Transcriptional drifts associated with environmental changes in endothelial cells

Yalda Afshar, Feiyang Ma, Austin Quach, Anhyo Jeong, Hannah Louise Sunshine, Vanessa Freitas, Yasaman Jami-Alahmadi, Raphael Helaers, Xinmin Li, Matteo Pellegrini, James Wohlschlegel, Casey E. Romanoski, Miikka Vikkula, M. Luisa Iruela-Arispe*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

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 RNAseq and protein expression by LC-MS 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.

Original languageEnglish (US)
Article numbere81370
JournaleLife
Volume12
DOIs
StatePublished - Mar 2023

Funding

Acknowledgments: This work was supported by a grant from the National Institutes of Health R35HL140014 (M.L.I.A), Leducq Foundation (M.L.I.A. and M.V), R01HL147187 (C.E.R.), FAPESP 2016/19968-3 (V.F.), and K12 HD000849 (Y.A.), awarded to the Reproductive Scientist Development Program by the Eunice Kennedy Shriver National Institute of Child Health & Human Development, by the American College of Obstetricians and Gynecologists, as part of the Reproductive Scientist Development Program (Y.A.), and the Ruth L. Kirschstein National Research Service Award T32HL069766 (Y.A.). We thank Bill Brancart for his contributions to the Flow Profiler.

ASJC Scopus subject areas

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

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