The mission of the Microscopy and Histopathology Core B is to provide access to basic and cutting-edge optical and electron microscopy equipment, expertise and methods for microscopy techniques, training, service, and histology/histopathology support for innovative and cross-disciplinary GI and liver research. Core B, which is located at the Beth Israel Deaconess Medical Center (site 1) and Boston Children?s Hospital (site 2) has the following Specific Aims: 1) to provide access to resources, technologies and services unavailable in members' labs, or inaccessible in other institutional cores; 2) to extend the resources of HDDC investigators by subsidizing the costs of services, materials and equipment use; 3) to enhance the technical capabilities of established and young HDDC investigators through training in advanced technologies; and 4) to research, develop and acquire new and emerging technologies that will accelerate digestive diseases research now and in the future. In the past 5-year funding cycle, seven services were offered for Core B. Sixteen or more HDDC members used one or more of the Core B services in every quarter as measured in billable hours of service. HDDC support significantly extended grant dollars by reducing the cost of services by 25% or more for HDDC members and more than 80 papers primarily benefited from core B use. New innovations and equipment updates in the past funding cycle benefited, in particular, the electron microscopy and confocal microscopy services and their users. In the next funding cycle, two new services are proposed for core B including advanced microscopy instrumentation and animal histopathology support. The electron microscopy service intends to add capacity for high pressure freezing/freeze substitution and the confocal service will add new instrumentation and the capacity for ratio imaging. Overall, fifty eight HDDC Members anticipate use of Core B in next funding cycle. Discounted services for HDDC members will continue to extend grant dollars and priority access for HDDC members to core services should facilitate greater productivity.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK034854-35
Application #
9850254
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2019-12-01
Budget End
2020-11-30
Support Year
35
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Boston Children's Hospital
Department
Type
DUNS #
076593722
City
Boston
State
MA
Country
United States
Zip Code
02115
Gornati, Laura; Zanoni, Ivan; Granucci, Francesca (2018) Dendritic Cells in the Cross Hair for the Generation of Tailored Vaccines. Front Immunol 9:1484
Blumberg, Richard S; Lillicrap, David; IgG Fc Immune Tolerance Group (2018) Tolerogenic properties of the Fc portion of IgG and its relevance to the treatment and management of hemophilia Blood 131:2205-2214
Yao, Lina; Seaton, Sarah Craven; Ndousse-Fetter, Sula et al. (2018) A selective gut bacterial bile salt hydrolase alters host metabolism. Elife 7:
Haghighi, Alireza; Krier, Joel B; Toth-Petroczy, Agnes et al. (2018) An integrated clinical program and crowdsourcing strategy for genomic sequencing and Mendelian disease gene discovery. NPJ Genom Med 3:21
Lee, Christine K; Mitchell, Paul D; Raza, Roshan et al. (2018) Validation of Transient Elastography Cut Points to Assess Advanced Liver Fibrosis in Children and Young Adults: The Boston Children's Hospital Experience. J Pediatr 198:84-89.e2
Santus, William; Mingozzi, Francesca; Vai, Marina et al. (2018) Deep Dermal Injection As a Model of Candida albicans Skin Infection for Histological Analyses. J Vis Exp :
Stein, Richard R; Tanoue, Takeshi; Szabady, Rose L et al. (2018) Computer-guided design of optimal microbial consortia for immune system modulation. Elife 7:
Chen, Peng; Tao, Liang; Wang, Tianyu et al. (2018) Structural basis for recognition of frizzled proteins by Clostridium difficile toxin B. Science 360:664-669
Shaw, Kelly A; Cutler, David J; Okou, David et al. (2018) Genetic variants and pathways implicated in a pediatric inflammatory bowel disease cohort. Genes Immun :
Lyons, Jesse; Ghazi, Phaedra C; Starchenko, Alina et al. (2018) The colonic epithelium plays an active role in promoting colitis by shaping the tissue cytokine profile. PLoS Biol 16:e2002417

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