2,624 research outputs found

    Glaucoma: from pathogenic mechanisms to retinal glial cell response to damage

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    Glaucoma is a neurodegenerative disease of the retina characterized by the irreversible loss of retinal ganglion cells (RGCs) leading to visual loss. Degeneration of RGCs and loss of their axons, as well as damage and remodeling of the lamina cribrosa are the main events in the pathogenesis of glaucoma. Different molecular pathways are involved in RGC death, which are triggered and exacerbated as a consequence of a number of risk factors such as elevated intraocular pressure (IOP), age, ocular biomechanics, or low ocular perfusion pressure. Increased IOP is one of the most important risk factors associated with this pathology and the only one for which treatment is currently available, nevertheless, on many cases the progression of the disease continues, despite IOP control. Thus, the IOP elevation is not the only trigger of glaucomatous damage, showing the evidence that other factors can induce RGCs death in this pathology, would be involved in the advance of glaucomatous neurodegeneration. The underlying mechanisms driving the neurodegenerative process in glaucoma include ischemia/hypoxia, mitochondrial dysfunction, oxidative stress and neuroinflammation. In glaucoma, like as other neurodegenerative disorders, the immune system is involved and immunoregulation is conducted mainly by glial cells, microglia, astrocytes, and Müller cells. The increase in IOP produces the activation of glial cells in the retinal tissue. Chronic activation of glial cells in glaucoma may provoke a proinflammatory state at the retinal level inducing blood retinal barrier disruption and RGCs death. The modulation of the immune response in glaucoma as well as the activation of glial cells constitute an interesting new approach in the treatment of glaucoma

    UMSL Bulletin 2023-2024

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    The 2023-2024 Bulletin and Course Catalog for the University of Missouri St. Louis.https://irl.umsl.edu/bulletin/1088/thumbnail.jp

    UMSL Bulletin 2022-2023

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    The 2022-2023 Bulletin and Course Catalog for the University of Missouri St. Louis.https://irl.umsl.edu/bulletin/1087/thumbnail.jp

    Effects of municipal smoke-free ordinances on secondhand smoke exposure in the Republic of Korea

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    ObjectiveTo reduce premature deaths due to secondhand smoke (SHS) exposure among non-smokers, the Republic of Korea (ROK) adopted changes to the National Health Promotion Act, which allowed local governments to enact municipal ordinances to strengthen their authority to designate smoke-free areas and levy penalty fines. In this study, we examined national trends in SHS exposure after the introduction of these municipal ordinances at the city level in 2010.MethodsWe used interrupted time series analysis to assess whether the trends of SHS exposure in the workplace and at home, and the primary cigarette smoking rate changed following the policy adjustment in the national legislation in ROK. Population-standardized data for selected variables were retrieved from a nationally representative survey dataset and used to study the policy action’s effectiveness.ResultsFollowing the change in the legislation, SHS exposure in the workplace reversed course from an increasing (18% per year) trend prior to the introduction of these smoke-free ordinances to a decreasing (−10% per year) trend after adoption and enforcement of these laws (β2 = 0.18, p-value = 0.07; β3 = −0.10, p-value = 0.02). SHS exposure at home (β2 = 0.10, p-value = 0.09; β3 = −0.03, p-value = 0.14) and the primary cigarette smoking rate (β2 = 0.03, p-value = 0.10; β3 = 0.008, p-value = 0.15) showed no significant changes in the sampled period. Although analyses stratified by sex showed that the allowance of municipal ordinances resulted in reduced SHS exposure in the workplace for both males and females, they did not affect the primary cigarette smoking rate as much, especially among females.ConclusionStrengthening the role of local governments by giving them the authority to enact and enforce penalties on SHS exposure violation helped ROK to reduce SHS exposure in the workplace. However, smoking behaviors and related activities seemed to shift to less restrictive areas such as on the streets and in apartment hallways, negating some of the effects due to these ordinances. Future studies should investigate how smoke-free policies beyond public places can further reduce the SHS exposure in ROK

    Dissecting Extracellular Matrix Internalisation Mechanisms using Functional Genomics

