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Artykuł

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Tytuł

Proteomic Profiling of Leukocytes Reveals Dysregulation of Adhesion and Integrin Proteins in Chronic Kidney Disease-Related Atherosclerosis

Autorzy

[ 1 ] Instytut Chemii Bioorganicznej Polskiej Akademii Nauk, Polska Akademia Nauk | [ P ] pracownik

Dyscyplina naukowa (Ustawa 2.0)

[7.5] Nauki biologiczne

Rok publikacji

2021

Opublikowano w

Journal of Proteome Research

Rocznik: 2021 | Tom: 20 | Numer: 6

Typ artykułu

artykuł naukowy

Język publikacji

angielski

Słowa kluczowe
EN
Streszczenie

EN A progressive loss of functional nephrons defines chronic kidney disease (CKD). Complications related to cardiovascular disease (CVD) are the principal causes of mortality in CKD; however, the acceleration of CVD in CKD remains unresolved. Our study used a complementary proteomic approach to assess mild and advanced CKD patients with different atherosclerosis stages and two groups of patients with different classical CVD progression but without renal dysfunction. We utilized a label-free approach based on LC-MS/MS and functional bioinformatic analyses to profile CKD and CVD leukocyte proteins. We revealed dysregulation of proteins involved in different phases of leukocytes' diapedesis process that is very pronounced in CKD's advanced stage. We also showed an upregulation of apoptosis-related proteins in CKD as compared to CVD. The differential abundance of selected proteins was validated by multiple reaction monitoring, ELISA, Western blotting, and at the mRNA level by ddPCR. An increased rate of apoptosis was then functionally confirmed on the cellular level. Hence, we suggest that the disturbances in leukocyte extravasation proteins may alter cell integrity and trigger cell death, as demonstrated by flow cytometry and microscopy analyses. Our proteomics data set has been deposited to the ProteomeXchange Consortium via the PRIDE repository with the data set identifier PXD018596.

Strony (od-do)

3053 - 3067

DOI

10.1021/acs.jproteome.0c00883

URL

https://pubs.acs.org/doi/pdf/10.1021/acs.jproteome.0c00883

Punktacja Ministerstwa / czasopismo

100

Punktacja Ministerstwa / czasopismo w ewaluacji 2017-2021

100