The in vivo endothelial cell translatome is highly heterogeneous across vascular beds.

Autor:	Cleuren ACA; Life Sciences Institute, University of Michigan, Ann Arbor, MI 48109., van der Ent MA; Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109., Jiang H; Department of Biostatistics, University of Michigan, Ann Arbor, MI 48109., Hunker KL; Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109., Yee A; Life Sciences Institute, University of Michigan, Ann Arbor, MI 48109., Siemieniak DR; Life Sciences Institute, University of Michigan, Ann Arbor, MI 48109.; Howard Hughes Medical Institute, University of Michigan, Ann Arbor, MI 48109., Molema G; Department of Pathology and Medical Biology, University of Groningen, 9700 RB Groningen, The Netherlands., Aird WC; Center for Vascular Biology Research, Beth Israel Deaconess Medical Center, Boston, MA 02215., Ganesh SK; Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109.; Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109., Ginsburg D; Life Sciences Institute, University of Michigan, Ann Arbor, MI 48109; ginsburg@umich.edu.; Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109.; Howard Hughes Medical Institute, University of Michigan, Ann Arbor, MI 48109.; Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109.; Department of Pediatrics, University of Michigan, Ann Arbor, MI 48109.
Jazyk:	angličtina
Zdroj:	Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2019 Nov 19; Vol. 116 (47), pp. 23618-23624. Date of Electronic Publication: 2019 Nov 11.
DOI:	10.1073/pnas.1912409116
Abstrakt:	Endothelial cells (ECs) are highly specialized across vascular beds. However, given their interspersed anatomic distribution, comprehensive characterization of the molecular basis for this heterogeneity in vivo has been limited. By applying endothelial-specific translating ribosome affinity purification (EC-TRAP) combined with high-throughput RNA sequencing analysis, we identified pan EC-enriched genes and tissue-specific EC transcripts, which include both established markers and genes previously unappreciated for their presence in ECs. In addition, EC-TRAP limits changes in gene expression after EC isolation and in vitro expansion, as well as rapid vascular bed-specific shifts in EC gene expression profiles as a result of the enzymatic tissue dissociation required to generate single-cell suspensions for fluorescence-activated cell sorting or single-cell RNA sequencing analysis. Comparison of our EC-TRAP with published single-cell RNA sequencing data further demonstrates considerably greater sensitivity of EC-TRAP for the detection of low abundant transcripts. Application of EC-TRAP to examine the in vivo host response to lipopolysaccharide (LPS) revealed the induction of gene expression programs associated with a native defense response, with marked differences across vascular beds. Furthermore, comparative analysis of whole-tissue and TRAP-selected mRNAs identified LPS-induced differences that would not have been detected by whole-tissue analysis alone. Together, these data provide a resource for the analysis of EC-specific gene expression programs across heterogeneous vascular beds under both physiologic and pathologic conditions. Competing Interests: The authors declare no competing interest.
Databáze:	MEDLINE
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