Paraventricular, subparaventricular and periventricular hypothalamic IRS4-expressing neurons are required for normal energy balance

Sutton, Amy K.; Gonzalez, Ian E.; Sadagurski, Marianna; Rajala, Michael; Lu, Chunxia; Allison, Margaret B.; Adams, Jessica M.; Myers, Martin G.; White, Morris F.; Olson, David P.

doi:10.1038/s41598-020-62468-z

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Published: 26 March 2020

Paraventricular, subparaventricular and periventricular hypothalamic IRS4-expressing neurons are required for normal energy balance

Amy K. Sutton¹^na1,
Ian E. Gonzalez¹^na1,
Marianna Sadagurski²,
Michael Rajala²,
Chunxia Lu⁴,
Margaret B. Allison¹,
Jessica M. Adams ORCID: orcid.org/0000-0002-6155-4213⁴,
Martin G. Myers ORCID: orcid.org/0000-0001-9468-2046^1,2,
Morris F. White³ &
…
David P. Olson ORCID: orcid.org/0000-0001-9249-7760^1,4

Scientific Reports volume 10, Article number: 5546 (2020) Cite this article

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Abstract

Understanding the neural components modulating feeding-related behavior and energy expenditure is crucial to combating obesity and its comorbidities. Neurons within the paraventricular nucleus of the hypothalamus (PVH) are a key component of the satiety response; activation of the PVH decreases feeding and increases energy expenditure, thereby promoting negative energy balance. In contrast, PVH ablation or silencing in both rodents and humans leads to substantial obesity. Recent studies have identified genetically-defined PVH subpopulations that control discrete aspects of energy balance (e.g. oxytocin (OXT), neuronal nitric oxide synthase 1 (NOS1), melanocortin 4-receptor (MC4R), prodynorphin (PDYN)). We previously demonstrated that non-OXT NOS1^PVH neurons contribute to PVH-mediated feeding suppression. Here, we identify and characterize a non-OXT, non-NOS1 subpopulation of PVH and peri-PVH neurons expressing insulin-receptor substrate 4 (IRS4^PVH) involved in energy balance control. Using Cre-dependent viral tools to activate, trace and silence these neurons, we highlight the sufficiency and necessity of IRS4^PVH neurons in normal feeding and energy expenditure regulation. Furthermore, we demonstrate that IRS4^PVH neurons lie within a complex hypothalamic circuitry that engages distinct hindbrain regions and is innervated by discrete upstream hypothalamic sites. Overall, we reveal a requisite role for IRS4^PVH neurons in PVH-mediated energy balance which raises the possibility of developing novel approaches targeting IRS4^PVH neurons for anti-obesity therapies.

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Introduction

Genetic polymorphisms associated with obesity are disproportionately clustered in pathways affecting neural function and architecture in the central nervous system (CNS)¹. Within the brain, the paraventricular nucleus of the hypothalamus (PVH) is a primary hypothalamic node that integrates neural and humoral information regarding energy balance and sends output signals to structures in the hindbrain and spinal cord to control satiety and energy expenditure^2,3,4. Dysregulation of the entire PVH with site-directed lesions or inhibition of PVH melanocortin-4 receptor (MC4R) action produce profound obesity^5,6,7. However, while disruption of MC4R^PVH activity leads to obesity due to hyperphagia, lesions of the entire PVH are associated with both feeding and energy expenditure dysregulation^7,8,9. While MC4R^PVH activity is necessary and sufficient to alter feeding behavior, MC4R action in the PVH cannot be ascribed to neural populations expressing oxytocin (OXT), vasopressin (AVP), or corticotropin-releasing hormone (CRH)⁷. Manipulation of other PVH populations, such as neuronal nitric oxide synthase 1 (NOS1^PVH) neurons, is sufficient to alter both feeding and energy expenditure¹⁰. This raises the possibility that distinct PVH cell types might independently or coordinately regulate feeding and/or energy expenditure. Even though substantial efforts have been made to define PVH neuronal populations and their distinct roles in energy balance control, few studies have revealed PVH populations that are capable of regulating multiple aspects of energy balance (i.e. energy expenditure and feeding), apart from the NOS1^PVH population.

Nos1 expression marks a relatively large percentage of PVH neurons that send projections to hindbrain and spinal cord sites. Chemogenetic activation of NOS1^PVH neurons suppresses feeding and increases energy expenditure by promoting both increased physical activity and thermogenesis¹⁰. OXT^PVH neurons are almost entirely contained within the NOS1^PVH field, yet their activation drives only small changes in energy expenditure and does not suppress feeding¹⁰. NOS1^PVH-dependent changes in energy expenditure are likely independent of MC4R-signaling in the PVH, since activation of MC4R^PVH neurons suppresses feeding but does not affect energy expenditure and selective PVH expression of Mc4R in an otherwise Mc4R-null background has little impact on energy expenditure^8,11. Given the important contribution of both energy expenditure and feeding dysregulation in the development of obesity, the identification of distinct targets that have the capability to modulate both aspects of energy balance is particularly pertinent.

Recent reports indicate that insulin receptor substrate-4 (IRS4) acts in synergy with insulin receptor substrate-2 (IRS2) in the hypothalamus to maintain normal bodyweight¹². We discovered that Irs4 is expressed in and adjacent to the PVH and that the paraventricular and periventricular IRS4-expressing cell population (referred to as IRS4^PVH) is both necessary and sufficient for normal feeding and bodyweight, suggesting a functional role for PVH and peri-PVH Irs4-expressing neurons in the control of energy homeostasis. Additionally, we find that NTS-projecting and PBN-projecting IRS4^PVH neurons are densely innervated by local PVH neurons, supporting a role for an intra-PVH network in the regulation of energy balance. Monosynaptic afferent neural tracing suggests that the inputs to IRS4^PVH neurons vary depending on the brain regions to which an IRS4^PVH subset projects. Overall, our study proposes a novel framework for the regulation of bodyweight consisting of multiple interconnected PVH populations that are potentially under independent control to modulate distinct energy balance parameters including feeding and energy expenditure.

