Adult male mice emit highly complex ultrasonic vocalizations(USVs)in response to female conspecifics.Such US Vs,thought to facilitate courtship behaviors,are routinely measured as a behavioral index in mouse models of...Adult male mice emit highly complex ultrasonic vocalizations(USVs)in response to female conspecifics.Such US Vs,thought to facilitate courtship behaviors,are routinely measured as a behavioral index in mouse models of neurodevelopmental and psychiatric disorders such as autism.While the regulation of US Vs by genetic factors has been extensively characterized,the neural mechanisms that control USV production remain largely unknown.Here,we report that optogenetic activation of the medial preoptic area(mPOA)elicited the production of USVs that were acoustically similar to courtship US Vs in adult mice.Moreover,mPOA vesicular GABA transporter-positive(Vgat +)neurons were more effective at driving USV production than vesicular glutamate transporter 2-positive neurons.Furthermore,ablation of mPOA Vgat+ neurons resulted in altered spectral features and syllable usage of USVs in targeted males.Together,these results demonstrate that the mPOA plays a crucial role in modulating courtship USVs and this may serve as an entry point for future dissection of the neural circuitry underlying USV production.展开更多
The raphe nucleus is critical for feeding, rewarding and memory. However, how the heterogenous raphe neurons are molecularly and structurally organized to engage their divergent functions remains unknown. Here, we gen...The raphe nucleus is critical for feeding, rewarding and memory. However, how the heterogenous raphe neurons are molecularly and structurally organized to engage their divergent functions remains unknown. Here, we genetically target a subset of neurons expressing VGLUT3. VGLUT3 neurons control the efficacy of spatial memory retrieval by synapsing directly with parvalbumin-expressing GABA interneurons(PGIs) in the dentate gyrus. In a mouse model of Alzheimer's disease(AD mice),VGLUT3→PGIs synaptic transmission is impaired by ETV4 inhibition of VGLUT3 transcription. ETV4 binds to a promoter region of VGLUT3 and activates VGLUT3 transcription in VGLUT3 neurons. Strengthening VGLUT3→PGIs synaptic transmission by ETV4 activation of VGLUT3 transcription upscales the efficacy of spatial memory retrieval in AD mice. This study reports a novel circuit and molecular mechanism underlying the efficacy of spatial memory retrieval via ETV4 inhibition of VGLUT3 transcription and hence provides a promising target for therapeutic intervention of the disease progression.展开更多
The lateral habenula(LHb),which is a critical neuroanatomical hub and a regulator of midbrain monoaminergic centers,is activated by events resulting in negative valence and contributes to the expression of both appeti...The lateral habenula(LHb),which is a critical neuroanatomical hub and a regulator of midbrain monoaminergic centers,is activated by events resulting in negative valence and contributes to the expression of both appetitive and aversive behaviors.However,whole-brain cell-type-specific monosynaptic inputs to the LHb in both sexes remain incompletely elucidated.In this study,we used viral tracing combined with in situ hybridization targeting vesicular glutamate transporter 2(vGlut2)and glutamic acid decarboxylase 2(Gad2)to generate a comprehensive whole-brain atlas of inputs to glutamatergic andγ-aminobutyric acid(GABA)ergic neurons in the LHb.We found>30 ipsilateral and contralateral brain regions that projected to the LHb.Of these,there were significantly more monosynaptic LHb-projecting neurons from the lateral septum,anterior hypothalamus,dorsomedial hypothalamus,and ventromedial hypothalamus in females than in males.More interestingly,we found a stronger GABAergic projection from the medial septum to the LHb in males than in females.Our results reveal a comprehensive connectivity atlas of glutamatergic and GABAergic inputs to the LHb in both sexes,which may facilitate a better understanding of sexual dimorphism in physiological and pathological brain functions.展开更多
基金the National Natural Science Foundation of China (31871066, 31471065)the National Basic Research Development Program (973 Program) of China (2015CB559201)+2 种基金the Thousand Young Talents Program of Chinathe Strategic Priority Research Program of the Chinese Academy of Sciences (XDB32010200)as part of the Chinese Academy of Science interdisciplinary innovation team
文摘Adult male mice emit highly complex ultrasonic vocalizations(USVs)in response to female conspecifics.Such US Vs,thought to facilitate courtship behaviors,are routinely measured as a behavioral index in mouse models of neurodevelopmental and psychiatric disorders such as autism.While the regulation of US Vs by genetic factors has been extensively characterized,the neural mechanisms that control USV production remain largely unknown.Here,we report that optogenetic activation of the medial preoptic area(mPOA)elicited the production of USVs that were acoustically similar to courtship US Vs in adult mice.Moreover,mPOA vesicular GABA transporter-positive(Vgat +)neurons were more effective at driving USV production than vesicular glutamate transporter 2-positive neurons.Furthermore,ablation of mPOA Vgat+ neurons resulted in altered spectral features and syllable usage of USVs in targeted males.Together,these results demonstrate that the mPOA plays a crucial role in modulating courtship USVs and this may serve as an entry point for future dissection of the neural circuitry underlying USV production.
