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2005, Nature
Neuronal polarization occurs shortly after mitosis. In neurons differentiating in vitro, axon formation follows the segregation of growth-promoting activities to only one of the multiple neurites that form after mitosis 1,2 . It is unresolved whether such spatial restriction makes use of an intrinsic program, like during C. elegans embryo polarization 3 , or is extrinsic and cue-mediated, as in migratory cells 4 . Here we show that in hippocampal neurons in vitro, the axon consistently arises from the neurite that develops first after mitosis. Centrosomes, the Golgi apparatus and endosomes cluster together close to the area where the first neurite will form, which is in turn opposite from the plane of the last mitotic division. We show that the polarized activities of these organelles are necessary and sufficient for neuronal polarization: (1) polarized microtubule polymerization and membrane transport precedes first neurite formation, (2) neurons with more than one centrosome sprout more than one axon and (3) suppression of centrosome-mediated functions precludes polarization. We conclude that asymmetric centrosome-mediated dynamics in the early post-mitotic stage instruct neuronal polarity, implying that pre-mitotic mechanisms with a role in division orientation may in turn participate in this event.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 2000
Hippocampal neurons developing in culture exhibit two types of differential, seemingly competitive, process outgrowth in the absence of external cues. During the initial acquisition of polarity, one of several equivalent undifferentiated minor neurites preferentially grows to become the axon. Once the axon has formed, it typically branches, and the branches grow differentially rather than concurrently. In axons with only two branches, growth alternates between branches. In both axon establishment and branch growth alternation, growth among sibling processes or branches must be differentially regulated. We found that elaborate and dynamic growth cones were associated with growth, whereas diminished growth cones were associated with nongrowing processes or branches. To test whether growth cones were necessary for differential growth, growth cone motility was eliminated by application of cytochalasin E. Although cytochalasin treatment before axon formation yielded longer processes over...
Developmental Biology, 1989
By the end of the first week in culture, hippocampal neurons have established a single axon and several dendrites. These 2 classes of processes differ in their morphology, in their molecular composition,
Final morphological polarization of neurons, with the development of a distinct axon and of several dendrites, is preceded by phases of non-polarized architecture. The earliest of these phases is that of the round neuron arising from the last mitosis. A second non polarized stage corresponds to the bipolar neuron, with two morphologically identical neurites. Both phases have their distinctive relevance in the establishment of neuronal polarity. During the round cell stage a decision is made as to where from the cell periphery a first neurite will form, thus creating the first sign of asymmetry. At the bipolar stage a decision is made as to which of the two neurites becomes the axon in neurons polarizing in vitro and the leading edge in neurons in situ. In this study we analysed cytoskeletal and membrane dynamics in cells at these two “pre-polarity” stages. By mean of time lapse imaging in dissociated hippocampal neurons and ex vivo cortical slices we show that both stages are characterized by polarized intracellular arrangements, however with distinct temporal hierarchies: polarized actin dynamics marks the site of first polarization in round cells, whereas polarized membrane dynamics precedes asymmetric growth in the bipolar stage.
Oncotarget, 2016
During the process of neurogenesis, the stem cell committed to the neuronal cell fate starts a series of molecular and morphological changes. The understanding of the physio-pathology of mechanisms controlling the molecular and morphological changes occurring during neuronal differentiation is fundamental to the development of effective therapies for many neurologic diseases. Unfortunately, our knowledge of the biological events occurring in the cell during neuronal differentiation is still poor. In this study, we focus preliminarily on the relevance of the cytoskeletal rearrangements, which earlier drive the morphology of the neuronal precursors, and later the migrating/mature neurons. In fact, neuritogenesis, neurite branching, outgrowth and retraction are seminal to the development of a fully functional nervous system. With this in mind, we highlight the importance of iPSC technology to study the processes of cytoskeletal-driven morphological changes during neuronal differentiation.
