United States

Background
Hydrocephalus (HC) is a common pediatric neurosurgical condition characterized by the accumulation of cerebrospinal fluid (CSF) and elevated intracranial pressure. Without treatment, HC causes substantial neurological morbidity and mortality. The gold-standard treatment for HC, CSF shunting, is associated with high rates of shunt infection, obstruction, and malfunction and requires lifelong access to prompt neurosurgical care. Endoscopic third ventriculostomy with choroid plexus cauterization (ETV-CPC) was thus developed as an alternative to CSF shunting in low and middle-income countries (LMICs); however, the impact of this treatment on neurological function or brain development remains unclear.

Methods
The current study details the technical development of an experimental, large animal model of ETV-CPC to examine the neurobiological and neurobehavioral effects of ETV-CPC versus CSF shunting.

Results
Hydrocephalus was induced in juvenile pigs by cisternal injection of 25% kaolin and confirmed with high-resolution MRI after 10-14 days post-induction. For surgical treatment of HC, frameless stereotactic Stealth neuronavigation was registered to the animal&#39;s head and an orthogonal trajectory to the foramen of Monro was planned with entry 1 cm lateral to midline. After incision, a burr hole was fashioned, the dura cauterized, and a ventricular catheter was passed into the right lateral ventricle. After the collection of ~1 ml of CSF for later analyses, the catheter was removed and a flexible ventriculoscope was inserted along the track. The endoscope was navigated through the foramen of Monro and into the 3rd ventricle, where a flexible Bugbee wire was used to make an ETV in the lamina terminalis. After completion of the ETV, the endoscope was withdrawn into the right lateral ventricule, and the choroid plexus was cauterized, beginning at the foramen of Monro and moving toward the atrium/glomus, and then into the temporal horn to the temporal tip. In most cases, the septum pellucidum was incompetent, and the same procedure was used to cauterize the entirety of the choroid plexus in the left lateral ventricle. After the ETV-CPC, the endoscope was removed and a ventricular catheter was affixed to a ventricular reservoir, inserted into the right lateral ventricle, and secured in place with pericranial sutures. The wound was irrigated and closed.

Conclusion
This experimental juvenile porcine model of ETV-CPC offers the opportunity to study the neurobiological and neurobehavioral effects of ETV-CPC and CSF shunting in a novel way. Understanding the long-term effects of these treatments is paramount in identifying the optimal treatment for children with HC.

AMA Research Challenge 2024 

Experimental  Endoscopic Third Ventriculostomy With Choroid Plexus Cauterization: A Novel Model For Physiological Investigation

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AMA Research Challenge 2025 

Join the AMA Research Challenge poster symposium and semifinals to explore top research posters and score posters in the semifinals (an AMA member exclusive opportunity).

Background
Hydrocephalus (HC) is a common pediatric neurosurgical condition characterized by the accumulation of cerebrospinal fluid (CSF) and elevated intracranial pressure. Without treatment, HC causes substantial neurological morbidity and mortality. The gold-standard treatment for HC, CSF shunting, is associated with high rates of shunt infection, obstruction, and malfunction and requires lifelong access to prompt neurosurgical care. Endoscopic third ventriculostomy with choroid plexus cauterization (ETV-CPC) was thus developed as an alternative to CSF shunting in low and middle-income countries (LMICs); however, the impact of this treatment on neurological function or brain development remains unclear.

Methods
The current study details the technical development of an experimental, large animal model of ETV-CPC to examine the neurobiological and neurobehavioral effects of ETV-CPC versus CSF shunting.

Results
Hydrocephalus was induced in juvenile pigs by cisternal injection of 25% kaolin and confirmed with high-resolution MRI after 10-14 days post-induction. For surgical treatment of HC, frameless stereotactic Stealth neuronavigation was registered to the animal's head and an orthogonal trajectory to the foramen of Monro was planned with entry 1 cm lateral to midline. After incision, a burr hole was fashioned, the dura cauterized, and a ventricular catheter was passed into the right lateral ventricle. After the collection of ~1 ml of CSF for later analyses, the catheter was removed and a flexible ventriculoscope was inserted along the track. The endoscope was navigated through the foramen of Monro and into the 3rd ventricle, where a flexible Bugbee wire was used to make an ETV in the lamina terminalis. After completion of the ETV, the endoscope was withdrawn into the right lateral ventricule, and the choroid plexus was cauterized, beginning at the foramen of Monro and moving toward the atrium/glomus, and then into the temporal horn to the temporal tip. In most cases, the septum pellucidum was incompetent, and the same procedure was used to cauterize the entirety of the choroid plexus in the left lateral ventricle. After the ETV-CPC, the endoscope was removed and a ventricular catheter was affixed to a ventricular reservoir, inserted into the right lateral ventricle, and secured in place with pericranial sutures. The wound was irrigated and closed.

