhanced tonic inhibition in the DG of 5xFAD mice
The high levels of astrocytic GAT3/4 can either uptake GABA into, or transport GABA outside of, astrocytes. Astrocytes have been shown to reverse GABA transporter to release GABA if stimulated by glutamate23. Since glutamate excitotoxicity is well documented in the AD mouse models24, we tested whether GAT3/4 in the reactive astrocytes of 5xFAD mice is capable of releasing GABA. If GABA is released by reactive astrocytes in the DG, the most sensitive detector will be the extrasynaptic GABAA-Rs in dentate granule cells, which have high affinity for GABA and will result in tonic GABA current when activated by ambient GABA13. Therefore, we performed patch clamp recordings in mouse hippocampal slices to record tonic GABA currents (ITonic) in dentate granule cells. In WT mice (6–8 months old), we detected a small tonic GABA current in dentate granule cells (Fig. 5c, left panel). However, in the dentate granule cells of 5xFAD animals (6–8 months old), the tonic current was significantly larger (Fig. 5c, right panel). To investigate whether this enhanced tonic GABA current is causally linked to the increased astrocytic GABA transporter, we incubated 5xFAD hippocampal slices with GAT3/4 inhibitor SNAP-5114 (50 μM) for 2 h. Chronically blocking GAT3/4 activity had no effect on WT dentate granule cells (Fig. 5d, left panel), but significantly diminished the tonic GABA current in 5xFAD dentate granule cells (Fig. 5d, right panel; quantified in Fig. 5e; P<0.001). Acute application of SNAP-5114 (50 μM) also reduced tonic GABA current in 5xFAD dentate granule cells (Fig. 5f, quantified in Fig. 5g,h), suggesting that astrocytic GABA release may contribute significantly towards tonic inhibition in 5xFAD brains. As a control, we recorded tonic GABA current in the dentate granule cells in young adult animals (3–4 months old) but found no difference between WT and 5xFAD individuals (Supplementary Fig. 2a,b; WT, 16.4±1.3 pA, n=16; 5xFAD, 16.5±1.6 pA, n=15; P>0.9), consistent with the very low level of GABA immunostaining in astrocytes of young adult animals (Fig. 2a). We further investigated whether neuronal GABA transporter GAT1 might be altered in 5xFAD mice. Application of a GAT1-specific blocker NO-711 (10 μM) revealed large tonic currents in both WT and 5xFAD animals with no significant difference (Supplementary Fig. 2c,d; WT, 97±20 pA, n=8; 5xFAD, 112±18 pA, n=7; P>0.4). Importantly, blocking GAT3/4 decreased tonic current, whereas blocking GAT1 enhanced tonic current (compare Fig. 5f with Supplementary Fig. 2c), indicating that GAT3/4 is releasing, whereas GAT1 is uptaking, GABA. Thus, the high GABA content in the reactive astrocytes of 5xFAD brains can be released through GABA transporter GAT3/4 to enhance tonic inhibition in dentate granule cells.
