Abstract
Thalamic reticular nucleus (TRN) is a group of inhibitory neurons surrounding the thalamus. Due to its important role in sensory information processing, TRN is considered as the target nucleus for the pathophysiological investigation of schizophrenia and autism spectrum disorder (ASD). Prepulse inhibition (PPI) of acoustic startle response, a phenomenon that strong stimulus-induced startle reflex is reduced by a weaker prestimulus, is always found impaired in schizophrenia and ASD. But the role of TRN in PPI modulation remains unknown. Here, we report that parvalbumin-expressing (PV+) neurons in TRN are activated by sound stimulation of PPI paradigm. Chemogenetic inhibition of PV+ neurons in TRN impairs PPI performance. Further investigations on the mechanism suggest a model of burst-rebound burst firing in TRN-auditory thalamus (medial geniculate nucleus, MG) circuitry. The burst firing is mediated by T-type calcium channel in TRN, and rebound burst firing needs the participation of GABAB receptor in MG. Overall, these findings support the involvement of TRN in PPI modulation.
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Introduction
Thalamic reticular nucleus (TRN) is a shell-like structure that is mainly composed of GABAergic neurons. TRN lies between cortex and thalamus, and receives inputs from both cortex and thalamus but sends outputs only to the thalamus1,2. Due to its specific position and synaptic connections, TRN is thought to play an important role in sensory information processing, such as sensory detection3, sensory selection4,5, and sensory gating6,7. Aberrant sensory processing is common in some major psychiatry disorders, so TRN is considered as the ideal target for the investigation of the pathophysiology of schizophrenia8,9,10 and autism spectrum disorder (ASD)11,12,13.
Prepulse inhibition (PPI) of the acoustic startle response is a cross-species sensorimotor phenomenon, which refers to the ability of a weak prestimulus to transiently inhibit the response to a closely following strong sensory stimulus14. PPI deficit has been known as one of the typical phenotypes of schizophrenia15,16 and ASD17,18. Although many studies on the mechanism of PPI have been conducted, the relationship between TRN and PPI remains unknown.
Previous studies on the neurobiology of PPI have shown that acoustic startle reflex circuit includes the ventral cochlear nucleus, nuclei of lateral lemniscus, nucleus reticularis pontis caudalis, spinal interneuron, and lower motor neuron19. However, recent studies have found that higher brain regions are also involved in the modulation of PPI of acoustic startle reflex, such as auditory cortex and prefrontal cortex20,21,22. This type of top-down modulation of PPI requires a pathway of auditory information transmission, including auditory thalamus, known as medial geniculate nucleus (MG), and auditory projecting TRN (audTRN). The involvement of MG in PPI has already been reported23, but there is no study on the involvement of audTRN in PPI. Besides, researchers also found that activation of the inhibitory TRN amplifies the sound response in MG and auditory cortex using in vivo electrophysiological technology24. These leave us a very interesting issue of what part of TRN plays in the modulation of PPI.
In the present study, we show that increased PV+ neuronal activity in the audTRN is tightly coupled with sound stimulus of PPI, and inhibition of PV+ neurons in the audTRN impairs PPI performance. Moreover, we introduce a burst-rebound burst firing model between audTRN and MG neurons which regulates PPI performance. These results indicate the essential role of the audTRN–MG circuit for regulating PPI of acoustic startle response.
Materials and methods
Animals
C57BL/6J mice (aged 8–12 weeks) were obtained from the Southern Medical University Animal Center (Guangzhou, China). PV-Cre and Ai14 mice were obtained from the Jackson Laboratory. Four to five mice were housed in one plastic cage (30 × 17 × 12 cm) at 24 ± 1 °C. The mice were maintained under standard laboratory conditions (12-h light/dark cycle, lights on from 8:00 a.m. to 8:00 p.m.) with access to food and water ad libitum. Only male mice were used in the study.
Ethics approval
Animal experiments were conducted following the Regulations for the Administration of Affairs Concerning Experimental Animals (China) and were approved by the Southern Medical University Animal Ethics committee.
