| MICROSCOPIC TECHNIQUES | LINK TO
ABSTRACT OR FULL TEXT |
PART NO | TITLE | Journal | Volume | JISSUE | JMONTH | JYEAR | ABSTRACT | SPECIES | TISSUE | ATCC DESC | MORPHOLOGY | CELL LINE | AUTHOR | COMPLETE AUTHORS | Company/Institution | KEYWORDS | MATERIALS & METHODS | |
| Time-Lapse | Time-lapsed video microscopy, laser scanning Confocal | 563 | Replication Of Cryptococcus Neoformans In Macrophages Is Accompanied By Phagosomal Permeabilization And Accumulation Of Vesiclescontaining Polysaccharide In The Cytoplasm | PNAS | 99 | 5 | March | 2002 | Cryptococcus
neoformans (CN), an encapsulated, ubiquitous environmental yeast, is pathogenic for humans, primarily those with compromised immune function. CN is believed to be a facultative intracellular pathogen. Time-lapsed video microscopy revealed |
MOUSE | BALB/c; Tumor: sarcoma, histiocytic cell | Morphology:
stellate Species: mouse, BALB/c; Tumor: sarcoma, histiocytic cell Properties: antigen presentation; phagocytosis; chemotaxis; cytotoxicity |
STELLATE | J774 | Tucker, Stephanie C. | Stephanie C. Tucker and Arturo Casadevall | Albert Einstein College of Medicine | replication,
phagosomal permeabilization, Cryptococcus neoformans, phagosome |
Infected
or treated cells [where infections or treatments were performed on glass
coverslips in MaTek (Ashland, MA)-brand dishes] were washed with PBS to remove trace serummedium. Monolayers were fixed with 3.7% formaldehyde in 1Fix Buffer pH 7.2 ( |
|
| Time-Lapse | time-lapse fluorescence microscopy, immunofluorescence microscopy | 555 | Baf Is Required For Emerin Assembly Into The Reforming Nuclear Envelope | Journal of Cell Science | 114 | 24 | December | 2001 | Mutations in emerin cause the X-linked recessive form of Emery-Dreifuss muscular dystrophy (EDMD). Emerin localizes at the inner membrane of the nuclear envelope (NE) during interphase, and diffuses into the ER when the NE disassembles during mitosis. |
HUMAN | cervix | IZSBS BS TCL20 Morphology: epithelial-like Species: human, Black female 31 years old; Tissue: cervix; Tumor: carcinoma, epitheloid Properties: antitumour testing; transformation; tumorigenicity; cytotoxicity; cell biology; bacterial invasiveness; virology |
epithelial-like | HeLa | Haraguchi, Tokuko | Tokuko Haraguchi, Takako Koujin, Miriam Segura-Totten, Kenneth
K. Lee, Yosuke Matsuoka, Yoshihiro Yoneda, Katherine L. Wilson and Yasushi Hiraoka |
Japan Science and Technology Corporation | Nuclear envelope, Lamin A, Lamin-associated polypeptide 2, MAN1, Emery-Dreifuss muscular dystrophy, Barrierto- autointegration factor, Chromosome |
Cells were grown in a glass-bottom culture dish (MatTech,
USA). GFP fusion plasmids (1 mg) were transfected into cells with LipofectaminePlus (Gibco BRL) according to manufacturer’s methods except that the incubation time with DNA was reduced to 1.5 h |
|
| Time-Lapse | time-lapse fluorescence microscopy | 425 | Identification Of Novel Principles Of Keratin Filament Network Turnover In Living Cells | Molecular Biology of the Cell | 15 | 5 | May | 2004 | It is generally assumed that turnover of the keratin filament
system occurs by exchange of subunits along its entire length throughout the cytoplasm. We now present evidence that a circumscribed submembranous compartment is actually the main site for ne |
eukaryotic | Windoffer, Reinhard | Reinhard Windoffer, Stefan Wo¨ ll, Pavel Strnad, and Rudolf E. Leube | Johannes Gutenberg University | keratin, intermediate filaments, Keratin filaments | For time-lapse fluorescence microscopy of living cells,
phenol-red–free Hanks’ medium (Invitrogen GmbH) was used. Images were recorded by epifluorescence microscopy using inverse optics (Olympus, Hamburg, Germany) and an attached IMAGO slow-scan CCD ca |
|||||
| Time-Lapse | 479 | Sindbis Virus-Induced Neuronal Death Is Both Necrotic And Apoptotic And Is Ameliorated By N-Methyl-D-Aspartate Receptor Antagonists | Journal of Virology | 75 | 15 | August | 2001 | Virus infection of neurons leads to different outcomes ranging
from latent and noncytolytic infection to cell death. Viruses kill neurons directly by inducing either apoptosis or necrosis or indirectly as a result of the host immune response. Sindbis vi |