Results

Irs4 expression marks a distinct PVH subpopulation

Hypothalamic IRS4 and IRS2 synergistically contribute to body weight maintenance¹². Since in situ hybridization (Allen Mouse Brain Atlas¹³) reveals dense Irs4 expression in and adjacent to the PVH, we sought to determine the role of IRS4^PVH neurons in energy homeostasis using Cre-dependent technologies in combination with a novel IRS4-iCre knock-in mouse model in which Cre recombinase expression is tethered to Irs4 (Fig. 1A). The Irs4 gene is located on the X chromosome. Since random X inactivation may lead to variable Cre activity in female mice, male mice were used exclusively in all studies. In situ hybridization of both Cre and Irs4 mRNA in the PVH of IRS4-iCre mice was used to verify the appropriate expression of Cre recombinase in the IRS4-iCre mouse line and demonstrated substantial overlap of Irs4 and Cre mRNA transcripts in the PVH (Fig. 1B). To investigate IRS4^PVH neuron overlap with other known PVH populations, IRS4^PVH neurons were labeled by injection of a Cre-dependent GFP reporter virus into the PVH of IRS4-iCre mice (Fig. 1C). This approach eliminates the possibility of overrepresentation of the IRS4^PVH reporter population due to developmental Irs4 expression and aligns with subsequent Cre-dependent viral technologies used to manipulate IRS4^PVH neurons in adult mice. Brains stained for GFP (indicating IRS4-iCre activity) and neurophysin I, the carrier protein for oxytocin, indicate that adult IRS4^PVH neurons do not substantially overlap with OXT^PVH neurons (Fig. 1D). To determine if IRS4^PVH neurons are contained within the NOS1^PVH population, we stained brain slices from IRS4-iCre mice injected with AAV-Flex-GFP for NOS1 peptide and GFP and found that IRS4^PVH neurons are a separate population from NOS1^PVH cells (Fig. 1E). As AVP^PVH neurons are also able to modestly control feeding, we examined the overlap of AVP and IRS4 within the PVH¹⁴. Indeed, GFP-identified PVH neurons representing IRS4-iCre activity do not overlap substantially with immunoreactivity for copeptin, the carrier molecule for AVP (Fig. 1F). To investigate the potential overlap between IRS4^PVH neurons and other subpopulations of the PVH recently reported to contribute to energy homeostasis, we conducted in situ hybridization for Irs4 mRNA in combination with Crh, Pdyn, and thyrotropin-releasing hormone (Trh) mRNAs (Supp. Fig. 1.1). The majority of IRS4^PVH neurons do not express Crh (9.76 + 2.94% of IRS4^PVH with Crh, n = 3 mice) or Pdyn (15.77 + 1.19% of IRS4^PVH with Pdyn, n = 3 mice), and a modest fraction of CRH^PVH and PDYN^PVH neurons express Irs4 mRNA (26.08 + 2.38% and 28.14 + 7.43% respectively). We do find that some IRS4^PVH neurons express Trh (40.54 + 1.10%), and more than half of the TRH^PVH neuronal population expresses Irs4 mRNA (60.43 + 3.14%). Taken together, these data suggest that Irs4 expression marks a circumscribed population of PVH neurons defined by the relative absence of OXT, AVP, and NOS1, but some overlap with CRH, PDYN, and TRH.

IRS4^PVH neurons are capable of regulating both feeding and energy expenditure

Given the published role of IRS4 in energy homeostasis and its expression in the PVH, we sought to determine the ability of these neurons to regulate distinct aspects of energy balance. To achieve this, we employed Cre-dependent DREADD (Designer Receptors Exclusively Activated by Designer Drugs) viruses to acutely modulate neuronal activity in response to peripheral injection of an otherwise inert compound, clozapine N-oxide (CNO)¹⁵. To achieve remote activation of IRS4^PVH neurons, we performed bilateral PVH injections of AAV-Flex-hM3Dq in IRS4-iCre mice (Fig. 2A,B). Following recovery, PVH-directed AAV-Flex-hM3Dq injected IRS4-iCre mice were fasted during the day and injected with either vehicle or CNO at the onset of the dark cycle, a time when feeding normally occurs. Activation of IRS4^PVH neurons results in robust suppression of feeding (Fig. 2C, p = 0.0005, paired t-test, t = 5.680). Feeding effects are not attributable to CNO or its metabolites as a separate cohort of wildtype mice injected with AAV-Flex-hM3Dq failed to suppress feeding with no change in nuclear Fos expression following injection of CNO (Supp. Fig. 2.1A,B). As pan-activation of PVH neurons suppresses feeding and increases energy expenditure, we placed IRS4^PVH mice injected with AAV-Flex-hM3Dq in metabolic chambers to measure energy expenditure and locomotor activity following CNO-mediated activation¹⁰. In the absence of food, activation of IRS4^PVH neurons increases energy expenditure, VO₂ and total activity without a significant change in RER (Fig. 2D–H; VO₂: p = 0.0027, t = 4.897; VO₂ lean body mass (LBM): p = 0.0025, t = 5.001; Energy Expenditure p = 0.0026, t = 4.946; total X activity: p = 0.0007, t = 6.297; all paired t-test). To examine the effect of IRS4^PVH activation on resting energy expenditure (REE), we measured VO₂ at timepoints before and after CNO injection in which physical activity was similar (Fig. 2I–K), as performed previously¹⁰. This demonstrates that IRS4^PVH activation results in increased VO₂ (normalized to bodyweight or LBM) that is independent of increased physical activity (VO₂ REE p = 0.0022, t = 5.113; VO₂/LBM p = 0.0019, t = 5.254). Thus, activation of IRS4^PVH neurons suppresses dark-cycle feeding and promotes energy expenditure in the absence of food.

IRS4^PVH neurons project to hindbrain and spinal cord regions

To identify the neural circuits engaged by IRS4^PVH neurons, we used injection of a Cre-dependent adenovirus, synaptophysin-mCherry (syn-mCherry) in the PVH area to label the IRS4^PVH synaptic terminals. Unilateral injection of syn-mCherry (Fig. 3A) in the PVH area of IRS4-iCre mice identifies robust IRS4^PVH projections to hindbrain projection targets including the parabrachial nucleus (PBN, Fig. 3B), nucleus of the solitary tract (NTS), and the dorsal motor nucleus of the vagus (DMV) (Fig. 3C). IRS4^PVH neurons also send projections to the median eminence, a site important for endocrine control of pituitary function (Fig. 3D). In addition to hindbrain regions, syn-mCherry projections were identified in the intermediolateral column (IML) of the thoracic spinal cord in close proximity to choline acetyltransferase (ChAT)-producing neurons, suggesting a circuit mechanism for the regulation of sympathetic activity by IRS4^PVH neurons (Fig. 3E). Of note, these results are strikingly similar to projections originating from NOS1^PVH neurons, despite the fact that these populations do not appear to overlap in the PVH¹⁰.