Virus
Adeno-associated viruses (AAVs) used in this study were purchased from BrainVTA, Wuhan, China and included AAV2/9-Efla-DIO-GCaMP6f-P2A-NLS-WPRE-pA (titer, 2.86 × 1012 v.g./mL), AAV2/9-Efla-DIO-hM4Di-P2A-NLS-mCherry-WPRE-pA (titer, 2.50 × 1012 v.g./mL), and AAV2/9-Efla-DIO-P2A-NLS-mCherry-WPRE-pA (titer, 2.58 × 1012 v.g./mL).
Surgery
Mice were anesthetized with sodium pentobarbital (1% wt/vol) via intraperitoneal injection. Viruses were injected into brain nuclei using stereotaxic equipment (Ruiwode Life Science). All coordinates for the injection sites are listed as measurements from the bregma. AudTRN:1.85 mm posterior, 2.45 mm lateral, 3.35 mm ventral; MG: 2.8 mm posterior, 2.0 mm lateral, and 3.2 mm ventral (for details, see Supplementary Methods).
Animal behavioral paradigm
Open field test (OFT)
The OFT was performed in 40 × 40 cm chambers. The mouse was gently placed in the center of the square for a 5-min recording period. The time spent in the center zone and the distances traveled were automatically calculated using the DigBehv animal behavior analysis program.
PPI of startle reflex
As previously described25, PPI was measured using the SR-Lab System (San Diego Instruments, San Diego, CA, USA). During all testing, the background was set at 65-dB white noise. The PPI test consisted of a 5 min acclimation period, followed by seven trial types presented six times each in pseudorandom order. Each trial consisted of a 20 ms prepulse, an 100 ms interval, and a 40 ms startle stimulus. Prepulse intensity was set at background, 74, 78, 82, 86, or 90 dB, and the startle stimulus in each case was 120 dB. One trial type consisted solely of background noise to control for the general movement of the subject. Trials were presented with a variable intertrial interval of 15–20 s. For each subject, the entire PPI test session lasted approximately 18 min. At the onset of the startle stimulus, maximum velocity (Vmax) in arbitrary units of the startle platform was recorded every 1 ms for 65 ms. The Vmax was averaged across trial type, with PPI calculated as the difference between Vmax after prepulse trials (Vmax-PP) and Vmax after startle stimulus alone trials (Vmax-startle), and was expressed as a percentage of Vmax-startle: PPI = ((Vmax-startle − Vmax-PP)/Vmax-startle)×100%.
Fiber photometry
Mice were allowed to recover from surgery for 14 days before the behavioral experiments. The fiber photometry system (ThinkerTech Nanjing Bioscience) was used in our study (for details, see Supplementary Methods). During the behavior experiment, the GCaMP6f fluorescence intensity from startle white noise (120 dB) and prepulse white noise (90 dB) was recorded. The signal during background white noise (65 dB) was set as the baseline.
For all behavioral tests, mice were separated into each group (N ≥ 8 mice) randomly. Analyses were performed blindly. All experiments were replicated more than three times in the laboratory.
In vitro electrophysiological recording
After slice preparation (refer to Supplementary Methods for details), slices were placed in the recording chamber that was superfused (3 mL/min) with ACSF at 30–32 °C. Whole-cell patch-clamp recordings of TRN and MG neurons were obtained under an infrared (IR)-differential interference contrast (DIC) microscope (Nikon). To record action potentials, pipettes (input resistance: 3–7 MΩ) were filled with an intracellular solution containing (in mM) 105 K-gluconate, 30 KCl, 10 HEPES, 10 phosphocreatine, 4 ATP-Mg, 0.3 GTP-Na, and 0.3 EGTA (pH 7.35, 290 mOsm). Depolarizing currents (60 pA, 500 ms) were injected into PV-positive neurons in audTRN of PV-Cre: Ai14 mice in the current-clamp configuration, and a recording was conducted at holding potentials of −70 mV. To isolate T-type calcium channel-dependent low threshold spike (LTS), 1 µM tetrodotoxin (TTX) was added to the ACSF. To block this LTS, T-type calcium channel antagonist NiCl2 (1 mM, Sigma Aldrich) was added to the ACSF. When the inhibitory synaptic response was recorded, a stimulating electrode was placed in the audTRN fiber path approximately 0.2 mm away from the recorded cell bodies in the MG. The electrical stimulation frequency was 300 Hz (0.2 and 50 ms), and a recording was conducted at holding potentials of −60 mV. To isolate the synaptic IPSPs, 20 μM CNQX and 100 μM D,L-APV were added to the ACSF. After the burst firing was induced, 20 µM GABAA receptor antagonist bicuculline methiodide (BMI) and 0.5 µM GABAB antagonist CGP55845 (ref. 26) were added to the ACSF. Data were recorded with a multiClamp 700B (Molecular Devices) software, digitized at 5 kHz, and filtered at 1 kHz. Data were collected when the series resistance fluctuated within 20% of the initial values and analyzed using pClamp10.7 software (Molecular Devices).