HIPPOCAMPAL | NEURONAL | Primary | Nargir-Aizenman, Jennifer L. | JENNIFER L. NARGI-AIZENMAN AND DIANE E. GRIFFIN | Johns Hopkins University | Neuronal Death, apoptosis, necrosis, Sindbis virus | Primary
cortical cells were prepared from gestational day 18 Long-Evans rats as previously described (56). Briefly, the cortex was dissected in Hanks balanced salt solution and digested in 10 U of papain (Worthington Biochemical, Lakewood, N.J.)/ml in |
||||
| Time-Lapse | Time-lapse imaging; FRAP | 225 | Mobile Foci Of Sp100 Do Not Contain Pml: Pml Bodies Are Immobile But Pml And Sp100 Proteins Are Not | Journal of Structural Biology | 140 | 1-3 | October | 2002 | PML bodies are nuclear organelles that are associated with various diseases and are suggested to be involved in multiple cellular activities including transcriptional regulation, apoptosis, and antiviral defence. Because many proteins with different funct | HUMAN | BONE | Morphology: epithelial-like Species: human, Caucasian female 15 years old; Tissue: bone; Tumor: osteosarcoma; Validated by isoenzymes: PGM1,1; PGM3,2; ES D,1; AK1,1; GLO-1,2; G6PD,B Properties: antitumour testing; cytotoxicity |
U2OS | Wiesmeijer, K. | Wiesmeijer, K., Molenaar, C., Bekeer, I., Tanke H., and Dirks R., Department of Molecular Cell Biology, Leiden University Medical Center, Leiden, The Netherlands. Journal of Structural Biology, 40, (-), 80-88, (00) | Leiden University | PML; Sp100; CBP; Time-lapse imaging; FRAP | "VH10 human primary fibroblasts and U2OS human osteosarcoma cells were cultured on 3.5-cm glass bottom petri dishes (Mattek, Ashland, MA) …" | ||
| Time-Lapse | time-lapse microscopy | 593 | A Preformed Complex of Postsynaptic Proteins Is Involved in Excitatory Synapse Development | Neuron | 49 | 4 | February | 2006 | Nonsynaptic clusters of postsynaptic proteins have been documented; however, their role remains elusive. We monitored the trafficking of several candidate proteins implicated in synaptogenesis, when nonsynaptic clusters of scaffold proteins are most abund | rat | neuronal | HIPPOCAMPAL | Gerrow, Kimberly | Kimberly Gerrow, Stefano Romorini, Shahin M. Nabi, Michael A. Colicos, Carlo Sala, and Alaa El-Husseini | University of British Columbia | postsynaptic proteins, synaptogenesis, scaffolding proteins, neuroligin-1, postsynaptic density (PSD) | Neurons were plated at 100,000 per 35mm glass-bottom microwell dish (MatTek). | |||
| Time-Lapse | Time-lapse video phase-contrast microscopy and time-lapse digital confocal-fluorescence microscopy | 341 | Macropinocytosis Is The Endocytic Pathway That Mediates Macrophage Foam Cell Formation With Native Low Density Lipoprotein | Journal of Biological Chemistry | 280 | 3 | January | 2005 | Previously, we reported that fluid-phase endocytosis of native LDL by PMA-activated human monocytederived macrophages converted these macrophages into cholesterol-enriched foam cells (Kruth, H. S., Huang, W., Ishii, I., and Zhang, W. Y. (2002) J. Biol |
HUMAN | FORESKIN | HFF | Kruth, H. | Kruth, H., Jones, N., Huang, W., Zhao, B., Ishii, I., Chang, J., Combs, C., Malide, D., and Zhang, W-Y. Section of Experimental Atherosclerosis, NHLBI, National Institutes of Health, Bethesda, MD., the Department of Pathology, Wake Forest Unive | National Institutes of Health | |||||
| Time-Lapse | Time-Lapse Video Microscopy | 474 | Dynamic Interactions Of Macrophages With T Cells During Antigen Presentation | Journal of Experimental Medicine | 190 | 12 | December | 1999 | We have established a method for real-time video analysis of the
interaction of antigen-presenting cells (APCs) with T cells. Green fluorescent protein expression controlled by a nuclear factor of activated T cells (NFAT)-responsive promoter permits the |
MOUSE | monocyte macrophage | ECACC 91062702 Morphology: Macrophage Mouse monocyte macrophage Depositor: Not registered No restrictions. Patent: None Specified By Depositor Properties: Receptors: Immunoglobulin, complement Products: Lysozyme Applications: Metabolic studies |
RAW 264.7 | Underhill, David M. | David M. Underhill, Michael Bassetti, Alexander Rudensky, and Alan Aderem |
University of Washington | nuclear factor of activated T cells, hybridoma, green
fluorescent protein, video microscopy |
RAW 264.7 cells were plated 48 h before use on 35-mm glass-bottomed microwell dishes (MatTek Corp.) with 20 U/ml IFNg , and OVA was added to 10 mg/ml for the final 16 h. DO11-GFP cells were added to the dish at fivefold excess, centrifuged onto the R |
