ABSTRACT
Nuclear migration of newly born neurons is essential for cortex formation in the brain. The nucleus is translocated by actin and microtubules, yet the actual force generated by the interplay of these cytoskeletons remains elusive. High-resolution time-lapse observation of migrating murine cerebellar granule cells revealed that the nucleus actively rotates along the direction of its translocation, independently of centrosome motion. Pharmacological and molecular perturbation indicated that spin torque is primarily generated by microtubule motors through the LINC complex in the absence of actomyosin contractility. In contrast to the prevailing view that microtubules are uniformly oriented around the nucleus, we observed that the perinuclear microtubule arrays are of mixed polarity and both cytoplasmic dynein complex and kinesin-1 are required for nuclear rotation. Kinesin-1 can exert a point force on the nuclear envelope via association with nesprins, and loss of kinesin-1 causes failure in neuronal migration in vivo Thus, microtubules steer the nucleus and drive its rotation and translocation via a dynamic, focal interaction of nesprins with kinesin-1 and dynein, and this is necessary for neuronal migration during brain development.
Subject(s)
Cell Movement , Cell Nucleus/physiology , Microfilament Proteins/physiology , Microtubules/physiology , Nerve Tissue Proteins/physiology , Neurons/physiology , Animals , Animals, Newborn , Cell Nucleus/metabolism , Cells, Cultured , Female , HEK293 Cells , Humans , Male , Mice , Mice, Inbred ICR , Mice, Transgenic , Microtubules/metabolism , Motion , NIH 3T3 CellsABSTRACT
Neural activity plays roles in the later stages of development of cortical excitatory neurons, including dendritic and axonal arborization, remodeling, and synaptogenesis. However, its role in earlier stages, such as migration and dendritogenesis, is less clear. Here we investigated roles of neural activity in the maturation of cortical neurons, using calcium imaging and expression of prokaryotic voltage-gated sodium channel, NaChBac. Calcium imaging experiments showed that postmigratory neurons in layer II/III exhibited more frequent spontaneous calcium transients than migrating neurons. To test whether such an increase of neural activity may promote neuronal maturation, we elevated the activity of migrating neurons by NaChBac expression. Elevation of neural activity impeded migration, and induced premature branching of the leading process before neurons arrived at layer II/III. Many NaChBac-expressing neurons in deep cortical layers were not attached to radial glial fibers, suggesting that these neurons had stopped migration. Morphological and immunohistochemical analyses suggested that branched leading processes of NaChBac-expressing neurons differentiated into dendrites. Our results suggest that developmental control of spontaneous calcium transients is critical for maturation of cortical excitatory neurons in vivo: keeping cellular excitability low is important for migration, and increasing spontaneous neural activity may stop migration and promote dendrite formation.
Subject(s)
Calcium/metabolism , Cell Differentiation/physiology , Cell Movement/physiology , Neocortex/growth & development , Neuroglia/cytology , Neurons/cytology , Animals , Dendrites/metabolism , Mice , Neocortex/metabolism , Neurogenesis/physiology , Neurons/physiologyABSTRACT
Elucidating the dynamic organization of nuclear RNA foci is important for understanding and manipulating these functional sites of gene expression in both physiological and pathological states. However, such studies have been difficult to establish in vivo as a result of the absence of suitable RNA imaging methods. Here, we describe a high-resolution fluorescence RNA imaging method, ECHO-liveFISH, to label endogenous nuclear RNA in living mice and chicks. Upon in vivo electroporation, exciton-controlled sequence-specific oligonucleotide probes revealed focally concentrated endogenous 28S rRNA and U3 snoRNA at nucleoli and poly(A) RNA at nuclear speckles. Time-lapse imaging reveals steady-state stability of these RNA foci and dynamic dissipation of 28S rRNA concentrations upon polymerase I inhibition in native brain tissue. Confirming the validity of this technique in a physiological context, the in vivo RNA labeling did not interfere with the function of target RNA nor cause noticeable cytotoxicity or perturbation of cellular behavior.