Immunostaining
For histological procedures, please refer to the Supplementary Materials.
Statistical analyses
Statistical comparisons were conducted in GraphPad Prism 8. The homoscedasticity and normality of the distributions of data were determined using GraphPad Prism 6 before assigning specific statistical tests. Data were analyzed using Student’s t-test or Mann–Whitney two-tailed t-test or two-way analysis of variance (ANOVA). Data are expressed as the means ± standard errors of the means (SEM), unless otherwise indicated, and a difference was considered statistically significant when P < 0.05. The sample size (N = number of neurons or mice) and statistical test results, such as p, t, and df are reported in results for all measurements.
Results
PV+ neurons in auditory TRN are activated during PPI process
In consideration of the fact that TRN has several subsections related to different types of sensory information processing1, we first focused on the auditory pathway for its wide usage in studies on PPI. To identify the position and cell type of auditory thalamus projecting TRN (audTRN), we injected retrobeads (RBs) into the MG of C57 mice (Fig. 1A and Supplementary Fig. S1). After the position of audTRN was confirmed (Fig. 1B), we tested whether parvalbumin-expressing (PV+) neurons are predominated as previously described27 by calculating the ratio of the co-label between RBs and PV+ neurons in audTRN. The result showed that about 88.00 ± 2.23% MG-projecting neurons in audTRN were PV positive (Fig. 1B, C), which indicated that PV+ neurons account for the majority of the auditory pathway of TRN.
Next, we determined whether PV+ neurons are activated during the sound stimuli of PPI paradigm. C57 mice were randomly divided into two groups. Mice were put into the startle reflex chamber without or with sound stimuli of PPI (Fig. 1D, F). After c-Fos staining, we found that PPI paradigm significantly increased c-Fos expression compared to the control group (Fig. 1H; number of c-Fos-positive neurons, control: 0.43 ± 0.20, PPI: 10.20 ± 1.01; P < 0.0001). The result revealed that audTRN was activated during sound stimuli of PPI. Among the c-Fos-positive neurons of the PPI group, approximately 89.38 ± 4.40% neurons were PV+ (Fig. 1I).
Given that c-Fos staining was carried out in slices in vitro, we further determined whether PV+ neuronal activation appears in audTRN in vivo during sound stimuli of PPI using fiber photometry. A Cre-dependent AAV for expression of the Ca2+ indicator Gcamp6f, AAV-DIO-GCaMP6f, was injected into audTRN in PV-Cre mice (Fig. 2A, B). Among the infected neurons, about 97.86 ± 0.93% neurons expressed PV (Fig. 2C). Different sound stimuli of PPI, 90 and 120 dB, were generated by a white noise generator and were given by a speaker in a behavioral chamber where ca2+ fluorescence (∆F/F(%)) was monitored by fiber photometry system (Fig. 2D). We found that GCaMP6f fluorescence in PV+ neurons in the audTRN increased when mice were presented with startle 120 dB sound stimulation (Fig. 2F, H. ∆F/F(%), 0 s: 0.55 ± 0.45, peak amplitude: 10.42 ± 1.31; P = 0.0005), and 90 dB sound stimulation (Fig. 2G, I; ∆F/F(%), 0 s: 0.11 ± 0.38, peak amplitude: 6.08 ± 1.74; P = 0.0307). Taken together, these results indicate that the activity of PV+ neurons in audTRN is tightly coupled with the sound stimuli of PPI.