Seminars in Cell & Developmental Biology, 1996
Development of neurons from neuroblasts involves the extension of cytoplasmic processes (neurites) that mature into axons and dendrites in response to distinct extracellular signals. Changes in the cytoskeleton are crucial for neurite outgrowth and maturation. The initial sprouting of neurites requires rearrangements of actin microfilaments which are possibly under the control of proteins belonging to the Rho subfamily of GTPases. Little is known about the extracellular stimuli which regulate the activity of these GTPases in developing neurons. Likewise, the molecular mechanisms by which actin microfilament dynamics and organization are modified after the activation of Rho subfamily GTPases are not yet clear. The consolidation and maturation of growing neurites that become axons and dendrites requires the participation of other cytoskeletal elements, particularly microtubules. The expression and phosphorylation of specific microtubule-associated proteins may be important for axon and dendrite development. There is some information about the protein kinases and phosphatases that act on microtubule-associated proteins. However, much less is known about the signal transduction pathways that regulated microtubule-associated protein expression and phosphorylation in response to distinct extracellular signals.
| The stereotyped circuitry of the adult nervous system is a result of instructive guidance of the neuronal processes to their respective synaptic targets. Signal-induced, choreographed remodeling of the cytoskeleton in the neuronal growth cones is at the core of this remarkable feat of establishing precise connectivity. Actin and microtubule cytoskeleton undergo dynamic reorganization in response to guidance cues and enable the growth cone to navigate accurately through the complex environment of the developing embryo.
nature cell …, 2007
Extension of neurites from a cell body is essential to form a functional nervous system; however, the mechanisms underlying neuritogenesis are poorly understood. Ena/VASP proteins regulate actin dynamics and modulate elaboration of cellular protrusions. We recently reported that cortical axon-tract formation is lost in Ena/VASP-null mice and Ena/VASP-null cortical neurons lack filopodia and fail to elaborate neurites. Here, we report that neuritogenesis in Ena/VASP-null neurons can be rescued by restoring filopodia formation through ectopic expression of the actin nucleating protein mDia2. Conversely, wildtype neurons in which filopodia formation is blocked fail to elaborate neurites. We also report that laminin, which promotes the formation of filopodia-like actin-rich protrusions, rescues neuritogenesis in Ena/VASP-deficient neurons. Therefore, filopodia formation is a key prerequisite for neuritogenesis in cortical neurons. Neurite initiation also requires microtubule extension into filopodia, suggesting that interactions between actin-filament bundles and dynamic microtubules within filopodia are crucial for neuritogenesis.
The Journal of Neuroscience : The Official Journal of the Society for Neuroscience
We monitored developmental alterations in the morphology of dendritic spines in primary cultures of hippocampal neurons using confocal laser scanning microscopy (CLSM) and the fluorescent marker Dil. Dissociated rat hippocampal neurons were plated on polylysine-coated glass cover slips and grown in culture for l-4 weeks. Fixed cultures were stained with Dil and visualized with the CLSM. Spine density, spine length, and diameters of spine heads and necks were measured. Some cultures were immunostained for synaptophysin and others prepared for EM analysis. In the 1-3 week cultures, 92-95% of the neurons contained spiny dendrites. Two subpopulations of spine morphologies were distinguished. At 1 week in culture, "headless" spines constituted 50% of the spine population and were equal in length to the spines with heads. At 2, 3, and 4 weeks in culture headless spines constituted a progressively smaller fraction of the population and were, on average, shorter than spines with heads. Spines with heads had narrower necks than headless spines. At 3 weeks in culture, spines were associated with synaptophysin-immunoreactive labeling, resembling synaptic terminals.
