Le but de ce travail est l'étude de la connectivité anatomique et fonctionnelle desréseaux neuronaux et le développement des nouveaux outils à cet effet. Car le dernieraspect est une préoccupation majeure de la neuroscience actuelle, nous avonsdeveloppé d'abord un nouveau traceur virale permettant la reconstruction neuronale.Nous avons ensuite appliqué cet et d'autres techniques pour sonder les défauts deconnectivité neuronale dans le syndrome de l'X fragile.Dans la première partie, nous avons discuté les avantages et inconvénients d'unetechnique émergente en utilisant un nouveau type de vecteur viral qui permet uneunique application pour l’étude du cerveau.Dans la deuxième partie, nous avons développé, au départ de ce vecteur viral, unenouvelle variante de faciliter le traçage et reconstruction des caractéristiquesmorphologiques de neurones. Nous avons montré la force de cette varianteantérograde du virus de la rage recombinant glycoprotéine supprimé pour lareconstruction de calcul de toutes les caractéristiques morphologiques clés deneurones: les dendrites, épines, les axones longs envergure dans tous les terminaux ducerveau et les boutons.Dans la troisième partie, nous avons examiné les modifications dans la connectivitédes structures cérébrales dans le syndrome du X fragile (FXS). FXS est le retardmental héréditaire la plus fréquente et la forme génétique la plus fréquente del'autisme, ce qui conduit à l'apprentissage et de la mémoire des déficits, lescomportements répétitifs, des convulsions et une hypersensibilité à des stimulisensoriels (visuels). Une des hypothèses éminents dans le domaine de l'autismesuppose une phénotype de hyper-connectivité locale mais de hypo-connectivité pourles connexions longue portée. Pour tester cette hypothèse dans un modèle de sourisFXS nous avons utilisé l'imagerie par résonance magnétique, pour balayer la totalitédu cerveau et de mesurer la connectivité anatomique et fonctionnel. Cela nous apermis d'identifier des altérations de connectivité dans plusieurs domains. Après nous8avons utilisé des traceurs viraux pour explorer un de ceux domains plus detaillé. Enutilisant le virus de la rage rétrograde à quantifier le nombre de neurones projetantvers ces zones, nous avons confirmé une connectivité d'entrée modifié pour le cortexvisuel primaire, ce qui pourrait contribuer au traitement visuel altéré de l'information.Nous avons découvert une connectivité réduite à longue portée globale anatomique etfonctionnelle entre plusieurs régions du cerveau, l'identification FXS comme unepathologie de la connectivité neuronale, ce qui pourrait expliquer les difficultés deplusieurs stratégies de sauvetage visant des cibles moléculaires sont actuellementconfrontés. / The goal of this work was the investigation of the anatomical and functionalconnectivity of neuronal networks and the development of novel tools for thispurpose. Since the latter aspect is a major focus of current neuroscience, we firstsought a novel viral tracer enabling sparse neuronal reconstruction and neuronclassification. We then applied this and other techniques to probe neuronalconnectivity defects in Fragile X Syndrome.In the first part we discussed the merits and drawbacks of a emergingtechnique using a new type of viral vector that allows in a unique manner mapping ofthe input of a given brain area.In the second part we developed, departing from this viral vector, a newvariant to facilitate the tracing and reconstructing of morphologic features of neurons.We showed the strength of this anterograde variant of the recombinant glycoproteindeletedrabies virus for computational reconstruction of all key morphologicalfeatures of neurons: dendrites, spines, long-ranging axons throughout the brain andbouton terminals.In the third part we examined alterations in the wiring of brain structures inthe Fragile X Syndrome (FXS). FXS is the most common inherited mental retardationand most frequent genetic form of autism, leading to learning and memory deficits,repetitive behavior, seizures and hypersensitivity to sensory (e.g. visual) stimuli. Oneof the eminent hypotheses in the autism field assumes a local hyper- connectivityphenotype but hypo-connectivity for long-ranging connections. To test this hypothesisin a FXS mouse model we used magnetic resonance imaging, to scan the entire brainand measure the anatomical and functional connectivity. This allowed us to identifyconnectivity alterations in several areas that we further explored using viral tracers.Using retrograde rabies virus to count the number of neurons projecting to such areaswe confirmed an altered input connectivity to the primary visual cortex, which couldcontribute to the altered visual information processing. We discovered an overallreduced anatomical and functional long-range connectivity between several brainareas, identifying FXS as pathology of neuronal connectivity, which might explain thedifficulties several rescue strategies aiming at molecular targets are currently facing.

by Priscilla Miu-kuen Poon. / Thesis (Ph.D.)--Chinese University of Hong Kong, 1997. / Includes bibliographical references (p. 176-193). / Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Mode of access: World Wide Web.

