Transcriptional drifts associated with environmental changes in endothelial cells

Author:

Afshar Yalda12ORCID,Ma Feyiang23,Quach Austin3,Jeong Anhyo1,Sunshine Hannah L45,Freitas Vanessa6ORCID,Jami-Alahmadi Yasaman7ORCID,Helaers Raphael8,Li Xinmin9,Pellegrini Matteo23,Wohlschlegel James A7,Romanoski Casey E10ORCID,Vikkula Miikka811,Iruela-Arispe M Luisa35ORCID

Affiliation:

1. Department of Obstetrics and Gynecology, University of California, Los Angeles

2. Molecular Biology Institute, University of California, Los Angeles

3. Department of Molecular, Cell, and Developmental Biology, University of California, Los Angeles

4. Department of Molecular, Cellular and Integrative Physiology, University of California, Los Angeles

5. Department of Cell and Developmental Biology, Northwestern University Feinberg School of Medicine

6. Departament of Cell and Developmental Biology, Institute of Biomedical Science, University of Sao Paulo

7. Department of Biological Chemistry, University of California

8. Human Molecular Genetics, de Duve Institute, University of Louvain

9. Department of Pathology and Laboratory Medicine, University of California

10. Department of Cellular and Molecular Medicine, University of Arizona

11. WELBIO department, WEL Research Institute

Abstract

Environmental cues, such as physical forces and heterotypic cell interactions play a critical role in cell function, yet their collective contributions to transcriptional changes are unclear. Focusing on human endothelial cells, we performed broad individual sample analysis to identify transcriptional drifts associated with environmental changes that were independent of genetic background. Global gene expression profiling by RNA sequencing and protein expression by liquid chromatography–mass spectrometry directed proteomics distinguished endothelial cells in vivo from genetically matched culture (in vitro) samples. Over 43% of the transcriptome was significantly changed by the in vitro environment. Subjecting cultured cells to long-term shear stress significantly rescued the expression of approximately 17% of genes. Inclusion of heterotypic interactions by co-culture of endothelial cells with smooth muscle cells normalized approximately 9% of the original in vivo signature. We also identified novel flow dependent genes, as well as genes that necessitate heterotypic cell interactions to mimic the in vivo transcriptome. Our findings highlight specific genes and pathways that rely on contextual information for adequate expression from those that are agnostic of such environmental cues.

Funder

National Institutes of Health

Foundation for the National Institutes of Health

Fondation Leducq

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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