Chemogenetic inhibition of audTRN PV neurons impairs PPI performance
To determine the role of PV+ neuronal activity in audTRN in mediating PPI performance, we examined the effect of chemogenetic inhibition of PV+ neurons. An AAV virus for expression of the engineered inhibitory G protein-coupled receptor (hM4Di), AAV-DIO-hM4Di-mCherry, or a control virus, AAV-DIO-mCherry, was injected into the audTRN in PV-Cre mice (Fig. 3A). Among the infected neurons, about 89.41 ± 1.08% neurons expressed PV (Fig. 3C). HM4Di suppressed neuronal activity in the presence of its agonist clozapine-N-oxide (CNO). The efficacy of hM4Di-mediated inhibition was tested in brain slices using whole-cell recordings from PV+ neurons expressing hM4Di (Fig. 3D). Infusions of CNO (5 µM) into audTRN slices from these mice resulted in blockage of action potential firing. For behavioral test, after CNO (3 mg/kg, i.p.) treatment, the hM4Di group showed no effect on the total distance of OFT (Fig. 3E and Supplementary Fig. S2), or startle reflex of PPI (Fig. 3F) compared to the mCherry group, which indicated that inhibition of PV+ neuron in audTRN does not affect the locomotor activity or startle system. In contrast, CNO treatment decreased the PPI of the hM4Di group significantly compared to the mCherry group (Fig. 3G, P < 0.0001). Together, these data indicated that the PV+ neurons in audTRN are critical for PPI of acoustic startle.
Inhibition of T-type calcium channel causes blockage of burst firing and PPI performance impairment
Previous studies have found that neurons in the sensory system exhibit two different firing modes, tonic and burst firing28,29. Tonic firing affords better linearity, whereas burst firing supports better signal detection30,31. Sound stimulation can induce burst firing in TRN3,6, and the activity of PV+ neurons in audTRN is tightly coupled with the sound stimuli of PPI (Fig. 2), we then hypothesized that burst firing of PV+ neurons in audTRN may be involved in the process of PPI modulation.
To testify this idea, we first confirmed that PV+ neurons in audTRN can fire in burst ways using whole-cell recordings from PV+ neurons of PV-Cre: Ai14 mice by inward current injection (Fig. 4A, B). It has been shown that burst firing was triggered by T-type calcium channel-mediated depolarization, known as the LTS29,32. LTS could be isolated by the addition of voltage-gated sodium channel blocker TTX (Fig. 4B). To prove the leading role of T-type calcium channel in burst firing, its antagonist NiCl2 was added into the ACSF33. One millimolar NiCl2 could block LTS (Fig. 4B, D, amplitude of LTS, TTX: 22.43 + 0.19 mV, TTX + NiCl2: 0.75 + 0.20 mV; P < 0.0001) as well as burst firing (Fig. 4C, E, number of burst, control: 1.2 + 0.20, NiCl2: 0; P = 0.0039) of PV+ neurons in audTRN. The results showed that NiCl2 attenuated the burst firing of PV+ neurons efficiently.
To test the involvement of burst firing in the PPI modulation, 6 mM NiCl2 (ref. 33) or vehicle was injected into audTRN of C57 mice by the micro-injection system (Fig. 4F and Supplementary Fig. S1). NiCl2 treatment showed no effect on the total distance of OFT (Fig. 4G and Supplementary Fig. S2), or startle reflex of PPI (Fig. 4H) compared to vehicle group, indicating that inhibition of burst firing in audTRN does not affect the locomotor activity or startle system. In contrast, NiCl2 treatment decreased PPI significantly compared to the vehicle group (Fig. 4I, P = 0.0002). These results inferred that burst firing of audTRN neurons plays an important role in the regulation of PPI of startle reflex.
