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1.
Dev Dyn ; 249(1): 141-153, 2020 01.
Article in English | MEDLINE | ID: mdl-31736174

ABSTRACT

BACKGROUND: At the earliest stages of brain development, the neuroepithelium works as an interdependent functional entity together with cerebrospinal fluid, which plays a key regulatory role in neuroepithelial cell survival, replication and neurogenesis; however, the underlying mechanism remains unknown in mammals. RESULTS: We show the presence of fibroblast growth factor 2 (FGF2) and epidermal growth factor (EGF), in 13.5-day rat embryo cerebrospinal fluid (eCSF). Immunohistochemical detection of FGF2 expression localized this factor inside neuroepithelial precursors close to the neuroepithelial-CSF interface, suggesting that FGF2 from eCSF could originate in the neuroepithelium by apical secretion. The colocalization of FGFR1 and FGF2 in some neuroepithelial cells close to the ventricular surface suggests they are target cells for eCSF FGF2. Brain neuroepithelium EGF expression was negative. By using a neuroepithelial organotypic culture, we demonstrate that FGF2 and EGF from eCSF plays a specific role in triggering the self-renewal and are involved in neurogenetic induction of mesencephalic neuroepithelial precursor cells during rat development. CONCLUSIONS: We propose eCSF as an intercommunication medium for neuroepithelial precursor behavior control during early rat brain development, and the neuroepithelial regulation of FGF2 and EGF presence in eCSF, as a regulative mechanism controlling precursor proliferation and neurogenesis.


Subject(s)
Epidermal Growth Factor/metabolism , Fibroblast Growth Factor 2/metabolism , Animals , Brain/embryology , Brain/metabolism , Cell Differentiation/genetics , Cell Differentiation/physiology , Cell Proliferation/genetics , Cell Proliferation/physiology , Cerebrospinal Fluid/metabolism , Embryo, Mammalian/metabolism , Epidermal Growth Factor/genetics , Fibroblast Growth Factor 2/genetics , Neurogenesis/genetics , Neurogenesis/physiology , Rats
2.
Cells Tissues Organs ; 198(5): 398-404, 2013.
Article in English | MEDLINE | ID: mdl-24401814

ABSTRACT

INTRODUCTION: There is a nondeveloped neurogenic potential in the adult mammalian brain, which could be the basis for neuroregenerative strategies. Many research efforts have been made to understand the control mechanisms which regulate the transition from a neural precursor to a neuron in the adult brain. Embryonic cerebrospinal fluid (CSF) is a complex fluid which has been shown to play a key role in neural precursor behavior during development, working as a powerful neurogenic inductor. We tested if the neurogenic properties of embryonic CSF are able to increase the neurogenic activity of neuronal precursors from the subventricular zone (SVZ) in the brains of adult mice. RESULTS: Our results show that mouse embryonic CSF significantly increases the neurogenic activity in precursor cells from adult brain SVZ. This intense neurogenic effect was specific for embryonic CSF and was not induced by adult CSF. CONCLUSIONS: Embryonic CSF is a powerful neurogenesis inductor in homologous neuronal precursors in the adult brain. This property of embryonic CSF could be a useful tool in neuroregeneration strategies.


Subject(s)
Brain/cytology , Cerebral Cortex/embryology , Cerebrospinal Fluid/physiology , Neurons/cytology , Animals , Cell Differentiation/physiology , Cell Growth Processes/physiology , Mice , Neurogenesis
3.
Dev Dyn ; 240(7): 1650-9, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21594951

ABSTRACT

Embryonic-cerebrospinal fluid (E-CSF) plays crucial roles in early brain development including the control of neurogenesis. Although FGF2 and lipoproteins present in the E-CSF have previously been shown to be involved in neurogenesis, the main factor triggering this process remains unknown. E-CSF contains all-trans-retinol and retinol-binding protein involved in the synthesis of retinoic acid (RA), a neurogenesis inducer. In early chick embryo brain, only the mesencephalic-rombencephalic isthmus (IsO) is able to synthesize RA. Here we show that in chick embryo brain development: (1) E-CSF helps to control RA synthesis in the IsO by means of the RBP and all-trans-retinol it contains; (2) E-CSF has retinoic acid activity, which suggests it may act as a diffusion pathway for RA; and (3) the influence of E-CSF on embryonic brain neurogenesis is to a large extent due to its involvement in RA synthesis. These data help to understand neurogenesis from neural progenitor cells.