Upregulation of α5-GABAA-Rs in 5xFAD dentate granule cells
Tonic GABA currents are typically mediated by extrasynaptic GABAA-Rs, including δ subunit- and α5-subunit-containing GABAA-Rs12,13. We next investigated which subtype of GABAA-Rs mediated the enhanced tonic GABA current in 5xFAD dentate granule cells. The δ subunit-containing GABAA-Rs are known to be expressed in the dentate granule cells25. Therefore, we applied THIP (2 μM), a selective agonist for δ-GABAA-Rs (EC50=6.3 μM (ref. 26)), to examine the tonic current in dentate granule cells in hippocampal slices. Surprisingly, the THIP-induced tonic currents did not show significant difference between WT and 5xFAD dentate granule cells (Supplementary Fig. 2e,f; WT, 65.2±6.6 pA, n=8; 5xFAD, 60.7±10.4 pA, n=8; P>0.7). Besides δ-GABAA-Rs, α5-GABAA-Rs were also reported to partially mediate the tonic current in dentate granule cells14. We therefore employed α5-specific inverse agonist L-655,708 to examine the contribution from the α5-GABAA-Rs. In WT animals, application of L-655,708 (100 nM) in the presence of 5 μM GABA partially reduced the tonic current in dentate granule cells (Fig. 6a, left), whereas in 5xFAD mice, L-655,708 blocked the majority of the tonic current activated by 5 μM GABA (Fig. 6a, right), suggesting a significant contribution of the α5-GABAA-Rs towards tonic inhibition in 5xFAD mice. Quantitatively, the tonic current blocked by L-655,708 in 5xFAD dentate granule cells was more than double of that in WT dentate granule cells (Fig. 6b; WT, 35.4±6.3 pA, n=12; 5xFAD, 98.7±12.9 pA, n=9; P<0.001). Since α5-GABAA-Rs are known to be expressed in CA1 pyramidal neurons, we further recorded the tonic current in CA1 region and found similar tonic currents between WT and 5xFAD animals (Fig. 6c; WT, 31.2±4.7 pA, n=11; 5xFAD, 36.1±6.7 pA, n=9; P>0.5), and the proportion of tonic current blocked by L-655,708 was also similar in CA1 neurons between WT and 5xFAD animals (Fig. 6d). In contrast, the proportion of L-655,708-sensitive tonic current significantly increased in 5xFAD dentate granule cells (Fig. 6d, P<0.001). These results suggest that the α5-GABAA-Rs are upregulated in the DG of 5xFAD mice.
To corroborate the electrophysiology data, we performed immunostaining and detected α5-immunopositive signal in the dentate granule layer (Fig. 6e), as reported before27. Interestingly, the α5 receptors were significantly increased in 5xFAD dentate granule cells (Fig. 6f,g; P<0.001), consistent with the enhanced tonic current mediated by α5-GABAA-Rs. Note that consistent with their typical extrasynaptic localization, the majority of α5 puncta were not colocalized with presynaptic GAD65 puncta (Fig. 6e,f, inset). GAD67 is the major GABA synthesis enzyme mainly localized in cell bodies, while GAD65 is localized at GABAergic nerve terminals and often used as a presynaptic marker. While the α5 receptors significantly increased in the DG of 5xFAD animals, the GAD65 puncta number did not change in the hippocampus (Fig. 6h). Therefore, the α5-GABAA-Rs are upregulated in 5xFAD dentate granule cells and contribute to the enhanced tonic inhibition in the DG.
Reducing tonic inhibition rescues the impairment of LTP
To investigate the functional consequence of enhanced tonic inhibition in the 5xFAD brain, we examined the LTP in the DG by performing hippocampal slice recordings. WT animals (6–8 months old) showed normal LTP in the DG after high-frequency stimulation (HFS; 100 Hz for 1 s, repeated three times with 20 s interval); however, the same age 5xFAD animals showed significantly decreased LTP (Fig. 7a, quantified in Fig. 7b; WT, green; 5xFAD, grey; P<0.01). Interestingly, suppression of tonic inhibition, either with SNAP-5114 (50 μM, blue) to block astrocytic GABA release or with L-655,708 (100 nM, orange) to block α5-GABAA-Rs, rescued the LTP impairment in the 5xFAD dentate granule cells (Fig. 7a,b, P<0.05). The LTP in the DG of WT animals was not affected by the drug treatment (Fig. 7b). Therefore, the enhanced tonic inhibition in the DG of 5xFAD mice may play a critical role in the suppression of LTP.
We further investigated the effect of tonic current on cell excitability in WT and 5xFAD dentate granule cells (Supplementary Fig. 3). It is known that dentate granule cells do not fire spontaneous action potentials (APs) because of hyperpolarized resting membrane potentials (typically −80 mV, Supplementary Fig. 3a–c). The intrinsic membrane conductance was found to be similar between WT and 5xFAD dentate granule cells (Supplementary Fig. 3d–e). We then injected currents (~70 pA) to make granule cells firing APs, similar to previously published work28,29. When 5 μM GABA was applied in the bath solution to activate tonic GABA currents, we found that WT granule cells showed little change in AP firing, but 5xFAD granule cells showed a significant decrease in AP firing (Supplementary Fig. 3f,g, quantified in h; P<0.001), consistent with the increased tonic current in 5xFAD granule cells (Fig. 6a). Importantly, blocking tonic current with the α5 GABAA-R inverse agonist L-655,708 rescued the AP firing in 5xFAD granule cells (Supplementary Fig. 3g,h; P<0.001), confirming an increased tonic inhibition in the DG of 5xFAD mice. In addition, blocking all GABAA-R-mediated inhibition with 100 μM picrotoxin increased AP firing in both WT and 5xFAD granule cells (Supplementary Fig. 3f–h), as expected. These results suggest that the enhanced tonic inhibition in the DG of 5xFAD mice plays a critical role in regulating neuronal activity.
