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 #
5P30DK052574-14
Application #
8427338
Study Section
Special Emphasis Panel (ZDK1-GRB-8)
Project Start
Project End
Budget Start
2012-12-01
Budget End
2013-11-30
Support Year
14
Fiscal Year
2013
Total Cost
$174,626
Indirect Cost
$59,740
Name
Washington University
Department
Type
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Stoka, Kellie V; Maedeker, Justine A; Bennett, Lisa et al. (2018) Effects of Increased Arterial Stiffness on Atherosclerotic Plaque Amounts. J Biomech Eng 140:
Yoshino, Jun; Almeda-Valdes, Paloma; Moseley, Anna C et al. (2018) Percutaneous muscle biopsy-induced tissue injury causes local endoplasmic reticulum stress. Physiol Rep 6:e13679
Sofia, M Anthony; Ciorba, Matthew A; Meckel, Katherine et al. (2018) Tryptophan Metabolism through the Kynurenine Pathway is Associated with Endoscopic Inflammation in Ulcerative Colitis. Inflamm Bowel Dis 24:1471-1480
Kulkarni, Devesha H; McDonald, Keely G; Knoop, Kathryn A et al. (2018) Goblet cell associated antigen passages are inhibited during Salmonella typhimurium infection to prevent pathogen dissemination and limit responses to dietary antigens. Mucosal Immunol 11:1103-1113
Bajpai, Geetika; Schneider, Caralin; Wong, Nicole et al. (2018) The human heart contains distinct macrophage subsets with divergent origins and functions. Nat Med 24:1234-1245
Onufer, Emily J; Tay, Shirli; Barron, Lauren K et al. (2018) Intestinal epithelial cell-specific Raptor is essential for high fat diet-induced weight gain in mice. Biochem Biophys Res Commun 505:1174-1179
Barron, Lauren; Courtney, Cathleen; Bao, James et al. (2018) Intestinal resection-associated metabolic syndrome. J Pediatr Surg 53:1142-1147
Higgins, Cassandra B; Zhang, Yiming; Mayer, Allyson L et al. (2018) Hepatocyte ALOXE3 is induced during adaptive fasting and enhances insulin sensitivity by activating hepatic PPAR?. JCI Insight 3:
Dolai, Subhankar; Liang, Tao; Orabi, Abrahim I et al. (2018) Pancreatitis-Induced Depletion of Syntaxin 2 Promotes Autophagy and Increases Basolateral Exocytosis. Gastroenterology 154:1805-1821.e5
Riehl, Terrence E; Alvarado, David; Ee, Xueping et al. (2018) Lactobacillus rhamnosus GG protects the intestinal epithelium from radiation injury through release of lipoteichoic acid, macrophage activation and the migration of mesenchymal stem cells. Gut :

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