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1.
Methods Mol Biol ; 1474: 269-78, 2016.
Article in English | MEDLINE | ID: mdl-27515087

ABSTRACT

Pre-embedding nanogold silver and gold intensification methods involve immunoreactions with nanogold-labeled antibodies and intensification of the nanogold particles before embedding and ultrathin sectioning. These highly sensitive methods show good resolution and ultrastructural preservation. They also are useful for simultaneous observation of immunolabeled cells under light and electron microscopes, and for three-dimensional immunoelectron microscopic analyses. Silver intensification is usually superior for immunolabeling. On the other hand, ultrastructural preservation is better when gold intensification is used. In this chapter, we introduce pre-embedding nanogold silver and gold intensification procedures for use primarily with cultured cells.


Subject(s)
Antibodies/chemistry , Gold Colloid/chemistry , Immunohistochemistry/methods , Microscopy, Immunoelectron/methods , Silver/chemistry , Tissue Fixation/methods , Aldehyde Dehydrogenase/genetics , Aldehyde Dehydrogenase/metabolism , Animals , COS Cells/metabolism , COS Cells/ultrastructure , Chlorocebus aethiops , Endoplasmic Reticulum/metabolism , Endoplasmic Reticulum/ultrastructure , Epoxy Resins/chemistry , Fixatives/chemistry , Formaldehyde/chemistry , Freezing , Gene Expression , Green Fluorescent Proteins/genetics , Green Fluorescent Proteins/metabolism , HSP47 Heat-Shock Proteins , Mice , Microtomy , NIH 3T3 Cells , Polymers/chemistry , Staining and Labeling/methods , Tissue Embedding/methods
2.
Genes Cells ; 20(2): 85-94, 2015 Feb.
Article in English | MEDLINE | ID: mdl-25440894

ABSTRACT

The dynamics of the cell membrane and submembrane structures are closely linked, facilitating various cellular activities. Although cell surface research and cortical actin studies have shown independent mechanisms for the cell membrane and the actin network, it has been difficult to obtain a comprehensive understanding of the dynamics of these structures in live cells. Here, we used a combined atomic force/optical microscope system to analyze membrane-based cellular events at nanometer-scale resolution in live cells. Imaging the COS-7 cell surface showed detailed structural properties of membrane invagination events corresponding to endocytosis and exocytosis. In addition, the movement of mitochondria and the spatiotemporal dynamics of the cortical F-actin network were directly visualized in vivo. Cortical actin microdomains with sizes ranging from 1.7×10(4) to 1.4×10(5) nm2 were dynamically rearranged by newly appearing actin filaments, which sometimes accompanied membrane invaginations, suggesting that these events are integrated with the dynamic regulation of submembrane organizations maintained by actin turnovers. These results provide novel insights into the structural aspects of the entire cell membrane machinery which can be visualized with high temporal and spatial resolution.


Subject(s)
Actin Cytoskeleton/ultrastructure , Actins/metabolism , Cell Membrane/ultrastructure , Mitochondrial Dynamics , Animals , COS Cells/ultrastructure , Cell Membrane/metabolism , Endocytosis , Exocytosis , Microscopy, Atomic Force/methods , Microscopy, Fluorescence/methods
3.
J Electron Microsc (Tokyo) ; 61(2): 127-31, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22345710

ABSTRACT

Mitochondria in all eukaryotes are essential organelles responsible for adenosine triphosphate synthesis, calcium homeostasis and steroidogenesis. Because the structure and distribution of mitochondria are highly diverse depending on their function and cellular conditions, it is important to develop a rapid and accurate method to assess their morphology. In this study, we visualize whole mitochondria in cultured cells using high-voltage electron microscopy (HVEM). Compared with conventional transmission electron microscopic approaches, the present method does not require thin sectioning and thus requires less time for image acquisition and processing. Furthermore, compared with fluorescence-based light microscopic approaches, our method provides more accurate size information. Thus, we propose that HVEM is a useful tool for rapid and accurate analysis of mitochondrial morphology and distribution in a cell.