Reducing tonic inhibition alleviates memory deficit
We further conducted behavioural analysis to test the effect of enhanced tonic inhibition on the cognitive function of 5xFAD animals. It has been reported that 5xFAD mice show a significant memory deficit in the spontaneous alternation test in Y-maze17. We first confirmed that our 5xFAD mice indeed showed such memory deficit when placed in a Y-maze to test their sequential entries in each arm (Fig. 7c, P<0.05). Interestingly, intraperitoneal administration of SNAP-5114 (50 μmol kg−1, i.p., once per day for 1 week; blue) or L-655,708 (1 mg kg−1, i.p., once per day for 1 week; orange) rescued the memory deficit in 5xFAD animals (Fig. 7c, P<0.05). The total number of arm entry did not differ among WT, 5xFAD and 5xFAD plus drug treatment groups (Fig. 7d). Therefore, we conclude that the enhanced tonic inhibition in the DG of 5xFAD mice contributes to the impairment of memory.
Our studies discovered unusual GABA accumulation in the reactive astrocytes in the DG of both mouse and human AD brains, leading to enhanced tonic GABA inhibition. Functional and behavioural analyses demonstrated that such increased tonic inhibition suppresses LTP and results in memory deficit in 5xFAD animals. On the basis of these results, we propose a working model (Fig. 8) that in the DG of AD brains, excitotoxic/inflammatory stimulation, possibly originated from Aβ deposit, will stimulate reactive astrocytes to accumulate glutamate and convert it into GABA. The high level of GABA in reactive astrocytes will be released through GAT3/4 to increase ambient GABA concentration in the DG of AD brain. In the meanwhile, the α5-GABAA-Rs in AD dentate granule cells are upregulated to further enhance tonic inhibition. This increased tonic inhibition in the AD brain may initially be part of a compensatory mechanism to antagonize glutamate excitotoxicity. However, chronic increase of tonic inhibition in the DG of AD brain will suppress LTP and result in learning and memory deficits. Our studies suggest that reducing tonic inhibition in the DG of AD brains may lead to a potential new therapy for AD.
Astrocytes play a variety of functions in the brain including regulation of neuronal connectivity and activity, participation in the brain–blood barrier and maintenance of energy and ionic balance30,31. Astrocytes regulate neuronal synapse formation during brain development32 and also form tripartite synapses with neurons33, uptake glutamate released by nerve terminals and convert into glutamine to shuttle back to neurons34. Compared with the well-studied astrocytic glutamate–glutamine cycle, astrocytic GABA and GABA transporters are understudied, particularly in neurological disorders. Astrocytes are reported to be immunoreactive for GABA and can also release GABA35,36,37,38,39. Our present study suggests that astrocytes may have very low level of GABA in the adult brain under physiological conditions, compared with the high level of GABA immunostaining in GABAergic neurons. However, under pathological conditions such as AD, reactive astrocytes start to accumulate a significant amount of GABA. Consistent with our study, GABA immunostaining also increases significantly in reactive astrocytes after ischaemic insult40. Notably, we observed no significant change in astrocytic GABA content in young adult 5xFAD mice, which also lack Aβ plaques. By the age of 6–8 months, Aβ plaques were spreading throughout the DG of 5xFAD mice and astrocytic GABA content increased dramatically, suggesting a progressive accumulation of astrocytic GABA that might correlate with Aβ pathology. Astrocytes may uptake GABA through astrocyte-specific GABA transporter GAT3/4 (ref. 41). Alternatively, they may convert glutamate into GABA through GAD67. Astrocytic glutamate is normally converted into glutamine by glutamine synthetase. However, it is widely reported that glutamine synthetase is significantly reduced under pathological conditions31. Our study discovered that GAD67 can be upregulated in AD-reactive astrocytes; a possible compensation for the reduction of glutamine synthetase in order to process glutamate accumulated in astrocytes. In agreement with our study, an increased GABA synthesis in astrocytes has been reported in a different transgenic mouse model for AD42. Therefore, high levels of astrocytic GABA content may be a novel biomarker for brain pathology including AD.