||
| Time-Lapse | Time-lapse microscopy | 475 | A Pseudomonas Aeruginosa Quorum-Sensing Molecule Influences Candida Albicans Morphology | Molecular Microbiology | 54 | 5 | December | 2004 | Candida albicans is an opportunistic pathogen that is commonly found as a member of the human microflora. The ability of C. albicans to alter its cellular morphology has been associated with its virulence; yeast cells are more prevalent in commensa |
YEAST | CANDIDA ALBICAN | Hogan, Deborah A. | Deborah A. Hogan, Åshild Vik and Roberto Kolter |
Harvard Medical School | Candida albicans, 3OC12HSL, fungal morphology, pathogen, Pseudomonas aeruginosa |
Candida albicans was grown in 5 ml of YNBNP medium
incubated in a rollerdrum overnight at 378C. The morphological state of C. albicans was determined microscopically using a 100¥ objective lens on a Nikon Eclipse TE300 inverted microscope equipped wit |
||||
| Time-Lapse | Time-lapse movies | 318 | A Critical Step In Metastasis: In Vivo Analysis Of Intravasation At The Primary Tumor | Cancer Research | 60 | 9 | May | 2000 | Detailed evaluation of all steps in tumor cell metastasis is critical for evaluating the cell mechanisms controlling metastasis. Using green fluorescent protein transfectants of metastatic (MTLn3) and nonmetastatic (MTC) cell lines derived from the rat ma | MTLn3-GFP | Wyckoff, Jb. | Wyckoff, JB., Jones, JG., Condeelis, , JS., Segall, JE. Department of Anatomy and Structural Biology, Pathology, and the Analytical Imaging Facility Albert Einstein College of Medicine, Bronx, NY, USA. Cancer Research, 60, (9), 504-5, (00 | Albert Einstein College of Medicine | The lungs were then placed in matTek dishes (MatTek Corporation, Ashland, MA) with 1 ml of L15 medium (Life Technologies, Inc.) to keep them moist. | ||||||
| Time-Lapse | 733 | 35-mm poly-d-lysine-coated glass bottom dishes | Spatiotemporal control of spindle midzone formation by PRC1 in human cells | PNAS | 106 | 16 | April | 2006 | We have examined the role of PRC1, a midzone-associated,
microtubule bundling, Cdk substrate protein, in regulating the spatiotemporal formation of the midzone in HeLa cells. Cdk-mediated phosphorylation of PRC1 in early mitosis holds PRC1 in an inactive |
HeLa | Zhu, Changjun | Changjun Zhu, Eric Lau, Robert Schwarzenbacher, Ella Bossy-Wetzel, and Wei Jiang | Burnham Institute for Medical Research | Cdk phosphorylation
mitosiscytokinesis
microtubule-associated proteins microtubule bundling |
HeLa cells grown on a 35-mm polylysinecoated glass-bottom microwell dish (MatTek, Ashland, MA) were transfected with mammalian expression plasmids andor siRNA by using Lipofectamine 2000 or Oligofectamine (Invitrogen). |
|||||
| Time-Lapse | Time-lapse microscopy | 500 | Retinal Axon Growth Cones Respond To Ephb Extracellular Domains Asinhibitory Axon Guidance Cues | Development | 128 | 15 | August | 2001 | Axon pathfinding relies on cellular signaling mediated by growth cone receptor proteins responding to ligands, or guidance cues, in the environment. Eph proteins are a family of receptor tyrosine kinases that govern axon pathway development, including |
E14 | Birgbauer, Eric | Eric Birgbauer, Stephen F. Oster, Christophe G. Severin and David W. Sretavan | University of Californa, San Francisco (UCSF) | Axon pathfinding, Ephrins, Extracellular domains, Retinal axons, Reverse signaling, Mouse |
E14 dorsal retinal explants were grown overnight in 35 mm coverslip culture dishes (MatTek Corporation). Cultures were overlaid with prewarmed mineral oil (Sigma or Fisher) and equilibrated on a 37°C microscope stage incubator with CO2 influx. Glass m |
|||||
| Time-Lapse | 884 | 35-mm glass bottom dishes | mDia2 induces the actin scaffold for the contractile ring and
stabilizes its position during cytokinesis in NIH 3T3 cells |
Molecular Biology of the Cell | 19 | 5 | May | 2008 | mDia proteins are mammalian homologs of Drosophila diaphanous
and belong to the formin family proteins that catalyze actin nucleation and polymerization. While formin family proteins of nonmammalian species such as Drospohila diaphanous are essential in |
NIH 3T3 | Sadanori Watanabe | Sadanori Watanabe, Yoshikazu Ando, Shingo Yasuda, Hiroshi