Subject(s)
Microscopy, Electron, Transmission/methods , Mitochondria/ultrastructure , Animals , COS Cells/ultrastructure , Cells, Cultured , Chlorocebus aethiops , Green Fluorescent Proteins/genetics , Green Fluorescent Proteins/metabolism , HeLa Cells/ultrastructure , Humans
4.
PLoS One ; 7(12): e51849, 2012.
Article in English | MEDLINE | ID: mdl-23284788

ABSTRACT

We previously demonstrated that endogenous hNUDC and Mpl co-localized in the perinuclear and cytoplasmic regions of megakaryocyte cells by indirect immunofluorescence. We further reported that hNUDC accumulated in the Golgi when NIH 3T3 cells were transfected with an hNUDC expression vector alone. However, co-transfection with hNUDC and Mpl expression vectors caused both proteins to co-localize predominantly in the cytosol. These observations led us to hypothesize that a complex containing hNUDC and Mpl may alter hNUDC subcellular location and induce its secretion. In the present study, we test this hypothesis by employing bimolecular fluorescence complementation (BiFC) to detect and visualize the complex formation of hNUDC/Mpl in living cells. We further examined in detail the subcellular locations of the hNUDC/Mpl complex by co-transfection of BiFC chimeras with known subcellular markers. The distribution of hNUDC/Mpl in the endoplasmic reticulum (ER), Golgi and cell surface was determined. Furthermore, the N-terminal 159 amino acids of hNUDC, but not C-terminal half, bound to Mpl in vivo and exhibited a similar localization pattern to that of full-length hNUDC in Cos-1 cells. Adenovirus-mediated overexpression of hNUDC or its N-terminal 159 residues in a human megakaryocyte cell line (Dami) resulted in increased levels of hNUDC or hNUDC(1-159) secretion. In contrast, depletion of Mpl by transfecting Dami cells with adenovirus bearing Mpl-targeting siRNA significantly blocked hNUDC secretion. Thus, we provide the first evidence that the N-terminal region of hNUDC contains all of the necessary information to complex with Mpl and traffic through the secretory pathway.


Subject(s)
Cell Cycle Proteins/metabolism , Cell Membrane/metabolism , Endoplasmic Reticulum/metabolism , Golgi Apparatus/metabolism , Nuclear Proteins/metabolism , Receptors, Thrombopoietin/metabolism , Adenoviridae/genetics , Animals , Blotting, Western , COS Cells/metabolism , COS Cells/ultrastructure , Cell Cycle Proteins/genetics , Chlorocebus aethiops , Culture Media, Conditioned/pharmacology , Flow Cytometry , Fluorescence Resonance Energy Transfer , Humans , Microscopy, Confocal , Nuclear Proteins/genetics , RNA, Small Interfering/genetics , Receptors, Thrombopoietin/antagonists & inhibitors , Receptors, Thrombopoietin/genetics , Subcellular Fractions
5.
J Struct Biol ; 174(3): 552-62, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21440635

ABSTRACT

Three-dimensional (3D) maps of proteins within the context of whole cells are important for investigating cellular function. However, 3D reconstructions of whole cells are challenging to obtain using conventional transmission electron microscopy (TEM). We describe a methodology to determine the 3D locations of proteins labeled with gold nanoparticles on whole eukaryotic cells. The epidermal growth factor receptors on COS7 cells were labeled with gold nanoparticles, and critical-point dried whole-mount cell samples were prepared. 3D focal series were obtained with aberration-corrected scanning transmission electron microscopy (STEM), without tilting the specimen. The axial resolution was improved with deconvolution. The vertical locations of the nanoparticles in a whole-mount cell were determined with a precision of 3nm. From the analysis of the variation of the axial positions of the labels we concluded that the cellular surface was ruffled. To achieve sufficient stability of the sample under electron beam irradiation during the recording of the focal series, the sample was carbon coated. A quantitative method was developed to analyze the stability of the ultrastructure after electron beam irradiation using TEM. The results of this study demonstrate the feasibility of using aberration-corrected STEM to study the 3D nanoparticle distribution in whole cells.


Subject(s)
Eukaryotic Cells , Gold/chemistry , Image Processing, Computer-Assisted/methods , Imaging, Three-Dimensional/methods , Microscopy, Electron, Scanning Transmission/methods , Proteins/chemistry , Animals , COS Cells/ultrastructure , Chlorocebus aethiops , Nanoparticles/chemistry , Nanoparticles/ultrastructure
6.
Med Mol Morphol ; 42(4): 201-3, 2009 Dec.
Article in English | MEDLINE | ID: mdl-20033364

ABSTRACT

This review article covers the molecular mechanisms of secretory granule formation by chromogranin transfection. Recently, a few investigators have reported that the transfection of chromogranin A and B produces the structures of secretory granules. We used the GFP-chromogranin A transfection method to nonendocrine cells, COS-7 cells, which are not equipped with secretory granules. Despite the absence of endogenous secretory granules in nontransfected COS-7 cells, COS-7 cells transfected with chromogranin A contained granule-like structures in electron micrographs. The granules were composed of an outer limiting membrane with core structures that were interpreted as secretory granules. Human chromogranin A (CgA) labeled with 5-nm gold particles was present in several dense-core granules in our previous electron microscopy study. This review depicts the role of chromogranin A in the formation of secretory granules. It emphasizes the application of recently developed new technologies and the genesis of secretory granules.