Projection-specific modified rabies tracing identifies unique inputs to IRS4^PVH subpopulations

As IRS4^PVH neurons project to various brain regions implicated in feeding and energy expenditure, we hypothesized that the afferent input to distinct IRS4^PVH circuits might differ based on IRS4^PVH neuronal projection site. To test this hypothesis, we labeled monosynaptic inputs to either NTS-projecting or PBN-projecting IRS4^PVH neurons in the same animal using a modified rabies virus approach that requires Cre-dependent helper virus (AAV-Flex-TVA-B19G) expression. Due to the limited efficacy and applicability of available helper virus reagents for our desired approach, we generated a Cre-dependent helper virus that co-expresses both the TVA receptor and B19 glycoprotein (B19G) via a self-cleaving 2A peptide linker (Fig. 4A). Modified rabies virus (EnvA-ΔG-mCherry (rabies-mCherry, Fig. 4B) or EnvA-ΔG-GFP (rabies-GFP, Fig. 4C)) cannot enter cells without the TVA receptor and is modified to express a fluorescent protein (mCherry or GFP) instead of B19G^16,17. Therefore, infection of the modified rabies virus requires viral expression of the TVA receptor and retrograde transport of rabies-mCherry or rabies-GFP requires viral expression of the B19G (Fig. 4D). The fidelity of this system is demonstrated by a lack of rabies-mCherry expression in the brain of Sim1-Cre mice in which the helper virus injection missed the PVH (determined by a lack of 2A staining in the PVH), despite rabies-mCherry injection into the NTS (Supp. Fig. 4.1A,B). In this approach, neurons upstream of primary infected neurons theoretically do not express Cre recombinase, and therefore do not produce B19G; this limits rabies-mCherry or rabies-GFP expression to monosynaptic inputs to IRS4^PVH neurons.

Cre-dependent expression of the TVA receptor throughout the cell body and synaptic terminals of transduced neurons allows terminal-specific rabies infection¹⁸. To determine if subpopulations of IRS4^PVH neurons might be engaged by discrete afferent inputs, we performed dual rabies virus injections at anatomically separable projection targets in the same mouse (Fig. 4D). Three weeks following helper virus injection, rabies-mCherry was injected in the NTS whereas rabies-GFP was injected in the PBN. Following 5 days of incubation, we found that IRS4^PVH neurons that project to the NTS or PBN are largely distinct as evidenced by the lack of significant fluorescence colocalization in the PVH (colocalized cells: n = 27 ± 5.7 cells, n = 2 mice). The fact that some co-localization between GFP and mCherry occurs in the PVH suggests the existence of PVH neurons capable of regulating both the NTS and PBN presumably either through collateralization or intra-PVH microcircuitry (Fig. 4E–G).

Consistent with published literature examining PVH circuitry, our rabies monosynaptic labeling demonstrates that the arcuate nucleus (ARC) is an upstream site of NTS-projecting IRS4^PVH neurons (Fig. 4H,H^II)¹⁹. Additional hypothalamic sites engaging NTS-projecting IRS4^PVH neurons include the lateral hypothalamic area (LHA, Fig. 4H^I) and the dorsomedial hypothalamus (DMH, Fig. 4H), whereas sites upstream of PBN-projecting IRS4^PVH neurons largely include the ventromedial hypothalamus (VMH) and LHA (Fig. 4H). Although monosynaptic rabies tracing is not a quantitative methodology, a small number of LHA neurons co-express GFP and mCherry, suggesting LHA modulation of both IRS4^PVH-PBN and IRS4^PVH-NTS circuits (Fig. 4H^I, n = 8 ± 11.3 cells, n = 2 mice). In contrast, very few afferent neurons in the ARC co-express GFP and mCherry (n = 2 ± 2.1 cells, n = 2 mice). Forebrain sites including the preoptic area (POA, Fig. 4L^II) and bed nucleus of the stria terminalis (BNST, Fig. 4L^I) include largely non-overlapping populations upstream of both IRS4^PVH circuits, suggesting distinct forebrain circuits may modulate IRS4^PVH neuronal function.

IRS4^PVH neurons are necessary for normal feeding and energy balance

To test the necessity of IRS4^PVH neuron activity in physiologic body weight regulation, we permanently silenced IRS4^PVH neurons using a Cre-dependent tetanus toxin virus (AAV-Flex-TetTox) that cleaves the SNARE protein, synaptobrevin, and inhibits synaptic vesicle release²⁰. This construct has been modified to express the A subunit and does not travel retrogradely, therefore limiting neuronal silencing to IRS4 Cre-expressing neurons²¹. We performed bilateral PVH injections of AAV-Flex-TetTox in IRS4-iCre mice (Fig. 5A,B). In comparison to control Cre-dependent viral injections into the PVH of IRS4-iCre mice (PVH^Flex) or AAV-Flex-TetTox injections in the PVH of wildtype mice (WT^TetTox), mice with IRS4^PVH neuronal silencing show modest obesity within one week of injection (Fig. 5C: PVH^TetTox v. WT^TetTox p = 0.0162; Fig. 5D: PVH^TetTox v. WT^TetTox p = 0.0008, PVH^TetTox v. PVH^Flex p = 0.0003; mixed effects analysis followed by Tukey’s post-hoc). Obesity following elimination of IRS4^PVH signaling is likely driven primarily by early hyperphagia, demonstrated by increased food intake in the second week of the study (Fig. 5E, PVH^TetTox v. WT^TetTox p = 0.0303; one-way ANOVA followed by Tukey’s post-hoc). Mice with silenced IRS4^PVH neurons demonstrate a non-significant trend towards decreased energy expenditure during the second and third weeks of the study (Fig. 5G,I,J, energy expenditure p = 0.074; RER p = 0.075; one-way ANOVA), without changes in total X activity (Fig. 5H). Body composition analysis indicates that IRS4^PVH neuronal silencing leads to an increased fat percentage at both early (Fig. 5F, left; PVH^TetTox v. PVH^Flex p = 0.0259, one-way ANOVA followed by Tukey’s post-hoc) and late (Fig. 5F, right; PVH^TetTox v. WT^TetTox p = 0.0377; one-way ANOVA followed by Tukey’s post-hoc) time points after injection. Unilateral IRS4^PVH neuronal silencing was also associated with increased bodyweight throughout the course of the experiment, with trends toward similar effects on feeding and energy expenditure (Supp. Table 5.1, one-way ANOVA followed by Tukey’s post-hoc if applicable).