Le syndrome du X fragile est la première cause monogénique de déficience intellectuelle héréditaire affectant un garçon sur 5161 et une fille sur 6000. La maladie résulte de mutations dynamiques dans le gène FMR1 (expansion de trinucléotides CGG et méthylation du gène) conduisant à l'absence ou à la diminution importante d'expression de la protéine FMRP (Fragile X Mental Retardation Protein).Le syndrome du X fragile est difficile à identifier étant donné la grande variabilité des manifestations cliniques entre les individus. La déficience intellectuelle est variable et elle est moins profonde chez les femmes et les individus mosaïques.Le phénotype atténué chez ces patients serait dû à la présence d'un allèle fonctionnel permettant la synthèse de la protéine FMRP dans une portion des cellules. Ainsi, il est suggéré qu'une relation existerait entre la quantité de synthèse de FMRP au cerveau et le phénotype cognitif des individus avec le syndrome du X fragile.Le but de notre projet de recherche est de développer un test diagnostique pour le syndrome du X fragile, basé sur la mesure quantitative de la protéine FMRP dans les plaquettes sanguines. D'abord, les niveaux de FMRP ont été mesurés dans une population d'individus sans déficience intellectuelle d'âge et de sexe différents. Nos résultats montrent que les niveaux mesurés suivent une distribution normale et ne seraient pas influencés par le sexe ou l'âge. Ensuite, ces niveaux de FMRP ont été comparés avec ceux mesurés chez les individus diagnostiqués avec le syndrome du X fragile. Comme attendu, les niveaux de FMRP des individus avec le X fragile sont inférieurs à ceux des contrôles et permettent d'établir une valeur seuil pour le diagnostic de la maladie. En combinant les résultats obtenus chez les femmes et hommes avec la maladie, une relation positive entre FMRP, le quotient intellectuel et le comportement adaptatif a été observée. Dans le groupe des femmes avec le syndrome du X fragile, la relation entre FMRP et le comportement adaptatif demeure statistiquement significative. L'approche que nous proposons permet non seulement de détecter les cas de syndrome du X fragile, mais également de donner des informations prédictives des capacités cognitives des individus atteints. Ce nouvel outil diagnostique pourrait avoir des impacts significatifs dans l'investigation et la prise en charge des individus avec le syndrome du X fragile.

This dissertation examines low-income fathers’ involvement with their young children using the Fragile Families and Child Wellbeing (FFCW) data. Chapter 3 entitled, “He Said, She Said: Comparing Father and Mother Reports of Father Involvement,” compares mother and father reports of fathers’ frequency of involvement in various activities and in measures of emotional involvement. This chapter finds that fathers report spending 17.6 percent more time engaged in 11 activities with their young children than mothers report the father spending. How parental disagreement is measured yields starkly different results given the underlying distribution of these data. Chapter 4 entitled, “Estimating the Impact of Child Support and Welfare Policies on Fathers’ Involvement,” is a longitudinal analysis combining three waves of the FFCW data with annual, state-level policy data on child support enforcement and welfare policies. This chapter examines the impact of policies on fathers’ involvement over time. Fathers’ involvement is operationalized as accessibility, responsibility, and engagement. Using parents that are unmarried at the time of the focal child’s birth, this chapter finds that public policies do influence fathers’ involvement after controlling for individual social and demographic characteristics. Policies may be operating in conflicting ways to both increase and decrease fathers’ involvement. For example, fathers’ daily engagement is positively affected by stronger paternity establishment policies but is negatively affected by stronger child support enforcement collection rates and the welfare family cap policy. Chapter 5 entitled, “Two Dads Are Better Than One: Biological and Social Father Involvement,” examines whether biological and social fathers are substitutes or complements in a child’s life and how biological fathers and social fathers impact the mother’s frequency of involvement. This chapter finds that resident social fathers contribute as much time to the focal child as resident biological fathers. Factors that increase the overall parental frequency of involvement include having: a resident biological or social father, native-born parents, a biological father who had a very involved father, and a positive relationship between the biological parents. Factors that decrease overall parental frequency of involvement include: the father’s new partner, the father’s incarceration, a mother’s other children, and the child’s increasing age. / text

