Targeting pulmonary vascular endothelial cells for the treatment of respiratory diseases

Pulmonary vascular endothelial cells (VECs) are the main damaged cells in the pathogenesis of various respiratory diseases and they mediate the development and regulation of the diseases. Effective intervention targeting pulmonary VECs is of great significance for the treatment of respiratory diseas...

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Published inFrontiers in pharmacology Vol. 13; p. 983816
Main Authors Li, Yi-Xuan, Wang, Hong-Bo, Li, Jing, Jin, Jian-Bo, Hu, Jing-Bo, Yang, Chun-Lin
Format Journal Article
LanguageEnglish
Published Frontiers Media S.A 30.08.2022
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ISSN1663-9812
1663-9812
DOI10.3389/fphar.2022.983816

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Summary:Pulmonary vascular endothelial cells (VECs) are the main damaged cells in the pathogenesis of various respiratory diseases and they mediate the development and regulation of the diseases. Effective intervention targeting pulmonary VECs is of great significance for the treatment of respiratory diseases. A variety of cell markers are expressed on the surface of VECs, some of which can be specifically combined with the drugs or carriers modified by corresponding ligands such as ICAM-1, PECAM-1, and P-selectin, to achieve effective delivery of drugs in lung tissues. In addition, the great endothelial surface area of the pulmonary vessels, the “first pass effect” of venous blood in lung tissues, and the high volume and relatively slow blood perfusion rate of pulmonary capillaries further promote the drug distribution in lung tissues. This review summarizes the representative markers at the onset of respiratory diseases, drug delivery systems designed to target these markers and their therapeutic effects.
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Yuan Tang, University of Toledo, United States
Edited by: Richard D. Minshall, University of Illinois at Chicago, United States
This article was submitted to Inflammation Pharmacology, a section of the journal Frontiers in Pharmacology
Reviewed by: Alexander Verin, Medical College of Georgia, Augusta University, United States
ISSN:1663-9812
1663-9812
DOI:10.3389/fphar.2022.983816