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    Breast and ovarian malignancies account for one third of female cancers. The role of the stroma in supporting invasive growth in breast cancer has become clear. Breast cancer cells interact and respond to the cues from the surrounding extracellular matrix (ECM). Integrins are main cell adhesion receptors and key players in invasive migration by linking the ECM to the actin cytoskeleton. In addition, integrins mediate distinctive biochemical and biomechanical signals to support cancer invasion. The role of matrix proteases in promoting ECM degradation and cancer dissemination has been extensively studied; however, cancer cells possess additional means to support those processes, such as integrin-mediated ECM endocytosis and consequent degradation in the lysosomes. Internalisation of the extracellular matrix is upregulated in invasive breast cancer. Nonetheless, the mechanisms by which cancer cells regulate this process are poorly understood. We developed a high throughput pH sensitive system to detect ECM uptake. Here, we show that MDA-MB-231 breast cancer cells converge in macropinocytosis to internalise diverse ECM components and we confirm that this process is modulated by PAK1. To unravel which ECM components breast cancer cells internalise in a complex environment (namely, cell derived matrices), we performed mass spectrometry. Proteomic analysis identified Annexin A6, Collagen VI, Tenascin C and fibronectin, among other matrisome proteins, to be internalised by invasive breast cancer cells. Following ECM endocytosis, ECM is targeted for lysosomal degradation. To unravel the molecular mechanisms behind this process, we performed a trafficking screen and identified the AP3 complex, VAMP7, Arf1 and ARFGEF2. Our results suggest that the AP3 complex may regulate ECM-integrin delivery to lysosomes. To gain more insight on the signalling pathways governing macropinocytosis in breast cancer cells, we performed a kinase and phosphatase screen that unravelled MAP3K1 and PPP2R1A, a subunit of protein phosphatase 2A (PP2A) as relevant regulators of ECM endocytosis. Furthermore, our data suggests that p38 mitogen-activated protein kinase (MAPK) activation upon binding to the ECM is required for ECM macropinocytosis. Outstandingly, inhibiting p38 MAPK led to profound changes in the ability of breast cancer cells to migrate in cell derived matrices. Previous work from the Rainero lab focused on characterising the receptors involved in ECM internalisation; α2β1 integrin was identified as the main regulator of ECM uptake in MDA-MB-231 cells. In particular, α2β1 integrin has been shown to activate p38 MAPK pathway. Taken together, we hypothesise that binding of ECM to α2β1 integrin results in the activation of PAK1 and MAP3K1, which in turn leads to ECM endocytosis. p38 MAPK activity may induce changes in actin polymerisation via PPP2R1A and/or focal adhesion turnover, which consequently promotes ECM macropinocytosis and invasive migration

    2023-2024 Graduate School Catalog

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    You and your peers represent more than 67 countries and your shared scholarship spans 140 programs - from business administration and biomedical engineering to history, horticulture, musical performance, marine science, and more. Your ideas and interests will inform public health, create opportunities for art and innovation, contribute to the greater good, and positively impact economic development in Maine and beyond

    Endogenous analgesic systems and neuropathic pain

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    Purpose: Neuropathic pain is a debilitating condition that deeply affects quality of life and is a major socioeconomic burden. The endogenous analgesic system can be modelled by assessing responses to stress known as stress induced analgesia. Quite often, the anticipation of pain is a major source of fear and anxiety for chronic pain sufferers, leading to or compounding stress and anxiety related disorders. Thus, responses to conditioned fear were modelled utilising a fear conditioned analgesia protocol on an animal model of neuropathic pain. Methods: Electric foot-shock stimulation was used as a stressor to activate the endogenous analgesic system in C57BL/6 mice. Neuropathic pain was modelled via the chronic constriction injury method. The resultant analgesia from the stressor was measured by two thermal pain assays: the hotplate and Hargreaves test, engaging unique supraspinal and spinal pain pathways. The immediate response to stress was the experimentally produced stress induced analgesia. A two-day fear conditioning protocol was setup to assess fear conditioned analgesia. The engagement of endogenous opioids and cannabinoids were tested via systemic administrations of drugs. The neuronal activity within the PAG was assessed using c-fos immunohistochemistry. Results: Stress induced analgesia induced by brief continuous footshock was largely mediated by endogenous opioids. By contrast, both opioids and cannabinoids mediated the analgesia induced by intermittent footshock. Extended continuous footshock produced supramaximal responses which prevented the assessment of endogenous opioids and cannabinoids. The immediate response to stress was opioid mediated whilst both endogenous opioid and cannabinoids was necessary to mediate fear expression and fear conditioned analgesia. Neuropathic pain disrupts the stress response but interestingly did not alter fear expression. Neuronal activity within the PAG was increased with neuropathic pain mice