The GABA accumulation in the reactive astrocytes of 5xFAD mice seems to have reached a significant level that can be detected by GABA ELISA or a newly developed BHP assay. Both assays demonstrated that the 5xFAD hippocampal tissue has higher GABA content than WT hippocampal tissue. It should be noted that GABA concentration in brain homogenate is the summation of total GABA in both astrocytes and neurons. Under normal conditions, GABAergic neurons may contain the majority of GABA in brain tissue. However, under pathological conditions such as AD, high GABA content in reactive astrocytes may account for a substantial proportion. Nevertheless, if GABAergic neurons degenerate significantly such as at the late stages of AD, the total GABA content in the brain homogenate might reduce. Therefore, the net GABA level in brain tissue may vary under different pathological conditions, or even change at different stages of the same disease. In contrast, GABA content in reactive astrocytes may be a better pathological marker than the total GABA concentration in the brain tissue.
The high GABA content in AD-reactive astrocytes has to be released to accommodate newly converted GABA from glutamate. One study reports that cerebellar glial cells may release GABA through an anion channel Bestrophin 1 (ref. 36). Alternatively, GABA transporter in astrocytes may reverse its direction to release GABA under stimulation of glutamate37. Indeed, GABA transporter has been reported to reverse its transport direction under both physiological and pathological conditions43. In the adult hippocampus, GABA uptake is mainly mediated by GAT1, the major GABA transporter in neurons44. In accordance, we demonstrated that blocking GAT1 with NO-711 induced a large tonic current in WT animals, indicating an increase in ambient GABA because of the blockage of GABA uptake by GAT1. In contrast, blocking astrocytic GAT3/4 with SNAP-5114 induced no significant change in tonic current in WT animals. In 5xFAD animals, however, blocking GAT3/4 reduced rather than increased tonic current, suggesting that GAT3/4 in 5xFAD-reactive astrocytes normally releases GABA to increase ambient GABA concentration. Since the expression level of GAT3/4 is significantly increased in AD-reactive astrocytes, both in 5xFAD animals and human AD patients, we propose that GAT3/4 may serve as a novel drug target for developing a new therapy to treat AD.
The GABAA-R α5-subunit is widely expressed in the early-embryonic brain and later restricted to the hippocampus and olfactory bulb in the adult brain45. The α5-GABAA-Rs are known to be involved in learning and memory because of their specific localization in the hippocampus46,47,48. GABA inhibition, including tonic inhibition mediated by α5-GABAA-Rs, has been reported to affect the induction and maintenance of LTP49,50,51,52. Our studies demonstrate that α5-GABAA-Rs are upregulated in the DG of 5xFAD animals and blocking α5-GABAA-Rs rescues the impairment of LTP and memory deficit. Consistent with our finding, the α5-GABAA-Rs have been found to enhance the tonic inhibition after stroke53 and are involved in the inflammation-induced memory deficit54. Therefore, α5-GABAA-Rs may serve as a common pathological marker for both brain injury and neurological disorders. However, inverse agonists of α5-GABAA-Rs, developed for the purpose of treating human memory deficit, failed clinical trials55, possibly because of their potential side effect on other synaptic GABAA-Rs. This may make the astrocytic GABA transporter GAT3/4 a more attractive drug target because GAT3/4 inhibitors are more specific to astrocytes and may have fewer side effects on neurons.