IRS4^PVH neurons are dispensable for melanocortin-induced feeding suppression

Given the important role of the PVH in mediating melanocortin-induced satiety, and the identification of numerous ARC inputs to IRS4^PVH neurons, we hypothesized that IRS4^PVH neurons might contain melanocortin 4 receptors (MC4R) and participate in melanocortin agonist-induced anorexia. To test this, we performed in situ hybridization for Mc4r and Irs4 in wildtype mice (Fig. 6A). Although most IRS4^PVH neurons do not contain Mc4r mRNA (9.67% + 1.11% of IRS4^PVH with Mc4R, n = 3 mice), a significant fraction of MC4R^PVH neurons do express Irs4 mRNA (53.66% + 1.13%). To test the physiologic importance of melanocortin action in IRS4 neurons, we attempted to delete MC4R expression from IRS4 neurons by crossing IRS4-iCre and the Cre-dependent lox-Mc4R mouse line⁷. Unfortunately, developmental expression of Cre recombinase from the IRS4-iCre allele resulted in germline deletion of Mc4R (data not shown). We then tested the ability of the melanocortin agonist melanotan-II (MTII) to suppress dark cycle feeding in mice with AAV-Flex-TetTox or control injections in the PVH at 4–5 weeks post-injection. Despite the inability to transmit information from IRS4^PVH neurons (and therefore a significant portion of MC4R^PVH neurons), MTII injection (150 ug/mouse) still suppressed both two and four hour feeding in all cohorts of mice, suggesting that IRS4^PVH neuron activity is not required for the melanocortin feeding response (Fig. 6B,C; two-way repeated measures ANOVA vehicle vs. MT2; two hour PVH^TetTox p = 0.0312, t = 2.714, WT^TetTox p = 0.0001, t = 4.763, PVH^Flex p < 0.0001, t = 6.113; four-hour PVH^TetTox p = 0.0535, t = 2.486, WT^TetTox p = 0.0025, t = 3.681, PVH^Flex p = −0.0004, t = 4.355).

Discussion

The combination of genetic mouse models with site-specific delivery of chemogenetic and optogenetic tools has greatly advanced our understanding of the role of the PVH in modulating energy balance through feeding and/or energy expenditure. Nonetheless, few studies have genetically identified specific PVH populations crucial for these functions. Our previous work suggests the importance of a non-OXT Nos1^PVH population in feeding regulation¹⁰. Here, we identify a different (non-OXT and non-NOS1^PVH) population expressing insulin receptor substrate-4 (Irs4) that is necessary for normal bodyweight maintenance.

Genetic deletion of Irs4 results in modest obesity and altered glucose homeostasis; whether this phenotype reflects simply a loss of Irs4 function or developmental compensation in response to Irs4 loss is unknown^12,22. In our approach, we used site and temporal specific manipulations in adult organisms to circumvent developmental issues and directly examine the function of IRS4-expressing cells predominantly within the PVH. Whereas chemogenetic activation reveals the potential function of IRS4^PVH neuronal function in adult mice, neuronal silencing with tetanus toxin addresses the physiologic necessity of this population in various energy balance parameters. Indeed, permanent inhibition of IRS4^PVH-specific synaptic release results in obesity due to altered feeding and a trend toward lower energy expenditure.

An important caveat to this study flows from its methodologic approach. Stereotaxic injections to defined brain regions are not always exclusively limited to cells within a classically defined neuroanatomical region. In our study we have excluded data for physiologic analyses from animals with significant extra-PVH viral transduction. All analyses were performed using data from animals with limited extra-PVH viral expression. However, post-hoc immunocytochemistry of brain sections from analyzed animals revealed transduction of IRS4 Cre-expressing cells adjacent to the PVH. The contribution of these subparaventricular and periventricular IRS4 cells to the outputs measured cannot be determined from the current study. In our study there were no cases of PVH-targeted injections that were limited to just the subparaventricular or periventricular IRS4-expressing cells that would allow physiologic comparisons with the PVH and peri-PVH-transduced cohort. Highly refined injections limited to cells solely in the PVH or solely in adjacent areas would be needed to completely define the contributions of these peri-PVH IRS4-expressing cells to energy balance control.

Cre-dependent efferent tract tracing suggests that the circuitries engaged by IRS4^PVH neurons used to regulate feeding and energy expenditure are similar to those identified for both NOS1^PVH and MC4R^PVH neurons and include the PBN and NTS and sparse projections to the spinal cord^7,10,11. While our current studies cannot discriminate which projection site is relevant for controlling feeding and energy expenditure, it is possible that IRS4^PVH neurons projecting to the PBN contribute to feeding modulation since the PBN is the relevant output in MC4R-mediated feeding suppression¹¹. However, our data indicate that IRS4^PVH neurons and MC4R^PVH neurons overlap only in part, and that MC4R-mediated feeding suppression is unaffected by IRS4^PVH neuronal silencing. Therefore, it remains possible that other projection output sites may drive the IRS4^PVH-mediated satiety response.

Given their minimal overlap in the PVH, the functional redundancy of the IRS4^PVH and NOS1^PVH neuronal populations in energy expenditure and feeding control is intriguing. A recent report suggests that nonoverlapping MC4R^PVH and PDYN^PVH neuron populations function together to coordinate a full PVH satiety response²³. The contribution of other non-MC4R PVH neurons in energy expenditure control is less clear. Here, we demonstrate that despite neuronal silencing of IRS4^PVH neurons, which includes half of the MC4R^PVH population, the satiety response to the melanocortin agonist MT-II remains intact. Thus, the anorectic response to melanocortin agonist is not dependent on IRS4^PVH neurons, even though they compromise ~50% of the MC4R^PVH population. Although most IRS4^PVH neurons do not express Pdyn, chemogenetic activation of IRS4^PVH will activate a subset of PDYN^PVH neurons. Whether this subset is responsible for the feeding effects seen following IRS4^PVH activation remains to be determined. IRS4 and TRH overlap significantly in the PVH. However, feeding suppression following IRS4^PVH activation is unlikely mediated by TRH^PVH neurons since activation of this population has been shown to promote feeding by targeting orexigenic AgRP neurons in the ARC²⁴. Future studies will be needed to determine whether the IRS4/TRH^PVH subset modulates energy expenditure through direct effects on autonomic output or alterations in the pituitary-thyroid axis. In addition, whether distinct PVH populations control feeding and energy expenditure via disparate projection sites (e.g. PBN vs. NTS vs. spinal cord) requires additional investigation.

The PVH is a hypothalamic relay station for energy balance control. It receives dense innervation from sites critical for feeding and energy expenditure regulation, integrates this incoming energy balance information and then transmits an output signal to hindbrain sites to achieve appropriate physiologic and behavioral responses^19,25,26,27. Whether PVH inputs can be mapped on to distinct PVH outputs (either anatomical or physiological) is not known. Here, we used monosynaptic rabies tracing to identify the possibility of unique afferent inputs to NTS-projecting versus PBN-projecting IRS4^PVH neurons. We demonstrate that NTS-projecting IRS4^PVH neurons receive dense innervation from the ARC, confirming this approach in a historically defined circuit. Additionally, PBN-projecting IRS4^PVH neurons receive innervation from the VMH. Given the role for direct PVH connections to the PBN in mediating MC4R-induced satiety, it is possible that the VMH-IRS4^PVH-PBN circuit is relevant in feeding control, though future studies will be necessary to test the function of this circuit and better characterize its genetic signature¹¹. It is of interest that a few LHA neurons appear to be upstream of both PBN and NTS-projecting IRS4^PVH neurons. Given the role for the LHA in controlling both energy expenditure and feeding behavior, this raises the possibility that the PVH input neurons originating in the LHA might be coordinating distinct energy balance parameters via divergent IRS4^PVH circuits^28,29,30.

