Abstract

The overall objectives of the Proteomics Core are (1) to provide high throughput comparative quantitative proteome analysis capabilities for analyzing large scale clinical time course samples including blood leukocyte subpopulations and blood plasma samples from trauma and burn patients;(2) to provide high quality quantitative proteomic data that will lead to the identification of protein """"""""fingerprints"""""""" or """"""""signatures"""""""" from blood leukocyte populations and blood plasma that are associated with specific clinical trajectories in patients with severe trauma or burn injury, and the extraction of novel biological information regarding signaling networks from inflammatory cells in severely injured patients with different clinical outcomes;and, (3) to integrate objectives (1) and (2) into an overall functional proteomic view of enriched T-cells and monocytes in the context of their cellular phenotype. To achieve these goals, highly coordinated efforts with other cores and a multitude of developments within the Proteomics Core including high throughput sample processing, high throughput and high sensitivity instrumentation, and efficient data handling and processing are required.

  Funding Agency

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
5U54GM062119-10
Application #
8142231
Study Section
Special Emphasis Panel (ZGM1)
Project Start
Project End
2013-08-31
Budget Start
2010-09-01
Budget End
2011-08-31
Support Year
10
Fiscal Year
2010
Total Cost
$914,094
Indirect Cost

  Institution

Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02199

  Publications

Gale, Stephen C; Kocik, Jurek F; Creath, Robert et al. (2016) A comparison of initial lactate and initial base deficit as predictors of mortality after severe blunt trauma. J Surg Res 205:446-455
Agarwal, Shailesh; Loder, Shawn; Brownley, Cameron et al. (2016) Inhibition of Hif1? prevents both trauma-induced and genetic heterotopic ossification. Proc Natl Acad Sci U S A 113:E338-47
Lopez, Maria-Cecilia; Efron, Philip A; Ozrazgat-Baslanti, Tezcan et al. (2016) Sex-based differences in the genomic response, innate immunity, organ dysfunction, and clinical outcomes after severe blunt traumatic injury and hemorrhagic shock. J Trauma Acute Care Surg 81:478-85
Sood, Ravi F; Gibran, Nicole S; Arnoldo, Brett D et al. (2016) Early leukocyte gene expression associated with age, burn size, and inhalation injury in severely burned adults. J Trauma Acute Care Surg 80:250-7
Mathias, Brittany; Lipori, Gigi; Moldawer, Lyle L et al. (2016) Integrating ""big data"" into surgical practice. Surgery 159:371-4
Mason, Stephanie A; Nathens, Avery B; Finnerty, Celeste C et al. (2016) Hold the Pendulum: Rates of Acute Kidney Injury are Increased in Patients Who Receive Resuscitation Volumes Less than Predicted by the Parkland Equation. Ann Surg 264:1142-1147
Winfield, Robert D; Southard, Robert E; Turnbull, Isaiah R et al. (2015) Angiotensin Inhibition Is Associated with Preservation of T-Cell and Monocyte Function and Decreases Multiple Organ Failure in Obese Trauma Patients. J Am Coll Surg 221:486-94.e4
Peltan, Ithan D; Vande Vusse, Lisa K; Maier, Ronald V et al. (2015) An International Normalized Ratio-Based Definition of Acute Traumatic Coagulopathy Is Associated With Mortality, Venous Thromboembolism, and Multiple Organ Failure After Injury. Crit Care Med 43:1429-38
Nacionales, Dina C; Szpila, Benjamin; Ungaro, Ricardo et al. (2015) A Detailed Characterization of the Dysfunctional Immunity and Abnormal Myelopoiesis Induced by Severe Shock and Trauma in the Aged. J Immunol 195:2396-407
Seok, Junhee; Xu, Weihong; Davis, Ronald W et al. (2015) RASA: Robust Alternative Splicing Analysis for Human Transcriptome Arrays. Sci Rep 5:11917

Showing the most recent 10 out of 199 publications