Inhibition of GABAB receptor prevents rebound bursting in the MG and impairs PPI of acoustic startle
How does the burst firing in audTRN regulate PPI performance of startle reflex? TRN is an inhibitory nucleus which sends inhibitory outputs to thalamic relay cells. Burst firing of interneurons in TRN can provide a short but strong hyperpolarization for relay cells. Previous studies have found that thalamic relay cells’ bursts potently activate cortical circuits31,34 served as a “wake-up call” from thalamus30. This suggests that burst firing of thalamic relay cells is responsible for the detection of sensory information. So we wondered whether bursting in audTRN neurons regulates burst firing in thalamic relay neurons.
First, an electrical stimulus was given by a stimulating electrode placed in the audTRN fiber path while whole-cell recording was conducted in relay neurons in MG. To mimic the burst firing in audTRN, the electrical stimulation parameters were set up as follows: 300 Hz, 50 ms duration, 0.2 ms pulse width28,35,36. CNQX, and APV were added to the ACSF to block the effect of excitatory synaptic inputs (Fig. 5A). We found that after a strong hyperpolarization from inhibitory synaptic inputs of TRN, MG relay neurons exhibited a rebound burst firing28 afterward (Fig. 5B). Furthermore, this kind of hyperpolarization and rebound burst could be blocked by GABAB receptor antagonist CGP55845, rather than GABAA receptor antagonist bicuculline methiodide (BMI) (Fig. 5C–E). These data suggest that GABAB receptor-mediated hyperpolarization plays an important role in triggering rebound burst firing in MG. Next, we used CGP55845 to block the rebound burst in MG in the behavioral tests. In all, 0.1 mM CGP55845 or vehicle was injected into the MG of C57 mice by the micro-injection system (Fig. 5F and Supplementary Fig. S1). CGP55845 treatment showed no effect on the total distance of OFT (Fig. 5G and Supplementary Fig. S2), or startle reflex of PPI (Fig. 5H) compared to the vehicle group, indicating that inhibition of rebound burst firing of neurons in MG does not affect the locomotor activity or startle system. In contrast, CGP55845 treatment decreased PPI significantly compared to the vehicle group (Fig. 5I, P < 0.0001). All these data suggested that there may exist a burst-rebound firing pathway from audTRN to MG and this pathway is critical to the regulation of PPI of startle reflex.
Discussion
Using cell-type-specific fiber photometry, electrophysiology, chemogenetics, and pharmacology, we report three major findings. First, PV+ neurons in the audTRN are activated by sound stimulation. Second, chemogenetic inhibition of PV+ neurons in the audTRN impairs PPI performance. Last, pharmacological inhibition of burst firing in audTRN, or rebound burst firing in MG also impairs PPI performance. Together, these findings revealed an audTRN–MG circuit that controls PPI of acoustic startle.
What do these findings inspire us about the relationship between TRN and psychiatry disorders? Previous studies on TRN and sensory gating were often conducted using anesthetized animals3,6. Lack of in vivo experimental evidence makes TRN’s role in PPI of acoustic startle unclear. To overcome this obstacle, we first identified the position of auditory related TRN to obtain a better recording of neuronal activity. Then we found that Gcamp6f fluorescence in PV+ neurons in audTRN was increased during sound stimulation of PPI in awake mice, suggesting the involvement of TRN in PPI. Furthermore, the participation of PV+ neurons in the modulation of PPI performance in our chemogenetic study is consistent with a previous human postmortem study in schizophrenia10. They found a marked decrease in the number of PV neurons in TRN of schizophrenia patients. All these findings suggest that PV+ neuron abnormalities are a potential cellular mechanism of schizophrenia. As to the relationship between TRN and ASD, plenty of studies have been done. TRN may be involved with the hyperactivity, attention deficits, and hypersensitivity of ASD11,12,13. An animal model of autism, the PTCHD1 knockout mouse, was reported. During development, Ptchd1 is selectively enriched in TRN. In their study, the PTCHD1 knockout mice showed reduced repetitive bursting of TRN neurons, but no change in PPI performance12. In consideration of our findings, different kinds of burst firing modes, like single burst firing or repetitive burst firing, may modulate sensory processing in different ways2,37. Undoubtedly, complete blockage of burst firing can impair PPI performance.