The DG is the gateway to the hippocampus, playing an important role in detecting, sorting and encoding information input from the entorhinal cortex. Compared with other hippocampal areas, the DG of 5xFAD animals has higher level of Aβ deposit and more reactive astrocytes. The high level of Aβ deposit in DG suggests that DG is subjected to severe excitotoxic and inflammatory stimulation. The reactive astrocytes are likely a reaction to the Aβ stimulation and may play both a detrimental and neuroprotective role in the AD brain18,56,57. We demonstrate here that reactive astrocytes in the 5xFAD brain have high GABA content, which enhances tonic inhibition in DG. This increased tonic inhibition may be the result of Aβ stimulation in order to offset glutamate excitotoxicity. The upregulation of α5-GABAA-Rs may also be a compensatory mechanism to reduce excitotoxicity in DG. While tonic inhibition may initially exert a neuroprotective role, chronic enhancement of tonic inhibition in DG will eventually impair LTP and cognitive functions in AD brains, possibly through suppressing AP firing. Therefore, while Aβ and other factors may trigger the initial neurodegenerative process, it is important to correct the downstream changes, such as the increased tonic inhibition discovered in this study, to effectively treat AD. Our study may offer a potential explanation as to why simply reducing Aβ production in AD patients may not have worked in clinical trials. One of the reasons might be that the downstream alterations that are already triggered by Aβ deposit cannot be corrected by reducing Aβ production, at least not easily. We propose here that reducing tonic inhibition may offer a novel treatment for AD patients.
The 5xFAD transgenic mice were purchased from the Jackson Laboratory (stock number: 006554), carrying mutations on both human APP (Swedish (K670N/M671L), Florida (I716V) and London (V717I)) and human PS1 proteins (M146L and L286V)17. This transgenic line was crossed with the C57BL/6 mice for breeding. Both male and female mice at the age of 6–8 months (5xFAD and age-matched WT littermates) were used in the present study. Young adult mice at the age of 3–4 month were also used as control. Mice were housed in a 12-h light–dark cycle and supplied with food and water. Experimental protocols were approved by Pennsylvania State University IACUC, in accordance with the guidelines of the National Institutes of Health for the Care and Use of Laboratory Animals.
Human case material
Human hippocampal tissues were provided by the Emory University Alzheimer’s Disease Center and Center for Neurodegenerative Disease Brain Bank from nine cases meeting CERAD58, NIA-Reagan59 and National Institute on Aging-Alzheimer’s Association60 criteria for the neuropathologic diagnosis of AD (see Supplementary Table 1 for case information). Tissue from nine controls with no history of neurological disease and no significant neuropathologic changes was also provided.
For mouse brain tissue immunostaining, mice were deeply anaesthetized with 2.5% Avertin and then perfused with saline solution (0.9% NaCl) to wash off blood in the brain, followed by perfusing ice-cold 4% paraformaldehyde (PFA) to fix the brain. The brain was dissected out and post-fixed overnight in 4% PFA at 4 °C. A vibratome (Leica) was used to cut coronal sections at 40 μm and these sections were stored in 0.1 M PB at 4 °C. For human brain tissue staining, 50-μm sections of 4% PFA-fixed human hippocampus were cut on a freezing microtome. Sections were rinsed three times in phosphate-buffered saline (PBS; 12 min each time) after removal from the storage protection solution. Both mouse and human brain sections were pretreated with blocking solution (0.3% Triton-X and 10% normal donkey and goat serum in 0.1 M PBS) for 2 h, and then incubated for 48 h with the following primary antibodies (in blocking solution at 4 °C): polyclonal anti-GFAP (chicken, 1:1,000, Millipore, AB5541); polyclonal anti-GABA (guinea pig, 1:1,000, Millipore, AB175); polyclonal anti-glutamate (rabbit, 1:300, Abcam, ab9440); polyclonal anti-Glutamate decarboxylase 67 (GAD67, rabbit, 1:100, AnaSpec, 53501); polyclonal anti-GAT3/4 (Abcam, rabbit, 1:100, ab431; and Millipore, rabbit, 1:500, AB1574), both specific for human and rat GAT3 and mouse GAT4); monoclonal anti-GAD65 (Mouse, 1:200, Developmental Studies Hybridoma Bank); polyclonal anti-GABAA-R α5-subunit (rabbit, 1:200, Abcam, ab10098); monoclonal anti-beta amyloid 1–42 (rabbit, 1:2,000, Invitrogen, 700254). After washing three times in PBS with 0.01% triton-X, the brain sections were incubated with appropriate secondary antibodies conjugated to Alexa Fluor 488, Alexa Fluor 546 or Alexa Fluor 647 (1:300, Molecular Probes), FITC or TRITC (1:500, Jackson ImmunoResearch) for 2 h at room temperature. To reveal the location of Aβ plaques, the brain sections were incubated in PBS containing 2 μg ml−1 thioflavin-s for 12 min, followed by washing in PBS for three times (3 × 12 min). To reduce lipofuscin like-autofluorescence in human brain sections, the Autofluorescence Eliminator Reagent (Millipore, 2160) was used, which did not adversely affect other fluorescent labelling in the section. The brain sections were mounted on a glass slide with an antifading mounting solution with or without 4′,6-diamidino-2-phenylindole (Invitrogen). Fluorescent images were obtained with an Olympus confocal microscope (FV1000) and analysed using the Image J software.