The accurate development of the wiring between the billions of neurons in our brain is fundamental to brain function. Development of this connectivity relies on activity-dependent modification of synapses similar to those that underlie learning and memory. Glutamate is the principal excitatory neurotransmitter in the mammalian brain and several brain disorders result from altered glutamatergic receptor signalling (Catania et al., 2007; Lau and Zukin, 2007). Genes encoding glutamate receptor associated proteins have a high incidence of mutation in cognitive disorders, especially X-linked mental retardation (MR)(Laumonnier et al., 2007). MR has long been associated with altered cortical connectivity, particularly dendritic spine dysgenesis. There is also an emerging view that aberrant local protein synthesis within dendrites and protein trafficking to dendrites underlies some forms of MR (Kelleher and Bear, 2008; Pfeiffer and Huber, 2006; Zalfa and Bagni, 2005). Most studies examining the role of glutamatergic receptors in MR have focused on adults. Little is known about how these MR genes regulate brain development despite their neurodevelopmental aetiology. Fragile X mental retardation (FXS) is the most common form of inherited MR and results from the loss of fragile X mental retardation protein (FMRP). FMRP is a RNA binding protein and is hypothesised to have a role in protein trafficking from nucleus to sites of synapses, and regulating local protein synthesis at sites of synapses (Bagni and Greenough, 2005). A prevalent theory of FXS causation is ‘metabotropic glutamate receptor (mGluR) theory of fragile X’, which postulates that all functional consequences of mGluR (predominantly mGluR5)-dependent protein synthesis maybe exaggerated in FXS (Bear et al., 2004). Primary somatosensory cortex (S1) of rodents provides an excellent model system to study the role of MR genes in development because of its stereotypic, glutamate receptor-dependent, anatomical development (Barnett et al., 2006b; Erzurumlu and Kind, 2001). Hannan et al., (2001) reported that genetic deletion of mGluR5 results in loss of ‘barrels’, the anatomical correlates of rodent whiskers in S1. Chapter 3 extends these findings to show that there is expression of mGluR5 as early as P4 in S1 prior to segregation of layer 4 cells into barrels suggesting a tropic role for glutamate in barrel formation. The expression of mGluR5 is postsynaptic during barrel formation and does not regulate tangential or radial cortical development. Its effects on barrel segregation are dose dependent and are not due to a developmental delay. During late S1 development, loss of mGluR5 results in decreased spine density suggesting a role in synaptogenesis. Supporting this hypothesis in mGluR5 mutant mice there is a general decrease in expression of synaptic markers in early S1 development. Chapter 4 explores the role of FMRP in cortical development. FMRP is expressed early in S1 development with peak expression prior to synaptogenesis at P14. It is expressed postsynaptically at P7 and pre and postsynaptically at P14. FMRP does not regulate cortical arealisation during barrel formation but results in decreased barrel segregation. In the absence of FMRP, biochemical studies show altered expression of glutamatergic receptors in the neocortex P7 and P14 suggesting altered glutamatergic receptor composition at synaptic sites. During late S1 development, loss of FMRP results in increased spine density in layer 4 spiny cells. Together these data indicate a role for FMRP during early and late S1 development. Chapter 5 directly tests the mGluR theory of FXS by examining whether genetic reduction of mGluR5 levels rescues anatomical phenotypes characterised in Fmr1-/y mice. The defect in barrel formation in Fmr1-/y mice is partially rescued by reducing mGluR5 levels. However, layer 4 spine density in Fmr1-/y mice does not appear to be rescued. Chapter 6 explores the expression patterns of three key synaptic MAGUKs (Membrane associated guanylate kinases) PSD95, SAP102 and PSD93, one of which (PSD95) is regulated by FMRP (Zalfa et al., 2007) and the others which have putative binding sites for FMRP. MAGUKs tether glutamatergic receptors to their associated signalling complexes at the postsynaptic membrane and also regulate glutamatergic receptor trafficking (Collins and Grant, 2007; Kim and Sheng, 2004). The immunohistochemical expression profiles of PSD95, SAP102 and PSD93 show dynamic regulation during S1 development that is unaffected by loss of FMRP (at P7), and biochemical data indicates that basal levels of these MAGUKs in neocortex are unaltered at P7 and P14 in Fmr1-/y mice. In Sap102-/y and Psd95-/- mice, there is altered expression of several synaptic proteins biochemically providing evidence for differential roles of SAP102 and PSD95 in regulating expression of glutamatergic receptors at synaptic sites during early S1 development. This thesis demonstrates that synaptic proteins associated with MR are expressed early in development and display regulatory roles in cellular processes governing S1 formation. An understanding of their role in early brain development would be critical in fully appreciating when and where they exert their regulatory effects, and this in turn would be beneficial in designing therapeutic interventions.

