Morphologic analysis remains an essential tool for visualizing the spatial relationships of different cell types, and studying cellular components in the Gl tract. The unique feature of this Morphology Core Facility is the expertise it provides to participating investigators on the structural biology of the Gl tract. Its primary function has been to train and assist investigators in the morphologic analysis of the Gl tract It has also served as an important resource for rapid processing of tissue specimens and for providing investigators with newly developed methods/protocols and reagents for labeling tissue sections. Before the establishment of this Core, DDRCC investigators had poor access to histology services (limited availability, long turn-around, variable quality, and high fees). Because many DDRCC investigators are junior faculty with limited resources, funding for, and access to, the Morphology core has benefited this group, as well as more senior investigators (see Exhibit). This core has provides expert technical service related to the processing of Gl tissue and cell samples. These functions require investment in expensive equipment, and sample preparation and operation of sophisticated instrumentation require highly trained experienced technicians. It is, therefore, much more cost effective to concentrate instrumentation and highly skilled technical support in a centrally managed facility where they can be utilized a high percentage ofthe time. The DDRCC Morphology Core is the onlv histology facilitv at this institution that provides immunohistochemical staining on a fee for service basis. The Morphology Core also serves as a focus for the collective expertise at this institution and rapid dissemination of new techniques. It facilitates exchange of reagents such as antibodies and tissue blocks, and has fostered many collaborations between DDRCC members.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
2P30DK052574-11
Application #
7777674
Study Section
Special Emphasis Panel (ZDK1-GRB-8 (M1))
Project Start
2009-12-01
Project End
2014-11-30
Budget Start
2009-12-01
Budget End
2010-11-30
Support Year
11
Fiscal Year
2010
Total Cost
$137,184
Indirect Cost
Name
Washington University
Department
Type
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Song, Wilbur M; Joshita, Satoru; Zhou, Yingyue et al. (2018) Humanized TREM2 mice reveal microglia-intrinsic and -extrinsic effects of R47H polymorphism. J Exp Med 215:745-760
Bockerstett, Kevin A; Osaki, Luciana H; Petersen, Christine P et al. (2018) Interleukin-17A Promotes Parietal Cell Atrophy by Inducing Apoptosis. Cell Mol Gastroenterol Hepatol 5:678-690.e1
Willet, Spencer G; Lewis, Mark A; Miao, Zhi-Feng et al. (2018) Regenerative proliferation of differentiated cells by mTORC1-dependent paligenosis. EMBO J 37:
Bando, Jennifer K; Gilfillan, Susan; Song, Christina et al. (2018) The Tumor Necrosis Factor Superfamily Member RANKL Suppresses Effector Cytokine Production in Group 3 Innate Lymphoid Cells. Immunity 48:1208-1219.e4
Gathungu, Grace; Zhang, Yuanhao; Tian, Xinyu et al. (2018) Impaired granulocyte-macrophage colony-stimulating factor bioactivity accelerates surgical recurrence in ileal Crohn's disease. World J Gastroenterol 24:623-630
Feng, Jing; Luo, Jialie; Yang, Pu et al. (2018) Piezo2 channel-Merkel cell signaling modulates the conversion of touch to itch. Science 360:530-533
Eberth, Jan M; Josey, Michele J; Mobley, Lee R et al. (2018) Who Performs Colonoscopy? Workforce Trends Over Space and Time. J Rural Health 34:138-147
Zhang, Daoxiang; Li, Lin; Jiang, Hongmei et al. (2018) Tumor-Stroma IL1?-IRAK4 Feedforward Circuitry Drives Tumor Fibrosis, Chemoresistance, and Poor Prognosis in Pancreatic Cancer. Cancer Res 78:1700-1712
Sullender, Meagan E; Baldridge, Megan T (2018) Norovirus interactions with the commensal microbiota. PLoS Pathog 14:e1007183
Brenot, Audrey; Knolhoff, Brett L; DeNardo, David G et al. (2018) SNAIL1 action in tumor cells influences macrophage polarization and metastasis in breast cancer through altered GM-CSF secretion. Oncogenesis 7:32

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