Although several investigations have shown that the local GABAergic circuit in the rat hippocampus is functional very early in development, this result has not been yet completed by the investigation of the full dendritic and axonal arborization of the neonatal interneurones. In the present study, intracellular injection of biocytin was used to assess the branching pattern of interneurones in the hippocampal CA3 region of rat between 2 and 6 days of age. Based on their dendritic morphology, the biocytin-filled interneurones were divided into four classes: bipolar, stellate, pyramidal-like and fusiform interneurones. About half of the biocytin-filled neonatal interneurones exhibited dendritic or somatic filopodial processes. The axonal arbors of the filled-interneurones were widely spread into the CA3 region, and in four out of nine cases extended beyond the CA3 region to branch into the CA1 region. These results show that, despite immature features, the filopodial processes, the hippocampal interneurones are well developed early in development at a time when their target cells, the pyramidal neurones, are still developing. These observations are consistent with a trophic role that GABA may play early in development.
The Journal of Cell Biology, 1984
TO examine the role in neurite growth of actin-mediated tensions within growth cones, we cultured chick embryo dorsal root ganglion cells on various substrata in the presence of cytochalasin B. Time-lapse video recording was used to monitor behaviors of living cells, and cytoskeletal arrangements in neurites were assessed via immunofluorescence and electron microscopic observations of thin sections and whole, detergent-extracted cells decorated with the $1 fragment of myosin. On highly adhesive substrata, nerve cells were observed to extend numerous (though peculiarly oriented) neurites in the presence of cytochalasin, despite their lack of both filopodia and lamellipodia or the orderly actin networks characteristic of typical growth cones. We concluded that growth cone activity is not necessary for neurite elongation, although actin arrays seem important in mediating characteristics of substratum selectivity and neurite shape.
Brain Research, 1978
Neurobiologists have traditionally assumed that with maturation the neurones of the central nervous system gradually lose much or all of their capacity for growth and structural change (see ref. 2, page 330, for discussion). Recent studies on the various 'sprouting' responses of intact axons in partially deafferented brain sites have provided information which is germane to this issue. Specifically, it appears that while fiber growth, including collateral sprouting and synaptogenesis, does occur after lesions in the adult brain, these effects are more restricted than those observed after comparable damage in neonates. This developmental difference is well illustrated by the responses of the intact afferents of the rat dentate gyrus following removal of that structure's primary input. These projections are precisely laminated such that axons originating within the ipsilateral entorhinal cortex densely innervate the distal 75 ~ of the dendritic field of the dentate granule cells (the 'middle' and 'outer' molecular layers), whereas fibers from the regio inferior of the ipsilateral and contralateral hippocampi (the 'associational' and 'commissural' systems), form a dense plexus which occupies the dendritic region proximal to cell bodies (the 'inner' molecular layer). In the adult rat deafferentation of the outer portions of the dendritic field by removal of the ipsilateral entorhinal cortex induces an expansion of the commissural and associational terminal fields resulting in the repopulation of the adjacent 50 #m of the denervated territory. The more distal regions of the dentate molecular layer, similarly deafferented by the lesion, are not penetrated by the growing collateral sprouts of the inner plexus axons. However, if the lesion of the entorhinal cortex is performed within the first two postnatal weeks, the commissural and associational projections do not observe this limitation and occupy the deafferented region in its entiretyS, la. These effects provide a striking demonstration of the influence of maturation on axon plasticity and lead to a number of questions about the cellular nature of such influences. However, testable hypotheses regarding questions of this type will require a more complete comparison of the sprouting effect in young and adult brains. Particularly needed are data pertinent to the possibility that sprouting is initiated by different triggers and is governed by different rate limiting steps in the neonate and the adult; in other words, information on the postlesion interval required for the initiation of sprouting and the rate at which it proceeds once it has begun.
Current Biology, 2008
The Journal of Neuroscience, 2018
In 1988, Carlos Dotti, Chris Sullivan, and I published a paper on the establishment of polarity by hippocampal neurons in culture, which continues to be frequently cited 30 years later (Dotti et al., 1988). By following individual neurons from the time of plating until they had formed well developed axonal and dendritic arbors, we identified the five stages of development that lead to the mature expression of neuronal polarity. We were surprised to find that, before axon formation, the cells pass through a multipolar phase, in which several, apparently identical short neurites undergo periods of extension and retraction. Then one of these neurites begins a period of prolonged growth, becoming the definitive axon; the remaining neurites subsequently become dendrites. This observation suggested that any of the initial neurites were capable of becoming axons, a hypothesis confirmed by later work. In this Progressions article, I will try to recall the circumstances that led to this work...