Subject(s)
Brain/embryology , Brain/metabolism , Cerebrospinal Fluid/metabolism , Neurogenesis/physiology , Tretinoin/metabolism , Animals , Cell Line , Cells, Cultured , Chick Embryo , Chickens , Coculture Techniques , Mice , Retinol-Binding Proteins, Cellular/metabolism , Tubulin/metabolism
4.
Cells Tissues Organs ; 189(6): 391-402, 2009.
Article in English | MEDLINE | ID: mdl-18836253

ABSTRACT

Previous studies have demonstrated that during neural fold fusion in different species, an apical extracellular material rich in glycoconjugates is involved. However, the composition and the biological role of this material remain undetermined. In this paper, we show that this extracellular matrix in rat increases notably prior to contact between the neural folds, suggesting the dynamic behaviour of the secretory process. Immunostaining has allowed us to demonstrate that this extracellular matrix contains chondroitin sulphate proteoglycan (CSPG), with a spatio-temporal distribution pattern, suggesting a direct relationship with the process of adhesion. The degree of CSPG involvement in cephalic neural fold fusion in rat embryos was determined by treatment with specific glycosidases.In vitro rat embryo culture and microinjection techniques were employed to carry out selective digestion, with chondroitinase AC, of the CSPG on the apical surface of the neural folds; this was done immediately prior to the bonding of the cephalic neural folds. In all the treated embryos, cephalic defects of neural fold fusion could be detected. These results show that CSPG plays an important role in the fusion of the cephalic neural folds in rat embryos, which implies that this proteoglycan could be involved in cellular recognition and adhesion.


Subject(s)
Chondroitin Sulfate Proteoglycans/metabolism , Neural Crest/metabolism , Animals , Brain/metabolism , Cells, Cultured , Rats , Rats, Wistar
5.
Cytokine ; 37(2): 128-37, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17449272

ABSTRACT

Interleukin-1beta (IL-1beta) is an important trophic factor in the nervous system (NS). IL-1beta is ubiquitously expressed from very early stages during the development of the amphibian NS and its action has been demonstrated in vitro on survival, proliferation and differentiation in mammalian embryos. In this report, we show that IL-1beta is immunocytochemically expressed in embryonic spinal cord from early stages, both in rat (embryonic day 12) and in chicken (stage 17-HH), in neuroepithelial cells and nerve fibres, dorsal root ganglia, anterior and posterior roots of the spinal nerves, and in the fibres of these nerves. Our in vivo experiments on chick embryos, with microbeads impregnated with IL-1beta implanted laterally to the spinal cord at the level of the wing anlage, demonstrate that this cytokine produces a statistically significant increase in nuclear incorporation of BrdU at the dorsal level and a reduction of this at the ventral level, whereas local immunoblocking with anti-IL-1beta antibodies causes a dorsal reduction of BrdU incorporation and alters ventral differentiation. These data demonstrate that IL-1beta plays a part in controlling proliferation and early differentiation during the development of the spinal cord in chick embryos.


Subject(s)
Cell Differentiation/physiology , Cell Proliferation , Interleukin-1beta/metabolism , Neuroepithelial Cells/physiology , Spinal Cord , Animals , Chick Embryo , Morphogenesis , Neuroepithelial Cells/cytology , Rats , Rats, Wistar , Spinal Cord/cytology , Spinal Cord/growth & development
6.
Dev Biol ; 297(2): 402-16, 2006 Sep 15.
Article in English | MEDLINE | ID: mdl-16916506

