» Articles » PMID: 29485616

Whole-Transcriptome Sequencing: a Powerful Tool for Vascular Tissue Engineering and Endothelial Mechanobiology

Overview
Journal High Throughput
Publisher MDPI
Date 2018 Feb 28
PMID 29485616
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Among applicable high-throughput techniques in cardiovascular biology, whole-transcriptome sequencing is of particular use. By utilizing RNA that is isolated from virtually all cells and tissues, the entire transcriptome can be evaluated. In comparison with other high-throughput approaches, RNA sequencing is characterized by a relatively low-cost and large data output, which permits a comprehensive analysis of spatiotemporal variation in the gene expression profile. Both shear stress and cyclic strain exert hemodynamic force upon the arterial endothelium and are considered to be crucial determinants of endothelial physiology. Laminar blood flow results in a high shear stress that promotes atheroresistant endothelial phenotype, while a turbulent, oscillatory flow yields a pathologically low shear stress that disturbs endothelial homeostasis, making respective arterial segments prone to atherosclerosis. Severe atherosclerosis significantly impairs blood supply to the organs and frequently requires bypass surgery or an arterial replacement surgery that requires tissue-engineered vascular grafts. To provide insight into patterns of gene expression in endothelial cells in native or bioartificial arteries under different biomechanical conditions, this article discusses applications of whole-transcriptome sequencing in endothelial mechanobiology and vascular tissue engineering.

Citing Articles

Deciphering the role of non-coding RNAs involved in sorafenib resistance.

Jing F, Shi Y, Jiang D, Li X, Sun J, Zhang X Heliyon. 2024; 10(8):e29374.

PMID: 38644890 PMC: 11031791. DOI: 10.1016/j.heliyon.2024.e29374.


Change of Title: From to .

Iadarola P, Negrini M BioTech (Basel). 2022; 9(4).

PMID: 35822821 PMC: 9258314. DOI: 10.3390/biotech9040018.


Characterization of Endothelial and Smooth Muscle Cells From Different Canine Vessels.

Oosterhoff L, Kruitwagen H, van Wolferen M, van Balkom B, Mokry M, Lansu N Front Physiol. 2019; 10:101.

PMID: 30809157 PMC: 6379353. DOI: 10.3389/fphys.2019.00101.

References
1.
Berg E . Systems biology in drug discovery and development. Drug Discov Today. 2013; 19(2):113-25. DOI: 10.1016/j.drudis.2013.10.003. View

2.
Jansen I, Ye H, Heetveld S, Lechler M, Michels H, Seinstra R . Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing. Genome Biol. 2017; 18(1):22. PMC: 5282828. DOI: 10.1186/s13059-017-1147-9. View

3.
Wernig M, Meissner A, Foreman R, Brambrink T, Ku M, Hochedlinger K . In vitro reprogramming of fibroblasts into a pluripotent ES-cell-like state. Nature. 2007; 448(7151):318-24. DOI: 10.1038/nature05944. View

4.
Boyer M, Townsend L, Vogel L, Falk J, Trevor K, Villalba M . Isolation of endothelial cells and their progenitor cells from human peripheral blood. J Vasc Surg. 2000; 31(1 Pt 1):181-9. DOI: 10.1016/s0741-5214(00)70080-2. View

5.
Suzuki Y, Yamamoto K, Ando J, Matsumoto K, Matsuda T . Arterial shear stress augments the differentiation of endothelial progenitor cells adhered to VEGF-bound surfaces. Biochem Biophys Res Commun. 2012; 423(1):91-7. DOI: 10.1016/j.bbrc.2012.05.088. View