基金supported by the National Natural Science Foundation of China (31721002, 81920208014, 31930051, 81800133)China Postdoctoral Science Foundation Funded Project (2018M642853)。
文摘The raphe nucleus is critical for feeding, rewarding and memory. However, how the heterogenous raphe neurons are molecularly and structurally organized to engage their divergent functions remains unknown. Here, we genetically target a subset of neurons expressing VGLUT3. VGLUT3 neurons control the efficacy of spatial memory retrieval by synapsing directly with parvalbumin-expressing GABA interneurons(PGIs) in the dentate gyrus. In a mouse model of Alzheimer's disease(AD mice),VGLUT3→PGIs synaptic transmission is impaired by ETV4 inhibition of VGLUT3 transcription. ETV4 binds to a promoter region of VGLUT3 and activates VGLUT3 transcription in VGLUT3 neurons. Strengthening VGLUT3→PGIs synaptic transmission by ETV4 activation of VGLUT3 transcription upscales the efficacy of spatial memory retrieval in AD mice. This study reports a novel circuit and molecular mechanism underlying the efficacy of spatial memory retrieval via ETV4 inhibition of VGLUT3 transcription and hence provides a promising target for therapeutic intervention of the disease progression.
基金This work was supported by the NSFC-Guangdong Joint Fund(U20A6005)the National Natural Science Foundation of China(31630031 and 31930047)+2 种基金the Key-Area Research and Development Program of Guangdong Province(2018B030340001 and 2018B030331001)the Guangdong Provincial Key Laboratory of Brain Connectome and Behavior(2017B030301017)the Shenzhen Key Laboratory of Translational Research for Brain Diseases(ZDSYS20200828154800001).
文摘The lateral habenula(LHb),which is a critical neuroanatomical hub and a regulator of midbrain monoaminergic centers,is activated by events resulting in negative valence and contributes to the expression of both appetitive and aversive behaviors.However,whole-brain cell-type-specific monosynaptic inputs to the LHb in both sexes remain incompletely elucidated.In this study,we used viral tracing combined with in situ hybridization targeting vesicular glutamate transporter 2(vGlut2)and glutamic acid decarboxylase 2(Gad2)to generate a comprehensive whole-brain atlas of inputs to glutamatergic andγ-aminobutyric acid(GABA)ergic neurons in the LHb.We found>30 ipsilateral and contralateral brain regions that projected to the LHb.Of these,there were significantly more monosynaptic LHb-projecting neurons from the lateral septum,anterior hypothalamus,dorsomedial hypothalamus,and ventromedial hypothalamus in females than in males.More interestingly,we found a stronger GABAergic projection from the medial septum to the LHb in males than in females.Our results reveal a comprehensive connectivity atlas of glutamatergic and GABAergic inputs to the LHb in both sexes,which may facilitate a better understanding of sexual dimorphism in physiological and pathological brain functions.