ABSTRACT

During early stages of brain development, neuroepithelial stem cells undergo intense proliferation as neurogenesis begins. Fibroblast growth factor 2 (FGF2) has been involved in the regulation of these processes, and although it has been suggested that they work in an autocrine-paracrine mode, there is no general agreement on this because the behavior of neuroepithelial cells is not self-sufficient in explants cultured in vitro. In this work, we show that during early stages of development in chick embryos there is another source of FGF2, besides that of the neuroepithelium, which affects the brain primordium, since the cerebrospinal fluid (E-CSF) contains several isoforms of this factor. We also demonstrate, both in vitro and in vivo, that the FGF2 from the E-CSF has an effect on the regulation of neuroepithelial cell behavior, including cell proliferation and neurogenesis. In order to clarify putative sources of FGF2 in embryonic tissues, we detected by in situ hybridization high levels of mRNA expression in notochord, mesonephros and hepatic primordia, and low levels in brain neuroectoderm, corroborated by semiquantitative PCR analysis. Furthermore, we show that the notochord segregates several FGF2 isoforms which modify the behavior of the neuroepithelial cells in vitro. In addition, we show that the FGF2 ligand is present in the embryonic serum; and, by means of labeled FGF2, we prove that this factor passes via the neuroepithelium from the embryonic serum to the E-CSF in vivo. Considering all these results, we propose that, in chick embryos, the behavior of brain neuroepithelial stem cells at the earliest stages of development is influenced by the action of the FGF2 contained within the E-CSF which could have an extraneural origin, thus suggesting a new and complementary way of regulating brain development.


Subject(s)
Cerebrospinal Fluid/metabolism , Fibroblast Growth Factor 2/physiology , Neuroepithelial Cells/cytology , Stem Cells/cytology , Animals , Cell Differentiation , Cell Proliferation , Cerebrospinal Fluid Proteins/physiology , Chick Embryo , Embryonic Development , Fibroblast Growth Factor 2/metabolism , Neurons/metabolism , PC12 Cells , Rats
7.
J Neurochem ; 77(3): 786-95, 2001 May.
Article in English | MEDLINE | ID: mdl-11331407

ABSTRACT

The importance of individual members of the fibroblast growth factor gene family during innervation of the vertebrate inner ear is not clearly defined. Here we address the role of fibroblast growth factor 2 (FGF-2 or basic FGF) during development of the chicken inner ear. We found that FGF-2 stimulated survival of isolated cochlear and vestibular neurons during distinct phases of inner ear innervation. The potential neurotrophic role of FGF-2 was confirmed by its expression in the corresponding sensory epithelia and the detection of one of its high-affinity receptors in inner ear neurons. Finally, we have analysed the potential of the amplicon system based on defective herpes simplex virus type 1 (HSV-1) vectors to express FGF-2 in cochlear neurons. Overexpression of FGF-2 in cochlear neurons resulted in neuronal differentiation demonstrating the presence of biologically active growth factor. This study underlines the potential of FGF-2 to control innervation and development of sensory epithelia in the avian inner ear. Furthermore, amplicon vectors may provide a useful tool to analyse gene function in isolated neurons of the vertebrate inner ear.


Subject(s)
Ear, Inner/innervation , Fibroblast Growth Factor 2/physiology , Animals , Blotting, Western , Cells, Cultured , Chick Embryo , Chickens , Cochlea/embryology , Cochlea/innervation , Ear, Inner/embryology , Fibroblast Growth Factor 2/genetics , Fibroblast Growth Factor 2/pharmacology , Gene Expression , Genetic Vectors , Herpesvirus 1, Human/genetics , Immunohistochemistry , Neurons, Afferent/chemistry , Neurons, Afferent/drug effects , Neurons, Afferent/physiology , Receptor Protein-Tyrosine Kinases/analysis , Receptor, Fibroblast Growth Factor, Type 1 , Receptors, Fibroblast Growth Factor/analysis , Transfection , Vestibule, Labyrinth/embryology , Vestibule, Labyrinth/innervation
8.
Development ; 127(10): 2011-9, 2000 May.
Article in English | MEDLINE | ID: mdl-10769226

ABSTRACT

Loss-of-function experiments in avians and mammals have provided conflicting results on the capacity of fibroblast growth factor 3 (FGF3) to act as a secreted growth factor responsible for induction and morphogenesis of the vertebrate inner ear. Using a novel technique for gene transfer into chicken embryos, we have readdressed the role of FGF3 during inner ear development in avians. We find that ectopic expression of FGF3 results in the formation of ectopic placodes which express otic marker genes. The ectopically induced placodes form vesicles which show the characteristic gene expression pattern of a developing inner ear. Ectopic expression of FGF3 also influences the formation of the normal orthotopic inner ear, whereas another member of the FGF family, FGF2, shows no effects on inner ear induction. These results demonstrate that a single gene can induce inner ear fate and reveal an unexpectedly widespread competence of the surface ectoderm to form sensory placodes in higher vertebrates.