Conclusion
This experimental juvenile porcine model of ETV-CPC offers the opportunity to study the neurobiological and neurobehavioral effects of ETV-CPC and CSF shunting in a novel way. Understanding the long-term effects of these treatments is paramount in identifying the optimal treatment for children with HC.

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Background: 
The unfolded protein response (UPR) is activated by stresses in tumor cells, including hypoxia, acidosis, reactive oxygen species, radiation, and chemotherapy. It responds to unfolded/misfolded proteins in the endoplasmic reticulum (ER) by initiating pathways to enhance chaperone expression, boost protein degradation, and reduce protein synthesis, thereby regulating ER stress. If ER homeostasis cannot be restored, the UPR can shift from promoting cell survival to cell death. Targeting the UPR is a novel therapeutic approach for glioblastoma (GBM), especially against GBM stem-like cells (GSCs) that drive tumor regrowth, heterogeneity, and resistance. This strategy also shows potential for use before surgical resection of this aggressive brain tumor.

Methods
We evaluated a series of curcumin derivatives against three GSC lines. MTS assay was used to determine the IC50 of the compounds. Western blot analysis determined protein expression of targets and downstream effectors, including C/EBP Homologous Protein (CHOP), GRP78/Bip, caspase 7, and PARP.

Results
A trimethoxy bis-chalcone compound was identified that induces robust cell death in GSCs, with an average IC50 of just below 300 nM — 100-fold increase in potency compared to curcumin. This bis-chalcone showed minimal toxicity towards normal human mesenchymal stem cells. Western blot revealed that this compound effectively activated the pro-death UPR protein CHOP while reducing the expression of the pro-survival chaperone GRP78/Bip. It also induced caspase 7 expression and PARP cleavage, indicating apoptosis.

Conclusion
Most ER stress-inducing agents activate both survival pathways and cell death pathways of UPR. In contrast, our identified compound selectively promotes UPR cell death signaling and is highly toxic against radiation and temozolomide-resistant GSCs, while showing no toxicity to non-tumor cells. This bis-chalcone compound is a promising lead for developing UPR-targeted therapies, particularly for GBM. Its potential application in pre-surgical resection of GBM is noteworthy due to its ability to reduce cell migration and tumor size.

Identification of ER Stress-Inducing Agents for Glioblastoma: Advancing Therapeutic Strategies

Background 
The blood brain barrier (BBB) is a selective, semi-permeable boundary in the central nervous system (CNS) that plays a critical role in maintaining the homeostasis of the brain microenvironment. While clinical experiments can accurately determine which compounds effectively cross the BBB, these are time-consuming and labor-intensive. Machine Learning (ML) and computational techniques can alleviate this burden by rapidly screening a large set of potential drug candidates for those that should be prioritized for experimentation validation. In this study, we use ML to predict BBB permeability and then use Parallel Artificial Membrane Permeability Assays (PAMPA) as the in vitro method to assess the accuracy and reliability of these predictions. 

Methods 
The dataset used is B3DB, one of the largest public BBB datasets consisting of seven thousand compounds compiled from 50 published resources. We trained and validated models on this dataset with methods including support vector machines (SVMs), deep neural networks (DNNs), and graph convolutional neural networks (GCNNs). The transfer learning model consisted of an initial DNN trained to the task of quantum chemical property before retraining to the task of BBB permeability. After using these models to screen the Emory Enriched Bioactive Library, a test dataset of two thousand compounds, the top 50 compounds will be prioritized for in vitro experimental confirmation with PAMPA permeability assays. These assays consist of an artificial lipid membrane that simulates BBB properties. Samples will be collected from both sides at specific intervals and analyzed spectrophotometrically post-incubation. 

