Toxicité cellulaire d’un herbicide organophosphoré, le glufosinate d’ammonium, et de son principal métabolite : Induction d’un stress oxydatif et modifications des voies de différenciation sur un modèle murin in vitro de culture primaire de cellules souches neurales

The glufosinate-ammonium (GLA) is an organophosphorus herbicide commonly used in agriculture. Many cases of intentional ingestions have highlighted its neurotoxicity. However, its effects on neurodevelopment are not well studied. Indeed, the brain is an important target of GLA due to its structural homology with glutamate, the main excitatory neurotransmitter of the central nervous system. Our previous data are shown that a perinatal exposure to low doses of GLA induces disturbances in neurogenesis and in neuroblasts migration from the subventricular zone to the olfactory bulbs. These changes are associated with the development of autism spectrum disorders in the offspring. My thesis is in the continuity of his work and addresses the cellular and molecular aspects involved in early exposure to GLA. Since we are continuously exposed to pesticides, but also to their metabolites, I studied in parallel the effects of the main metabolite of GLA, the 4 methylphosphinyl-2-oxo-butanoic acid (PPO).The first work of my thesis was to develop an in vitro protocol for the primary culture of neural stem cells from the subventricular zone of mice, for the analysis of the neurotoxic effects of GLA and PPO. The results of the first study of my thesis showed an induction of related oxidative stress involving the glutamatergic system, and associated with a disruption of calcium homeostasis. Since neural stem cells are sensitive to the effects of oxidative stress, in a second study, I studied the impact of these effects on the cellular differentiation mechanisms of neural stem cells. My results indicated a significant effect of exposure to GLA and PPO on the formation and maintenance of the subventricular neurogenic niche in vitro. GLA and PPO interfere with the formation of ependyma and induce a disruption in the neuroglial differentiation of neural stem cells, without influencing their growth or proliferation capacity.All these data highlight on the interest of studying the cellular and molecular mechanisms linked to the neurotoxicity of the active substances of pesticides, the metabolites of these same pesticides, but also the mixtures of active substances and metabolites to which we are continuously exposed in our environment.Le glufosinate d’ammonium (GLA) est un herbicide organophosphoré couramment utilisé en agriculture. De nombreux cas d’ingestions intentionnelles ont mis en évidence sa neurotoxicité. Cependant, ses effets sur le neurodéveloppement ne sont peu étudiés. En effet, le cerveau est une cible importante du GLA en raison de son homologie de structure avec le glutamate, principal neurotransmetteur excitateur du système nerveux central. Des résultats précédents du laboratoire ont permis de montrer qu’une exposition périnatale à de faibles doses de GLA induisait des perturbations de la neurogenèse et de la migration des neuroblastes au niveau de la zone sous ventriculaire vers les bulbes olfactifs. Ces modifications sont associées à l’apparition de troubles du spectre autistique dans la descendance. Ma thèse s’inscrit dans la continuité de ses travaux en abordant les aspects cellulaires et moléculaires mis en jeux lors d’une exposition précoce au GLA. Etant donné que dans la vie de tous les jours, nous sommes continuellement exposés aux pesticides mais également à leurs métabolites, j’ai étudié en parallèle les effets du principal métabolite du GLA, l’acide 4-méthylphosphinyl-2-oxo-butanoïque (PPO).Le premier travail de ma thèse a été de développer un protocole in vitro de culture primaire de cellules souches neurales issues de la zone sous-ventriculaire de souris pour l’analyse des effets neurotoxiques du GLA et du PPO. Les résultats de la première étude de ma thèse montrent une induction d’un stress oxydatif lié impliquant le système glutamatergique et associé à une perturbation de l’homéostasie calcique. Etant donné que les cellules souches neurales sont sensibles aux effets d’un stress oxydatif, dans une seconde étude, j’ai étudié l’impact de ces effets sur les mécanismes de différenciation cellulaire des cellules souches neurales. Mes résultats indiquent un effet significatif d’une exposition au GLA et au PPO sur la formation et le maintien de la niche neurogénique sous-ventriculaire in vitro. Le GLA et le PPO interfèrent avec la formation de l’épithélium épendymaire et induisent une perturbation dans la différenciation neurogliale des cellules souches neurales, sans influencer leur capacité de croissance ou de prolifération.L’ensemble des données de cette thèse mettent l’accent sur l’intérêt d’étudier les mécanismes cellulaires et moléculaires liés à la neurotoxicité des substances actives des pesticides, des métabolites de ces mêmes pesticides, mais également des mélanges substances actives-métabolites auxquels nous sommes continuellement exposés dans notre environnement

Cellular toxicity of an organophosphate herbicide, ammonium glufosinate, and its main metabolite : Induction of oxidative stress and alteration in cell differentiation in an in vitro mouse model of primary neural stem cell culture