Subject(s)
In Situ Hybridization, Fluorescence/methods , RNA/analysis , Animals , Cell Movement , Cell Nucleus/genetics , Cerebellum/chemistry , Cerebellum/cytology , Chick Embryo , HeLa Cells , Humans , MCF-7 Cells , Mice, Inbred ICR , Oligonucleotide Probes/chemical synthesis , Oligonucleotide Probes/chemistry , Optical Imaging , RNA/metabolism , RNA, Ribosomal, 28S/analysis , RNA, Small Nucleolar/analysis , Time-Lapse ImagingABSTRACT
BACKGROUND: Neurons in the central nervous system (CNS) are generated by symmetric and asymmetric cell division of neural stem cells and their derivative progenitor cells. Cerebellar granule cells are the most abundant neurons in the CNS, and are generated by intensive cell division of granule cell precursors (GCPs) during postnatal development. Dysregulation of GCP cell cycle is causal for some subtypes of medulloblastoma. However, the details and mechanisms underlying neurogenesis from GCPs are not well understood. RESULTS: Using long-term live-cell imaging of proliferating GCPs transfected with a fluorescent newborn-granule cell marker, we found that GCPs underwent predominantly symmetric divisions, generating two GCPs or two neurons, while asymmetric divisions generating a GCP and a neuron were only occasionally observed, in both dissociated culture and within tissues of isolated cerebellar lobules. We found no significant difference in cell cycle length between proliferative and neurogenic divisions, or any consistent changes in cell cycle length during repeated proliferative division. CONCLUSIONS: Unlike neural stem cells in the cerebral cortex and spinal cord, which generate many neurons by repeated asymmetric division, cerebellar GCPs produce neurons predominantly by terminal symmetric division. These results indicate diverse mechanisms of neurogenesis in the mammalian brain.
Subject(s)
Cerebellum/cytology , Neural Stem Cells/cytology , Neurogenesis/physiology , Neurons/cytology , Animals , Asymmetric Cell Division , Biomarkers , Cell Cycle , Cell Division , Cells, Cultured , Culture Media, Conditioned , Cyclin-Dependent Kinase Inhibitor p27/biosynthesis , Cyclin-Dependent Kinase Inhibitor p27/genetics , Doublecortin Domain Proteins , Fluorescent Dyes/analysis , Genes, Reporter , HEK293 Cells , Hedgehog Proteins/physiology , Humans , Mice, Inbred ICR , Microtubule-Associated Proteins/biosynthesis , Microtubule-Associated Proteins/genetics , Nerve Tissue Proteins/analysis , Nerve Tissue Proteins/biosynthesis , Nerve Tissue Proteins/genetics , Neuropeptides/biosynthesis , Neuropeptides/genetics , Signal Transduction , Time-Lapse ImagingABSTRACT
Caprice [C19orf21 actin-bundling protein in characteristic epithelial cells, also called mitotic interactor and substrate of Plk1 (MISP)] is a novel actin-related protein identified in the highly-insoluble subcellular scaffold proteins. This protein contains multiple actin-binding sites, forms characteristic mesh-like F-actin bundles in vitro, and exhibits capricious localization and expression patterns in vivo. Overexpression or knock-down of Caprice resulted in a dramatic effect on cellular morphology by inducing stress fiber-like thick filaments or filopodial formations, respectively. Caprice is expressed and localized in distinct cells and tissues with specialized actin-based structures, such as growth cones of migrating neurons and stereocilia of inner ear hair cells. However, Caprice gene expression is varied among different cell types; especially enriched in several epithelial cells whereas relatively suppressed in a subset of epithelial cells, fibroblasts, and neuroblastoma cells at the transcriptional level. Thus, this protein is expected to be an effector for cell type-specific actin reorganization with its direct actin-binding properties and provides a novel model of cell morphology regulation by a non-ubiquitous single actin-bundling protein.
Subject(s)
Actin Cytoskeleton/metabolism , Actins/metabolism , Cell Cycle Proteins/metabolism , Microfilament Proteins/metabolism , Phosphoproteins/metabolism , Actin Cytoskeleton/ultrastructure , Animals , Cell Cycle Proteins/genetics , Cells, Cultured , Dogs , Humans , Mice , Microfilament Proteins/genetics , Phosphoproteins/genetics , Protein Binding , Protein Interaction Domains and Motifs , Pseudopodia/metabolismABSTRACT
The cerebellar granule cell is a unique neuron which undergoes tangential migration along axonal tracts and radial migration along glial fibers sequentially during postnatal development. Little is known about molecular bases of the differential kinetics of tangential and radial migration. Here we developed a time-lapse imaging assay for tangential migration of cerebellar granule cells, and investigated comparative contributions of cyclin-dependent kinase 5 (CDK5), a key regulator of neuronal migration, in tangential and radial migration of granule cells in vivo and in organotypic cultures. Overexpression of a dominant-negative form of CDK5 severely disrupted cell morphology and somal movement during radial migration, while it only moderately affected tangential migration. Dominant-negative inhibition of CDK5 induced formation of ectopic radial processes in granule cells in vivo which aberrantly elongated into the white matter in the cerebellum. Live imaging of granule cell migration in cerebellar slices revealed that CDK5 regulates not only nuclear migration but also centrosome movement during radial migration. These findings suggest a mode-specific function of CDK5 in neuronal migration.
