Search

PCDH19 gene-related epilepsy or epileptic encephalopathy, early infantile, 9 (EIEE9) is an infantile onset epilepsy syndrome characterized by psychiatric (including autistic) sensory and cognitive impairment of varying degrees. EIEE9 is caused by X-linked PCDH19 protein loss of function. Due to random X-chromosome inactivation, EIEE9-affected females present a mosaic population of healthy and Pcdh19-mutant cells. Unfortunately, no mouse models recapitulate to date both the brain histological and behavioural deficits present in people with EIEE9. Thus, the search for a proper understanding of the disease, and possible future treatment is hampered. By inducing a focal mosaicism of Pcdh19 expression using in utero electroporation in rat, we found here that Pcdh19 signaling in specific brain areas is implicated in neuronal migration, as well as in core behaviors related to autism and cognitive function.

Inherited retinal dystrophies (IRDs) are a large and heterogeneous group of degenerative diseases caused by mutations in various genes. Given the favorable anatomical and immunological characteristics of the eye, gene therapy holds great potential for their treatment. Our goal is to validate the preservation of visual functions by viral-free homology directed repair (HDR) in an autosomal recessive loss of function mutation. We used a tailored gene editing system based on clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) to prevent retinal photoreceptor death in the retinal degeneration 10 (Rd10) mouse model of retinitis pigmentosa. We tested the gene editing tool in vitro and then used in vivo subretinal electroporation to deliver it to one of the retinas of mouse pups at different stages of photoreceptor differentiation. Three months after gene editing, the treated eye exhibited a higher visual acuity compared to the untreated eye. Moreover, we observed preservation of light-evoked responses both in explanted retinas and in the visual cortex of treated animals. Our study validates a CRISPR/Cas9-based therapy as a valuable new approach for the treatment of retinitis pigmentosa caused by autosomal recessive loss-of-function point mutations.

Inherited retinal dystrophies are a large and heterogeneous group of degenerative diseases caused by mutations in various genes. Given the favourable anatomical and immunological characteristics of the eye, gene therapy holds great potential for their treatment. We used a tailored CRISPR/Cas9-based gene editing system to prevent retinal photoreceptor death in the Rd10 mouse model of retinitis pigmentosa. We tested the gene editing toolin vitroand then usedin vivosubretinal electroporation to deliver it to one of the retinas of mouse pups at different stages of photoreceptor differentiation. Three months after gene editing, the treated eye exhibited a higher visual acuity compared to the untreated eye. Moreover, we observed preservation of light-evoked responses both in explanted retinas and in the visual cortex of treated animals. Our study validates a CRISPR/Cas9-based therapy as a valuable new approach for the treatment of retinitis pigmentosa caused by autosomal recessive loss-of-function point mutations.