Hosoya, Naoki Watanabe, Toshimasa Ishizaki and Shuh Narumiya |
mDia2, Actin Scaffold, Contractile Ring, NIH 3T3, Cytokinesis | NIH 3T3 cells were seeded on 35-mm glass-bottom dishes (Mat Tek)
with or without siRNA transfection. |
||||||
| Time-Lapse | 886 | glass bottom dishes | Calpain-mediated regulation of the distinct signaling
pathways and cell migration in human neutrophils |
Journal of Leukocyte Biology | 84 | July | 2008 | We studied the mechanisms underlying calpain inhibition-mediated human neutrophil migration. MAPKs, including ERK, p38, and JNK, MEK1/2, MAPK kinase 3/6 (MKK3/6), PI-3K/Akt, c-Raf, and p21-activated kinase (PAK; an effector molecule of Rac) were rapi |
HL-60 | Masataka Katsube | Masataka Katsube, Takayuki Kato, Maki Kitagawa, Haruyoshi Noma,
Hisakazu Fujita, and Seiichi Kitagawa |
Mitogen-activated protein kinases, pertussis toxin phosphatidylinositol 3-kinase, Rac | Cells (3.5105/ml) suspended in HBSS were placed in a
glass-bottom dish (MatTek Co., Ashland, MA, USA) |
|||||||
| Time-Lapse | 912 | P50G-1.5-3x14-F | Cell and fibronectin dynamics during branching morphogenesis |
Journal of Cell Science | 119 | 16 | August | 2006 | Branching morphogenesis is a dynamic developmental process shared by many organs, but the mechanisms that reorganize cells during branching morphogenesis are not well understood. We hypothesized that extensive cell rearrangements are involved, and inv |
E12 and E13 SMGs | Melinda Larsen | Melinda Larsen, Cindy Wei and Kenneth M. Yamada | Branching morphogenesis, Migration, Salivary gland, Fibronectin |
Whole SMGs were cultured as previously described (Hoffman et
al., 2002) except that for imaging they were cultured submerged in glass-bottom culture dishes (MatTek) coated with FN. |
||||||
| Time-Lapse | 761 | glass bottom culture dishes | Microtubule function in fibroblast spreading is modulated
according to the tension state of cell–matrix interactions |
PNAS | 104 | 13 | March | 2007 | Mechanical and physical features of the extracellular
environment dramatically impact cell shape. Fibroblasts interacting with
3D relaxed collagen matrices appear much different from cells on 2D collagen-coated surfaces and form dendritic cell extension |
Human | foreskin fibroblasts | Rhee, Sangmyung | Sangmyung Rhee, Hongmei Jiang, Chin-Han Ho, and Frederick Grinnell | University of Texas Southwestern Medical Center | adhesion cell
plasticity cytoskeleton extracellular matrix mechanosignaling |
Time-lapse microscopy was carried out with glass bottom culture dishes (MatTek, Ashland, MA) placed in a 37°C environment chamber. |
||||
| Time-Lapse | time-lapse microscopy | 418 | Imaging Movement Of Malaria Parasites During Transmission By Anopheles Mosquitoes | Cellular Microbiology | 6 | 7 | July | 2004 | Malaria is contracted when Plasmodium sporozoites are inoculated into the vertebrate host during the blood meal of a mosquito. In infected mosquitoes, sporozoites are present in large numbers in the secretory cavities of the salivary glands at the m |
SALIVARY | Frischknecht, Friedrich | Friedrich Frischknecht, Patricia Baldacci, Béatrice Martin, Christophe Zimmer, Sabine Thiberge, Jean-Christophe Olivo-Marin, Spencer L. Shorte and Robert Ménard |
Institut Pasteur | Malaria, mosquito, Plasmodium sporozoites |
The Plasmodium berghei NK65 strain transformed to express GFP at the sporozoite stage was described previously (Natarajan et al., 2001). Parasite stocks were refreshed after several months by natural transmission from mosquitoes to mice. Mice developin |
|||||
| Time-Lapse | Time-Lapse Videomicroscopy | 578 | Apoptotic Membrane Blebbing Is Regulated By Myosin Light Chain Phosphorylation | Journal of Cell Biology | 140 | 3 | February | 1998 | The evolutionarily conserved execution phase of apoptosis is defined by characteristic changes occurring during the final stages of death; specifically cell shrinkage, dynamic membrane blebbing, condensation of chromatin, and DNA fragmentation. Mechan |
RAT | ADRENAL MEDULLA | PC12 | Mills, Jason C. | Jason C. Mills, Nicole L. Stone, Joseph Erhardt, and Randall N. Pittman | University of Pennsylvania | membrane blebbing, apoptosis, z-VAD-FMK, myosin light chain kinase inhibitors, cell contraction, execution phase | For Hoechst staining after serum removal or staurosporine