Subject(s)
Ear, Inner/embryology , Fibroblast Growth Factors/physiology , Proto-Oncogene Proteins/physiology , Animals , Chick Embryo , Ectoderm , Fibroblast Growth Factor 2/genetics , Fibroblast Growth Factor 2/physiology , Fibroblast Growth Factor 3 , Fibroblast Growth Factors/genetics , Genetic Vectors/physiology , Herpesvirus 1, Human/physiology , Humans , Morphogenesis , Proto-Oncogene Proteins/genetics
9.
Nat Cell Biol ; 2(2): 57-61, 2000 Feb.
Article in English | MEDLINE | ID: mdl-10655583

ABSTRACT

Activation of calcium-ion (Ca2+) channels on the plasma membrane and on intracellular Ca2+ stores, such as the endoplasmic reticulum, generates local transient increases in the cytosolic Ca2+ concentration that induce Ca2+ uptake by neighbouring mitochondria. Here, by using mitochondrially targeted aequorin proteins with different Ca2+ affinities, we show that half of the chromaffin-cell mitochondria exhibit surprisingly rapid millimolar Ca2+ transients upon stimulation of cells with acetylcholine, caffeine or high concentrations of potassium ions. Our results show a tight functional coupling of voltage-dependent Ca2+ channels on the plasma membrane, ryanodine receptors on the endoplasmic reticulum, and mitochondria. Cell stimulation generates localized Ca2+ transients, with Ca2+ concentrations above 20-40 microM, at these functional units. Protonophores abolish mitochondrial Ca2+ uptake and increase stimulated secretion of catecholamines by three- to fivefold. These results indicate that mitochondria modulate secretion by controlling the availability of Ca2+ for exocytosis.


Subject(s)
Adrenal Medulla/metabolism , Calcium Signaling , Calcium/metabolism , Chromaffin Cells/metabolism , Mitochondria/metabolism , Acetylcholine/pharmacology , Adrenal Medulla/cytology , Animals , Biological Transport , Caffeine/pharmacology , Calcium Channels , Carbonyl Cyanide m-Chlorophenyl Hydrazone/pharmacology , Catecholamines/metabolism , Cattle , Cell Membrane/metabolism , Chromaffin Cells/cytology , Clonazepam/analogs & derivatives , Clonazepam/pharmacology , Endoplasmic Reticulum/metabolism , Potassium/pharmacology , Ryanodine Receptor Calcium Release Channel/metabolism , Sodium-Calcium Exchanger/antagonists & inhibitors , Thiazepines/pharmacology
10.
J Neurovirol ; 5(3): 280-8, 1999 Jun.
Article in English | MEDLINE | ID: mdl-10414518

ABSTRACT

Replication-defective mutants of herpes simplex virus type 1 (HSV-1) are powerful tools to transfer genes into postmitotic neurons and show promise for gene therapy protocols in vivo. To evaluate the efficacy and safety of these vectors for the treatment of deafness we infected dissociated cochlear ganglia with HSV mutants defective in the immediate early genes IE 2 (5dl1.2) or IE 3 (d120). Our results reveal striking differences in the survival of neuronal and non-neuronal cells caused by these mutants. Surprisingly, cochlear neurons infected with 5dl1.2 at various concentrations show a significant increase in survival after 2 days in culture. In contrast, many non-neuronal cells undergo apoptosis reducing cell number to less than 50%. In both neuronal and non-neuronal cell types we also observe a population of cells with important changes in morphology. Analysis of dissociated cochlear ganglia infected with d120 reveals a decrease of neuronal survival, whereas non-neuronal cells were almost unaffected. To further characterize and compare the effects of 5dl1.2 and d120 we transduced central nervous system-derived cell types including cortical neurons and astrocytes. Similarly, as observed for cochlear neurons, infection with 5dl1.2 results in increased survival of cortical neurons, whereas d120 shows cytotoxic effects. Survival of astrocytes is equally reduced by both HSV deletion mutants. We conclude that HSV-1 mutants defective in immediate early genes cause very distinct cytopathic phenotypes depending on the cellular context. Possible reasons for these differences, like various patterns of cellular and viral gene expression, and the implications for the use of HSV-1 vectors for gene transfer are discussed.