Subject(s)
Chromogranin A/metabolism , Secretory Vesicles/metabolism , Animals , COS Cells/ultrastructure , Chlorocebus aethiops , Chromogranin A/genetics , Green Fluorescent Proteins/genetics , Green Fluorescent Proteins/metabolism , Humans , Immunohistochemistry , Microscopy, Electron , Secretory Vesicles/ultrastructure , Transfection
7.
J Microbiol Biotechnol ; 19(9): 904-10, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19809246

ABSTRACT

The development of effective cellular imaging requires a specific labeling method for targeting, tracking, and monitoring cellular/molecular events in the living organism. For this purpose, we studied the cellular uptake of isocyanide functionalized silver and gold nanoparticles by surface enhanced Raman scattering (SERS). Inside a single mammalian cell, we could monitor the intracellular behavior of such nanoparticles by measuring the SERS spectra. The NC stretching band appeared clearly at approximately 2,100 cm-1 in the well-isolated spectral region from many organic constituents between 300 and 1,700 or 2,800 and 3,600 cm-1. The SERS marker band at approximately 2,100 cm-1 could be used to judge the location of the isocyanide-functionalized nanoparticles inside the cell without much spectral interference from other cellular constituents. Our results demonstrate that isocyanide-modified silver or gold nanoparticle-based SERS may have high potential for monitoring and imaging the biological processes at the single cell level.


Subject(s)
Cells/ultrastructure , Animals , COS Cells/ultrastructure , Chlorocebus aethiops , Cyanides , Gold , Indicators and Reagents , Isocyanates , Mammals/physiology , Microscopy, Electron , Nanoparticles , Scattering, Radiation , Silver , Spectrum Analysis, Raman/methods
8.
Genes Cells ; 14(6): 751-7, 2009 Jun.
Article in English | MEDLINE | ID: mdl-19486166

ABSTRACT

In recent years, several novel types of disorder caused by the expansion of triplet repeats in specific genes have been characterized; in the "polyalanine diseases", these expanded repeats result in proteins with aberrantly elongated polyalanine tracts. In this study, we fused expanded polyalanine tracts to yellow fluorescent protein to examine their physical interaction with mitochondria. Tracts containing more than 23 alanine repeats were found to physically associate with mitochondria, strongly suggesting that an interaction between polyalanine tracts and mitochondria is a contributing factor in the pathology of polyalanine diseases. Furthermore, in in vitro experiments, polyalanine tracts induced release of cytochrome c from mitochondria and caspase-3 activation, independently of the mitochondrial permeability transition pore. These results suggest that oligomerized polyalanine tracts might induce the rupture of the mitochondrial membrane, the subsequent release of cytochrome c, and apoptosis. This novel mechanism for polyalanine tract cytotoxicity might be common to the pathogenesis of all polyalanine diseases. Further investigation of this mechanism might aid the development of therapies for these diseases.


Subject(s)
Apoptosis/physiology , Cytochromes c/metabolism , Mitochondria , Mitochondrial Membrane Transport Proteins/metabolism , Peptides/metabolism , Peptides/pharmacology , Animals , COS Cells/ultrastructure , Caspase 3/metabolism , Chlorocebus aethiops , Enzyme Activation , Humans , Mice , Mitochondria/enzymology , Mitochondria/metabolism , Mitochondria, Liver/enzymology , Mitochondria, Liver/metabolism , Mitochondrial Permeability Transition Pore
9.
J Neurochem ; 108(2): 319-30, 2009 Jan.
Article in English | MEDLINE | ID: mdl-19012746

ABSTRACT

Alzheimer's amyloid precursor protein (APP) sorting and processing are modulated through signal transduction mechanisms regulated by protein phosphorylation. Notably, protein kinase C (PKC) appears to be an important component in signaling pathways that control APP metabolism. PKCs exist in at least 11 conventional and unconventional isoforms, and PKCalpha and PKCepsilon isoforms have been specifically implicated in controlling the generation of soluble APP and amyloid-beta (Abeta) fragments of APP, although identification of the PKC substrate phospho-state-sensitive effector proteins remains challenging. In the current study, we present evidence that chronic application of phorbol esters to cultured cells in serum-free medium is associated with several phenomena, namely: (i) PKCalpha down-regulation; (ii) PKCepsilon up-regulation; (iii) accumulation of APP and/or APP carboxyl-terminal fragments in the trans Golgi network; (iv) disappearance of fluorescence from cytoplasmic vesicles bearing a green fluorescent protein tagged form of APP; (v) insensitivity of soluble APP release following acute additional phorbol application; and (vi) elevated cellular APP mRNA levels and holoprotein, and secreted Abeta. These data indicate that, unlike acute phorbol ester application, which is accompanied by lowered Abeta generation, chronic phorbol ester treatment causes differential regulation of PKC isozymes and increased Abeta generation. These data have implications for the design of amyloid-lowering strategies based on modulating PKC activity.