Le glufosinate d’ammonium (GLA) est un herbicide organophosphoré couramment utilisé en agriculture. De nombreux cas d’ingestions intentionnelles ont mis en évidence sa neurotoxicité. Cependant, ses effets sur le neurodéveloppement ne sont peu étudiés. En effet, le cerveau est une cible importante du GLA en raison de son homologie de structure avec le glutamate, principal neurotransmetteur excitateur du système nerveux central. Des résultats précédents du laboratoire ont permis de montrer qu’une exposition périnatale à de faibles doses de GLA induisait des perturbations de la neurogenèse et de la migration des neuroblastes au niveau de la zone sous ventriculaire vers les bulbes olfactifs. Ces modifications sont associées à l’apparition de troubles du spectre autistique dans la descendance. Ma thèse s’inscrit dans la continuité de ses travaux en abordant les aspects cellulaires et moléculaires mis en jeux lors d’une exposition précoce au GLA. Etant donné que dans la vie de tous les jours, nous sommes continuellement exposés aux pesticides mais également à leurs métabolites, j’ai étudié en parallèle les effets du principal métabolite du GLA, l’acide 4-méthylphosphinyl-2-oxo-butanoïque (PPO).Le premier travail de ma thèse a été de développer un protocole in vitro de culture primaire de cellules souches neurales issues de la zone sous-ventriculaire de souris pour l’analyse des effets neurotoxiques du GLA et du PPO. Les résultats de la première étude de ma thèse montrent une induction d’un stress oxydatif lié impliquant le système glutamatergique et associé à une perturbation de l’homéostasie calcique. Etant donné que les cellules souches neurales sont sensibles aux effets d’un stress oxydatif, dans une seconde étude, j’ai étudié l’impact de ces effets sur les mécanismes de différenciation cellulaire des cellules souches neurales. Mes résultats indiquent un effet significatif d’une exposition au GLA et au PPO sur la formation et le maintien de la niche neurogénique sous-ventriculaire in vitro. Le GLA et le PPO interfèrent avec la formation de l’épithélium épendymaire et induisent une perturbation dans la différenciation neurogliale des cellules souches neurales, sans influencer leur capacité de croissance ou de prolifération.L’ensemble des données de cette thèse mettent l’accent sur l’intérêt d’étudier les mécanismes cellulaires et moléculaires liés à la neurotoxicité des substances actives des pesticides, des métabolites de ces mêmes pesticides, mais également des mélanges substances actives-métabolites auxquels nous sommes continuellement exposés dans notre environnement.The glufosinate-ammonium (GLA) is an organophosphorus herbicide commonly used in agriculture. Many cases of intentional ingestions have highlighted its neurotoxicity. However, its effects on neurodevelopment are not well studied. Indeed, the brain is an important target of GLA due to its structural homology with glutamate, the main excitatory neurotransmitter of the central nervous system. Our previous data are shown that a perinatal exposure to low doses of GLA induces disturbances in neurogenesis and in neuroblasts migration from the subventricular zone to the olfactory bulbs. These changes are associated with the development of autism spectrum disorders in the offspring. My thesis is in the continuity of his work and addresses the cellular and molecular aspects involved in early exposure to GLA. Since we are continuously exposed to pesticides, but also to their metabolites, I studied in parallel the effects of the main metabolite of GLA, the 4 methylphosphinyl-2-oxo-butanoic acid (PPO).The first work of my thesis was to develop an in vitro protocol for the primary culture of neural stem cells from the subventricular zone of mice, for the analysis of the neurotoxic effects of GLA and PPO. The results of the first study of my thesis showed an induction of related oxidative stress involving the glutamatergic system, and associated with a disruption of calcium homeostasis. Since neural stem cells are sensitive to the effects of oxidative stress, in a second study, I studied the impact of these effects on the cellular differentiation mechanisms of neural stem cells. My results indicated a significant effect of exposure to GLA and PPO on the formation and maintenance of the subventricular neurogenic niche in vitro. GLA and PPO interfere with the formation of ependyma and induce a disruption in the neuroglial differentiation of neural stem cells, without influencing their growth or proliferation capacity.All these data highlight on the interest of studying the cellular and molecular mechanisms linked to the neurotoxicity of the active substances of pesticides, the metabolites of these same pesticides, but also the mixtures of active substances and metabolites to which we are continuously exposed in our environment

Neurodevelopmental effects of natural and synthetic ligands of estrogen and progesterone receptors in zebrafish eleutheroembryos