treatment, 300,000 cells were plated on collagen-coated, glass bottom 35-mm tissue culture dishes (Mat-Tek, Ashland, MA). After experimental treatments, cells were rinsed three times with PBS |
|||
| Time-Lapse | three-dimensional time-lapse microscopy | 430 | Cdc25B cooperates with Cdc25A to induce mitosis but has a unique role in activating cyclin B1–Cdk1 at the centrosome |
Journal of Cell Biology | 171 | 1 | October | 2005 | Cdc25 phosphatases are essential for the activation of mitotic cyclin–Cdks, but the precise roles of the three mammalian isoforms (A, B, and C) are unclear. Using RNA interference to reduce the expression of each Cdc25 isoform in HeLa and HEK293 cells |
HUMAN | cervix | IZSBS BS TCL20 Morphology: epithelial-like Species: human, Black female 31 years old; Tissue: cervix; Tumor: carcinoma, epitheloid Properties: antitumour testing; transformation; tumorigenicity; cytotoxicity; cell biology; bacterial invasiveness; virology |
epithelial-like | HeLa | Lindqvist, Arne | Arne Lindqvist, Helena Källström, Andreas Lundgren, Emad Barsoum, and Christina Karlsson Rosenthal | Karolinska Institutet | mitosis, cyclin B1–Cdk1, phosphorylation | Cells growing on a glass-bottomed dish (MatTek) or a coverslip
were microinjected with 10 nM siRNA and 0.008 g/ l plasmid CFP (pCFP)- Golgi as a marker in the first release of a double thymidine block. As for time-lapse microscopy, different si |
|
| Time-Lapse | time-lapse microscopy, fluorescent stereomicroscopy | 453 | Using Green Fluorescent Malaria Parasites To Screen For Permissive Vector Mosquitoes | Malaria Journal | 5 | 23 | March | 2006 | The Plasmodium species that infect rodents, particularly
Plasmodium berghei and Plasmodium yoelii, are useful to investigate host-parasite interactions. The mosquito species that act as vectors of human plasmodia in South East Asia, Africa and South Ame |
zebrafish | NEUROEPITHELIA | MOSQUITOES | Frischknecht | Friedrich Frischknecht, Beatrice Martin, Isabelle Thiery, Catherine Bourgouin and Robert Menard |
Institut Pasteur | malaria, sporozoites, Plasmodium berghei | Whole mosquitoes or isolated midguts were observed at 10–18 days (A. stephensi and A. gambiae) or 10–26 days (A. albimanus) after the infectious blood meal. Sporozoites were isolated from infected salivary glands 15–22 days (A. stephensi) and 15–35 da |
|||
| Time-Lapse | Time-lapse Microscopy, Indirect Immunofluorescence | 236 | Role Of Pi 3-Kinase And Pip3 In Submandibular Gland Branching Morphogenesis, Developmental Biology | Developmental Biology | 255 | 1 | March | 2003 | The mouse submandibular gland (SMG) epithelium undergoes extensive morphogenetic branching during embryonic development as the first step in the establishment of its glandular structure. However, the specific signaling pathways required for SMG branching | E13 | Larsen, M. | Larsen, M., Hoffman, M.P., Sakai, T., Neibaur, J.C., Mitchell, J.M, and Yamada, K.M., Craniofacial Developmental Biology and Regeneration Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, USA. Develop | National Institutes of Health | Branching morphogenesis; Salivary gland; Submandibular gland; Organ culture; Phosphatidylinositol 3-kinase; Phosphatidylinositol 3,4,5-trisphosphate; Akt; Inhibitors; Mouse; Time-lapse microscopy | The SMG were cultured on membranes at the air/medium interface at 37°C for 1–72 h. Five or more glands were placed on Nuclepore Track-Etch Membranes (Whatman, Clifton, NJ) (13 mm, 0.1 µM) floating on 250 µL of DMFTV standard media [DMEM/F12 (1:1) (Invitro | |||||
| Time-Lapse | Time-lapse video microscopy | 435 | Lfa-1/Icam-1 Interaction Lowers The Threshold Of B Cell Activation By Facilitating B Cell Adhesion And Synapse Formation | Immunity | 20 | 5 | May | 2004 | The integrin LFA-1 and its ligand ICAM-1 mediateB cell adhesion, but their role in membrane-bound antigen recognition is still unknown. Here, using planar lipid bilayers and cells expressing ICAM-1 fused to green fluorescence protein, we found that the |
LYMPHOCYTE | adipocyte | Carrasco, Yolanda R. | Yolanda R. Carrasco, Sebastian J. Fleire, Thomas Cameron, Michael L. Dustin, and Facundo D. Batista |
Lincoln's Inn Fields Laboratories | Cell Adhesion, synapse, B cell receptor (BCR) | Time-lapse video microscopy was performed using a Nikon