PVH neurons are predominantly glutamatergic and highly interconnected through PVH interneurons that may coordinate neural activity between PVH subsets^31,32,33. Our modified rabies tracing findings suggest that projection-defined IRS4^PVH neurons are likely innervated by other local PVH populations based on the dense expression of rabies virus throughout the PVH (Fig. 4E–G). Since some PVH populations suppress feeding without affecting energy expenditure (i.e. MC4R^PVH), whereas others increase energy expenditure absent of feeding regulation (i.e. OXT^PVH), it seems likely that separate circuitries exist to coordinate these nodes. By extension, this suggests that some PVH populations (such as OXT^PVH) are differentially connected and/or insulated from other PVH circuits in terms of feeding regulation. One potential model for PVH action could include a final common output from the PVH that is responsible for coordinating feeding regulation. In such a scenario, NOS1^PVH and/or IRS4^PVH neurons might lie upstream of or parallel to MC4R^PVH neurons and coordinate feeding suppression via projections to the PBN. Certainly, connections between separate PVH populations are well documented^34,35,36. Moreover, the dense PVH interconnectivity highlighted by projection-specific monosynaptic retrograde tracing suggests the possibility that anatomically and functionally separable IRS4^PVH neuronal circuits can be coordinately regulated in order to promote an orchestrated physiologic output through simultaneous transmission to multiple brain sites.

Taken together, our results clearly demonstrate that IRS4^PVH neurons are a genetically defined PVH population capable of controlling feeding behavior and overall energy balance, presumably through projections to hindbrain and spinal cord regions. Moreover, tetanus toxin sensitive vesicle fusion in IRS4^PVH cells is essential in preventing hyperphagia and obesity. Furthermore, our studies support the concept of a complex, intra-PVH network that regulates hindbrain structures previously shown to control energy balance parameters. While the significance of this local communication between PVH subpopulations in the control of distinct aspects of energy balance remains to be elucidated, further characterization of the composition and connectivity of individual PVH populations is necessary to fully understand the control of feeding and energy expenditure by an essential hypothalamic output center.

Materials and Methods

Experimental animals

IRS4-ires-Cre (IRS4-iCre) mice were generated using methods previously described³⁷. Briefly, genomic DNA including the 3’ UTR of the murine Irs4 gene was PCR amplified from R1 ES cells and cloned into a plasmid for insertion of an Frt-flanked neomycin selection cassette followed by an internal ribosomal entry sequence fused to a Cre recombinase transgene (iCre) between the STOP codon and the polyadenylation site. Constructs were linearized and electroporated into R1 ES cells by the University of Michigan Transgenic Animal Model Core. Correctly targeted ES cells were identified by quantitative real-time PCR and Southern blots and then injected into C57Bl/6J blastocysts to generate chimeric animals. Chimeras were then bred to C57Bl/6J females to confirm germline transmission and generate the IRS4-neo-iCre mice. To remove the Frt-flanked neo cassette, IRS4-neo-iCre mice were then bred to Flp deleter mice (Jax 012930).

Adult male mice (8–16 weeks old) were used for all studies. Irs4 is located on the X-chromosome which confounds experiments using IRS4-iCre in females given the random lyonization of the X chromosome. All animals were bred and housed within our colony according to guidelines approved by the University of Michigan Committee on the Care and Use of Animals. Unless otherwise noted, mice were provided ad libitum access to food and water. All mice were acclimatized to intraperitoneal (i.p.) injections three days prior to any experimental i.p. injection.

Generation of modified rabies virus

Replication deficient modified rabies virus containing fluorescent reporters in place of the B19 glycoprotein (EnvA-ΔG-mCherry and EnvA-ΔG-GFP) were generated in the University of Michigan viral vector core using conditions previously described^16,17.

Stereotaxic injections

Stereotaxic injections were performed in IRS4-iCre and non-transgenic (WT) mice as previously described¹⁰. Briefly, mice were placed in a digital stereotaxic frame (Model 1900, Kopf Instruments) under isofluorane and provided with pre-surgical analgesia. Viral injections were performed using a pressurized picospritzer system coupled to a pulled glass micropipette (coordinates from bregma: PVH: A/P = −0.500, M/L = +/− 0.220, D/V = −4.800). For tract tracing experiments, 50 nl of the adenoviral synatophysin-mCherry terminal tracer (Ad-iN/syn-mCherry³⁸) was unilaterally injected in IRS4-iCre mice. For functional analysis of IRS4^PVH neurons, bilateral PVH injections of AAV-Flex-hM3Dq-mCherry (AAV-Flex-hM3Dq, purchased from UNC Vector Core), AAV-Flex-TetTox (purchased from the Stanford Viral Vector core) or control injections of AAV-Flex-GFP were performed in IRS4-iCre or WT mice (50 nl/side). For analysis of monosynaptic upstream inputs to IRS4^PVH neurons, IRS4-iCre mice were unilaterally injected with AAV-Flex-TVA-B19G in the PVH and allowed to recover for at least 21 days to ensure adequate helper virus expression throughout both cell bodies and terminals³⁹. Mice then underwent a second surgery with dual stereotaxic injections into ipsilateral PVH projection targets with rabies-GFP in the PBN (A/P = −4.770, M/L = +/− 1.35, D/V = −2.8) and rabies-mCherry injected into the NTS. NTS injections were performed as previously described, whereby the fourth ventricle was identified and used as a geographic landmark to determine the site of injection¹⁰. A glass micropipette was lowered into the site (D/V: −0.550) and ~25 nl of virus was injected. Mice injected with the Ad-iN/syn-mCherry tracer were individually housed for five days following injection to allow for viral transduction and protein transport before perfusion, whereas mice injected with modified rabies virus were perfused seven days following rabies virus injections. Mice injected with AAV-Flex-hM3Dq were allowed to recover for fourteen days following surgery before further experiments were performed.