Results 
For fair comparison, the same 75/25 train/test split of the B3DB dataset was used consistently across the various models. The DNN had a similar performance to the SVM with an accuracy of 83.09% and 82.33% respectively. For transfer learning, the most predictive model was of the DNN with target domain of polarizability of 76.89%. The results indicate that the GCNN was the best performing model of 87.14%. 

Conclusion 
Currently, GCCN’s demonstrate the best predictive capability, highlighting their ability to learn relevant molecular features to the predictive task in the message passing phase. After then comparing these predictions with the in vitro experiments, the next step is to conduct in vivo validation using small and large animal models. The intent is for this hybrid computational and experimental approach to accelerate the understanding of drug therapeutic effects on neuro-oncology and provide insights into key chemical properties that will guide the design of future compounds.

Machine Learning Prediction and In Vitro Validation of Drug Blood Brain Barrier Permeability

Background: Meningiomas are the most common primary intracranial tumor, accounting for over 30% of all primary brain tumors. Although most are benign, up to 20% recur and can be considered aggressive. Based on RNA and whole-exome sequencing data, we identified three molecular subtypes of meningioma. Meningioma Group B and C (MenG B/C) are characterized by deletion of Neurofibromatosis Type 2 (NF2) gene. Simultaneously, the deactivation of the Hippo pathway has been linked to meningioma growth. NF2 inactivation has previously been linked to deregulating the Hippo signaling pathway; however, the mechanism of this relationship is unclear in meningioma. This study aims to investigate the impact of common meningiomal NF2 mutations on Hippo pathway activity and identify which specific NF2-Hippo signaling interactions contribute to these effects. 

Methods: We conducted an extensive literature review to identify the most common NF2 mutations in meningioma. Six of these mutants were cloned and overexpressed in 293 cells with a N-terminal mono-GFP tag. Localization was assessed via fluorescence imaging and compared to wild-type (WT) NF2 localization. We then generated a split-luciferase Hippo pathway biosensor to quantify mutant NF2’s effects on downstream Hippo pathway activity. In this biosensor, one of two luciferase domains is attached to a small amino acid stretch of the YAP protein that harbors the phosphorylation site for degradation. The other part is attached to the phospho-dependent interactor 14-3-3. When Hippo is on, the YAP site gets phosphorylated, binds to 14-3-3 and completes a functional luciferase, which emits a luminescence signal upon substrate binding. WT and mutant NF2s were co-transfected with this biosensor and corresponding signals were quantified. In a second line of experiments WT and mutants were co-expressed with Hippo pathway kinases, MST1 and LATS1, then immunoprecipitated to investigate if these interact. 

Results: We found 19 articles and one database describing 205 NF2 mutations in meningioma, most of which were nonsense mutations. We investigated six of the most common mutants along with the three most common WT NF2 variations (v1, v2, v7). NF2 var7 and NF2 mutants showed aberrant protein aggregation compared to var1 or var2 NF2 which correlated with severity of truncation. Luciferase assay revealed that var7 NF2 as well as mutant NF2 decreased YAP phosphorylation and subsequent Hippo pathway activity. Immunoprecipitation and Western Blot results found that although NF2 v1 and v2 show normal MST1 and LATS interaction, var7 lost interaction with MST1. Interestingly, the NF2 mutants lacked LATS1 interaction, but MST1 interacted even with the smallest truncation of NF2. 

Conclusion: We propose that NF2 forms a tertiary complex with MST1 and LATS1 to activate the Hippo kinase cascade and prevent proliferation. NF2 nonsense mutations create aberrant non-functional proteins that disrupt this complex formation and attenuate Hippo signaling. The naturally occurring var7 NF2 loses MST1 interaction while the NF2 mutations lose LATS1 interaction. These findings have strong therapeutic implications in targeting the MST1-LATS interaction to suppress oncogenicity. Future directions suggest investigating the role of TRAF7 in Hippo signaling, enabling a complete picture of the Hippo pathway in meningioma.