Since the dawn of neuroscience, genetic alterations causing macroscopic brain defects have attracted the attention of scientists. However, in recent years, the increasing understanding of the biological causes of neurological disorders such as Autism Spectrum Disorder or Schizophrenia have indicated that affected patients do not display gross structural alterations in the brain. These findings have shifted the attention of scientists toward the study of genetic alterations that may cause subtle defects in brain architecture. The investigation on such microscopic brain alterations is currently favored by the progress in experimental techniques for brain research. In Perlini et al., 2015 [1], we took advantage of the in utero electroporation technique coupled with RNA interference to examine the role of Synapsin III (SynIII) in the developing neocortex. SynIII belongs to the Syn family, which comprises three phosphoproteins abundantly expressed in the brain. Whereas a large body of literature indicates that both SynI and SynII are mainly involved in synaptic transmission and plasticity in the adult brain, the available data suggest an involvement of SynIII in brain development. First, SynIII is expressed early during mammalian brain formation and is involved in early stages of neuronal development in vitro, while it is downregulated in the adult brain [2, 3]. Second, SynIII participates in adult neurogenesis [3], and often proteins involved in adult neurogenesis are also players in brain development. Third, SynIII SNPs have been implicated in neurodevelopmental disorders such as schizophrenia, and SynIII knockout (KO) mice display some behavioral traits of schizophrenia [4]. Finally, according to evolutionary studies, the Syn family originated from a single primordial Syn gene that was expressed in the brain since early development [5]. As in higher vertebrates SynI and II are expressed mostly in the adult brain, SynIII probably carries out the functions performed during development by the primitive single Syn. Interestingly, the emergence of a distinct SynIII gene correlates with the appearance of the telencephalic region during evolution [6]. Despite the evidence suggesting a developmental role for SynIII, the initial analysis of SynIII KO mice revealed a mild behavioral phenotype with no gross alterations in brain development. We hypothesized that the alterations caused by SynIII absence could be very subtle and difficult to detect with conventional histochemical techniques. In Perlini et al., 2015 [1], we demonstrated that SynIII KO brains do have aberrant brain development with defects in neuronal orientation as visualized by in utero transfection of a fluorescent (GFP) reporter. As the migration and orientation phenotypes were milder in SynIII KO mice than in animals where SynIII was acutely downregulated by RNA interference, we hypothesized that a partial compensation phenomenon could be triggered by the chronic depletion of the protein in KO animals. Interestingly, also animals with in utero upregulation of SynIII levels presented defects in radial migration with the appearance of ectopic cells at late stages. Thus, SynIII plays a key role in the orchestration of cortical development, and a tight regulation of its expression is essential for this function. In Perlini et al., 2015 [1], we also demonstrated that the migration and orientation defects upon SynIII depletion involved the Sema3A/CDK5 signaling cascade. Indeed, Sema3A stimulation caused SynIII phosphorylation by CDK5 on Ser404 and such CDK5-dependent phosphorylation was essential for Sema3A-induced SynIII activity. It would be interesting to investigate whether SynIII participates in other developmental events mediated by Sema3A. Indeed, Sema3A is also involved in axon/dendrite initiation during the early phase of neuronal polarization through its negative regulation of PKA activity. Interestingly, SynIII also carries a highly conserved phosphorylation site targeted by PKA (Ser9), and defects in neuronal polarization consequent to SynIII downregulation were recently observed [7]. Besides the findings in Perlini et al., 2015 [1] demonstrating that SynIII acts downstream Sema3A, the existence of multiple phosphorylation sites on SynIII indicates that SynIII may be potentially downstream to other signaling pathways. Interestingly, during development, migrating cortical neurons encounter an increasing gradient of both Sema3A and Reelin around the marginal zone, and mice defective in Sema3A- and Reelin-signaling share common phenotypic features, such as misoriented neurons, also found in SynIII-downregulated brains. This suggests that Sema3A/SynIII and Reelin signaling interact at least in part. Notably, this interaction might be important for proper brain development and function, as an increase in Sema3A with a concomitant decrease of Reelin was observed in brains from schizophrenic patients. Moreover, both Sema3A and Reelin activate the Src-family kinase Fyn. The presence of a phosphorylation site for Src-family kinases (Tyr301) on SynIII puts this protein again downstream of Sema3A, but potentially also downstream of Reelin signaling, as a potential link through these two pivotal pathways for brain development. Therefore, despite the recent advancements in the comprehension of the role of SynIII in brain development, many questions on other potential functions of this protein remain open.