Effect of PVH^IRS4 neuronal activation on feeding and energy expenditure

Following recovery, IRS4-iCre + AAV-Flex-hM3Dq mice underwent feeding and energy expenditure assays as previously described¹⁰. Briefly, to measure changes in energy expenditure, IRS4-iCre + AAV-Flex-hM3Dq mice were acclimatized for two consecutive days to the Comprehensive Laboratory Monitoring System (CLAMS, Columbus Instruments) in the University of Michigan’s Small Animal Phenotyping Core to obtain multi-parameter analysis including open circuit calorimetry and activity via optical beam breaks. Following acclimatization, food was removed from metabolic cages during the light cycle on experimental days beginning two hours prior to experiments. Mice received an i.p. injection of vehicle (10% β-cyclodextrin, Sigma) and CLAMS measurements were analyzed for the following four hours. Mice remained in the chambers with food access at the onset of the dark cycle and the experiment repeated at the same time the following day instead with i.p. injection of CNO (0.3 mg/kg in 10% B-cyclodextrin). While measurements were performed throughout the duration of the experiment, data shown are averaged over the 4 hours following injection of vehicle or CNO. Resting energy expenditure data shown was determined by analyzing data oxygen consumption values at data points in which activity levels were approximately matched during the four hours before and after CNO administration. In experiments aimed to identify feeding changes induced by IRS4^PVH neuronal activation, mice were fasted during the day and received an i.p. injection of vehicle at the onset of the dark cycle with the presentation of food. Food intake was measured at two and four hours after injection and the experiment repeated the following day upon injection of CNO at the onset of the dark cycle. In a separate cohort of mice, the effects of CNO were tested on wildtype mice injected with AAV-Flex-hM3Dq and compared to IRS4-iCre mice injected with AAV-Flex-hM3Dq. In these experiments, CNO or vehicle (0.9% sodium chloride) injections were counterbalanced and performed 4 days apart.

Longitudinal bodyweight, food intake, and calorimetry measurements

Mice injected with AAV-Flex-TetTox or control viruses were allowed to recover for 7 days before weekly body weight and food intake measurements began. Energy expenditure was determined using the Comprehensive Laboratory Monitoring System (CLAMS, Columbus Instruments) in the University of Michigan’s Small Animal Phenotyping Core to obtain multi-parameter analysis including open circuit calorimetry and activity via optical beam breaks between 11–24 days post-injection. Mice were allowed to acclimatize to the chambers for two days, followed by VO₂ and locomotor activity data collection for three consecutive days. Analysis of CLAMS data was averaged across all three days of recording. Body composition analysis (Minispec LF90 II, Bruker Optics) was performed at both two weeks and 7 weeks following injection.

MT-II-induced feeding suppression

Five weeks following viral injection, IRS4-iCre mice injected with AAV-Flex-TetTox and appropriate controls were fasted during the light cycle (10:00–18:00). At the onset of the dark cycle, mice received an i.p. injection of 0.9% sodium chloride (APP Pharmaceuticals, 63323-186-10) or melanotan-II (MT-II, 150 ug/mouse, Bachem) and ad libitum access to food. Food intake was measured two and four hours post injection. The following week, injections were counter balanced and corresponding food intake measured.

Perfusion and Immunohistochemistry (IHC)

At the end of all experiments, mice were perfused to verify viral injection sites. Briefly, mice were deeply anesthetized with an overdose of pentobarbital (150 mg/kg, IP) and transcardially perfused with sterile PBS followed by 10% neutral buffered formalin or 4% paraformaldehyde (for perfusions with spinal cord removal. Brains and spinal cords (syn-mCherry injections only) were removed, post-fixed, and dehydrated in 30% sucrose before sectioning into 30 μm slices on a freezing microtome (Leica). Coronal brain sections were collected in four representative sections whereas longitudinal thoracic spinal cord sections were collected in three representative sections and stored at −20 °C. For 2A peptide and cFos immunohistochemistry (IHC), free floating brain and spinal cord sections were pretreated with 30% H₂O₂ to remove endogenous peroxidase activity and then blocked with normal goat or donkey serum and incubated in primary antibody overnight (rabbit anti-2A 1:1,000, Millipore ABE457; rabbit anti-cFos). Detection of primary antibody was performed by avidin-biotin/diaminobenzidine (DAB) method (Biotin-SP-conjugated Donkey Anti-Rabbit, Jackson Immunoresearch, 1:200; ABC kit, Vector Labs; DAB reagents, Sigma). mCherry and choline acetyltransferase (ChAT) were detected using with primary antibodies for dsRed (rabbit 1:1000, Clontech, 632496) or TdTomato (rat, 1:1000, Kerafast 16D7) and ChAT (spinal cords only; goat, 1:500, Millipore AB144P) respectively followed by secondary immunofluorescence detection with donkey anti-rabbit-Alexa 568 or donkey anti-goat-Alexa 488 (1:200, Invitrogen). For PVH colocalization, rabies experiments, cFos (non-DAB method) and TetTox-GFP expression, IHC immunostaining was performed using primary antibodies for cFos (rabbit, 1:1000, Cell Signaling 9F6), GFP (rabbit 1:20,000, Invitrogen A6455), nNos1 (sheep 1:1500, (24), kindly provided by Dr. Vincent Prevot), neurophysin (goat, 1:1000, Santa Cruz Biotechnology, sc-7810) and copeptin (goat 1:1000, Santa Cruz Biotechnology, sc-7812). For all AAV-TetTox and AAV-hM3Dq injections, bilateral or unilateral PVH hit sites were verified and misses eliminated from data analysis, with viral injections that modestly leaked into the peri-PVH included in the PVH groups. Viral leak into any other area outside of this region were excluded. Imaging was performed using an Olympus BX-53 upright microscope with G6000 camera.

In situ hybridization

Mice were deeply anesthetized with an overdose of inhaled isofluorane and brains removed and flash frozen in 2-methylbutane. Brains were sectioned into 16 μm sections onto glass slides using a cryostat (Leica CM 1950) and stored at −80 °C. The probes were purchased from Advanced Cell Diagnostics, and the assays were performed according to the manufacturer’s protocol. The sections were fixed in cold 10% formalin for 1 hour, followed by dehydration in 50% and 75% ethanol for 5 minutes each, and 100% ethanol twice. Sections were dried at 40 °C for 30 minutes. For fluorescent staining, sections were pretreated in protease IV for 30 minutes, washed in PBS twice, and then incubated with the desired probes for 2 hours and then washed twice in 1x wash buffer (ACD, 310091) for 2 minutes each. Amplification and detection steps were performed using the RNAscope® Fluorescent Multiplex Reagent Kit (320850). Sections were incubated with Amp1 for 30 min, Amp2 for 15 min, Amp3 for 30 min, and Amp 4 Alt C for 15 min. There were 2 washes between each amplification, and all amplifications were performed at 40 °C in the EZ Hybridization oven. To demonstrate overlapping expression of IRS4 and Cre mRNA, IRS4 and Cre probes were used. To quantify overlapping expression of IRS4 and CRH, PDYN and TRH, fluorescent probes were used. For the tissues exposed to the IRS4, CRH, PDYN, TRH and Cre probes, the slides were stained with DAPI for 30 seconds before coverslipping using Prolong Gold antifade reagent (Invitrogen). To investigate MC4R and IRS4 expression in the PVH, chromogen staining was conducted using the RNAscope® 2.5 HD Duplex Reagent Kit (ACD 320701). The sections were treated with H₂O₂ for 10 min and then incubated with the protease K IV for 30 min. After hybridization with probes against MC4R and IRS4 mRNA, the sections were washed 2 times, followed with amplification from Amp1 to Amp6 with 2 washes in between. To detect the red signal component, Red-B was diluted 1:60 in component Red-A and incubated on the tissue for 10 minutes at room temperature. Slides were then rinsed two times in wash buffer to stop the chromogen reaction. Amplification continued with Amp7 through Amp10, followed by detection of the green signal, which was achieved by diluting component Green-B 1:50 in component Green-A and incubating for 10 minutes at room temperature. Counterstaining was performed by immersing the slides in 50% hematoxylin for 30 seconds. The slides were then dried and mounted in VectaMount mounting medium (Vector Laboratories, INC). Imaging for fluorescent staining was performed using an Olympus BX-53 microscope with a G6000 camera. Imaging for the chromogen staining used an Olympus BX-51 microscope with a DP80 camera (Olympus). For the purposes of quantification, images from the coronal sections were processed uniformly using Photoshop (Adobe) to remove background and to mark cells that expressed a given probe. Cells (indicated by DAPI/hematoxylin stain) determined to be positive for each probe were quantified using ImageJ and summed for each mouse, with the percentages of overlapping expression averaged between the mice.

