Many DERC investigators share a common need for high-speed fluorescence imaging of cells in both 2 and 3 dimensions. The instrumentation and software developments of the Biomedical Imaging Group are largely determined by the evolving needs of these studies. The work is performed on unique instruments and analysis software developed by the faculty of the Biomedical Imaging Group (BIG), in whose laboratory the core is located, and is highly collaborative in nature. The central instrumentation of the Cell Imaging Core are: 1) a high-resolution, Fluorescence Digital Imaging Microscope (F-DIM) for 2-D imaging and 3-D reconstruction of molecular distributions inside fixed and living cells; 2) a unique, custom-built high-speed F-DIM for 2-D imaging of very rapid molecular dynamics (e.g. local calcium signaling) and fast (< 1 sec.) 3-D imaging of molecular distributions in living cells; 3) a new Total Internal Reflection Fluorescence (TIRF) microscope for high-speed imaging of near membrane molecules; 4) a new Multi-photon fluorescence microscope with the ability to image deep into living tissue. In addition, the Imaging Core provides high-speed computational facilities, numerous 3-D graphical workstations with custom software for image processing, visualization and analysis, and for computer simulation of molecular interactions inside cells. Strong, grant-funded (NIH R01, PPG) collaborations with DERC members Czech, Corvera, and Ikebe have provided driving biological problems, and the ability to commit our resources to the development of complex instrumentation and software systems in the BIG laboratory. Funding from the DERC Imaging Core has enabled us to develop further and to refine these advances in instrumentation, and to offer assistance, training, and access to more DERC members (Davis, Doxsey, Rock, Bortell, Greiner, Mordes, Rossini, Mello). Support from the DERC has allowed us to commit to expanding (e.g. multi-photon microscopy) with a focus on future DERC utilization and collaborations. We were able recruit and hire an Optical Physicist (C. Standley) with expertise in optics, imaging, lasers, and image processing, to work on TIRF and multi-photon microscopy, two of the newest instruments available in BIG and to the DERC members.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK032520-25
Application #
7619909
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2008-04-01
Budget End
2009-03-31
Support Year
25
Fiscal Year
2008
Total Cost
$110,106
Indirect Cost
Name
University of Massachusetts Medical School Worcester
Department
Type
DUNS #
603847393
City
Worcester
State
MA
Country
United States
Zip Code
01655
Desai, Paurav B; San Agustin, Jovenal T; Stuck, Michael W et al. (2018) Ift25 is not a cystic kidney disease gene but is required for early steps of kidney development. Mech Dev 151:10-17
Ly, Socheata; Navaroli, Deanna M; Didiot, Marie-Cécile et al. (2017) Visualization of self-delivering hydrophobically modified siRNA cellular internalization. Nucleic Acids Res 45:15-25
Wang, Feng; McCannell, Kurtis N; Boškovi?, Ana et al. (2017) Rlim-Dependent and -Independent Pathways for X Chromosome Inactivation in Female ESCs. Cell Rep 21:3691-3699
Watkin, Levi B; Mishra, Rabinarayan; Gil, Anna et al. (2017) Unique influenza A cross-reactive memory CD8 T-cell receptor repertoire has a potential to protect against EBV seroconversion. J Allergy Clin Immunol 140:1206-1210
LeBlanc, Scott E; Wu, Qiong; Lamba, Pallavi et al. (2016) Promoter-enhancer looping at the PPAR?2 locus during adipogenic differentiation requires the Prmt5 methyltransferase. Nucleic Acids Res 44:5133-47
Wang, Feng; Shin, JongDae; Shea, Jeremy M et al. (2016) Regulation of X-linked gene expression during early mouse development by Rlim. Elife 5:
Kincaid, Eleanor Z; Murata, Shigeo; Tanaka, Keiji et al. (2016) Specialized proteasome subunits have an essential role in the thymic selection of CD8(+) T cells. Nat Immunol 17:938-45
Townsley, E; O'Connor, G; Cosgrove, C et al. (2016) Interaction of a dengue virus NS1-derived peptide with the inhibitory receptor KIR3DL1 on natural killer cells. Clin Exp Immunol 183:419-30
Wyss, Lena; Stadinski, Brian D; King, Carolyn G et al. (2016) Affinity for self antigen selects Treg cells with distinct functional properties. Nat Immunol 17:1093-101
Delong, Thomas; Wiles, Timothy A; Baker, Rocky L et al. (2016) Pathogenic CD4 T cells in type 1 diabetes recognize epitopes formed by peptide fusion. Science 351:711-4

Showing the most recent 10 out of 707 publications