Subject(s)
Cochlear Nucleus/cytology , Defective Viruses/physiology , Gene Transfer Techniques , Herpesvirus 1, Human/physiology , Neurons/virology , Animals , Animals, Newborn , Apoptosis , Cell Survival/physiology , Cells, Cultured/virology , Chick Embryo , Chlorocebus aethiops , Defective Viruses/genetics , Gene Deletion , Genes, Immediate-Early/genetics , Herpesvirus 1, Human/genetics , Neurons/cytology , Rats , Vero Cells
11.
J Cell Biol ; 144(2): 241-54, 1999 Jan 25.
Article in English | MEDLINE | ID: mdl-9922451

ABSTRACT

The presence and physiological role of Ca2+-induced Ca2+ release (CICR) in nonmuscle excitable cells has been investigated only indirectly through measurements of cytosolic [Ca2+] ([Ca2+]c). Using targeted aequorin, we have directly monitored [Ca2+] changes inside the ER ([Ca2+]ER) in bovine adrenal chromaffin cells. Ca2+ entry induced by cell depolarization triggered a transient Ca2+ release from the ER that was highly dependent on [Ca2+]ER and sensitized by low concentrations of caffeine. Caffeine-induced Ca2+ release was quantal in nature due to modulation by [Ca2+]ER. Whereas caffeine released essentially all the Ca2+ from the ER, inositol 1,4, 5-trisphosphate (InsP3)- producing agonists released only 60-80%. Both InsP3 and caffeine emptied completely the ER in digitonin-permeabilized cells whereas cyclic ADP-ribose had no effect. Ryanodine induced permanent emptying of the Ca2+ stores in a use-dependent manner after activation by caffeine. Fast confocal [Ca2+]c measurements showed that the wave of [Ca2+]c induced by 100-ms depolarizing pulses in voltage-clamped cells was delayed and reduced in intensity in ryanodine-treated cells. Our results indicate that the ER of chromaffin cells behaves mostly as a single homogeneous thapsigargin-sensitive Ca2+ pool that can release Ca2+ both via InsP3 receptors or CICR.


Subject(s)
Calcium/metabolism , Chromaffin Cells/metabolism , Endoplasmic Reticulum/metabolism , Aequorin , Animals , Caffeine/pharmacology , Calcium Channel Blockers/pharmacology , Cattle , Chromaffin Cells/drug effects , Histamine/pharmacology , Microscopy, Confocal , Ryanodine/pharmacology , Thapsigargin/pharmacology
12.
Cell Calcium ; 24(2): 87-96, 1998 Aug.
Article in English | MEDLINE | ID: mdl-9803309

