Publication

Role of bone marrow-derived lymphatic endothelial progenitor cells for lymphatic neovascularization

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Last modified
  • 02/20/2025
Type of Material
Authors
    Changwon Park, University of IllinoisJi Yoon Lee, Emory UniversityYoung Sup Yoon, Emory University
Language
  • English
Date
  • 2011-07
Publisher
  • Elsevier: 12 months
Publication Version
Copyright Statement
  • © 2012 Elsevier Inc. All rights reserved.
License
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 1050-1738
Volume
  • 21
Issue
  • 5
Start Page
  • 135
End Page
  • 140
Grant/Funding Information
  • This work was supported in part by Idea Grant Award from Department of Defense (W81XWH-09-1-0278); NIH grants DP3DK094346; and NIH contract, HHSN268201000043C (Program of Excellence in Nanotechnology Award); NSF-EBICS (Emergent Behaviors of Integrated Cellular Systems) grant, CBET-0939511.
Abstract
  • The lymphatic vasculature plays a pivotal role in maintaining tissue fluid homeostasis, immune surveillance, and lipid uptake in the gastrointestinal organs. Therefore, impaired function of the lymphatic vessels caused by genetic defects, infection, trauma, or surgery leads to the abnormal accrual of lymph fluid in the tissue and culminates in the swelling of affected tissues, known as lymphedema. Although millions of people suffer from lymphedema worldwide which causes impaired wound healing, compromised immune defense and, in rare case, lymphangiosarcoma, no effective therapy is currently available. In addition, recent advances in cancer biology have disclosed an indispensable function of the lymphatic vessel in tumor growth and metastasis. Therefore, understanding the detailed mechanisms governing lymphatic vessel formation and function in pathophysiologic conditions is essential to prevent or treat these diseases. Here, we will review the developmental processes of the lymphatic vessels and postnatal lymphatic neovascularization, focusing on the role of recently identified bone-marrow (BM) derived PODOPLANIN expressing (PODOPLANIN+) cells as lymphatic endothelial progenitor cells (LEPCs).
Author Notes
  • Correspondence: Young-sup Yoon, Department of Medicine, Division of Cardiology, Emory University School of Medicine, 101 Woodruff Circle, Woodruff Memorial Research Building, Atlanta, GA 30322, USA; Tel: 404-727-8176; Email: yyoon5@emory.edu
Research Categories
  • Health Sciences, Pharmacology
  • Health Sciences, Medicine and Surgery

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