EURYI project to understand how the brain wires during embryogenesisSeptember 24, 2007One of the great questions of neurobiology, how the brain is built up during embryonic development, could be resolved by a young French scientist in an award winning project organised by the European Science Foundation (ESF) and the European Heads of Research Councils (EuroHORCS). Sonia Garel has won one of the prestigious EURYI Awards granted annually to young scientists, to pursue her ground breaking research into mammalian forebrain development. She will tackle a number of fundamental questions relating both to the wiring of the brain during growth, and how evolution drove forward the sophisticated neural circuitry associated with mammals. Garel will focus on two key processes involved in development of neural circuitry in the forebrains of young mammals as they grow. One of these processes concerns the formation of connections between neurons, the nerve cells of the brain. These connections are needed to process sensory information, execute motor functions, and provide the network for cognitive abilities. They are made up of nerve fibres called axons, which conduct electrical impulses between neurons. The other key process involves migration of brain cells to their correct positions after their manufacture. As Garel noted, these two processes are coordinated in the development of the mammalian brain, and yet have until now been studied separately for the sake of simplicity. Garel and her colleagues have already broken new ground by demonstrating the link between axon formation, and migration of cells, within the brain. "While axon guidance and cell migration have been usually studied as independent processes, our group has shown for the first time that they are elegantly coordinated to ensure the formation of a major long-range connection of the mammalian brain, the thalamocortical projection," said Garel. The thalamocortical projection is one of the significant evolutionary developments of the forebrain, comprising bundles of axonal connections linking two key centres, the thalamus, which relays external sensory information, and the cerebral cortex, the most highly developed region comprising the so-called grey matter.
The thalamocortical projections, that first appeared in reptiles, have been remodelled in rodents and in primates, and are therefore of great interest in the study of neurological evolution. This phase of accelerated changes in connections correlates with an increase in cell migration in the brain. But there was a price to pay for this sophistication in the form of disorders associated with neurological dysfunctions, which particularly afflict humans. Garel hopes that her work will also advance understanding of some of these disorders, which can arise through defects both in the network of axonal connections and in the process of cell migration. "Understanding how neural circuits are elaborated during mammalian forebrain development is essential to gain insights into its normal functioning and to make progress in our comprehension of neurological and psychiatric disorders," said Garel. But malfunctions in cell migration can be just as harmful. "During development, cell migration is essential to control the positioning of cells in the brain, and cell migration defects have been associated with several neuropsychiatry diseases such as epilepsy, schizophrenia or bipolar disorders," said Garel. Garel will conduct her research in mice, aiming to improve understanding of how cell migration and axonal circuit development fit together. "We have showed that, in mice embryos, migrating cells act as dynamic guideposts to guide growing axons towards their final target in the brain," said Garel. "Our study thus opens a novel perspective of the role of cell migration in the formation of brain connections during normal and pathological development." The EURYI awards scheme, entering its fourth and final year, is designed to attract outstanding young scientists from around the world to create their own research teams at European research centres and launch potential world-leading research careers. Most awards are between €1,000,000 and €1,250,000, comparable in size to the Nobel Prize. Garel will receive her award in Helsinki, Finland on 27 September 2007 with other 19 young researchers. Sonia Garel, 35 year-old French citizen, is an independent young investigator at Paris' Ecole Normale Supérieur, studying forebrain regionalisation and formation of thalamocortical projections. Dr. Garel gained her doctorate in molecular and cellular pharmacology at the University of Paris VI, which she followed by a post-doctoral stay at the University of California in San Francisco. She came back to France in 2003 and was selected for a career development award from the Human Frontier Science Program Organisation. She has been a regular contributor to journals such as Development. European Science Foundation | |||||||||||||||||||||
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Related Embryogenesis Current Events and Embryogenesis News Articles Case Western Reserve University uncovers genetic basis for some birth defects A multidisciplinary research team at Case Western Reserve University led by Gary Landreth, Ph.D., a professor in the School of Medicine's Department of Neurosciences, has uncovered a common genetic pathway for a number of birth defects that affect the development of the heart and head. Abnormal development of the jaw, palate, brain and heart are relatively common congenital defects and frequently arise due to genetic errors that affect a key developmental pathway. Scientists identify genes capable of regulating stem cell function Scientists from The Forsyth Institute, Boston, MA, and the Howard Hughes Medical Institute at the University of Utah School of Medicine have developed a new system in which to study known mammalian adult stem cell disorders. Protein maintains cross talk between cells that control hair growth Genes, it turns out, are only as active as the signals that turn them on and off. Now scientists from Rockefeller University and the Howard Hughes Institute have identified the signaling molecule that ratchets up and clamps down the activity of key genes in dermal papilla, a type of skin cell whose unique collection of proteins ultimately instruct epithelial stem cells to make hair. Study examines genetic defects linked to body abnormalities in patients with childhood cancer Children with cancer have a higher prevalence of body abnormalities, such as asymmetric lower limbs and curvature of the spine, suggesting that the genetic defect responsible for the abnormality may play a role in the development of cancer, according to a study in the January 2 issue of JAMA. Cold Spring Harbor Protocols features innovative methods for embryology research Two methods that permit scientists to examine critical stages in early embryogenesis are featured in this month's release of Cold Spring Harbor Protocols. How stem cells are regulated Researchers from Biotech Research & Innovation Centre (BRIC) at University of Copenhagen have identified a new group of proteins that regulate the function of stem cells. The results are published in the new issue of Cell. Cleft palate in fetal mice prevented by treating Mice engineered to have cleft palates can be rescued in utero by injecting the mothers with a small molecule to correct the defect, say scientists at the Stanford University School of Medicine and Lucile Packard Children's Hospital. Jefferson researchers uncover new way nature turns genes on and off Peering deep within the cells of fruit flies, developmental biologists at the Kimmel Cancer Center at Thomas Jefferson University in Philadelphia may have discovered a new way that genes are turned on and off during development. Vax and Pax: Taking turns to build an eye Opposing ball clubs don't take the field at the same time, and neither do teams of proteins responsible for creating the eye. While one team builds the retina, in adjacent cellular turf the opponents are busy constructing the cord that carries visual signals to the brain. And these guys aren't supposed to mingle. Study will explore genetics of congenital limb and heart malformations New research published in the August issue of the Journal of Cell Biology explains for the first time why congenital heart defects so often occur with limb deformities. More Embryogenesis Current Events and Embryogenesis News Articles |
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