Burst firing is a popular firing mode in the sensory system. It has always been shown in thalamus during sleep and epilepsy38,39. Recent studies also found the appearance of burst firing in awake animals, such as cat and monkey34,40,41,42. In our study, blockage of the burst firing in TRN using T-type calcium channel antagonist disrupted PPI performance in awake mice. This testifies that burst firing may also be functional during awake states. Along with MG, we proposed a burst-rebound burst model that provides a new way of sensory information transmission. In this model, the rebound burst of auditory thalamus may increase cortical detection31,34, which in turn amplifies the auditory signal. This kind of rebound excitation was common in the rhythmic brain activity of asleep animals or anesthetized animals38,43, but little is known in awake animals. So further investigation of this model is needed, especially the role of the rebound burst in information processing during wakeful periods. Besides, rebound burst firing in MG relies on the GABAB receptor. This is understandable because the activation of the T-type calcium channel requires a slow time course of the GABAB synaptic response44,45. Together, these findings provide some molecular targets for the following studies on this issue.
How does the burst-rebound burst firing model regulate PPI of acoustic startle response? Crick F.46 has proposed a “searchlight hypothesis” about how TRN participates in the process of attention a long time ago and considered TRN as the gatekeeper of the thalamus. Recent studies on the mechanism of attention have found that TRN can filter out irrelevant information through its inhibition of the sensory thalamus4,47,48. Our studies suggest that instead of inhibiting the auditory signal, TRN amplifies the signal through a burst-rebound burst firing model which may work as follows: prepulse sound signal induces burst firing in audTRN PV+ neurons, and this kind of firing of inhibitory terminals produces strong hyperpolarization on MG neurons through GABAB receptors, which in turns activates T-type calcium channel and then triggers burst firing in these MG neurons. This kind of firing can be detected by higher brain regions, which can raise the attention level of an animal. Higher attention level can in turn inhibits following strong sound stimulation49, at last, this inhibition produces the PPI effect. In short, prepulse stimulation activates the top-down regulation of PPI through a burst-rebound burst firing model between audTRN and MG.
There are several limitations to our studies. Limited by the technology, we cannot record the firing activities of TRN, MG, or cortex in awake mice. Monitoring analysis of the firing properties in these regions is unavailable so that we cannot investigate the relationship between firing mode and animal behaviors. We are unable to record the neuronal activity of audTRN and MG in vivo at the same time either. This makes it impossible to prove the existence of a burst-rebound burst firing model between audTRN and MG in awake mice. Besides, in consideration of the fact that stimulation given by the bipolar electrode may unavoidably activate other inhibitory pathways to MG in the electrophysiological recording experiment, more specific methods such as optogentics will be used to verify such circuit in the future study.
In summary, our work identifies audTRN PV+ interneurons as an important cellular modulator in the regulation of PPI of acoustic startle response. The burst firing in the thalamus may be the mechanism underlying this kind of modulation. AudTRN PV+ neurons and its firing mode may, thus, serve as potential targets for the treatment of patients with schizophrenia and ASD.
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Acknowledgements
This work was supported by grants from the National Natural Science Foundation of China (31830033, 82090032), the Program for Changjiang Scholars and Innovative Research Team in University (IRT_16R37), and Key-Area Research and Development Program of Guangdong Province (2018B030334001).
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Q.-l.Y. and T.-m.G. conceived and designed the project, and wrote the manuscript. Q.-l.Y. and Z.-y.L. performed electrophysiological recordings and analysis. Q.-l.Y., Z.-c.L., Y.K., Z.-l.L., and X.-w.L. performed behavioral tests, immunofluorescence staining, and analysis. J.-m.Y. and T.-m.G. helped with data interpretation and provided instruction. T.-m.G. supervised the project.
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You, Ql., Luo, Zc., Luo, Zy. et al. Involvement of the thalamic reticular nucleus in prepulse inhibition of acoustic startle. Transl Psychiatry 11, 241 (2021). https://doi.org/10.1038/s41398-021-01363-1
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DOI: https://doi.org/10.1038/s41398-021-01363-1
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