Diaphot 200 inverted microscope equipped with a CCD camera (Hama-matsu Orca). ICAM-1-GFP APCs were split on 35 mm glass-bottom dishes (MatTek Corporation, Ashland, MA). The dish was placed on a 37 C |
||||
| Time-Lapse | 676 | P35G-1.5-14-C | A Surfactant Protein C Precursor Protein BRICHOS Domain Mutation Causes Endoplasmic Reticulum Stress…. | American Journal of Respiratory Cell and Molecular Biology | 32 | 6 | June | 2005 | BRICHOS is a domain found in several proteins consisting of 100 amino acids with sequence and structural similarities. Mutations in BRICHOS domain have been associated with both degenerative and proliferative diseases in several nonpulmonary organs, alt |
Human | embryonic kidney | HEK 293 | Mulugeta, Surafel | Surafel Mulugeta, Vu Nguyen, Scott J. Russo, Madesh Muniswamy, and Michael F. Beers | University of Pennsylvania School of Medicine | conformational disease; apoptosis; unfolded protein
response; epithelial cells; protein aggregation |
For time-lapse microscopy, the same procedure described above was followed with the exception of using glass-bottom 35-mm petri dishes with 0.16- to 0.19-mm coverglasses (MatTek Corporation, Ashland,MA) for live microscopic observation. |
|||
| Time-Lapse | Time-lapse videomicroscopy | 532 | Contrasting Effects Of Basic Fibroblast Growth Factor And Neurotrophin 3 On Cell Cycle Kinetics Of Mouse Cortical Stem Cells | Journal of Neuroscience | 22 | 15 | August | 2002 | Basic fibroblast growth factor (bFGF) exerts a mitogenic
effect on cortical neuroblasts, whereas neurotrophin 3 (NT3) promotes differentiation in these cells. Here we provide evidence that both the mitogenic effect of bFGF and the differentiationpromot |
MOUSE | CORTICAL | STEM CELLS | Lukaszewicz | Agnes Lukaszewicz, Pierre Savatier, Ve´ ronique Cortay, Henry Kennedy, and Colette Dehay | Institut National de la Sante et de la Recherche Medicale | G1 phase; cell cycle; proliferation; neuroblast; time-lapse videomicroscopy; bFGF; NT3; corticogenesis |
Cortical precursors from green fluorescent protein (GFP; Okabe
et al., 1997) / and / mice were seeded on poly-L-lysine- and laminin-coated glass coverslips to obtain 25% of GFP cells. This low proportion of GFP cells makes it possible to reliably |
|||
| Time-Lapse | Time-lapse video microscopy, Scanning Electron Microscopy, Immunofluorescence, Digital Immunofluorescence Microscopy | 337 | Early Molecular Events In The Assembly Of The Focal Adhesion-Stress Fiber Complex During Fibroblast Spreading | Cell Motility and the Cytoskeleton | 58 | 3 | July | 2004 | Cell adhesion to the extracellular matrix triggers the formation of integrin-mediated contact and reorganization of the actin cytoskeleton. Examination of nascent adhesions, formed during early stages of fibroblast spreading, reveals a variety of forms of | human | foreskin | FIBROBLAST | FOAM | Zimerman, B. | Zimerman, B., Volberg, T., and Geiger, B. Department of Molecular Cell Biology, The Weizmann Institute of Science, Rehovot, Israel. Cell Motility and the Cytoskeleton 58, (), 4-59, (004). | The Weizmann Institute of Science | After the electroporation, the cells were collected by centrifugation, resuspended in DMEM, and plated on glass-bottom microwell dishes (MatTek, Ashlend, MA) |
|||
| Time-Lapse | 702 | P35G-1.5-14-C | Shape Change Controls Supporting Cell Proliferation in Lesioned Mammalian Balance Epithelium | Journal of Neuroscience | 27 | 16 | April | 2007 | Mature mammals are uniquely vulnerable to permanent auditory and
vestibular deficits, because the cell proliferation that produces replacement hair cells in other vertebrates is limited in mammals. To investigate the cellular mechanisms responsible for th |
Mouse | Embryonic utricles | Embryonic urticles | Meyers, Jason R. | Jason R. Meyers and Jeffrey T. Corwin | University of Virginia | hair cell; regeneration; lysophosphatidic acid; LPA; vestibular; wound healing; cytoskeleton | Embryonic utricles were adhered with the nerve side down on poly-L-lysine-coated glass-bottom dishes (Mat- Tek, Ashland, MA). Utricles from postnatal animals were adhered nerve side down in MatTek dishes treated with CellTak (2l, air-dried onto the glass |
|||