ABSTRACT

Changes in the free calcium concentration of the endoplasmic reticulum ([Ca2+]er) play a central role controlling cellular functions like contraction, secretion or neuronal signaling. We recently reported that recombinant aequorin targeted to the endoplasmic reticulum (ER) [Montero M., Brini M., Marsault R. et al. Monitoring dynamic changes in free Ca2+ concentration in the endoplasmic reticulum of intact cells. EMBO J 1995; 14: 5467-5475, Montero M., Barrero M.J., Alvarez J. [Ca2+] microdomains control agonist-induced Ca2+ release in intact cells. FASEB J 1997; 11: 881-886] can be used to monitor selectively [Ca2+]er in intact HeLa cells. Here we have used a herpes simplex virus type 1 (HSV-1) based system to deliver targeted aequorin into a number of different cell types including both postmitotic primary cells (anterior pituitary cells, chromaffin cells and cerebellar neurons) and cell lines (HeLa, NIH3T3, GH3 and PC12 cells). Functional studies showed that the steady state lumenal [Ca2+]er ranged from around 300 microM in granule cells to 800 microM in GH3 cells. InsP3-coupled receptor stimulation with agonists like histamine (in HeLa, NIH3T3 and chromaffin cells), UTP and bradykinin (in PC12 cells) or thyrotropin-releasing hormone (TRH, in GH3 cells) produced a very rapid decrease in lumenal [Ca2+]er. Caffeine caused a rapid Ca2+ depletion of the ER in chromaffin cells, but not in the other cell types. Depolarization by high K+ produced an immediate and reversible increase of [Ca2+]er in all the excitable cells (anterior pituitary, GH3, chromaffin cells and granule neurons). We conclude that delivery of recombinant aequorin to the ER using HSV amplicon provides the first direct quantitative and dynamic measurements of [Ca2+]er in several primary non-dividing cells.


Subject(s)
Aequorin/genetics , Calcium/analysis , Endoplasmic Reticulum/chemistry , Gene Transfer Techniques , Simplexvirus/genetics , Aequorin/metabolism , Animals , Bradykinin/pharmacology , Caffeine/pharmacology , Calcium/metabolism , Chromaffin Cells/metabolism , Endoplasmic Reticulum/metabolism , Genetic Vectors , HeLa Cells/drug effects , HeLa Cells/metabolism , Histamine/pharmacology , Humans , Immunohistochemistry/methods , Luminescent Measurements , Mice , Neurons/metabolism , Neurons/virology , PC12 Cells/drug effects , PC12 Cells/metabolism , Pituitary Gland, Anterior/cytology , Pituitary Gland, Anterior/metabolism , Pituitary Gland, Anterior/virology , Rats , Recombinant Proteins/metabolism , Thyrotropin-Releasing Hormone/pharmacology , Uridine Triphosphate/pharmacology
13.
J Neurochem ; 70(6): 2336-46, 1998 Jun.
Article in English | MEDLINE | ID: mdl-9603198

ABSTRACT

The importance of individual members of the neurotrophin gene family for avian inner ear development is not clearly defined. Here we address the role of two neurotrophins, brain-derived neurotrophic factor (BDNF) and nerve growth factor (NGF), for innervation of the chicken cochlea. We have used defective herpes simplex virus type 1 (HSV-1) vectors, or amplicons, to express these neurotrophins in dissociated cultures of cochlear neurons. HSV-1-mediated expression of BDNF promotes neuronal survival similar to the maximal level seen by exogenously added BDNF and exceeds its potency to produce neurite outgrowth. In contrast, cochlear neurons transduced with an amplicon producing bioactive NGF show no response. These results confirm BDNF as an important mediator of neurotrophin signaling inside avian cochlear neurons. However, these neurons can be rendered NGF-responsive by transducing them with the high-affinity receptor for NGF, TrkA. This study underlines the usefulness of amplicons to study and modify neurotrophin signaling inside neurons.


Subject(s)
Brain-Derived Neurotrophic Factor/physiology , Gene Transfer Techniques , Herpesvirus 1, Human/genetics , Nerve Growth Factors/physiology , Neurons/physiology , Spiral Ganglion/cytology , Animals , Brain-Derived Neurotrophic Factor/biosynthesis , Brain-Derived Neurotrophic Factor/genetics , Cell Survival , Cells, Cultured , Chick Embryo , Genetic Vectors , Nerve Growth Factors/biosynthesis , Nerve Growth Factors/genetics , Neurites/physiology , Neurons/metabolism , Neurons/ultrastructure , Neurons/virology , Proto-Oncogene Proteins/biosynthesis , Proto-Oncogene Proteins/genetics , Receptor Protein-Tyrosine Kinases/biosynthesis , Receptor Protein-Tyrosine Kinases/genetics , Receptor, trkA , Receptors, Nerve Growth Factor/biosynthesis , Receptors, Nerve Growth Factor/genetics , Spiral Ganglion/metabolism , Spiral Ganglion/ultrastructure , Spiral Ganglion/virology , Transduction, Genetic
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