Subject(s)
Amyloid beta-Protein Precursor/metabolism , Gene Expression Regulation/drug effects , Phorbol Esters/pharmacology , Protein Kinase C-alpha/metabolism , Protein Kinase C-epsilon/metabolism , Amyloid Precursor Protein Secretases/metabolism , Amyloid beta-Protein Precursor/genetics , Analysis of Variance , Animals , COS Cells/drug effects , COS Cells/ultrastructure , Cerebral Cortex/drug effects , Cerebral Cortex/metabolism , Chlorocebus aethiops , Culture Media, Serum-Free/pharmacology , Green Fluorescent Proteins/genetics , Humans , Protein Kinase C-alpha/genetics , Protein Kinase C-epsilon/genetics , Qa-SNARE Proteins/metabolism , RNA, Messenger/metabolism , Rats , Subcellular Fractions/drug effects , Subcellular Fractions/metabolism , Time Factors , trans-Golgi Network/drug effects , trans-Golgi Network/metabolism
10.
J Neuropathol Exp Neurol ; 67(4): 299-308, 2008 Apr.
Article in English | MEDLINE | ID: mdl-18379438

ABSTRACT

Progressive multifocal leukoencephalopathy is a fatal demyelinating disorder due to human polyomavirus JC infection in which there are viral inclusions in enlarged nuclei of infected oligodendrocytes. We report that the pathogenesis of this disease is associated with distinct subnuclear structures known as promyelocytic leukemia nuclear bodies (PML-NBs). Postmortem brain tissues from 5 patients with the disease were examined. Affected cells with enlarged nuclei contained distinct dot-like subnuclear PML-NBs that were immunopositive for PML protein and nuclear body protein Sp100. Major and minor viral capsid proteins and proliferating cell nuclear antigen, an essential component for DNA replication, colocalized with PML-NBs. By in situ hybridization, viral genomic DNA showed dot-like nuclear accumulation, and by electron microscopy, virus-like structures clustered in subnuclear domains, indicating that PML-NBs are the site of viral DNA replication and capsid assembly. Molecules involved in the ubiquitin proteosome pathway (i.e. ubiquitin and small ubiquitin-like modifier 1) did not accumulate in the nuclei with viral inclusions, indicating that cell degeneration may not be dependent on this pathway. When viral progeny production was advanced, PML-NBs were disrupted. These data suggest that: 1) PML-NBs allow for efficient viral propagation by providing scaffolds, 2) disruption of PML-NBs is independent of the ubiquitin-proteasome pathway, and 3) this disruption probably heralds oligodendrocyte degeneration and the resulting demyelination.


Subject(s)
Inclusion Bodies, Viral/metabolism , JC Virus/physiology , Leukoencephalopathy, Progressive Multifocal , Neoplasm Proteins/metabolism , Nuclear Proteins/metabolism , Transcription Factors/metabolism , Tumor Suppressor Proteins/metabolism , Virus Replication/physiology , Adult , Aged , Aged, 80 and over , Animals , COS Cells/ultrastructure , COS Cells/virology , Capsid Proteins/metabolism , Chlorocebus aethiops , Female , Humans , Inclusion Bodies, Viral/diagnostic imaging , Inclusion Bodies, Viral/pathology , JC Virus/pathogenicity , JC Virus/ultrastructure , Leukoencephalopathy, Progressive Multifocal/etiology , Leukoencephalopathy, Progressive Multifocal/pathology , Leukoencephalopathy, Progressive Multifocal/virology , Male , Microscopy, Electron, Transmission/methods , Middle Aged , Promyelocytic Leukemia Protein , SUMO-1 Protein/metabolism , Transfection , Ubiquitin/metabolism , Ultrasonography
11.
J Neurosci Res ; 86(7): 1529-37, 2008 May 15.
Article in English | MEDLINE | ID: mdl-18214990