Fragile X Syndrome (FXS) is the most common form of inherited mental retardation, affecting approximately 1/4000 males and 1/6000 females worldwide. FXS is caused by loss of FMR1 gene expression, resulting in the lack of the protein product, Fragile X protein (FMRP). FMRP is an RNA-binding protein thought to regulate synaptic plasticity by controlling the localization and translation of specific mRNAs in neurons. To determine whether FMRP is also required in early brain development we examined the distribution of cell cycle markers in Drosophila FMR1 (dFmr1) mutant brains compared to wild-type brains. Our results indicate that the loss of dFmr1 leads to a significant increase in the number of mitotic neuroblasts and BrdU incorporation in the brain, consistent with the notion that FMRP controls proliferation in neural stem cells. To determine the role of FMRP in neuroblast division and differentiation, we used Mosaic Analysis with a Repressible Marker (MARCM) approaches in the developing larval brain and found that single dFmr1 neuroblasts generate significantly more neurons than controls. Developmental studies suggest that FMRP also inhibits neuroblast exit from quiescence, or reactivation, in early larval brains, as indicated by misexpression of the G1 to S phase transition marker Cyclin E. We have also identified a novel role for FMRP in the glia surrounding the neuroblasts, indicating that FMRP in these cells contributes to the regulation of neuroblast reactivation via signaling from the supporting glial cells. Our results demonstrate that FMRP is required during brain development to control the exit from quiescence and proliferative capacity of neuroblasts as well as neuron production, which may provide insights into Fragile X Syndrome and other Autism-Spectrum disorders.

The purpose of this study was to explore what contributes to resilience in females diagnosed with Fragile X Syndrome. Fragile X Syndrome can be defined as an inherited (genetic) condition that causes mental impairment, attention deficit and hyperactivity, anxiety and unstable mood, autistic behaviours, hyper-extensible joints, and seizures. I became aware of Fragile X Syndrome during my time as a live-in caretaker to an adolescent female who was diagnosed with Fragile X Syndrome. Because she coped with her disability so resiliently, I was encouraged to explore what contributes to resilience in females diagnosed with Fragile X Syndrome. I followed a qualitative approach, anchored in the interpretivist paradigm. This means that I tried to understand the resilience of females diagnosed with Fragile X Syndrome through the meanings that the participants in my study assigned to them. Furthermore, I worked from a transformative paradigm, which meant that I was interested in changing the traditionally negative ways in which females diagnosed with Fragile X Syndrome are seen. I followed a multiple case study approach, which included four case studies. I conveniently selected the first participant, but realised that convenience sampling was not very credible for a qualitative case study. An Advisory Panel was then used to purposefully recruit three more participants. In order to explore what contributed to their resilience, I made use of interviews, observations, and visual data collection. I also interviewed adults (e.g. parents, teachers and consulting psychologists) who were significantly involved in the lives of my participants. My findings suggest that resilience in females with Fragile X Syndrome is rooted in protective processes within the individual as well as within her family and environment. Because my findings do not point to one specific resource, my study underscores newer understandings of resilience as an Eco systemic transaction. Most of the resilience-promoting resources noted by the participants in my study as contributing to their resilience have been identified as resilience-promoting in previous studies. Although the themes that emerged in my study have been reported in resilience previously, I make a contribution to theory because I link traditional resilience-promoting resources to resilience in females diagnosed with Fragile X Syndrome. Peer support was previously reported as a resilience-promoting resource, but in my study I noticed that the main source of peer support came from peers who were also disabled. Furthermore, my study transforms how we see females diagnosed with Fragile X Syndrome. This transformation encourages communities and families to work together towards resilience in females diagnosed with Fragile X Syndrome. / Ph.D, North-West University, Vaal Triangle Campus, 2011

