Light microscopy The light microscopy arm of the MIC operates on 4 different aspects of imaging: Equipment maintenance and upgrade The MIC operates several confocal laser scanning microscopes optimized for different applications: The most recent acquisition is a confocal microscope by Zeiss, the LSM 780. This confocal microscope and is now made available for both live cell imaging and for fixed specimens. In addition the MIC maintains a Zeiss LSM 510 inverted for high-resolution confocal imaging of fixed specimen, Zeiss Live DuoScan for high-speed imaging of live cells, and a Zeiss LSM 510 NLO for two-photon imaging of live tissue sections and live animals. The NICHD DIR recently made funds available to acquire a new hybrid spinning disk confocal microscope from Nikon Microscopes, and an order has been placed. This acquisition will solve a long existing deficiency within the MIC since the decommissioning of a Perkin Elmer spinning disk confocal microscope in 2010. MIC operates a home-built Photo-Activation Localization (PALM) Microscope for sub-resolution microscopy. This microscope and the necessary software were implemented by Dr. Schram in the MIC. Two high-end wide-field fluorescence microscopes, one on an upright platform and another on an inverted platform are also now functional. Finally, a fluorescence stereo microscope is available for imaging large specimens such as whole embryos and large tissue sections in low magnifications. Live cell imaging is supported with temperature, CO2, humidity control and heated perfusion on most microscopes. The newly acquired microscopes including the ones currently under procurement processes are equipped with computer-controlled constant focus capabilities which allows for long term imaging of live cell preparations. Instrument downtime is kept to a minimum by providing full-time support to end users (phone and pager). For problems that require extensive repairs, most instruments are covered by service contracts provided by the manufacturers, and are usually serviced within a few days. User training and Support Each user then receives hands-on training on the light microscope required by the project. The training covers the principles of fluorescence microscopy, confocal imaging, and optimum operation of the hardware platform. During the Spring of 2012, the MC staff offered a series of classroom lessons as well as hands-on laboratory courses on various aspects of microscopy and practical microscopy modalities.These courses were attended by over 30 individual postdoctoral scientists and technical staff. The courses were so well received by all the participants and their PIs, that it will be repeated at least annually. Image analysis The MIC operates a data analysis center with three high-end workstations and image analysis, and image processing software (ImageJ/Fiji, Metamorph, Volocity, Imaris and Zeiss AIM, MatLab, LabView). At the users request, training and support are provided for each software package. When required, custom macros and high-throughput image analysis solutions are also provided. The facility offers extensive data storage and archival services with an enterprise-level file server and a data backup system. Method development MIC is actively involved in the development of newer microscopy and imaging methodologies denovo, and in collaborative effort with scientists within the NIH IRP. Recently, Dr. Schram completed installation of a Photo-Activatable Localization Microscopy (FPALM) platform. Similar method development efforts will be taken on according to needs within the Institute and availability of funds. Requests are actively entertained. MIC, in addition hosts a number of vendor-offered demonstrations and hands-on use of new microscopy platforms. Electron microscopy Because of the complex and delicate nature of Electron Microscopy (EM) sample preparation, the EM operations of the MIC function differently from the light microscopy imaging side. Sample processing Typically, all EM processing (fixation, embedding, cutting and staining) is done in-house by Mr. Dye. The MIC has a full-fledged EM laboratory with a LKB Pyramitome, a Leica CM3050-S Cryostat and a Reichert Ultracut-E Ultramicrotome. Due to the labor involved, the number of projects undertaken is comparatively fewer. By providing consistent and controlled incubation parameters, the PELCO Biowave Pro, programmable incubator (Ted Pella, Inc.) has been instrumental in improving the preservation of ultrastructure and the quality of immunolabeling. Imaging EM imaging is done most of the time by the microscopist, except in cases where the user has the necessary training and experience. The newly acquired JEM 1400 transmission electron microscope is currently fully operational. This scope was installed during the Spring of 2011 and it offers two new