| Time-Lapse | 641 | Rac1 null mouse embryonic fibroblasts are motile and respond to PDGF | Molecular Biology of the Cell | 17 | 5 | May | 2006 | Previous studies of Rac1 in fibroblasts have used dominant
negative constructs, which may have non-specific effects. We used a conditional Rac1 allele to critically examine Rac1 function in mouse fibroblasts. Lack of Rac1 had dramatic effects on non-confl |
MEF | Vidali, Luis | Luis Vidali*, Feng Chen, Gregor Cicchetti*, Yasutaka Ohta*, and David J. Kwiatkowski*‡ | Brigham and Women’s Hospital and Harvard Medical School, | Mouse alleles, PCR and Southern blot Rac1 conditional and null
alleles were generated as previously reported (Glogauer et al., 2003; Gu et al., 2003). The conditional Rac1 allele contains loxP sites flanking exon1; upon cremediated excision this allele ge |
|||||||
| Time-Lapse | 814 | P35G-1.5-14-C | The retromer complex and clathrin define an early endosomal retrograde exit site | Journal of Cell Science | 120 | 12 | June | 2007 | clathrin adaptors AP1 and epsinR, and the retromer complex in
retrograde sorting from early/recycling endosomes to the trans Golgi network
(TGN). However, it has remained unclear whether these protein machineries function on the same or parallel pathway |
HeLa | Popoff, Vincent | Vincent Popoff, Gonzalo A. Mardones, Danièle Tenza, Raúl Rojas,
Christophe Lamaze, Juan S. Bonifacino, Graça Raposo and Ludger Johannes |
The retromer complex and clathrin define an early endosomal retrograde exit site |
Retrograde transport, Retromer, Shiga toxin, Endosome, Golgi, Clathrin |
HeLa cells grown to 40-50% confluency on 35-mmglass- bottom culture dishes (MatTek Corporation, Ashland, MA) |
|||||
| Time-Lapse | 713 | glass-bottom microwell dishes | p120 catenin regulates lamellipodial dynamics and cell adhesion in cooperation with cortactin | PNAS | 104 | 26 | June | 2007 | The armadillo-family protein, p120 catenin (p120), binds to
the juxtamembrane domain of classical cadherins and increases cell– cell junction stability. Overexpression of p120 modulates the activity of Rho family GTPases and augments cell migratory abilit |
Mouse | cDNA in pRcCMV vector (46) | p120 | Boguslavsky, Shlomit | Shlomit Boguslavsky*, Inna Grosheva*, Elad Landau*, Michael
Shtutman, Miriam Cohen*, Katya Arnold*, Elena Feinstein‡, Benjamin Geiger*, and Alexander Bershadsky*§ |
The Weizmann Institute of Science, Ordway Research
Institute, Inc., QBI Enterprises Ltd., |
adherens junctions
Arp2/3 endocytic vesicles focal adhesions leading edge |
For live cell imaging, cells were plated on glass-bottom
microwell dishes (MatTek, Ashland, MA). Movies were taken using a DeltaVision microscopy system (Applied Precision, Issaquah, WA). |
|||
| Time-Lapse | time-lapse laser scanning microscopy | 482 | Effect Of Tumor-Associated Mutant E-Cadherin Variants With Defects In Exons 8 Or 9 On Matrix Metalloproteinase 3 | Journal of Cellular Physiology | 202 | 3 | August | 2004 | Tumor
progression is characterized by loss of cell adhesion and increase of
invasion and metastasis. The cell adhesion molecule E-cadherin is frequently down-regulated or mutated in tumors. In addition to down-regulation of cell adhesion, degradation of |
HUMAN | BREAST | Epithelial | MDA-MB-435S | Fuchs, Margit | MARGIT FUCHS, CHRISTINE HERMANNSTA¨ DTER, KATJA SPECHT, PJOTR
KNYAZEV, AXEL ULLRICH, ERIKA ROSIVATZ, RAYMONDE BUSCH, PETER HUTZLER, HEINZ HO¨ FLER, AND BIRGIT LUBER |
Technische Universitat Munchen | Tumor progression, cell adhesion, matrix metalloproteinase 3, E-cadherin, cell motility | For time-lapse laser scanning microscopy, cells were
seeded at a density of 2105 cells per 3.5-cm in collagen I-coated plates with a glass bottom which were purchased from MatTek Corporation (Ashland, MA). Uncoated plates were coated for 4hat 378Cwit |
||
| Time-Lapse | 731 | 35-mm glass bottom dishes | Different mitochondrial intermembrane space proteins are
released during apoptosis in a manner that is coordinately initiated but can vary in duration |
PNAS | 103 | 31 | August | 2006 | The
release of mitochondrial intermembrane space proteins to the cytosol is a key event during apoptosis. We used in situ fluorescent labeling of proteins tagged with a short tetracysteine-containing sequence to follow the release of Smac, Omi, adenylate |
HeLa | Munoz-Pinedo, Cristina | Cristina Mun˜ oz-Pinedo*, Ana Guı´o-Carrio´ n‡§, Joshua C.