NF2 mutations found in meningioma disrupt the kinase cascade of the Hippo pathway

INTRODUCTION
Marine organisms produce a wide variety of metabolites with unique scaffolds that are biologically active. Manzamines are marine-derived polycyclic alkaloids. Approximately 100 manzamine-type alkaloids have been isolated from 16 marine sponge species. Some of these compounds are reported to have anti-inflammatory and neuritogenic properties. Previous neurite outgrowth screens have identified manzamine A and 8-methoxymanzamine A for further analyses. 
METHODS
To assess the neuritogenic potential, this study conducted neurite outgrowth assays to build dose-response curves for manzamine A and 8-methoxymanzamine A in murine primary cortical cultures. Sytox assays were performed in the Celloger to assess cell toxicity. 
RESULTS
The neurite outgrowth analyses showed that 8-methoxymanzamine A induced neurite outgrowth in a statistically significant manner at 1 micromolar dose. Likewise, that dose and others demonstrated a statistically significant increase in neuronal complexity via number of processes and number of branches. However, at 10 micromolar dosage, 8-methoxymanzamine appears to be largely toxic, with reduced neurite outgrowth, number of processes and number of branches, accompanied by some nuclear blebbing indicative of apoptosis. In contrast, manzamine A doesn’t show increased neurite outgrowth or complexity at any dose. Moreover, like 8-methoxymanzamine A, it appears potentially toxic at the 10 micromolar dose. Initial studies with Sytox indicate substantial toxicity for manzamine A and 8-mehthoxymanzamine A between 1 and 10 micromolar dosage.
CONCLUSIONS
Together, these data suggest 8-methoxymanzamine A has the potential to increase neurite outgrowth, and shows similar indications of toxicity at the 10 micromolar dose as manzamine A. Further studies will be performed with Sytox to refine the concentration at which it is toxic to 50% of cells (LC50). Together, these studies will help identify novel neuroactive manzamine compounds for the marine natural products preclinical pipeline.
Study conducted with intramural funding from Midwestern University.

8-methoxymanzamine A, but not manzamine A, induced neurite outgrowth in murine cortical cultures

Background: Stuttering is a neurodevelopmental disorder of unclear etiology characterized by involuntary disruptions in speech fluency. Recently, stuttering has been shown to be related to a point mutation in GNPTAB, a housekeeping gene involved in cellular lysosomal enzyme-targeting pathway, though it remained unclear how such a mutation might cause the stuttering phenotype. Transcranial ultrasounds in adults who stutter detected mesencephalic hyperechogenicity, likely associated with iron deposits. The current study aims to confirm, assess, and alleviate iron accumulation in a transgenic mouse model engineered with a mutation associated with Gnptab. 
Methods: 
Animal studies: All procedures in this study were approved by the Animal Care and Use Committee of the Intramural Research Program of the National Institute of Neurological Disorders and Stroke. 
Vocalization studies: Ultrasonic vocalizations (USVs) in male mice were recorded via Avisoft Bioacoustics and SASLab Pro software, and the complexity and geometry of USVs were analyzed in Sonotrack (Metris Inc). 
Iron chelation therapy: Adult male Gnptab-mutant (n = 10) and control littermates (n = 10) were treated by 3- Hydroxy-1,2-dimethyl-4(1H)-pyridone (Deferiprone; 0.1 g/L) orally for 1 month via water supply. Animals' vocal behaviors were recorded and compared before and after the treatment. 
Histological processing: Mice were transcardially perfused with 4% paraformaldehyde (PFA) fixative. The brain was extracted and post-fixed for 3-5 days in PFA. Iron was detected by iron-sensitive DAB-enhanced Perl’s staining on coronal brain sections. Bright field images were taken and imported to Fiji, where regional iron content was quantified. 
Statistical analysis: All data was exported to Prism 9.0. Statistical significance was taken at p < 0.05. 
Results: Gnptab-mutant animals show higher percentage of complex USVs and higher iron deposition in the medial lateral striatum, dorsolateral striatum, and central striatum when analyzed for percent area of iron deposition following Perl’s staining. Alleviation of this iron accumulation via chelation therapy was confirmed by Perl’s staining. Strikingly, the percentage of complex vocal bouts decreased following iron chelator therapy. 
Conclusion: The mutation in Gnptab gene, associated with stuttering, leads to an accumulation of CNS iron that may be alleviated with iron chelation, ultimately improving the stuttering phenotype in mice. Accordingly, we posit a novel therapeutic option and long-awaited etiology of the disorder.

