The Inflammation and Metabolism Core (IMC) is focused on developing instrumentation and infrastructure that are required to enable advanced approaches to studies of metabolic and inflammatory functions at the University of New Mexico (UNM) Health Science Center (HSC). Inflammation and metabolism are multi- faceted and systemic networks. Their study requires measurements involving complex mixtures of cells from multiple organs and tissues using animal or human tissue. IMC will establish an integrated resource of expertise, cutting-edge equipment, and training to assess metabolic and inflammatory readouts within animal models and tissues. To support the goals and the aims of the Autophagy, Inflammation and Metabolism (AIM) in Disease Center of Biomedical Research Excellence (CoBRE), IMC will provide crucial new equipment for state-of-the-art assessment of inflammation and metabolism in whole animals. Furthermore, IMC will bring together disparate resources already existing at UNM HSC to enhance UNM investigator capability to study metabolism and inflammation. Each project that CoBRE mentored PIs (mPIs) propose requires metabolic or inflammatory assessment of unique animal models to perturb autophagy. IMC is essential to support these innovative studies. Experts in inflammation and metabolism will direct the core. IMC leadership will facilitate access to new and existing equipment. This centralization of resources and expertise will extend beyond CoBRE investigators and offer new opportunities and resources for investigators at UNM as well as in the region. IMC will support the following aims:
Specific Aim 1. Create a centralized resource to assess inflammatory and metabolic dysfunction in animal models.
Specific Aim 2. Support mPI research objectives and cultivate a new cohort of CoBRE investigators in their study of metabolic and inflammatory disorders.
Specific Aim 3. Provide leadership to facilitate the increased utilization of metabolic and inflammatory measures as disease readouts.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Exploratory Grants (P20)
Project #
1P20GM121176-01
Application #
9207189
Study Section
Special Emphasis Panel (ZGM1)
Project Start
Project End
Budget Start
2016-12-01
Budget End
2017-11-30
Support Year
1
Fiscal Year
2017
Total Cost
Indirect Cost
Name
University of New Mexico Health Sciences Center
Department
Type
DUNS #
829868723
City
Albuquerque
State
NM
Country
United States
Zip Code
87131
Tasnim, Humayra; Fricke, G Matthew; Byrum, Janie R et al. (2018) Quantitative Measurement of Naïve T Cell Association With Dendritic Cells, FRCs, and Blood Vessels in Lymph Nodes. Front Immunol 9:1571
Castillo, Eliseo F; Zheng, Handong; Yang, Xuexian O (2018) Orchestration of epithelial-derived cytokines and innate immune cells in allergic airway inflammation. Cytokine Growth Factor Rev 39:19-25
Zheng, Handong; Wu, Dandan; Wu, Xiang et al. (2018) Leptin Promotes Allergic Airway Inflammation through Targeting the Unfolded Protein Response Pathway. Sci Rep 8:8905
Deretic, Vojo; Klionsky, Daniel J (2018) Autophagy and inflammation: A special review issue. Autophagy 14:179-180
Zhang, Xing; Luo, Yan; Wang, Chunqing et al. (2018) Adipose mTORC1 Suppresses Prostaglandin Signaling and Beige Adipogenesis via the CRTC2-COX-2 Pathway. Cell Rep 24:3180-3193
Kumar, Suresh; Jain, Ashish; Farzam, Farzin et al. (2018) Mechanism of Stx17 recruitment to autophagosomes via IRGM and mammalian Atg8 proteins. J Cell Biol 217:997-1013
Claude-Taupin, Aurore; Bissa, Bhawana; Jia, Jingyue et al. (2018) Role of autophagy in IL-1? export and release from cells. Semin Cell Dev Biol 83:36-41
Deretic, Vojo; Levine, Beth (2018) Autophagy balances inflammation in innate immunity. Autophagy 14:243-251
Jia, Jingyue; Abudu, Yakubu Princely; Claude-Taupin, Aurore et al. (2018) Galectins Control mTOR in Response to Endomembrane Damage. Mol Cell 70:120-135.e8
Choi, Seong Won; Gu, Yuexi; Peters, Ryan Scott et al. (2018) Ambroxol Induces Autophagy and Potentiates Rifampin Antimycobacterial Activity. Antimicrob Agents Chemother 62:

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