Cell Differentiation, 1978
Nature Neuroscience, 2011
Polarization of a neuron begins with the appearance of the first neurite, thus defining the ultimate growth axis. Unlike late occurring polarity events (such as axonal growth), very little is known about this fundamental process. We show here that, in Drosophila melanogaster neurons in vivo, the first membrane deformation occurred 3.6 min after precursor division. Clustering of adhesion complex components (Bazooka , cadherin-catenin) marked this place by 2.8 min after division; the upstream phosphatidylinositol 4,5-bisphosphate, by 0.7 min after division; and the furrow components RhoA and Aurora kinase, from the time of cytokinesis. Local DE-cadherin inactivation prevented sprout formation, whereas perturbation of division orientation did not alter polarization from the cytokinesis pole. This is, to our knowledge, the first molecular study of initial neuronal polarization in vivo. The mechanisms of polarization seem to be defined at the precursor stage.
FEBS Journal, 2009
Journal of Cell Biology, 1989
In culture, hippocampal neurons develop a polarized form, with a single axon and several dendrites. Transecting the axons of hippocampal neurons early in development can cause an alteration of polarity; a process that would have become a dendrite instead becomes the axon (Dotti, C. G., and G. A. Banker. 1987. Nature (Lond.). 330:254-256). To investigate this phenomenon more systematically, we transected axons at varying lengths. The greater the distance of the transection from the soma, the greater the probability for regrowth of the original axon. However, it was not the absolute length of the axonal stump that determined the response to transection, but rather its length relative to the lengths of the cell's other processes. If one process was greater than 10 microns longer than the others, it invariably became the axon regardless of its identity before transection. Conversely, when a cell's processes were nearly equal in length, it was impossible to predict which would be...
Molecular and Cellular Neuroscience, 2011
Regulation of Ca 2+ concentrations is essential to maintain the structure and function of the axon initial segment (AIS). The so-called cisternal organelle of the AIS is a structure involved in this regulation, although little is known as to how this organelle matures and is stabilized. Here we describe how the cisternal organelle develops in cultured hippocampal neurons and the interactions that facilitate its stabilization in the AIS. We also characterize the developmental expression of molecules involved in Ca 2+ regulation in the AIS. Our results indicate that synaptopodin (synpo) positive elements considered to be associated to the cisternal organelle are present in the AIS after six days in vitro. There are largely overlapping microdomains containing the inositol 1,4,5-triphosphate receptor 1 (IP 3 R1) and the Ca 2+ binding protein annexin 6, suggesting that the regulation of Ca 2+ concentrations in the AIS is sensitive to IP 3 and subject to regulation by annexin 6. The expression of synpo, IP 3 R1 and annexin 6 in the AIS is independent of the neuron activity, as it was unaffected by tetrodotoxin blockage of action potentials and it was resistant to detergent extraction, indicating that these proteins interact with scaffolding and/or cytoskeleton proteins. The presence of ankyrin G seems to be required for the acquisition and maintenance of the cisternal organelle, while the integrity of the actin cytoskeleton must be maintained for the expression IP 3 R1 and annexin 6 to persist in the AIS.
Current Opinion in Cell Biology, 2012
In a biological sense, polarity refers to the extremity of the main axis of an organelle, cell, or organism. In neurons, morphological polarity begins with the appearance of the first neurite from the cell body. In multipolar neurons, a second phase of polarization occurs when a single neurite initiates a phase of rapid growth to become the neuron's axon, while the others later differentiate as dendrites. Finally, during a third phase, axons and dendrites develop an elaborate architecture, acquiring special morphological and molecular features that commit them to their final identities. Mechanistically, each phase must be preceded by spatial restriction of growth activity. We will review recent work on the mechanisms underlying the polarized growth of neurons.
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