ABSTRACT

In recent years, several novel types of disorders have been characterized, including what have been termed polyalanine diseases, in which patients have expanded triplet repeats in specific genes, resulting in the translation of aberrantly elongated polyalanine stretches. In this study, we showed that yellow fluorescent protein (YFP)-fused elongated polyalanine stretches localized exclusively to the cytoplasm and formed aggregates. Additionally, the polyalanine stretches themselves were toxic. We sought to identify proteins that bound directly to the polyalanine stretches, as factors that might be involved in triggering cell death. Many mitochondrial proteins were identified as polyalanine-binding proteins. We showed that one of the identified proteins, succinate dehydrogenase subunit A, was decreased in the mitochondria of cells expressing polyalanine stretches; as a result, succinate oxidative activity was decreased. Furthermore, the polyalanine stretches also associated directly with mitochondria. This suggests that polya-lanine stretches might directly induce cell death. Additionally, the mitochondrial membrane potential was reduced in cells expressing polyalanine stretches. We propose a novel mechanism by which polyalanine stretches may cause cytotoxicity through mitochondrial dysfunction. This may be a common mechanism underlying the pathogenesis of all polyalanine diseases.


Subject(s)
Mitochondria/metabolism , Peptides/metabolism , Trinucleotide Repeat Expansion/physiology , Animals , Bacterial Proteins , COS Cells/ultrastructure , Carrier Proteins , Chlorocebus aethiops , Cytochromes c/metabolism , Flow Cytometry/methods , Glutathione Transferase/metabolism , Luminescent Proteins , Mass Spectrometry/methods , Membrane Potential, Mitochondrial/physiology , Mitochondria/ultrastructure , Peptides/genetics , Subcellular Fractions/metabolism , Succinate Dehydrogenase/metabolism , Transfection , Trinucleotide Repeat Expansion/genetics
12.
Phys Chem Chem Phys ; 9(45): 5966-74, 2007 Dec 07.
Article in English | MEDLINE | ID: mdl-18004408

ABSTRACT

In this paper we present the application of alternating current scanning electrochemical microscopy (AC-SECM) to the study of living cells. Commercial AFM instrumentation was modified to allow for performing robust AC-SECM measurements. Constant height AC imaging of the Cos-7 cells, performed directly in cell culture medium without the addition of a redox mediator, provided topographical information of the cell. Stationary tip measurements on the AC current were carried out to investigate the cellular activity of a single cell. The dependence of AC current magnitude on tip-to-sample separation distance was used to monitor real time changes in cell height of individual Cos-7 cells. Furthermore, AC-SECM was employed to observe changes in metabolic cellular activity stimulated by ethanol and phorbol-1,2-myristate-acetate-3. The effect of changing cellular activity on constant height AC-SECM imaging was also studied.


Subject(s)
Biosensing Techniques/methods , Cell Physiological Phenomena , Animals , COS Cells/metabolism , COS Cells/ultrastructure , Chlorocebus aethiops , Electrochemistry , Ethanol/pharmacology , Microscopy, Electron, Scanning/methods , Tetradecanoylphorbol Acetate/pharmacology
13.
Neurosci Lett ; 413(3): 238-40, 2007 Feb 21.
Article in English | MEDLINE | ID: mdl-17207929

ABSTRACT

Kinectin has been identified as a kinesin receptor on endoplasmic reticulum (ER). The ER membrane binding domain of kinectin is still obscure and is thought to require a half of the molecule. To determine the ER insertion site, we produced several constructs around N-terminus of kinectin connected with green fluorescent protein (GFP) and visualized the distribution in Cos-7 cells. The fragment of residues 7-29 appeared in the reticular pattern exactly colocalized with the ER marker but did not remain for a long time. On the other hand, residues 1-106 maintained a reticular pattern for more than seven days. These results indicate that residues 7-29 of kinectin are sufficient for targeting to the ER membrane but insufficient for remaining on the ER.


Subject(s)
Endoplasmic Reticulum/metabolism , Membrane Proteins/metabolism , Animals , Biological Transport , COS Cells/ultrastructure , Chlorocebus aethiops , Cricetinae , Green Fluorescent Proteins/metabolism , Humans , Protein Structure, Tertiary , Transfection/methods
14.
Neurosci Res ; 55(2): 123-33, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16600410