Despite the broad discourse on fragile states and the threat they pose to the contemporary world order, the literature on the subject does to a large extent ignore the material factors behind the causes of state fragility. Scholars and organizations in the field have almost exclusively adopted the Social Contract Theory (SCT) in order to explain state fragility as a problem caused by social factors. This study broadens the discourse by applying SCT as well as the Actor-Network Theory (ANT) on the case study of Sudan, in order to do a deductive theory testing of the added value of each theory. The results of this study show that while the Social Contract Theory does explain many factors behind state fragility, the application of the Actor-Network Theory adds to this by also incorporating the networks between the social and material determinants in societies. This research contributes to the debate on fragile states by adding to the scarce research on the materiality of fragility through the use of the Actor-Network Theory. The positive results of this thesis encourage future use of this theory in the field as it has the potential to give new insights in how to deal with fragile states.

Student Number : 9901196J - MSc dissertation - School of Pathology - Faculty of Science / Fragile sites are highly unstable regions of the genome, which have a tendency to form gaps and breaks in metaphase chromosomes under replication stress conditions. There are many common fragile sites in the human genome and exposure to carcinogens may affect several genes localised in fragile sites within a single cell, which could lead to activation of oncogenes and inactivation of tumour-suppressor genes simultaneously. FRA3B on chromosome 3 and FRA16D on chromosome 16 are the two most commonly expressed fragile sites and contain the FHIT and WWOX genes respectively. These genes are tumour suppressor genes and are inactivated in a number of different ways. Carcinogens found in cigarette smoke have been found to increase fragile site expression and could alter the integrity of theses genes in active smokers. Ten healthy non-smoking (control) individuals and twenty active smokers were recruited for the purpose of this study. Fluorescence in situ hybridisation was performed with probes spanning spanning the FHIT gene and RT-PCR was performed to assess both FHIT and WWOX expression. No significant difference in breaks at fragile sites was observed between controls and active smokers in the FISH experiments. In addition, no aberrant transcripts were detected for either FHIT or WWOX with RT-PCR. Although the sampling group was limited and heterogenous, no increase in the expression of breaks at fragile sites was seen in active smokers in the present study.

Thesis advisor: Summer S. Hawkins / Preventing poor health in childhood is a national social work and public health priority in the United States. Importantly, child health and wellbeing is explicitly linked with maternal health. Thus, maternal depression, a common mental illness, is a concern not only for the mother, but for the health of her offspring. The purpose of this three-paper dissertation was to extend the understanding of child health and wellbeing at age 9 years old in the context of maternal depression. Analyses utilized data from the Fragile Families and Child Wellbeing study and were guided by a resilience perspective, life course perspective, family systems theory, and ecological systems theory. Paper 1 examined the unique impact of maternal depression on child physical health outcomes utilizing a series of logistic regression analyses. Findings indicated that multiple individual-, maternal-, and family-level risk and protective factors influenced the association between maternal depression and child physical health. Paper 2 utilized latent profile analysis and multinomial logistic regression analyses to examine child physical health and psychosocial wellbeing in the context of maternal depression. Five distinct profiles of child health and wellbeing were identified, suggesting the traditional dichotomy of healthy versus unhealthy may fail to capture the complex nature of child health and wellbeing for those experiencing maternal depression. Results showed that maternal depression was associated with increased risk of poor health and wellbeing, yet also emphasized the ability for children to achieve resilient functioning. Paper 3 explored the impact of maternal depression on the maternal-child relationship and the protective nature of interpersonal supports and community resources. Findings indicated that interpersonal and community resources directly and indirectly supported a positive maternal-child relationship for mothers with depression. Altogether, results extend the literature base by providing a more nuanced and complete examination of child health and wellbeing in the context of maternal depression, with a focus on the potential for resilient functioning among this at-risk population. Findings provide evidence that even in the context of risk, protective factors exist that support resilient functioning. Results have important policy and practical implications, including continued screenings for maternal depression in a primary care setting. / Thesis (PhD) — Boston College, 2017. / Submitted to: Boston College. Graduate School of Social Work. / Discipline: Social Work.