Human proteome distribution atlas for tissue-specific plasma proteome dynamics
(2025) In Cell p.1-13- Abstract
The plasma proteome is maintained by the influx and efflux of proteins from surrounding organs and cells. To quantify the extent to which different organs and cells impact the plasma proteome in healthy and diseased conditions, we developed a mass-spectrometry-based proteomics strategy to infer the tissue origin of proteins detected in human plasma. We first constructed an extensive human proteome atlas from 18 vascularized organs and the 8 most abundant cell types in blood. The atlas was interfaced with previous RNA and protein atlases to objectively define proteome-wide protein-organ associations to infer the origin and enable the reproducible quantification of organ-specific proteins in plasma. We demonstrate that the resource can... (More)
The plasma proteome is maintained by the influx and efflux of proteins from surrounding organs and cells. To quantify the extent to which different organs and cells impact the plasma proteome in healthy and diseased conditions, we developed a mass-spectrometry-based proteomics strategy to infer the tissue origin of proteins detected in human plasma. We first constructed an extensive human proteome atlas from 18 vascularized organs and the 8 most abundant cell types in blood. The atlas was interfaced with previous RNA and protein atlases to objectively define proteome-wide protein-organ associations to infer the origin and enable the reproducible quantification of organ-specific proteins in plasma. We demonstrate that the resource can determine disease-specific quantitative changes of organ-enriched protein panels in six separate patient cohorts, including sepsis, pancreatitis, and myocardial injury. The strategy can be extended to other diseases to advance our understanding of the processes contributing to plasma proteome dynamics.
(Less)
- author
- organization
-
- Translational Sepsis research (research group)
- epIgG (research group)
- Infection Medicine Proteomics (research group)
- Lung Biology (research group)
- Neurological injury in acute type A aortic dissection (research group)
- Minimal invasive cardiac surgery in valvular heart disease (research group)
- Bleeding disorders and acute typ-A dissection (research group)
- LUCC: Lund University Cancer Centre
- Hepato-Pancreato-Biliary Surgery (research group)
- Surgery (research group)
- Urological cancer, Malmö (research group)
- Division of Molecular Medicine and Gene Therapy
- Stem cell and Cancer stem cell Regulation (research group)
- StemTherapy: National Initiative on Stem Cells for Regenerative Therapy
- Breast and Ovarian Cancer Genomics (research group)
- EpiHealth: Epidemiology for Health
- Advanced ovarian cancer (research group)
- Neurosurgery
- WCMM-Wallenberg Centre for Molecular Medicine
- Hand Surgery, Malmö (research group)
- Clinical Protein Science and Imaging (research group)
- Clinical Chemistry, Malmö (research group)
- Heparin bindning protein in cardiothoracic surgery (research group)
- SEBRA Sepsis and Bacterial Resistance Alliance (research group)
- Breast cancer Proteogenomics (research group)
- LTH Profile Area: Engineering Health
- BioMS (research group)
- publishing date
- 2025-04-04
- type
- Contribution to journal
- publication status
- epub
- subject
- in
- Cell
- pages
- 1 - 13
- publisher
- Cell Press
- external identifiers
-
- pmid:40203824
- ISSN
- 1097-4172
- DOI
- 10.1016/j.cell.2025.03.013
- language
- English
- LU publication?
- yes
- additional info
- Copyright © 2025 The Author(s). Published by Elsevier Inc. All rights reserved.
- id
- 7223fc38-11ce-43ec-afd9-05f61b0b9a74
- date added to LUP
- 2025-04-10 09:43:27
- date last changed
- 2025-04-10 12:21:58
@article{7223fc38-11ce-43ec-afd9-05f61b0b9a74, abstract = {{<p>The plasma proteome is maintained by the influx and efflux of proteins from surrounding organs and cells. To quantify the extent to which different organs and cells impact the plasma proteome in healthy and diseased conditions, we developed a mass-spectrometry-based proteomics strategy to infer the tissue origin of proteins detected in human plasma. We first constructed an extensive human proteome atlas from 18 vascularized organs and the 8 most abundant cell types in blood. The atlas was interfaced with previous RNA and protein atlases to objectively define proteome-wide protein-organ associations to infer the origin and enable the reproducible quantification of organ-specific proteins in plasma. We demonstrate that the resource can determine disease-specific quantitative changes of organ-enriched protein panels in six separate patient cohorts, including sepsis, pancreatitis, and myocardial injury. The strategy can be extended to other diseases to advance our understanding of the processes contributing to plasma proteome dynamics.</p>}}, author = {{Malmström, Erik and Malmström, Lars and Hauri, Simon and Mohanty, Tirthankar and Scott, Aaron and Karlsson, Christofer and Gueto-Tettay, Carlos and Åhrman, Emma and Nozohoor, Shahab and Tingstedt, Bobby and Regner, Sara and Elfving, Peter and Bjermer, Leif and Forsvall, Andreas and Doyle, Alexander and Magnusson, Mattias and Hedenfalk, Ingrid and Kannisto, Päivi and Brandt, Christian and Nilsson, Emma and Dahlin, Lars B and Malm, Johan and Linder, Adam and Niméus, Emma and Malmström, Johan}}, issn = {{1097-4172}}, language = {{eng}}, month = {{04}}, pages = {{1--13}}, publisher = {{Cell Press}}, series = {{Cell}}, title = {{Human proteome distribution atlas for tissue-specific plasma proteome dynamics}}, url = {{http://dx.doi.org/10.1016/j.cell.2025.03.013}}, doi = {{10.1016/j.cell.2025.03.013}}, year = {{2025}}, }