An etiology and novel therapeutic opportunity: iron dysregulation in a mouse model of stuttering disorder

Abstract Title 
Hyperexcitation of Mediobasal Hypothalamic Glutamatergic Neurons Induces a Phenotype Resembling Anorexia Nervosa

Background
Anorexia Nervosa (AN) is an eating disorder characterized by a voluntary restriction in food intake resulting in a sustained critically low body weight, hyperactivity, and increased anxiety. AN is among the deadliest psychiatric disorders, and the primary method of assessing its neurobiological basis is with animal models. However, current animal models restrict feeding, exogenously induce stress, and/or show unrelated phenotypes like normoactivity, dissimilar from the hyperactivity and self-induced starvation seen in AN. 
The Mediobasal hypothalamus (MBH) is known to be involved in the regulation of feeding and anxiety-related behaviors. In particular, once activated, glutamatergic neurons within the MBH promote these behaviors. However, these approaches acutely activated the neurons, and the behavioral changes were usually transient. Whether chronic activation of glutamatergic MBH neurons is involved in AN is unknown. 
Previous studies identified a bacterial sodium channel (NachBac), which is more readily activated and takes more time to inactivate than mammalian counterparts. This leads to constantly increased activity when expressed in mammalian neurons. Recent treatment-based rationale suggested chronic glutamatergic signaling may contribute to AN. Based on these observations, we hypothesized that chronic activation of glutamatergic neurons in the MBH will recapitulate the self-induced starvation observed in AN.

Methods
We used the Cre-LoxP technique to achieve neuron-specific gene expression, where genes flanked with LoxP were expressed in the presence of Cre recombinase. We used mice expressing Cre driven by the promoter of vesicular glutamate transporter 2 (Vglut2, a marker gene for glutamatergic neurons), Vglut2-Cre, to target hypothalamic glutamatergic neurons. We stereotaxically injected an Adeno-Associated Virus with a FLip-EXcision vector, AAV-FLEX-NaChBac-GFP, into the MBH to express NaChBac in a Cre-dependent manner.

Results
Interestingly, not only did we observe decreased feeding behavior, but we also observed increased locomotion, increased anxiety, and drastically decreased body weight, classically resembling AN.

Conclusion
These results demonstrate that constitutive activation of glutamatergic MBH neurons recapitulates the AN phenotype. In contrast to the most-used AN mouse models, our model exhibits AN phenotype without feeding restriction or stress induction. Importantly, these results complement the growing rationale of increased glutamatergic signaling in the pathophysiology of AN, based on the use of the glutamate receptor antagonist, ketamine, in treating AN in mice and humans. These findings reveal neurobiological evidence of glutamatergic signaling hyperexcitation contributing to the AN phenotype and provide a more clinically relevant animal model to examine mechanistic insights on AN pathogenesis.

Chronic Activation of Ventral Hypothalamic Glutamatergic Neurons Induces Anorexia Nervosa Phenotype in Mice

Background
Glaucoma is a group of optic neuropathies that affects approximately 2.7 million people in the United States and 76 million people worldwide. Glaucoma is irreversible and can result in permanent blindness if it is not treated. The main risk factor is elevated intraocular pressure (IOP) which predominantly affects retinal ganglion cells (RGC), resulting in cell death and permanent vision loss. Current therapeutics for glaucoma involve reducing IOP and halting progression of disease, but no current treatments can revive degenerated RGCs. Our project aims to evaluate the therapeutic effect of a neurotrophic factor, human Neuritin 1 (NRN1), in regenerating and protecting RGCs lost due to glaucomatous disease progression. Human NRN1 has been proven to enhance plasticity and maturation of RGC axons and dendrites in an acute glaucoma mouse model. The present study utilized non-glaucomatous and glaucomatous induced pluripotent stem cells (iPSC) derived RGCs seeded within in vitro collagen scaffolds. By administering NRN1 to the scaffolds, we hope to elucidate the ability of the therapeutic to increase survival of glaucomatous RGCs.