Hippocampal slice preparation and recording
Mice were anaesthetized with 2.5% Avertin. After decapitation, brains were rapidly dissected out and placed in ice-cold cutting solution containing (in mM): 79 NaCl, 80 sucrose, 26 NaHCO3, 10 glucose, 2.5 KCl, 1.25 NaH2PO4, 7 MgSO4 and 0.5 CaCl2 for tonic current recordings. The cutting solution for field EPSP recordings contained (in mM): 230 sucrose, 26 NaHCO3, 20 glucose, 2.5 KCl, 1.25 NaH2PO4, 10 MgSO4 and 0.5 CaCl2. Both solutions were bubbled with 95% O2/5% CO2. Hippocampal slices were cut at 350 μm with a vibratome (VT1200S, Leica, Germany) and transferred to a transitional chamber containing one half cutting solution and one half standard artificial cerebrospinal fluid (ACSF). The ACSF was composed of (in mM): 125 NaCl, 2.5 KCl, 1.3 MgSO4, 26 NaHCO3, 1.25 NaH2PO4, 2.0 CaCl2 and 10 glucose (290–300 mOsm l−1; bubbled with 95% O2/5% CO2, pH~7.4). Slices were then incubated in ACSF at 32 °C for 30 min to recover. Subsequently, slices were maintained at room temperature for another 30 min before recording. Individual slices were then transferred to a submerged recording chamber where they were continuously perfused (2-3 ml min−1) with ACSF saturated by 95% O2/5% CO2 at 32 °C.
Whole-cell voltage clamp recordings were performed on dentate granule cells using a pipette solution containing (in mM): 135 CsCl, 5 Na-phosphocreatine, 10 HEPES, 5 EGTA, 4 MgATP, 5 QX-314 and 0.5 Na2GTP (pH 7.3 adjusted with CsOH, 280–290 mOsm l−1). Pipette resistance was 2–5 MΩ, and series resistance was typically 20–40 MΩ. To record tonic GABA current, 10 μM CNQX and 50 μM DL-APV were added into the ACSF to block glutamate receptors. In some experiments, 5 μM GABA was also added into the ACSF to reveal larger tonic GABA current and increase the signal-to-noise ratio. The total tonic GABA current was revealed by the change of holding current after local perfusion of 100 μM BIC (sigma) to block all GABAA-Rs. The tonic current mediated by α5-GABAA-Rs was revealed by local application of 100 nM L-655,708 (Tocris), a selective inverse agonist for α5-GABAA-Rs. The membrane potential was held at −70 mV. Data were acquired using the pClamp 9 software (Molecular Devices; sampled at 10 kHz and filtered at 1 kHz) and analysed with the Clampfit 9.0 software (Molecular Devices).
To test neuronal excitability in dentate granule cells, whole-cell current clamp recordings were performed using a pipette solution containing (in mM): 135 K-Gluconate, 10 KCl, 5 Na-phosphocreatine, 10 HEPES, 2 EGTA, 4 MgATP and 0.5 Na2GTP (pH 7.3 adjusted with KOH, 280–290 mOsm l−1). As dentate granule cells were usually silent under normal condition, we injected appropriate current (~70 pA) to facilitate AP firing at a stable level (~2 Hz) for at least 5 min (serving as control). Then, brain slices were perfused with different drugs for 3–5 min. The AP fire frequency in the last minute of each drug treatment was quantified.