imaging methodologies, cryo-EM and tomography. The main advantage of cryo-EM is preservation of a high level of immuno-reactivity and imaging of specimen in a near native state. Cryo-EM will improve the quality of studies relying on immunogold labeling. Tomography provides the ability to image three-dimensional structures at the EM level. This feature offers the ability to create 3D views of identified structures of interest which have been functionally characterized by other methods (for example, electrophysiology). Method development Mr. Dye has set up techniques for EM-level immuno-histochemistry, and double immunolabeling to mark two separate antigens at the same time. The use of specialized grids (LUXFilm) has also been developed. LUXFilm EM grids allow a view of the entire specimen and are crucial for imaging large structures, tracing features, searching for special details and for tomography. The MIC has implemented a digital archival system for all EM images and parameters. More recently Mr. Dye has been involved in the development of the use of the newly developed molecular probe for correlative light microscopy and electron microscopy of the same specimen. Minisog is a protein probe which when expressed in cells functions as a photo-induced superoxide generator, and fluorophore. This property allows for initial fluorescence detection of the protein distribution in cells followed by EM level ultrastructural localization of protein distribution of the same cells. Community outreach The MIC is committed to promoting light and electron microscopy in the NICHD, DIR research community. Efforts are being made to educate investigators on the benefits and pitfalls of advanced imaging techniques. These initiatives include a) coaching users on the principles of confocal microscopy, during training and via publication of comprehensive operating protocols for each microscope, b) on-campus demonstrations of new instruments and software by vendors such as Zeiss, Olympus, Photometrics, Nikon and Perkin-Elmer, and c) on-site assistance to investigators in their own laboratories operating their imaging equipment to optimize the quality of the data recorded. Furthermore, the MIC web site ( is an important resource for tutorials and protocols for both fixed and live cell microscopy. Looking ahead Over the last year, a number of the light microscopy platforms received significant upgrades. Chief among them is the acquisition of a new LSM 780 from Zeiss Microscopes. This state-of-the-art platform provides for a number of imaging techniques which were not possible beforehand. The portfolio of instruments within the MIC needs to be maintained at peak levels of performance at all times to adequately serve the needs of NICHD scientists. The quality of data acquired data is heavily influenced by the quality of the optics.

Project Start
Project End
Budget Start
Budget End
Support Year
Fiscal Year
Total Cost
Indirect Cost
Zip Code
Russell, James T (2010) Imaging calcium signals In vivo: A powerful tool in pharmacology. Br J Pharmacol :
Uveges, Thomas E; Kozloff, Kenneth M; Ty, Jennifer M et al. (2009) Alendronate treatment of the brtl osteogenesis imperfecta mouse improves femoral geometry and load response before fracture but decreases predicted material properties and has detrimental effects on osteoblasts and bone formation. J Bone Miner Res 24:849-59
Wollert, Thomas; Wunder, Christian; Lippincott-Schwartz, Jennifer et al. (2009) Membrane scission by the ESCRT-III complex. Nature 458:172-7
Tanaka, Nobuaki K; Ito, Kei; Stopfer, Mark (2009) Odor-evoked neural oscillations in Drosophila are mediated by widely branching interneurons. J Neurosci 29:8595-603
Besser, Limor; Chorin, Ehud; Sekler, Israel et al. (2009) Synaptically released zinc triggers metabotropic signaling via a zinc-sensing receptor in the hippocampus. J Neurosci 29:2890-901
Balla, Tamas; Varnai, Peter (2009) Visualization of cellular phosphoinositide pools with GFP-fused protein-domains. Curr Protoc Cell Biol Chapter 24:Unit 24.4
Koshimizu, Hisatsugu; Senatorov, Vladimir; Loh, Y Peng et al. (2009) Neuroprotective protein and carboxypeptidase E. J Mol Neurosci 39:1-8
Park, Joshua J; Cawley, Niamh X; Loh, Y Peng (2008) Carboxypeptidase E cytoplasmic tail-driven vesicle transport is key for activity-dependent secretion of peptide hormones. Mol Endocrinol 22:989-1005
Woronowicz, Alicja; Koshimizu, Hisatsugu; Chang, Su-Youne et al. (2008) Absence of carboxypeptidase E leads to adult hippocampal neuronal degeneration and memory deficits. Hippocampus 18:1051-63
Jung, Sung-Cherl; Kim, Jinhyun; Hoffman, Dax A (2008) Rapid, bidirectional remodeling of synaptic NMDA receptor subunit composition by A-type K+ channel activity in hippocampal CA1 pyramidal neurons. Neuron 60:657-71

Showing the most recent 10 out of 22 publications