Statistical analysis

Paired t-tests, one-way ANOVAs followed by Tukey post-hoc tests (if applicable), two-way ANOVAs followed by Sidak’s multiple comparisons (if applicable), or mixed model analyses were calculated using GraphPad Prism 8 as appropriate. Significance was determined for p < 0.05.

Data availability

All data generated or analysed during this study are included in this published article (and its Supplementary Information files).

References

Locke, A. E. et al. Genetic studies of body mass index yield new insights for obesity biology. Nature 518, 197–206 (2015).
Article CAS Google Scholar
Sawchenko, P. E. & Swanson, L. W. Immunohistochemical identification of neurons in the paraventricular nucleus of the hypothalamus that project to the medulla or to the spinal cord in the rat. Journal of Comparative Neurology 205, 260–272 (1982).
Article CAS Google Scholar
Schwartz, M. W., Woods, S. C., Porte, D., Seeley, R. J. & Baskin, D. G. Central nervous system control of food intake. Nature 404, 661 (2000).
Article CAS Google Scholar
Caverson, M. M., Ciriello, J. & Calaresu, F. R. Paraventricular nucleus of the hypothalamus: an electrophysiological investigation of neurons projecting directly to intermediolateral nucleus in the cat. Brain Research 305, 380–383 (1984).
Article CAS Google Scholar
Gold, R. M. Hypothalamic Obesity: The Myth of the Ventromedial Nucleus. Science 182, 488–490 (1973).
Article CAS ADS Google Scholar
Sims, J. S. & Lorden, J. F. Effect of paraventricular nucleus lesions on body weight, food intake and insulin levels. Behavioural Brain Research 22, 265–281 (1986).
Article CAS Google Scholar
Shah, B. P. et al. MC4R-expressing glutamatergic neurons in the paraventricular hypothalamus regulate feeding and are synaptically connected to the parabrachial nucleus. PNAS 111, 13193–13198 (2014).
Article CAS ADS Google Scholar
Balthasar, N. et al. Divergence of Melanocortin Pathways in the Control of Food Intake and Energy Expenditure. Cell 123, 493–505 (2005).
Article CAS Google Scholar
Xi, D., Gandhi, N., Lai, M. & Kublaoui, B. M. Ablation of Sim1 Neurons Causes Obesity through Hyperphagia and Reduced Energy Expenditure. PLOS ONE 7, e36453 (2012).
Article CAS ADS Google Scholar
Sutton, A. K. et al. Control of Food Intake and Energy Expenditure by Nos1 Neurons of the Paraventricular Hypothalamus. J. Neurosci. 34, 15306–15318 (2014).
Article Google Scholar
Garfield, A. S. et al. A neural basis for melanocortin-4 receptor–regulated appetite. Nature Neuroscience 18, 863–871 (2015).
Article CAS Google Scholar
Sadagurski, M., Dong, X. C., Myers, M. G. & White, M. F. Irs2 and Irs4 synergize in non-LepRb neurons to control energy balance and glucose homeostasis. Molecular Metabolism 3, 55–63 (2014).
Article CAS Google Scholar
Lein, E. S. et al. Genome-wide atlas of gene expression in the adult mouse brain. Nature 445, 168–176 (2007).
Article CAS ADS Google Scholar
Pei, H., Sutton, A. K., Burnett, K. H., Fuller, P. M. & Olson, D. P. AVP neurons in the paraventricular nucleus of the hypothalamus regulate feeding. Molecular Metabolism 3, 209–215 (2014).
Article CAS Google Scholar
Alexander, G. M. et al. Remote Control of Neuronal Activity in Transgenic Mice Expressing Evolved G Protein-Coupled Receptors. Neuron 63, 27–39 (2009).
Article CAS Google Scholar
Wickersham, I. R. et al. Monosynaptic Restriction of Transsynaptic Tracing from Single, Genetically Targeted Neurons. Neuron 53, 639–647 (2007).
Article CAS Google Scholar
Wall, N. R., Wickersham, I. R., Cetin, A., Parra, M. D. L. & Callaway, E. M. Monosynaptic circuit tracing in vivo through Cre-dependent targeting and complementation of modified rabies virus. PNAS 107, 21848–21853 (2010).
Article CAS ADS Google Scholar
Betley, J. N., Cao, Z. F. H., Ritola, K. D. & Sternson, S. M. Parallel, Redundant Circuit Organization for Homeostatic Control of Feeding Behavior. Cell 155, 1337–1350 (2013).
Article CAS Google Scholar
Cowley, M. A. et al. Integration of NPY, AGRP, and Melanocortin Signals in the Hypothalamic Paraventricular Nucleus: Evidence of a Cellular Basis for the Adipostat. Neuron 24, 155–163 (1999).
Article CAS Google Scholar
Verderio, C. et al. Tetanus Toxin Blocks the Exocytosis of Synaptic Vesicles Clustered at Synapses But Not of Synaptic Vesicles in Isolated Axons. J. Neurosci. 19, 6723–6732 (1999).
Article CAS Google Scholar
McMahon, H. T. et al. Tetanus toxin and botulinum toxins type A and B inhibit glutamate, gamma-aminobutyric acid, aspartate, and met-enkephalin release from synaptosomes. Clues to the locus of action. J. Biol. Chem. 267, 21338–21343 (1992).
CAS Google Scholar
Fantin, V. R., Wang, Q., Lienhard, G. E. & Keller, S. R. Mice lacking insulin receptor substrate 4 exhibit mild defects in growth, reproduction, and glucose homeostasis. American Journal of Physiology-Endocrinology and Metabolism 278, E127–E133 (2000).
Article CAS Google Scholar
Li, M. M. et al. The Paraventricular Hypothalamus Regulates Satiety and Prevents Obesity via Two Genetically Distinct Circuits. Neuron, https://doi.org/10.1016/j.neuron.2019.02.028 (2019).
Krashes, M. J. et al. An excitatory paraventricular nucleus to AgRP neuron circuit that drives hunger. Nature 507, 238–242 (2014).
Article CAS ADS Google Scholar
Marsh, D. J. et al. Response of melanocortin–4 receptor–deficient mice to anorectic and orexigenic peptides. Nature Genetics 21, 119–122 (1999).
Article CAS Google Scholar
Kishi, T. et al. Expression of melanocortin 4 receptor mRNA in the central nervous system of the rat. Journal of Comparative Neurology 457, 213–235 (2003).
Article CAS Google Scholar
Swanson, L. W. & Kuypers, H. G. The paraventricular nucleus of the hypothalamus: cytoarchitectonic subdivisions and organization of projections to the pituitary, dorsal vagal complex, and spinal cord as demonstrated by retrograde fluorescence double-labeling methods. J. Comp. Neurol. 194, 555–570 (1980).
Article CAS Google Scholar
Brown, J. A., Woodworth, H. L. & Leinninger, G. M. To ingest or rest? Specialized roles of lateral hypothalamic area neurons in coordinating energy balance. Front. Syst. Neurosci. 9 (2015).
Woodworth, H. L. et al. Lateral Hypothalamic Neurotensin Neurons Orchestrate Dual Weight Loss Behaviors via Distinct Mechanisms. Cell Reports 21, 3116–3128 (2017).
Article CAS Google Scholar
Pei, H. et al. Lateral Hypothalamic Mc3R-Expressing Neurons Modulate Locomotor Activity, Energy Expenditure, and Adiposity in Male Mice. Endocrinology 160, 343–358 (2019).
Article CAS Google Scholar
Daftary, S. S., Boudaba, C., Szabó, K. & Tasker, J. G. Noradrenergic Excitation of Magnocellular Neurons in the Rat Hypothalamic Paraventricular Nucleus via Intranuclear Glutamatergic Circuits. J. Neurosci. 18, 10619–10628 (1998).
Article CAS Google Scholar
Csáki, Á., Kocsis, K., Halász, B. & Kiss, J. Localization of glutamatergic/aspartatergic neurons projecting to the hypothalamic paraventricular nucleus studied by retrograde transport of [3H]d-aspartate autoradiography. Neuroscience 101, 637–655 (2000).
Article Google Scholar
Latchford, K. J. & Ferguson, A. V. ANG II-induced excitation of paraventricular nucleus magnocellular neurons: a role for glutamate interneurons. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 286, R894–R902 (2004).
Article CAS Google Scholar
Pol, A. N. V. D. The magnocellular and parvocellular paraventricular nucleus of rat: Intrinsic organization. Journal of Comparative Neurology 206, 317–345 (1982).
Article Google Scholar
Herman, J. P., Cullinan, W. E., Ziegler, D. R. & Tasker, J. G. Role of the paraventricular nucleus microenvironment in stress integration*. European Journal of Neuroscience 16, 381–385 (2002).
Article Google Scholar
Liposits, Z., Paull, W. K., Sétáló, G. & Vigh, S. Evidence for local corticotropin releasing factor (CRF)-immunoreactive neuronal circuits in the paraventricular nucleus of the rat hypothalamus. An electron microscopic immunohistochemical analysis. Histochemistry 83, 5–16 (1985).
Article CAS Google Scholar
Greenwald-Yarnell, M. L. et al. ERα in Tac2 Neurons Regulates Puberty Onset in Female Mice. Endocrinology 157, 1555–1565 (2016).
Article CAS Google Scholar
Opland, D. et al. Loss of neurotensin receptor-1 disrupts the control of the mesolimbic dopamine system by leptin and promotes hedonic feeding and obesity. Molecular Metabolism 2, 423–434 (2013).
Article CAS Google Scholar
Meek, T. H. et al. Functional identification of a neurocircuit regulating blood glucose. PNAS 113, E2073–E2082 (2016).
Article CAS Google Scholar

