The Tissue and Neurobehavioral Phenotyping Core, designated as Core C, is a centralized facility that will provide investigators with a well-established and reproducible model of influenza A?induced pneumonia. Quantitative tools such as Flexivent measurements of lung mechanics, magnetic resonance imaging to evaluate lung repair and remodeling, and multiplex measures of pro-inflammatory cytokines will be conducted by Core C according to the research plan outlined in Projects 1, 2, and 3. Core C will use advanced flow cytometry capabilities to quantify, phenotype, and sort specific inflammatory and parenchymal cell populations from the murine lung, brain, and muscle. The sorting and isolation capabilities of the Core will allow cell-type- specific assessment of proteostasis networks via mass spectroscopy (as outlined by Core B). Core C will breed mice to generate the cell-type- or tissue-specific Cre recombinase lines to induce tissue-specific knockout mice. Core C will perform the genotyping of all the murine strains proposed by Project Leaders. Core C will maintain a uniform environment in which wild-type and genetically engineered mice will be aged. Importantly, Core C will assess the impact of influenza A?induced pneumonia on age-related changes in neurobehavioral phenotypes. Briefly, Core C will examine motor coordination and balance by means of an accelerating rotarod test. Response latency on a hot plate will be tested to assess nociceptive functions. Exploratory behaviors and locomotor activity will be examined in an open field assay and by continuous monitoring with running wheels. Learning and memory will be examined in novel object recognition and Barnes maze tests. Collectively, these tools provide a unique resource for Project Investigators, which would be difficult to reproduce without the support of this PPG.

Public Health Relevance

It is not required per instructions stated on the Funding Opportunity Announcement PAR-18-297, Section IV. Application and Submission Information, Project, Research & Related Other Project Information (Core), ?Project Narrative: Do not complete?.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
2P01AG049665-06
Application #
9937138
Study Section
Special Emphasis Panel (ZAG1)
Project Start
Project End
Budget Start
2020-06-01
Budget End
2021-03-31
Support Year
6
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Northwestern University at Chicago
Department
Type
DUNS #
005436803
City
Chicago
State
IL
Country
United States
Zip Code
60611
Hutt, Darren M; Loguercio, Salvatore; Roth, Daniela Martino et al. (2018) Correcting the F508del-CFTR variant by modulating eukaryotic translation initiation factor 3-mediated translation initiation. J Biol Chem 293:13477-13495
Lu, Ziyan; Casalino-Matsuda, S Marina; Nair, Aisha et al. (2018) A role for heat shock factor 1 in hypercapnia-induced inhibition of inflammatory cytokine expression. FASEB J 32:3614-3622
Mutlu, Gökhan M; Budinger, G R Scott (2018) Letter by Mutlu and Budinger Regarding Article, ""Particulate Matter Exposure and Stress Hormone Levels: A Randomized, Double-Blind, Crossover Trial of Air Purification"". Circulation 137:1203-1204
Radigan, Kathryn A; Nicholson, Trevor T; Welch, Lynn C et al. (2018) Influenza A Virus Infection Induces Muscle Wasting via IL-6 Regulation of the E3 Ubiquitin Ligase Atrogin-1. J Immunol :
Steinert, Elizabeth M; Chandel, Navdeep S (2018) Mitochondria-ER Pas de Deux Controls Memory T Cell Function. Immunity 48:479-481
Coates, Bria M; Staricha, Kelly L; Koch, Clarissa M et al. (2018) Inflammatory Monocytes Drive Influenza A Virus-Mediated Lung Injury in Juvenile Mice. J Immunol 200:2391-2404
Sala, Marc A; Chen, Cong; Zhang, Qiao et al. (2018) JNK2 up-regulates hypoxia-inducible factors and contributes to hypoxia-induced erythropoiesis and pulmonary hypertension. J Biol Chem 293:271-284
Sala, Marc A; Balderas-Martínez, Yalbi Itzel; Buendía-Roldan, Ivette et al. (2018) Inflammatory pathways are upregulated in the nasal epithelium in patients with idiopathic pulmonary fibrosis. Respir Res 19:233
Dela Cruz, Charles S; Wunderink, Richard G; Christiani, David C et al. (2018) Future Research Directions in Pneumonia. NHLBI Working Group Report. Am J Respir Crit Care Med 198:256-263
Galluzzi, Lorenzo; Vitale, Ilio; Aaronson, Stuart A et al. (2018) Molecular mechanisms of cell death: recommendations of the Nomenclature Committee on Cell Death 2018. Cell Death Differ 25:486-541

Showing the most recent 10 out of 58 publications