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Emerging Approaches to Understanding Microvascular Endothelial Heterogeneity: A Roadmap for Developing Anti-Inflammatory Therapeutics

期刊

出版社

MDPI
DOI: 10.3390/ijms22157770

关键词

microvascular endothelial cells; heterogeneity; inflammation; endothelial barrier permeability; leukocytes; transmigration; microphysiological systems; bMFA; sepsis; protein kinase C delta

资金

  1. National Institutes of Health [GM114359, GM134701]
  2. Defense Threat Reduction Agency [HDTRA11910012]
  3. U.S. Department of Defense (DOD) [HDTRA11910012] Funding Source: U.S. Department of Defense (DOD)

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The endothelium, the inner layer of blood vessels, plays a crucial role in hemostasis and regulation of systemic inflammatory response. However, there are concerns about the phenotypic heterogeneity of microvascular endothelial cells between different organs and species, which may pose challenges in developing therapeutics targeting endothelium inflammation.
The endothelium is the inner layer of all blood vessels and it regulates hemostasis. It also plays an active role in the regulation of the systemic inflammatory response. Systemic inflammatory disease often results in alterations in vascular endothelium barrier function, increased permeability, excessive leukocyte trafficking, and reactive oxygen species production, leading to organ damage. Therapeutics targeting endothelium inflammation are urgently needed, but strong concerns regarding the level of phenotypic heterogeneity of microvascular endothelial cells between different organs and species have been expressed. Microvascular endothelial cell heterogeneity in different organs and organ-specific variations in endothelial cell structure and function are regulated by intrinsic signals that are differentially expressed across organs and species; a result of this is that neutrophil recruitment to discrete organs may be regulated differently. In this review, we will discuss the morphological and functional variations in differently originated microvascular endothelia and discuss how these variances affect systemic function in response to inflammation. We will review emerging in vivo and in vitro models and techniques, including microphysiological devices, proteomics, and RNA sequencing used to study the cellular and molecular heterogeneity of endothelia from different organs. A better understanding of microvascular endothelial cell heterogeneity will provide a roadmap for developing novel therapeutics to target the endothelium.

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