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 #
5P30DK052574-15
Application #
8574511
Study Section
Special Emphasis Panel (ZDK1-GRB-8)
Project Start
Project End
Budget Start
2013-12-01
Budget End
2014-11-30
Support Year
15
Fiscal Year
2014
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
Luo, Jialie; Qian, Aihua; Oetjen, Landon K et al. (2018) TRPV4 Channel Signaling in Macrophages Promotes Gastrointestinal Motility via Direct Effects on Smooth Muscle Cells. Immunity 49:107-119.e4
Nywening, Timothy M; Belt, Brian A; Cullinan, Darren R et al. (2018) Targeting both tumour-associated CXCR2+ neutrophils and CCR2+ macrophages disrupts myeloid recruitment and improves chemotherapeutic responses in pancreatic ductal adenocarcinoma. Gut 67:1112-1123
Liss, Kim H H; McCommis, Kyle S; Chambers, Kari T et al. (2018) The impact of diet-induced hepatic steatosis in a murine model of hepatic ischemia/reperfusion injury. Liver Transpl 24:908-921
Anderson, Neil W; Tarr, Phillip I (2018) Multiplex Nucleic Acid Amplification Testing to Diagnose Gut Infections: Challenges, Opportunities, and Result Interpretation. Gastroenterol Clin North Am 47:793-812
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
Stoka, Kellie V; Maedeker, Justine A; Bennett, Lisa et al. (2018) Effects of Increased Arterial Stiffness on Atherosclerotic Plaque Amounts. J Biomech Eng 140:
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
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
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
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

Showing the most recent 10 out of 899 publications