    FGFR1-5HT1AR heteroreceptor complexes differently modulate GIRK currents in the hippocampus and the raphe nucleus of control rats and of a genetic rat model of depression

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    The midbrain raphe serotonin neurons provide the main ascending serotonergic projection to the forebrain, including the hippocampus, which has a recognized role in the pathophysiology of depressive disorder. The activation of G protein-coupled inwardly-rectifying potassium (GIRK) channels by serotonin 5HT1A receptors at the soma-dendritic level of serotonergic raphe neurons and glutamatergic hippocampal pyramidal neurons reduces neuronal activity. The presence of FGFR1-5HT1A heteroreceptor complexes in this raphe-hippocampal serotonin neuron system has been demonstrated, but functional receptor-receptor interactions in the heterocomplexes have only been studied in CA1 pyramidal neurons of control Sprague Dawley (SD) rats. In the present research, the short-term effects of FGFR1-5HT1A complex activation were studied in hippocampal pyramidal neurons, both in CA1 and CA2 areas, and midbrain dorsal raphe serotonergic neurons of SD rats and a genetic rat model of depression, the Flinders sensitive line (FSL) rats selected from SD strain, using an electrophysiological technique. The results obtained demonstrate that FGFR1-5HT1A heteroreceptor activation by specific agonists reduced the ability of the 5HT1AR protomer to open the GIRK channels via the allosteric inhibitory interplay produced by agonist activation of the FGFR1 protomer, resulting in increased neuronal firing in the raphe-hippocampal 5HT system of SD rats. In contrast, apart from CA2 neurons, the inhibitory allosteric effects of FGFR1 agonist on the 5HT1AR protomer were unable to have this influence on GIRK channels in FSL rats. According to these data, 5HT1AR activation impaired hippocampal plasticity in both SD and FSL rats, as determined by long-term potentiation induction capability in the CA1 field, but not in SD rats following simultaneous FGFR1-5HT1A heterocomplex activation. While, due to the impairment in heterocomplex activation, long-term potentiation was precluded in FSL rats. It is thus hypothesized that in the genetic FSL model of depression, there is a considerable decrease of the allosteric inhibition mediated by the FGFR1 protomer on the 5HT1AR protomer, resulting in a reduced opening of the GIRK channels in the raphe-hippocampal serotonin pathway. The consequent increase in inhibition in dorsal raphe 5HT nerve cells and glutamatergic hippocampal CA1 pyramidal nerve cell firing may contribute to the onset of major depression