Methods
The iPSCs derived from non-glaucomatous and glaucomatous donor corneal fibroblasts were differentiated to retinal organoids (RO) to generate RGCs in vitro. After around 30 days of differentiation, the ROs were dissociated to isolate RGCs. The RGCs were seeded at one end of three different in vitro collagen scaffolds. The first scaffold received no NRN1 treatment, the second received NRN1 at the cell body, and the third received NRN1 at the opposite end of the cultured RGCs. Downstream immunofluorescence with the TRA-1-60 antibody was performed on iPSCs to confirm that they were successfully reprogrammed from donor fibroblasts. Additionally, gene expression experiments for iPSC markers were performed to further verify successful iPSC reprogramming. Karyotyping procedures were performed on iPSCs to ensure no reprogramming induced chromosomal aberrations were evident.

Results
We successfully generated iPSC-derived RGCs from both non-glaucomatous and glaucomatous donor eyes. These RGCs effectively integrated within the three collagen scaffolds. After NRN1 treatment, both cell types demonstrated differential expression of apoptotic markers. Downstream iPSC experimentation confirmed that iPSCs were successfully reprogrammed from donor fibroblasts with no chromosomal aberrations.

Conclusion
Our study demonstrates that NRN1 exhibits a therapeutic effect on glaucomatous RGCs. NRN1 could potentially be a useful intervention to restore vision in patients suffering from severe glaucoma. The results also indicate that iPSC-derived RGCs can successfully be obtained from donor eyes and used in collagen scaffolds for future research.

Determining the Restorative Role of Human Neuritin 1 in Protecting Retinal Ganglion Cells from Glaucoma Patients

Background
Glaucoma is a neurodegenerative ocular disorder involving the degeneration of retinal ganglion cells (RGCs), thinning of the retinal nerve fiber layer, and atrophy of the optic nerve. Disease progression is often characterized by increased intraocular pressure (IOP) and visual field loss. Currently, the only efficacious therapy for treating glaucoma is modification of IOP through pharmacological eye drops or surgical intervention. Even though these interventions slow disease progression, they do not prevent RGC death entirely thus emphasizing the need for targeting RGC survival. Decreased axonal transport of essential neurotrophic factors contributes to RGC death. Neurotrophic factor supplementation has shown to improve survival of RGCs and sustain retinal function. Neuritin-1 (NRN1), a neurotrophic protein downstream of the neurotrophin family, has shown to play a protective role in non-glaucomatous eyes exposed to high pressure via the ex vivo ocular perfusion model, Translaminar Autonomous System (TAS). We will investigate the effects of NRN1 in glaucomatous human donor eyes within the TAS to understand if NRN1 can protect RGC loss in diseased retinas.

Methods
Three sets of glaucomatous human donor eyes were obtained from eye banks in accordance with the Declaration of Helsinki. Eyes were dissected, and posterior cups were perfused using the TAS model for 6-7 days under high and normal pressure conditions with and without NRN1. We then assessed RGC survival by measuring apoptosis, inflammation, and retinal markers using qRT-PCR and immunohistochemistry. Retinal activity was compared between treated and untreated retinas using OcuScience® Ex Vivo electroretinogram.

Results
The posterior eye cups were successfully maintained in the TAS model under normal and high-pressure conditions for 6-7 days. NRN1 treated eyes showed differential expression of various inflammatory and apoptotic markers. NRN1 treated eyes showed no difference in extra cellular matrix deposition following perfusion. Improved retinal activity was seen within the treated glaucomatous eyes. 

Conclusion
The TAS model can mimic pressure induced pathogenesis in human glaucomatous eyes. Data from this study shows that NRN1 may serve as a potential therapeutic target by promoting RGC survival under glaucomatous conditions.


Evaluating the Therapeutic Effect of Neuritin 1 on Human Retinal Ganglion Cell Survival

Innate Immune Memory refers to the ability of innate immune cells to display altered responses upon secondary exposure to pathogens. This phenomenon is driven by dynamic and heritable histone protein modifications, which influence post-translational gene transcription. Currently, while the broader MAPK and PI3K/AKT pathways of α-MSH are well established, there is little existing research on the direct link between α-MSH and histone modifications. Our study aims to investigate the effects of alpha-melanocyte-stimulating hormone (α-MSH), a neuropeptide with notable anti-inflammatory properties, on Histone 3 (H3) post-translational markers and their epigenetic impact on mouse macrophages.