Goldstein‡, Patrick Fitzgerald*, Donald D. Newmeyer‡, and Douglas R. Green |
St. Jude Children’s Research Hospital, Institut de Recerca Oncolo` gica–Institut d’Investigacio´ Biome` dica de Bellvitge (IDIBELL), ‡La Jolla Institute for Allergy and Immunology | apoptosis-inducing factor cytochrome c mitochondria Omi Smac | For time-lapse analysis, cells were grown in poly-D-lysine coated 35-mm glass-bottom microwell dishes (MatTek), and treated in 3 ml of DMEM (GIBCO) supplemented with 10% FCS/20 mM Hepes, pH 7.3/2 mM L-glutamine/200 mg/ml penicillin/100 mg/ml streptomycin | |||||
| Time-Lapse | 697 | 35 mm glass bottom culture dishes |
Proteolysis restricts localiztion of CID, the centromere-specific histone H3 variant of Drosophila, to centromeres | Nucleic Acids Research | 34 | 21 | December | 2006 | Centromere identity is determined by the formation of a specialized chromatin structure containing the centromere-specific histone H3 variant CENP-A. The precise molecular mechanism(s) accounting for the specific deposition of CENP-A at centromeres are st |
D.melanogaster | Kc167 | Moreno-Moreno, Olga | Olga Moreno-Moreno, Monica Torras-Llort and Fernando Azorın | Parc Cientıfic de Barcelona | For in vivo time-lapse analysis, 1.2 · 106 cells were
plated 48 h post-transfection on 35 mm glass-bottomed culture dishes (Mattek Inc.), |
|||||
| Time-Lapse | time-lapse microscopy, Confocal | 530 | Mitochondrial Metabolism Reveals A Functional Architecture In Intact Islets Of Langerhans From Normal And Diabetic Psammomys Obesus | American Journal of Physiology- Endocrinology and Metabolism | 287 | 6 | December | 2004 | The cells within the intact islet of Langerhans function as a metabolic syncytium, secreting insulin in a coordinated and oscillatory manner in response to external fuel. With increased glucose, the oscillatory amplitude is enhanced, leading to the hy |
Islet | Katzman, S. M. | S. M. Katzman, M. A. Messerli, D. T. Barry, A. Grossman, T.
Harel, J. D. Wikstrom, B. E. Corkey, P. J. S. Smith, and O. S. Shirihai |
Tufts University | diabetes; metabolic oscillations; mitochondrial membrane
potential; rhodamine 123 |
Mitochondrial membrane potential was measured using the potentiometric dye Rh123 (Molecular Probes, Eugene, OR) loaded at a final concentration of 13 M. This concentration of dye is not harmful to the cells; in studies of isolated -cells, exposure o |
|||||
| Time-Lapse | 261 | Distinct Functions Of The Unique C Terminus Of Lap2 A In Cell Proliferation And Nuclear Assembly | Journal of Biological Chemistry | 277 | 27 | May | 2002 | The non-membrane-bound lamina-associated polypeptide 2 isoform, LAP2, forms nucleoskeletal structures with A-type lamins and interacts with chromosomes in a cell cycle-dependent manner. LAP2 contains a LEM (LAP2, emerin, and MAN1) domain in the constant N | HUMAN | cervix | IZSBS BS TCL20 Morphology: epithelial-like Species: human, Black female 31 years old; Tissue: cervix; Tumor: carcinoma, epitheloid Properties: antitumour testing; transformation; tumorigenicity; cytotoxicity; cell biology; bacterial invasiveness; virology |
epithelial-like | HeLa | Vlcek, S. | Vlcek, S., Barbara Korbei , B., and Foisner, R., Department of Biochemistry and Molecular Cell Biology, Vienna Biocenter, University of Vienna, Vienna, Austria. Journal of Biol. Chem., 77, (), 8898-8907, (00). | University of Vienna | For time lapse microscopy, cells were seeded on glass-bottom culture dishes (MatTek Corp., Ashland, MA), grown for 8-48 h after transfection, and incubated … | |||
| Time-Lapse | 382 | Macrophages Promote The Invasion Of Breast Carcinoma Cells Via A Colony-Stimulating Factor-1/Epidermal Growth Factor Paracrine Loop | Cancer Research | 65 | 12 | June | 2005 | Previous studies have shown that macrophages and tumor cells are comigratory in mammary tumors and that these cell types are mutually dependent for invasion. Here we show that macrophages and tumor cells are necessary and sufficient for comigration and in | Breast | MTLN3-GFP | Goswami, Sumanta | Sumanta Goswami, Erik Sahai, Jeffrey B. Wyckoff, Michael Cammer,
Dianne Cox, Fiona J. Pixley, E. Richard Stanley, Jeffrey E. Segall, and John S. Condeelis |
Albert Einstein College of Medicine | Colony-Stimulating Factor-1/Epidermal Growth Factor, chemotactic factor |
MTLn3-GFP and RAW264.7 (LR5) cells were cultured in a-MEM with 5% fetal bovine serum (FBS). BAC1.2F51.2F5 cells were cultured in a-MEM with 10% FBS and 36 ng/mL of Human recombinant CSF-1 (a gift from Chiron Corp., Emeryville, CA). MTLn3-GFP (n = 50,00 |
|||||