    Characterizing of Robo downstream signalling to promote direct neurogenesis

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    The size and degree of folding of the mammalian cortex are pivotal factors that affect species’ cognitive abilities and sensorimotor skills. The cerebral cortex is the main region in the mammalian brain that governs complex cognitive behaviors. The development of the cortex depends on the amplification of neural stem cells (NSCs), neural progenitors (NPs) and the generation and differentiation of postmitotic neurons. There are two main types of NPs in the mouse neocortex (NCx): apical radial glia (aRGCs) and intermediate progenitor cells (IPCs). Robo receptors play an important role in regulating the amplification of cortical progenitors. The absence of Robo receptor signalling plus the alteration of the Notch signalling pathway in the mouse NCx leads to an overproduction of poorly functional IPCs. Ancient amniotic cortices exhibit a predominance of direct neurogenesis during development, where aRGCs produce neurons directly. Intriguingly, Robo receptors as well as Notch signalling play a major role in attenuating the mode of neurogenesis. This hypothesis was validated in several brain structures with phyletic antiquity, confirming that Robo receptors are essential in the shift towards indirect neurogenesis during the evolution and expansion of the cerebral cortex. However, little is known about the precise signalling cascade or interactors employed by Robo to initiate direct neurogenesis. In this thesis, we demonstrated the transcriptomic differences between the developing mouse NCx and OB (where direct neurogenesis is predominant in the OB vs NCx) using single cell RNA sequencing (scRNA). We showed aRGCs populations that are differently enriched between these regions. We traced lineage trajectories of indirect and direct neurogenesis, as well as validating the expression of several differentially expressed genes between the two regions. We used Robo intracellular domain (ICD)—this region is considered a constitutively active form of Robo receptor—and demonstrated the protein interactors that bind it. Following that, we demonstrated Robo ICD localization to the nucleus. We discovered that Robo conserved cytoplasmic domains play an important role in Robo ICD nucleocytoplasmic localization and direct neurogenesis induction in the mouse NCx. Next, we showed that Robo ICD localizes to chromatin, and causes transcriptional changes that occur upon the experimental gain of function of Robo ICD in the NCx and in vitro. Additionally, we showed that loss of function of Nup107, a nuclear pore complex (NPC) protein and one of Robo ICD protein interactors, induces direct neurogenesis in mouse NCx and chick lateral pallium. Taken together, our findings suggest the transcriptional role Robo ICD exerts by binding DNA and, consequently, its conserved role in moderating direct neurogenesis. El tamaño y el grado de plegamiento de la corteza cerebral son factores fundamentales que afectan a las capacidades cognitivas y habilidades sensoriomotoras de los mamíferos. La corteza cerebral es la principal región del cerebro que gobierna conductas cognitivas complejas. El desarrollo de la corteza depende de la amplificación de células madre neurales (CMN), progenitores neurales (PN) y de la generación y diferenciación de neuronas postmitóticas. Hay dos tipos principales de PN en la neocorteza o neocórtex (NCx) del ratón: las células de glía radial apical (CGRa) y las células progenitoras intermedias (CPI). Los receptores Robo juegan un papel importante en la regulación de la amplificación de los progenitores corticales. La ausencia de señalización del receptor Robo sumada a la alteración de la vía de señalización de Notch en el NCx de ratón conduce a una sobreproducción de CPI poco funcionales. La corteza de especies amniotas anteriores en la evolución a los mamíferos (como los reptiles y las aves) exhiben un predominio de neurogénesis directa durante el desarrollo, por el cual las CGRa producen neuronas directamente. Curiosamente, los receptores Robo, así como la señalización de Notch, desempeñan un papel importante en la atenuación de esta modalidad de neurogénesis a lo largo de la evolución. Esta hipótesis ha sido validada en varias estructuras cerebrales con antigüedad filética, confirmando que los receptores Robo son esenciales en el cambio hacia la neurogénesis indirecta durante la evolución y la consecuente expansión de la corteza cerebral. Sin embargo, se sabe poco sobre la cascada de señalización de Robo, así como de los mensajeros secundarios empleados por este receptor para iniciar el proceso de neurogénesis directa. En esta tesis, demostramos las diferencias transcriptómicas que existen entre el NCx y el bulbo olfatorio (BO) de ratón en desarrollo (sabiendo que la neurogénesis directa es predominante en BO frente al NCx). Para ello usamos la técnica de secuenciación de ARN de células individuales (single-cell RNA sequencing (scRNAseq) en inglés). Mostramos que hay poblaciones de RGCa que están diferentemente enriquecidas entre estas regiones. Trazamos trayectorias de linaje de neurogénesis indirecta y directa y validamos la expresión de varios genes expresados diferencialmente entre las dos regiones. Utilizamos el dominio intracelular (DIC) de Robo (esta región se considera una forma constitutivamente activa del receptor) y demostramos los mensajeros secundarios que se unen. Después, demostramos la localización del DIC de Robo en el núcleo. Descubrimos que sus dominios citoplasmáticos, muy conservados a lo largo de la evolución, tienen un papel importante en la localización núcleo-citoplasmática del DIC y la inducción directa de neurogénesis en el NCx de ratón. A continuación, mostramos que una vez en el núcleo, el DIC se une a la cromatina y provoca cambios transcripcionales que tienen como resultado una la ganancia de función de Robo tanto en el NCx como in vitro. Además, demostramos que la pérdida de función de Nup107, una proteína que forma parte del complejo del poro nuclear (CPN) además de ser una proteína de interacción del DIC de Robo, induce neurogénesis directa en el NCx de ratón y en el palio lateral de pollo. En conjunto, nuestros resultados sugieren el papel de modulación transcripcional que ejerce el DIC de Robo al unirse al ADN y, en consecuencia, su rol conservado a lo largo de la evolución en la disminución de la neurogénesis directa
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