Summary of Study ST002461
This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001588. The data can be accessed directly via it's Project DOI: 10.21228/M8F71Q This work is supported by NIH grant, U2C- DK119886.
See: https://www.metabolomicsworkbench.org/about/howtocite.php
Study ID | ST002461 |
Study Title | Untargeted metabolomics of HUVECs subjected to hypoxia-reoxygenation |
Study Summary | Acute hemorrhage commonly leads to coagulopathy and organ dysfunction or failure. Recent evidence suggests that damage to the endothelial glycocalyx contributes to these adverse outcomes. The physiological events mediating acute glycocalyx shedding are undefined, however. Here, we show that succinate accumulation within endothelial cells drives glycocalyx degradation through a membrane reorganization-mediated mechanism. We investigated this mechanism in a cultured endothelial cell hypoxia-reoxygenation model, in a rat model of hemorrhage, and in trauma patient plasma samples. We found that succinate metabolism by succinate dehydrogenase mediates glycocalyx damage through lipid oxidation and phospholipase A2-mediated membrane reorganization (increasing lysophospholipids), promoting the interaction of MMP24 and MMP25 with glycocalyx constituents. In trauma patients, we found that succinate levels were associated with glycocalyx damage and the development of coagulopathy, and that interaction of MMP24 and syndecan-1 were elevated compared to healthy controls. This establishes a novel metabolic cascade mediating the endotheliopathy of traumatic hemorrhage. |
Institute | Tulane University School of Medicine |
Department | Surgery |
Laboratory | Tulane Trauma and Critical Care Research Lab |
Last Name | Jackson-Weaver |
First Name | Olan |
Address | 1430 Tulane Ave, Department of Surgery, School of Medicine |
ojacksonweaver@tulane.edu | |
Phone | 5049885111 |
Submit Date | 2023-01-30 |
Num Groups | 2 |
Total Subjects | 12 |
Analysis Type Detail | LC-MS |
Release Date | 2023-03-31 |
Release Version | 1 |
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Factors:
Subject type: Cultured cells; Subject species: Homo sapiens (Factor headings shown in green)
mb_sample_id | local_sample_id | Treatment |
---|---|---|
SA246367 | HR3 | hypoxia/reoxygenation |
SA246368 | HR4 | hypoxia/reoxygenation |
SA246369 | HR6 | hypoxia/reoxygenation |
SA246370 | HR2 | hypoxia/reoxygenation |
SA246371 | HR5 | hypoxia/reoxygenation |
SA246372 | HR1 | hypoxia/reoxygenation |
SA246373 | N3 | normoxia |
SA246374 | N2 | normoxia |
SA246375 | N4 | normoxia |
SA246376 | N5 | normoxia |
SA246377 | N6 | normoxia |
SA246378 | N1 | normoxia |
Showing results 1 to 12 of 12 |