ABSTRACT

Mutations in the dynamin family GTPase OPA1 are reportedly the cause of autosomal dominant optic atrophy, the most frequently occurring form of hereditary optic neuropathy. But although the involvement of structural abnormalities of the enzyme in this neurodegenerative disease is clear, little is known about the cell biological and biochemical functions of OPA1. Therefore, to better understand the pathogenesis of autosomal dominant optic atrophy, we precisely analyzed the effects of exogenously introducing mouse OPA1 (mOPA1) on mitochondrial morphology in COS-7 cells. We found that exogenously introducing wild type mOPA1 caused the mitochondria to become fragmented, and moreover caused the intermembrane space to accumulate on one side of the ring-shaped mitochondrial fragments. Immunoelectron microscopic observation of the mOPA1 transfectants confirmed that the structure of the mitochondrial inner membrane had changed dramatically, accumulating on one side of the mitochondrial structures. When cells were transfected with mOPA1 containing a loss of function mutation (K301A) within the G1 GTP-binding domain, mitochondrial fragmentation still occurred. The markers for intermembrane space and matrix showed the similar morphology, which was distinctly different from the finding obtained with wild type mOPA1 transfectants. Notably, we also observed that the effect of two OPA1 missense mutations (E270K and D273A) associated with autosomal dominant optic atrophy elicit effects similar to those seen with the dominant negative K301A mutant.


Subject(s)
GTP Phosphohydrolases/metabolism , Mitochondria/ultrastructure , Mitochondrial Membranes/metabolism , Animals , Blotting, Western/methods , COS Cells/metabolism , COS Cells/ultrastructure , Chlorocebus aethiops , Cytochromes c/metabolism , GTP Phosphohydrolases/genetics , Immunohistochemistry/methods , Luminescent Proteins/biosynthesis , Mice , Microscopy, Immunoelectron/methods , Mitochondrial Membranes/ultrastructure , Molecular Biology/methods , Mutagenesis/physiology , Proto-Oncogene Proteins c-myc/metabolism , Transfection/methods
15.
Methods Enzymol ; 406: 665-76, 2006.
Article in English | MEDLINE | ID: mdl-16472696

ABSTRACT

Semaphorins are a family of growth cone guidance molecules. When associated with their receptors and coreceptors, plexins and neuropilins, they act as chemorepellents for an extensive range of neuronal populations. The prototypic semaphorin, Sema3A, has a potent inhibitory effect on sensory axons emanating from dorsal root ganglia. This has formed the basis of the most famous assay for semaphorin activity, the chick dorsal root ganglia collapse assay. Recently, a heterologous, highly tractable assay has been used to investigate semaphorin signaling. In this system, the binding of recombinant semaphorins to COS cells expressing plexins and neuropilins induces a morphological collapse that may correlate with growth cone collapse. This chapter describes the optimization of this assay and outlines the subtle differences required to enable Sema3A-Fc and Sema4D-Fc to induce identical collapse phenotypes in COS cells expressing Plexin-A1 and neuropilin-1, or Plexin-B1, respectively.


Subject(s)
Cell Adhesion Molecules/pharmacology , Nerve Tissue Proteins/pharmacology , Animals , Antigens, CD/biosynthesis , COS Cells/drug effects , COS Cells/ultrastructure , Chlorocebus aethiops , Cytoskeleton/drug effects , Humans , Nerve Tissue Proteins/metabolism , Neuropilin-1/physiology , Receptors, Cell Surface/metabolism , Semaphorin-3A/biosynthesis , Semaphorins/biosynthesis
16.
FASEB J ; 18(3): 592-4, 2004 Mar.
Article in English | MEDLINE | ID: mdl-14734633

ABSTRACT

Plexins encode receptors for semaphorins, molecular signals guiding cell migration, and axon pathfinding. The mechanisms mediating plexin function are poorly understood. Plexin activation in adhering cells rapidly leads to retraction of cellular processes and cell rounding "cell collapse"). Here we show that, unexpectedly, this response does not require the activity of Rho-dependent kinase (ROCK) nor the contraction of F-actin cables. Interestingly, integrin-based focal adhesive structures are disassembled within minutes upon plexin activation; this is followed by actin depolymerization and, eventually, by cellular collapse. We also show that plexin activation hinders cell attachment to adhesive substrates, blocks the extension of lamellipodia, and thereby inhibits cell migration. We conclude that plexin signaling uncouples cell substrate-adhesion from cytoskeletal dynamics required for cell migration and axon extension.


Subject(s)
Antigens, CD , Cytoskeleton/physiology , Integrins/antagonists & inhibitors , Nerve Tissue Proteins , Pseudopodia/physiology , Receptors, Cell Surface/physiology , Receptors, Peptide/physiology , Semaphorins , Signal Transduction/physiology , Actins/metabolism , Animals , Axons/physiology , Axons/ultrastructure , COS Cells/physiology , COS Cells/ultrastructure , Cell Movement , Cell Size , Chlorocebus aethiops , Cytoskeleton/ultrastructure , Focal Adhesions , Intracellular Signaling Peptides and Proteins , Membrane Glycoproteins/physiology , Mice , Protein Serine-Threonine Kinases/physiology , Protein Structure, Tertiary , Receptors, Cell Surface/chemistry , Receptors, Cell Surface/genetics , Receptors, Peptide/chemistry , Receptors, Peptide/genetics , Recombinant Fusion Proteins/physiology , rho-Associated Kinases
17.
Mol Cell Biol ; 23(6): 1983-93, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12612072