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Acknowledgements

Core support (Animal Phenotyping) was provided by the Michigan Diabetes Research and Training Center and Nutrition and Obesity Research Center. This work was supported by the US National Institutes of Health (F31 NS082027 to AKS, F31 DK122753-01 to IEG, DK104999 to DPO), the Rackham Graduate School Pre-Doctoral Fellowship to AKS, the Michigan Diabetes Research, the Systems and Integrative Biology Training Grant (T32-GM008322 to IEG) and the Training Center Pilot and Feasibility Award (NIH5P60 DK20572 to DPO). We thank Tom Lanigan and the UM Vector Core for generation of the modified rabies virus. We also thank Korri Burnett for technical assistance and members of both the Olson and Myers labs for helpful discussions and technical support.

Author information

These authors contributed equally: Amy K. Sutton and Ian E. Gonzalez.

Authors and Affiliations

Department of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, MI, USA
Amy K. Sutton, Ian E. Gonzalez, Margaret B. Allison, Martin G. Myers & David P. Olson
Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA
Marianna Sadagurski, Michael Rajala & Martin G. Myers
Department of Endocrinology, Children’s Hospital Boston, Boston, MA, USA
Morris F. White
Division of Pediatric Endocrinology, Department of Pediatrics, Michigan Medicine, Ann Arbor, MI, USA
Chunxia Lu, Jessica M. Adams & David P. Olson

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Amy K. Sutton
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Ian E. Gonzalez
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Marianna Sadagurski
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Michael Rajala
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Chunxia Lu
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Margaret B. Allison
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Martin G. Myers
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David P. Olson
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Contributions

A.K.S., I.E.G., M.G.M. and D.P.O. conceived and designed the experiments. A.K.S., I.E.G., J.M.A. and C.L. conducted the studies and collected the data. M.S., M.R., M.B.A. and M.F.W. provided reagents. A.K.S., I.E.G. and D.P.O. analyzed the data and wrote the manuscript.

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Correspondence to David P. Olson.

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Competing interests

D.P.O. and M.G.M. receive research funding from Novo Nordisk and MedImmune. The other authors declare no other competing interests.

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Sutton, A.K., Gonzalez, I.E., Sadagurski, M. et al. Paraventricular, subparaventricular and periventricular hypothalamic IRS4-expressing neurons are required for normal energy balance. Sci Rep 10, 5546 (2020). https://doi.org/10.1038/s41598-020-62468-z

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Received: 13 June 2019
Accepted: 12 March 2020
Published: 26 March 2020
DOI: https://doi.org/10.1038/s41598-020-62468-z

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