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Sci Rep. 2017 Sep 5;7(1):10462. doi: 10.1038/s41598-017-09058-8.

Transcriptome analysis of inflammation-related gene expression in endothelial cells activated by complement MASP-1.

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Department 3rd of Internal Medicine, Semmelweis University, Budapest, Hungary.
Department of Pathogenetics, National Institute of Oncology, Budapest, Hungary.
Institute of Enzymology, Research Centre for Natural Sciences, Hungarian Academy of Sciences, Budapest, Hungary.
First Department of Obstetrics and Gynecology, Semmelweis University, Budapest, Hungary.
MTA-SE Molecular Biophysics Research Group, Hungarian Academy of Sciences, Sciences and Institute of Biophysics and Radiation Biology, Semmelweis University, Budapest, Hungary.
Department 3rd of Internal Medicine, Semmelweis University, Budapest, Hungary.


Mannan-binding lectin-associated serine protease 1 (MASP-1), the most abundant enzyme of the complement lectin pathway, is able to stimulate human umbilical vein endothelial cells (HUVECs) to alter the expression of several cytokines and adhesion molecules. This study has assessed to what extent MASP-1 is able to modify the transcriptional pattern of inflammation-related (IR) genes in HUVECs. We utilized Agilent microarray to analyse the effects of recombinant MASP-1 (rMASP-1) in HUVECs, on a set of 884 IR genes. Gene Set Enrichment Analysis showed an overall activation of inflammation-related genes in response to rMASP-1. rMASP-1 treatment up- and down-regulated 19 and 11 IR genes, respectively. Most of them were previously unidentified, such as genes of chemokines (CXCL1, CXCL2, CXCL3), inflammatory receptors (TLR2, BDKRB2) and other inflammatory factors (F3, LBP). Expression of IR genes changed early, during the first 2 hours of activation. Both p38-MAPK inhibitor and NFκB inhibitor efficiently suppressed the effect of rMASP-1. We delineated 12 transcriptional factors as possible regulators of rMASP-1-induced IR genes. Our microarray-based data are in line with the hypothesis that complement lectin pathway activation, generating active MASP-1, directly regulates inflammatory processes by shifting the phenotype of endothelial cells towards a more pro-inflammatory type.

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