Subject(s)
Cell Movement/physiology , Cerebellum/growth & development , Cerebellum/metabolism , Cyclin-Dependent Kinase 5/metabolism , Neurons/metabolism , Animals , Electroporation , Fluorescent Antibody Technique , Gene Transfer Techniques , Mice , Neurons/cytology , Reverse Transcriptase Polymerase Chain ReactionABSTRACT
CCCTC-binding factor (CTCF) has a key role in higher-order chromatin architecture that is important for establishing and maintaining cell identity by controlling gene expression. In the mature cerebellum, CTCF is highly expressed in Purkinje cells (PCs) as compared with other cerebellar neurons. The cerebellum plays an important role in motor function by regulating PCs, which are the sole output neurons, and defects in PCs cause motor dysfunction. However, the role of CTCF in PCs has not yet been explored. Here we found that the absence of CTCF in mouse PCs led to progressive motor dysfunction and abnormal dendritic morphology in those cells, which included dendritic self-avoidance defects and a proximal shift in the climbing fibre innervation territory on PC dendrites. Furthermore, we found the peculiar lamellar structures known as "giant lamellar bodies" (GLBs), which have been reported in PCs of patients with Werdnig-Hoffman disease, 13q deletion syndrome, and Krabbe disease. GLBs are localized to PC dendrites and are assumed to be associated with neurodegeneration. They have been noted, however, only in case reports following autopsy, and reports of their existence have been very limited. Here we show that GLBs were reproducibly formed in PC dendrites of a mouse model in which CTCF was deleted. GLBs were not noted in PC dendrites at infancy but instead developed over time. In conjunction with GLB development in PC dendrites, the endoplasmic reticulum was almost absent around the nuclei, the mitochondria were markedly swollen and their cristae had decreased drastically, and almost all PCs eventually disappeared as severe motor deficits manifested. Our results revealed the important role of CTCF during normal development and in maintaining PCs and provide new insights into the molecular mechanism of GLB formation during neurodegenerative disease.
Subject(s)
Neurodegenerative Diseases , Purkinje Cells , Animals , Mice , Lamellar Bodies , Cerebellum , DendritesABSTRACT
Somal translocation in long bipolar neurons is regulated by actomyosin contractile forces, yet the precise spatiotemporal sites of force generation are unknown. Here we investigate the force dynamics generated during somal translocation using traction force microscopy. Neurons with a short leading process generated a traction force in the growth cone and counteracting forces in the leading and trailing processes. In contrast, neurons with a long leading process generated a force dipole with opposing traction forces in the proximal leading process during nuclear translocation. Transient accumulation of actin filaments was observed at the dipole center of the two opposing forces, which was abolished by inhibition of myosin II activity. A swelling in the leading process emerged and generated a traction force that pulled the nucleus when nuclear translocation was physically hampered. The traction force in the leading process swelling was uncoupled from somal translocation in neurons expressing a dominant negative mutant of the KASH protein, which disrupts the interaction between cytoskeletal components and the nuclear envelope. Our results suggest that the leading process is the site of generation of actomyosin-dependent traction force in long bipolar neurons, and that the traction force is transmitted to the nucleus via KASH proteins.