ABSTRACT

It is widely thought that the biological outcomes of Raf-1 activation are solely attributable to the activation of the MEK/extracellular signal-regulated kinase (ERK) pathway. However, an increasing number of reports suggest that some Raf-1 functions are independent of this pathway. In this report we show that mutation of the amino-terminal 14-3-3 binding site of Raf-1 uncouples its ability to activate the MEK/ERK pathway from the induction of cell transformation and differentiation. In NIH 3T3 fibroblasts and COS-1 cells, mutation of serine 259 resulted in Raf-1 proteins which activated the MEK/ERK pathway as efficiently as v-Raf. However, in contrast to v-Raf, RafS259 mutants failed to transform. They induced morphological alterations and slightly accelerated proliferation in NIH 3T3 fibroblasts but were not tumorigenic in mice and behaved like wild-type Raf-1 in transformation assays measuring loss of contact inhibition or anchorage-independent growth. Curiously, the RafS259 mutants inhibited focus induction by an activated MEK allele, suggesting that they can hyperactivate negative-feedback pathways. In primary cultures of postmitotic chicken neuroretina cells, RafS259A was able to sustain proliferation to a level comparable to that sustained by the membrane-targeted transforming Raf-1 protein, RafCAAX. In contrast, RafS259A was only a poor inducer of neurite formation in PC12 cells in comparison to RafCAAX. Thus, RafS259 mutants genetically separate MEK/ERK activation from the ability of Raf-1 to induce transformation and differentiation. The results further suggest that RafS259 mutants inhibit signaling pathways required to promote these biological processes.


Subject(s)
Cell Transformation, Neoplastic/genetics , MAP Kinase Kinase Kinase 1 , MAP Kinase Signaling System , Mitogen-Activated Protein Kinase 1/metabolism , Mitogen-Activated Protein Kinases/metabolism , Protein Serine-Threonine Kinases/metabolism , Proto-Oncogene Proteins c-raf/genetics , 14-3-3 Proteins , 3T3 Cells/metabolism , 3T3 Cells/transplantation , 3T3 Cells/ultrastructure , Active Transport, Cell Nucleus , Alleles , Animals , Binding Sites , COS Cells/metabolism , COS Cells/ultrastructure , Cell Differentiation/genetics , Cell Division/drug effects , Chlorocebus aethiops , Contact Inhibition , Enzyme Activation , Feedback, Physiological , Genes, Reporter , Mice , Mice, SCID , Mitogen-Activated Protein Kinase 3 , Mutagenesis, Site-Directed , PC12 Cells/cytology , Protein Serine-Threonine Kinases/genetics , Proto-Oncogene Proteins c-raf/physiology , Rats , Transfection , Tyrosine 3-Monooxygenase/metabolism
18.
Blood ; 101(8): 3021-8, 2003 Apr 15.
Article in English | MEDLINE | ID: mdl-12515716

ABSTRACT

Human blood platelets are anucleate cells whose response to extracellular stimuli results in actin cytoskeleton rearrangements, thereby providing the critical initial step in the regulation of hemostasis. The serine protease alpha-thrombin, known to activate platelets by cleavage of a family of protease-activated receptors (PARs), is the most potent physiologic activator of human platelets, though downstream effector proteins uniquely linked to platelet cytoskeletal actin polymerization remain largely uncharacterized. The gene encoding the putative rac1/cdc42 effector protein IQGAP2 was identified within the PAR gene cluster at 5q13, flanked telomeric by PAR1 and encompassing PAR3. Immunofluorescence microscopy demonstrated IQGAP2 expression in filopodial extensions of activated platelets and colocalized with F-actin in lamellipodia and filopodia of IQGAP2-transfected COS1 cells. Platelet activation by alpha-thrombin, but not saturating concentrations of fibrillar collagen or adenosine 5'-diphosphate, uniquely assemble an IQGAP2/arp2/3-actin cytoplasmic complex, an association regulated by guanosine triphosphate rac1 ([GTP]rac1) but not by [GTP]cdc42. Likewise, only thrombin-activated platelets resulted in rapid translocation of IQGAP2 to the platelet cytoskeleton. These observations identify a physiologic scaffolding function for IQGAP2 and establish the presence of a functional genomic unit in humans uniquely evolved to regulate thrombin-induced platelet cytoskeletal actin reorganization.