International audienceNatural and synthetic estrogens and progestins are widely used in human and veterinary medicine and are detected in waste and surface waters. Our previous studies have clearly shown that a number of these substances targets the brain to induce the estrogen-regulated brain aromatase expression but the consequences on brain development remain virtually unexplored. The aim of the present study was therefore to investigate the effect of estradiol (E2), progesterone (P4) and norethindrone (NOR), a 19-nortestosterone progestin, on zebrafish larval neurogenesis. We first demonstrated using real-time quantitative PCR that nuclear estrogen and progesterone receptor brain expression is impacted by E2, P4 and NOR. We brought evidence that brain proliferative and apoptotic activities were differentially affected depending on the steroidal hormone studied, the concentration of steroids and the region investigated. Our findings demonstrate for the first time that steroid compounds released in aquatic environment have the capacity to disrupt key cellular events involved in brain development in zebrafish embryos further questioning the short- and long-term consequences of this disruption on the physiology and behavior of organisms

Perinatal exposure to glufosinate ammonium herbicide impairs neurogenesis and neuroblast migration through cytoskeleton destabilization

Neurogenesis, a process of generating functional neurons from neural precursors, occurs throughout life in restricted brain regions such as the subventricular zone (SVZ). During this process, newly generated neurons migrate along the rostral migratory stream to the olfactory bulb to replace granule cells and periglomerular neurons. This neuronal migration is pivotal not only for neuronal plasticity but also for adapted olfactory based behaviors. Perturbation of this highly controlled system by exogenous chemicals has been associated with neurodevelopmental disorders. We reported recently that perinatal exposure to low dose herbicide glufosinate ammonium (GLA), leads to long lasting behavioral defects reminiscent of Autism Spectrum Disorder-like phenotype in the offspring (Laugeray, Herzine et al. 2014) . Herein, we demonstrate that perinatal exposure to low dose GLA induces alterations in neuroblast proliferation within the SVZ and abnormal migration from the SVZ to the olfactory bulbs. These disturbances are not only concomitant to changes in cell morphology, proliferation and apoptosis, but are also associated with transcriptomic changes. Therefore, we demonstrate for the first time that perinatal exposure to low dose GLA alters SVZ neurogenesis. Jointly with our previous work, the present results provide new evidence on the link between molecular and cellular consequences of early life exposure to the herbicide GLA and the onset of ASD-like phenotype later in life

Perinatal Exposure to the Cyanotoxin β-N-Méthylamino-l-Alanine (BMAA) Results in Long-Lasting Behavioral Changes in Offspring—Potential Involvement of DNA Damage and Oxidative Stress

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Multiple effects of the herbicide glufosinate-ammonium and its main metabolite on neural stem cells from the subventricular zone of newborn mice

International audienceThe globally used herbicide glufosinate-ammonium (GLA) is structurally analogous to the excitatory neurotransmitter glutamate, and is known to interfere with cellular mechanisms involved in the glutamatergic system. In this report, we used an in vitro model of murine primary neural stem cell culture to investigate the neurotoxicity of GLA and its main metabolite, 4-methylphosphinico-2-oxobutanoic acid (PPO). We demonstrated that GLA and PPO disturb ependymal wall integrity in the ventricular-subventricular zone (V-SVZ) and alter the neuro-glial differentiation of neural stem cells. GLA and PPO impaired the formation of cilia, with reduced Celsr2 expression after PPO exposure. GLA promoted the differentiation of neuronal and oligodendroglial cells while PPO increased B1 cell population and impaired neuronal fate of neural stem cells. These results confirm our previous in vivo report that developmental exposure to GLA alters neurogenesis in the SVZ, and neuroblast migration along the rostral migratory stream. They also highlight the importance of investigating the toxicity of pesticide degradation products. Indeed, not only GLA, but also its metabolite PPO disrupts V-SVZ homeostasis and provides a novel cellular mechanism underlying GLA-induced neurodevelopmental toxicity. Furthermore, we were able to demonstrate a neurotoxic activity of a metabolite of GLA different from that of GLA active substance for the very first time

XLF/Cernunnos loss impairs mouse brain development by altering symmetric proliferative divisions of neural progenitors

Summary: XLF/Cernunnos is a component of the ligation complex used in classical non-homologous end-joining (cNHEJ), a major DNA double-strand break (DSB) repair pathway. We report neurodevelopmental delays and significant behavioral alterations associated with microcephaly in Xlf−/− mice. This phenotype, reminiscent of clinical and neuropathologic features in humans deficient in cNHEJ, is associated with a low level of apoptosis of neural cells and premature neurogenesis, which consists of an early shift of neural progenitors from proliferative to neurogenic divisions during brain development. We show that premature neurogenesis is related to an increase in chromatid breaks affecting mitotic spindle orientation, highlighting a direct link between asymmetric chromosome segregation and asymmetric neurogenic divisions. This study reveals thus that XLF is required for maintaining symmetric proliferative divisions of neural progenitors during brain development and shows that premature neurogenesis may play a major role in neurodevelopmental pathologies caused by NHEJ deficiency and/or genotoxic stress