Subject(s)
Cell Movement , Cell Nucleus/physiology , Neurons/physiology , Actomyosin/physiology , Animals , Biomechanical Phenomena , Cells, Cultured , Mice, Inbred ICR , Microscopy, Atomic ForceSubject(s)
Cell Movement/genetics , Cerebellum/cytology , Cerebellum/embryology , Neurons/cytology , 1-Alkyl-2-acetylglycerophosphocholine Esterase , Cell Differentiation/genetics , Cell Movement/physiology , Embryonic Induction/genetics , Humans , Intercellular Signaling Peptides and Proteins/physiology , Microtubule-Associated Proteins/physiology , Neurons/physiologyABSTRACT
Lissencephaly is a devastating neurological disorder caused by defective neuronal migration. LIS1 (official symbol PAFAH1B1, for platelet-activating factor acetylhydrolase, isoform 1b, subunit 1) was identified as the gene mutated in individuals with lissencephaly, and it was found to regulate cytoplasmic dynein function and localization. Here we show that inhibition or knockdown of calpains protects LIS1 from proteolysis, resulting in the augmentation of LIS1 amounts in Lis1(+/-) mouse embryonic fibroblast cells and rescue of the aberrant distribution of cytoplasmic dynein, mitochondria and beta-COP-positive vesicles. We also show that calpain inhibitors improve neuronal migration of Lis1(+/-) cerebellar granular neurons. Intraperitoneal injection of the calpain inhibitor ALLN to pregnant Lis1(+/-) dams rescued apoptotic neuronal cell death and neuronal migration defects in Lis1(+/-) offspring. Furthermore, in utero knockdown of calpain by short hairpin RNA rescued defective cortical layering in Lis1(+/-) mice. Thus, calpain inhibition is a potential therapeutic intervention for lissencephaly.
Subject(s)
1-Alkyl-2-acetylglycerophosphocholine Esterase/metabolism , Calpain/antagonists & inhibitors , Gene Expression Regulation, Developmental , Lissencephaly , Microtubule-Associated Proteins/metabolism , Models, Neurological , 1-Alkyl-2-acetylglycerophosphocholine Esterase/genetics , Animals , Calpain/genetics , Cell Movement/genetics , Cell Movement/physiology , Cells, Cultured , Cerebral Cortex/metabolism , Cysteine Proteinase Inhibitors/pharmacology , Disease Models, Animal , Dyneins/genetics , Dyneins/metabolism , Embryo, Mammalian/metabolism , Female , Fibroblasts/metabolism , Leucine/analogs & derivatives , Leucine/pharmacology , Leupeptins/pharmacology , Mice , Mice, Knockout , Microtubule-Associated Proteins/genetics , Neurons/cytology , Neurons/metabolism , Neurons/physiology , Phenotype , PregnancyABSTRACT
During neuronal migration in the developing brain, it is thought that the centrosome precedes the nucleus and provides a cue for nuclear migration along the microtubules. In time-lapse imaging studies of radially migrating granule cells in mouse cerebellar slices, we observed that the movements of the nucleus and centrosome appeared to occur independently of each other. The nucleus often migrated ahead of the centrosome during its saltatory movement, negating the supposed role of the centrosome in pulling the nucleus. The nucleus was associated with dynamic microtubules enveloping the entire nucleus and stable microtubules extending from the leading process to the anterior part of the nucleus. Neither of these perinuclear microtubules converged at the centrosome. Disruption or excess formation of stable microtubules attenuated nuclear migration, indicating that the configuration of stable microtubules is crucial for nuclear migration. The inhibition of LIS1 function, a regulator of a microtubule motor dynein, specifically blocks nuclear migration without affecting the coupling of the centrosome and microtubules in the leading process, suggesting that movements of the nucleus and centrosome are differentially regulated by dynein motor function. Thus, the nucleus moves along the microtubules independently of the position of the centrosome in migrating neurons.
Subject(s)
Cell Nucleus/physiology , Microtubules/physiology , Neurons/cytology , Neurons/physiology , 1-Alkyl-2-acetylglycerophosphocholine Esterase/metabolism , Animals , Cell Movement/physiology , Centrosome/ultrastructure , Cerebellum/cytology , Dyneins/metabolism , Mice , Mice, Inbred ICR , Microtubule-Associated Proteins/metabolism , Movement , Neurons/ultrastructureABSTRACT
During lamination of the cerebellar cortex, granule cells initially migrate tangentially along the external granule layer, and then make a vertical turn and migrate radially to the internal granule layer. We comparatively analyzed the properties of biphasic migration of granule cells in a microexplant culture in which quantitation of morphology and subcellular localization of molecules were readily accomplished. Tangential migration was guided by a leading process that later formed a parallel fiber axon. Translocation of the soma within the axonal process occurred independently of the rapid displacement of the large growth cone. On the other hand, radial migration was guided by a leading process that differentiated into a dendrite after completion of migration. Displacement of the soma and the tiny growth cone were linked so that the radial leading process adopted locomotion and kept a constant length. We propose that the dual phases of granule cell migration are achieved by distinct cellular mechanisms guided by the leading processes forming an axon and a dendrite, respectively.