Subject(s)
Blood Platelets/ultrastructure , Carrier Proteins/physiology , Chromosomes, Human, Pair 5/genetics , Cytoskeleton/ultrastructure , Platelet Activation/drug effects , Thrombin/pharmacology , ras GTPase-Activating Proteins , Actin-Related Protein 2 , Actin-Related Protein 3 , Actins/metabolism , Adenosine Diphosphate/pharmacology , Adult , Animals , Blood Platelets/drug effects , COS Cells/chemistry , COS Cells/ultrastructure , Carrier Proteins/genetics , Chlorocebus aethiops , Collagen/pharmacology , Cytoskeletal Proteins/metabolism , Cytoskeleton/drug effects , Guanosine Triphosphate/metabolism , Humans , Macromolecular Substances , Microscopy, Fluorescence , Physical Chromosome Mapping , Pseudopodia/chemistry , Transfection , cdc42 GTP-Binding Protein/physiology , rac1 GTP-Binding Protein/physiology
19.
Blood ; 101(5): 1928-33, 2003 Mar 01.
Article in English | MEDLINE | ID: mdl-12424202

ABSTRACT

Some cells undergo apoptosis in response to DNA damage, whereas others do not. To understand the biochemical pathways controlling this differential response, we have studied the intracellular localization of cyclin B1 in cell types sensitive or resistant to apoptosis induced by DNA damage. We found that cyclin B1 protein accumulates in the nucleus of cells that are sensitive to gamma radiation-induced apoptosis (thymocytes, lymphoid cell lines), but remains cytoplasmic in apoptosis-resistant cells (primary and transformed fibroblasts). Treatment of both cell types with leptomycin B, an inhibitor of CRM1-dependent cyclin B1 nuclear export, induces apoptosis. Furthermore, ectopic expression of cyclin B1-5xE, a protein that preferentially localizes to the nucleus, is sufficient to trigger apoptosis. Conversely, expression of cyclin B1-5xA, a predominantly cytoplasmic protein, fails to induce apoptosis. This suggests that nuclear accumulation is necessary for cyclin B1-dependent apoptosis. Our observations are consistent with the idea that localization of cyclin B1 is among the factors determining the cellular decision to undergo apoptosis in response to DNA damage.


Subject(s)
Apoptosis/physiology , Cell Nucleus/chemistry , Cyclin B/physiology , DNA Damage , 3T3 Cells/cytology , 3T3 Cells/radiation effects , 3T3 Cells/ultrastructure , Active Transport, Cell Nucleus/drug effects , Animals , Apoptosis/drug effects , Apoptosis/radiation effects , Burkitt Lymphoma/pathology , COS Cells/cytology , COS Cells/radiation effects , COS Cells/ultrastructure , Chlorocebus aethiops , Cyclin B/analysis , Cyclin B/genetics , Cyclin B1 , Cytoplasm/chemistry , DNA, Neoplasm/radiation effects , Fatty Acids, Unsaturated/pharmacology , Gamma Rays , Humans , Mice , Microscopy, Confocal , Radiation Tolerance , Recombinant Fusion Proteins/physiology , Transfection , Tumor Cells, Cultured/cytology , Tumor Cells, Cultured/radiation effects , Tumor Cells, Cultured/ultrastructure
20.
Proc Natl Acad Sci U S A ; 99(25): 16018-23, 2002 Dec 10.
Article in English | MEDLINE | ID: mdl-12466501

ABSTRACT

We have developed a method for simultaneous recording of high-resolution topography and cell surface fluorescence in a single scan which we call scanning surface confocal microscopy. The resolution of the system allows imaging of individual fluorescent particles in the nanometer range on fixed or live cells. We used this technique to record the interaction of single virus-like particles with the cell surface and demonstrated that single particles sink into the membrane in invaginations reminiscent of caveolae or pinocytic vesicles. This method provides a technique for elucidating the interaction of individual viruses and other nanoparticles, such as gene therapy vectors, with target cells. Furthermore, this technique should find widespread application for studying the relationship of fluorescently tagged molecules with components of the cell plasma membrane.


Subject(s)
COS Cells/virology , Capsid/ultrastructure , Microscopy, Confocal/methods , Microscopy, Fluorescence/methods , Nanotechnology/methods , Animals , COS Cells/ultrastructure , Capsid/physiology , Carbocyanines , Cell Membrane/ultrastructure , Cell Membrane/virology , Chlorocebus aethiops , Equipment Design , Fluorescent Dyes , Genes, Synthetic , Microscopy, Confocal/instrumentation , Microscopy, Fluorescence/instrumentation , Particle Size , Surface Properties
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