Field excitatory postsynaptic potentials were recorded with glass electrodes filled with 1 M NaCl and 25 mM HEPES (pH 7.3) and were evoked every 20 s with a parallel bipolar tungsten electrode (MicroProbes, USA), which was placed at the medial perforant path in the DG. Three evoked responses were averaged to obtain a data point. Stimulation strength was set to a level that produced a field excitatory postsynaptic potential amplitude at ~30% of the maximum response. After stable 20-min baseline recording, LTP was induced by HFS (100 pulses at 100 Hz, three trains in 20-s interval).
Y-maze spontaneous alternation task
Spontaneous alternation performance was tested as described previously17. This learning task does not involve any training, reward or punishment. It allows the assessment of hippocampus-dependent spatial working memory. Each mouse was placed in the centre of a symmetrical Y-maze and was allowed to explore freely through the maze during an 8-min session. The first 2 min were not included for data analysis because mice were exploring new environment. The total number and the sequence of arm entries in the last 6 min were recorded and analysed. Arm entry was defined as the hind paws of the mice had been completely placed in the arm. Analysis was performed in a blind manner. The percentage of alternation is the number of triads containing entries into all three arms divided by the maximum possible alternations (the total number of arms entered−2) × 100.
For in vivo i.p. injection of drugs, L-655,708 (1 mg ml−1) and SNAP-5114 (50 mM) were dissolved in dimethylsulphoxide and frozen in storage aliquots. The working solution was diluted 10 times in normal saline solution. In order to chronically block the tonic inhibition mediated by α5-GABAA-Rs or astrocytic GABA release through GAT3/4, L-655,708 (1 mg kg−1) or SNAP-5114 (50 μmol kg−1) or vehicle was injected once every day for 1 week. The last injection was administrated 30 min before behavioural test.
Three pairs of 6- to 8-month-old WT and 5xFAD littermates were killed with 2.5% Avertin and the brain quickly removed and put into iced-cold PBS to wash out the residual blood. Hippocampi were then dissected out on a cold platform, the wet weight of each sample was recorded, put into autoclaved EP tube and flash-frozen in liquid nitrogen immediately. The samples were stored in a −80° freezer. To make hippocampal homogenate, two freeze-thaw cycles were performed to break the cell membrane before adding 20-μl bath solution per mg tissue into the EP tube. To further fracture the cell, the hippocampal tissue in the EB tube was sonicated for 1 min on ice. The homogenate was centrifuged for 5 min at 5,000 g. The supernatant was then aliquoted and stored at −20° freezer. To test GABA responses evoked by the brain homogenate, HEK293T cells were transfected with α2β3γ2 plasmids and electrophysiology was performed 24–48 h after transfection. A bundle of 3-barrel glass pipette was pulled by a P-97 pipette puller. Before electrophysiological recordings, the stored hippocampal homogenate was further diluted by 100 times in bath solution and then used for puffing experiments.
GABA ELISA assay
GABA concentration in the mouse hippocampal homogenate was also quantified using mouse GABA ELISA kit (NB-E20434, Novatein Biosciences, Boston, MA, USA), performed according to the manufacturer’s instructions. Data analysis was performed blindly. Hippocampal homogenate was prepared similar to that described above for BHP assay.
Data were represented as mean±s.e.m. Student’s t-test (paired or unpaired) was used for statistical analysis in two-group comparison. For comparison among multiple groups, one-way or two-way analysis of variance with post hoc tests were used. Statistical significance was set at P<0.05. Behavioural analysis, BHP assay and GABA ELISA analysis were performed blindly.
How to cite this article: Wu, Z. et al. Tonic inhibition in dentate gyrus impairs long-term potentiation and memory in an Alzheimer’s disease model. Nat. Commun. 5:4159 doi: 10.1038/ncomms5159 (2014).
We would like to thank Dr Ian Simpson, Dr Gangyi Wu and Kate Simpson for critical reading of the manuscript, and Chen lab members for rigorous discussion during the progress of this project. This work was supported by grants from the National Institutes of Health (MH083911 and AG045656) and Pennsylvania State University Eberly College of Science Stem Cell Fund to G.C. M.G. was supported by NIH grants P50 AG025688 and P30 NS055077.
Supplementary Figures 1-3 and Supplementary Table 1