Synapsin III (SynIII) is a neuron-specific phosphoprotein that plays a unique role in neuronal development. SynIII is phosphorylated by cAMP-dependent protein kinase (PKA) at a highly conserved phosphorylation site and by cyclin-dependent kinase-5 (Cdk5) at a newly described site. Although SynIII is known to be involved in axon elongationin vitro, the role of its phosphorylation by PKA and Cdk5 in the modulation of this process is unknown. We expressed either wild-type (WT) or phosphorylation-site mutants of SynIII in primary SynIII knock-out (KO) mouse neurons at early stages ofin vitrodevelopment. Whereas the neurite elongation phenotype of SynIII KO neurons was fully rescued by the expression of WT SynIII, the expression of nonphosphorylatable and pseudo-phosphorylated PKA mutants was ineffective. Also, the nonphosphorylatable Cdk5 mutant was unable to rescue the neurite elongation phenotype of SynIII KO neurons. By contrast, the pseudo-phosphorylated mutant rescued the delay in neuronal maturation and axonal elongation, revealing a Cdk5-dependent regulation of SynIII function. Interestingly, SynIII KO neurons also exhibited decreased survival that was fully rescued by the expression of WT SynIII, but not by its phosphorylation mutants, and was associated with increased activated caspase3 and altered tropomyosin receptor kinase B isoform expression. These results indicate that PKA and Cdk5 phosphorylation is required for the physiological action of SynIII on axon specification and neurite outgrowth and that the expression of a functional SynIII is crucial for cell survival.SIGNIFICANCE STATEMENTSynapsin III is an atypical member of the synapsin family of synaptic vesicle-associated phosphoproteins that is precociously expressed in neurons and is downregulated afterward. Although experimental evidence suggests a specific role for Synapsin III in neuronal development, the molecular mechanisms are still largely unknown. We found that Synapsin III plays a central role in early stages of neuronal development involving neuronal survival, polarization, and neuritic growth and that these effects are dependent on phosphorylation by cAMP-dependent protein kinase and cyclin-dependent protein kinase-5. These results explain the recently described neurodevelopmental defects in the migration and orientation of Synapsin III-depleted cortical neurons and support the potential association of Synapsin III with neurodevelopmental disorders such as schizophrenia.

Summary Synapsin III (SynIII) is a phosphoprotein that is highly expressed at early stages of neuronal development. Whereas in vitro evidence suggests a role for SynIII in neuronal differentiation, in vivo evidence is lacking. Here, we demonstrate that in vivo downregulation of SynIII expression affects neuronal migration and orientation. By contrast, SynIII overexpression affects neuronal migration, but not orientation. We identify a cyclin-dependent kinase-5 (CDK5) phosphorylation site on SynIII and use phosphomutant rescue experiments to demonstrate its role in SynIII function. Finally, we show that SynIII phosphorylation at the CDK5 site is induced by activation of the semaphorin-3A (Sema3A) pathway, which is implicated in migration and orientation of cortical pyramidal neurons (PNs) and is known to activate CDK5. Thus, fine-tuning of SynIII expression and phosphorylation by CDK5 activation through Sema3A activity is essential for proper neuronal migration and orientation., Graphical Abstract, Highlights • Precise regulation of SynIII expression is essential during brain development • SynIII regulates neuronal migration, orientation, and morphological maturation • SynIII acts downstream of the Sema3A pathway, which involves NP1 and kinase CDK5 • Phosphorylation of SynIII by CDK5 on Ser404 is essential for SynIII function, During brain development, newborn pyramidal neurons radially migrate to shape the neocortex. Perlini et al. show that the neuronal phosphoprotein Synapsin III (SynIII) is part of the Sema3A/NP1/CDK5 pathway and contributes to the regulation of proper neuronal migration and orientation/morphological maturation of cortical neurons.

International audience; Synapsins are synaptic vesicle (SV)-associated proteins that regulate synaptic transmission and neuronal differentiation. At early stages, Syn I and II phosphorylation at Ser9 by cAMP-dependent protein kinase (PKA) and Ca2+/calmodulin-dependent protein kinase I/IV modulates axon elongation and SV-precursor dynamics. We evaluated the requirement of Syn I for synapse formation by siRNA-mediated knockdown as well as by overexpression of either its wild-type (WT) form or its phosphorylation mutants. Syn1 knockdown at 14 days in vitro caused a decrease in the number of synapses, accompanied by a reduction of SV recycling. Although overexpression of WT Syn I was ineffective, overexpression of its phosphorylation mutants resulted in a complex temporal regulation of synapse density. At early stages of synaptogenesis, phosphomimetic Syn I S9E significantly increased the number of synapses. Conversely, dephosphomimetic Syn I S9A decreased synapse number at more advanced stages. Overexpression of either WT Syn I or its phosphomimetic S9E mutant rescued the decrease in synapse number caused by chronic treatment with tetrodotoxin at early stages, suggesting that Syn I participates in an alternative PKA-dependent mechanism that can compensate for the impairment of the activity-dependent synaptogenic pathway. Altogether these results indicate that Syn I is an important regulator of synapse formation, which adjusts synapse number in response to extracellular signals.