We conducted a comprehensive analysis of H3 modifications to identify key changes, focusing on H3K4 global methylation, H3K9 dimethylation, and H3K14 acetylation levels in response to varying concentrations of α-MSH. Methylation and acetylation of histone proteins, such as H3K4, H3K9, and H3K14, regulate the accessibility of transcriptional start sites and promoters, thereby influencing gene transcription. In immune cells, these histone modifications alter the transcription of genes associated with immune responses, particularly inflammation.

Utilizing enzyme-linked immunosorbent assays (ELISA) to quantify the H3 methylation and acetylation levels, the response of histone modifications to α-MSH treatment was measured, highlighting the potential of α-MSH as a modulator of epigenetic marks in innate immune cells. Such findings enhance our understanding of how neuropeptides like α-MSH can influence immune responses through epigenetic mechanisms, providing insights into new therapeutic strategies for controlling inflammation and enhancing immune memory.

Our results demonstrate significant effects of α-MSH on histone modifications, with notable demethylation of H3K4, increased dimethylation of H3K9, and elevated acetylation of H3K14 observed in treated macrophages. Specifically, significant changes in H3K4 global methylation and H3K14 acetylation were detected at 1 ng/mL and 10 ng/mL α-MSH, while H3K9 dimethylation was significantly affected at 30 pg/mL α-MSH. Additionally, low-dose α-MSH (30 pg/mL) induced demethylation and deacetylation of H3K4 and H3K14, respectively.

These findings suggest that α-MSH exerts anti-inflammatory effects by modulating histone methylation and acetylation patterns. Changes in H3 histone modifications decrease the expression of proinflammatory molecules and enhance the expression of anti-inflammatory molecules in macrophages. This epigenetic regulation may contribute to the innate immune memory, eliciting trained responses to subsequent exposures.

In summary, α-MSH modulates histone H3 post-translational modifications in a concentration-dependent manner, altering the epigenetic landscape of macrophages to promote anti-inflammatory responses. This research underscores the significance of histone modifications in the regulation of innate immune memory and the potential for targeting these pathways in immunotherapy. 



Histone Epigenetic Effects of α-MSH

Background
Age-related cataract affects 22% of individuals over the age of 75 years, and data suggest that delaying the progression rate by 10 years would decrease cataract surgery by 50%. When rodent lenses are incubated in culture medium, they lose their transparency after 24-48 hours due to protein aggregation, which changes the index of refraction resulting in light scattering and opacity. We hypothesized that finding ways to prevent or delay this process through manipulation of the culture medium would provide important clues toward cataract prevention and present a solid foundation for a drug testing model on specific mutated mice lenses for cataract treatment.
Methods
13 culture conditions, each comprising 4-6 adult C57BL6 mice lenses, were tested. Variations in glucose, pyruvate, fructose, antioxidant, osmolality (sorbitol), and crowding agent (polyethylene glycol) were used. The extent of opacification, the type of opacity (nuclear vs cortical), and the lens diameter were determined as a function of incubation time.
Results
Results show that compared to the baseline conditions (Medium TC199), basic nutrition materials that lenses need for survival and antioxidants that prevent oxidative stress in lenses show no improvement in preventing lens opacification. Next, we mimicked the lens environment in the eye and tested hyperosmolarity. PEG 1000 stood out among the rest by successfully preventing cataract formation in all of its lenses. We also noticed the lens size difference between the PEG 1000 condition and the rest. PEG 1000 successfully prevents the lens from swelling and keeps lens volume low. Thus, from our results, we tested another set of biopolymers which could prevent massive intake of medium to the lens that we saw in previous conditions. We saw that Lymphoprep successfully kept lenses clear until day 4 (96 hours), which was a major improvement compared to the rest of the conditions that we tested.
Conclusion
This project is novel in its approach as the first to develop a system of drug testing lens model for cataract by keeping mice lenses clear and transparent for 7-14 days. While we are still in the process of reaching 7-14 days of clarity in lenses, we have already tested some strong potential conditions that improved lens transparency in vitro incubations, such as PEG 1000 and Lymphoprep. We plan to further test possible conditions for optimizing lens culture medium for in vitro lens transparency, specifically focusing on mimicking the lens environment in the eye to maintain lens homeostasis.

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