Global Transcriptome Analysis Reveals Distinct Phases of the Endothelial Response to TNF

Author:

Struck Eike C.1,Belova Tatiana2,Hsieh Ping-Han2,Odeberg Jacob O.1345,Kuijjer Marieke L.267ORCID,Dusart Philip J.38ORCID,Butler Lynn M.1389ORCID

Affiliation:

1. *Department of Clinical Medicine, The Arctic University of Norway, Tromsø, Norway

2. †Centre for Molecular Medicine Norway, Nordic EMBL Partnership, University of Oslo, Oslo, Norway

3. ‡Science for Life Laboratory, Department of Protein Science, Royal Institute of Technology, Stockholm, Sweden

4. §The University Hospital of North Norway, Tromsø, Norway

5. ¶Coagulation Unit, Department of Hematology, Karolinska University Hospital, Stockholm, Sweden

6. ‖Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands

7. #Leiden Center for Computational Oncology, Leiden University Medical Center, Leiden, the Netherlands

8. **Clinical Chemistry and Blood Coagulation Research, Department of Molecular Medicine and Surgery, Karolinska Institute, Stockholm, Sweden

9. ††Clinical Chemistry, Karolinska University Laboratory, Karolinska University Hospital, Stockholm, Sweden

Abstract

Abstract The vascular endothelium acts as a dynamic interface between blood and tissue. TNF-α, a major regulator of inflammation, induces endothelial cell (EC) transcriptional changes, the overall response dynamics of which have not been fully elucidated. In the present study, we conducted an extended time-course analysis of the human EC response to TNF, from 30 min to 72 h. We identified regulated genes and used weighted gene network correlation analysis to decipher coexpression profiles, uncovering two distinct temporal phases: an acute response (between 1 and 4 h) and a later phase (between 12 and 24 h). Sex-based subset analysis revealed that the response was comparable between female and male cells. Several previously uncharacterized genes were strongly regulated during the acute phase, whereas the majority in the later phase were IFN-stimulated genes. A lack of IFN transcription indicated that this IFN-stimulated gene expression was independent of de novo IFN production. We also observed two groups of genes whose transcription was inhibited by TNF: those that resolved toward baseline levels and those that did not. Our study provides insights into the global dynamics of the EC transcriptional response to TNF, highlighting distinct gene expression patterns during the acute and later phases. Data for all coding and noncoding genes is provided on the Web site (http://www.endothelial-response.org/). These findings may be useful in understanding the role of ECs in inflammation and in developing TNF signaling–targeted therapies.

Funder

Hjärt-Lungfonden

Vetenskapsrådet

Stockholm läns landsting

Publisher

The American Association of Immunologists

Subject

Immunology,Immunology and Allergy

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