Medical Journals

Cxcr4 Down-regulation by Small Interfering Rna Inhibits Invasion and Tubule Formation of Human Retinal Microvascular Endothelial Cells.

Authors:
  • Yu Keming
  • Zhuang Jing
  • Kaminski Joseph M
  • Ambati Bala
  • Gao Qianying
  • Ma Ping
  • Liao Dongjiang
  • Li Fan
  • Liu Xuan
  • Ge Jian

From: State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou 510060, PR China.

Biochemical and biophysical research communications

  • Publish Date: Jul 2007
  • ISSN: 0006-291X
  • Volume: 358
  • Issue: 4
  • Pages: 990-6
  • Medium: Print
  • Language: English
  • Citation (JAMA): Yu Keming, Zhuang Jing, Kaminski Joseph M, et al. Cxcr4 Down-regulation by Small Interfering Rna Inhibits Invasion and Tubule Formation of Human Retinal Microvascular Endothelial Cells.. Biochem. Biophys. Res. Commun. Jul 2007;358:990-6

Abstract

The progressive alterations to the retinal microvasculature in diabetic retinopathy are known to cause vision loss. Chemokines are characterized by their ability to induce cell invasion, adhesion and migration. In this study, we used double siRNA transfection to transiently and selectively decrease the level of the endogenous CXCR4 in human retinal microvascular endothelial cells (HRMECs). The functional consequences of silencing CXCR4 expression in HRMECs were investigated using an endothelial cell migration assay and tubule formation in Matrigel. When CXCR4 expression was decreased with siRNA, HRMECs were less invasive and also resulted in markedly diminished vascular networks on Matrigel as compared to the controls. Additionally, hypoxia and VEGF, the factors affecting microvascular, regulate the expression level of CXCR4 in HRMECs, respectively, which have synergistic, additive effect in the HRMECs. As such, CXCR4 antagonists may become a therapeutic target for the treatment of retinal angiopathies.

Mesh Headings (Keywords): Blood Vessels, Cells, Cultured, Down-Regulation, Endothelial Cells, Gene Silencing, Humans, Neovascularization, Physiologic, RNA, Small Interfering, Receptors, CXCR4, Retinal Vessels


Check for Full Text / PubMed Unique Identifier (PMID): 17521613


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.

The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


Advertisements

About | Privacy Policy | Business Solutions | Advertise | Contact | Add Healia to your site

©2012. Healia / Meredith Corporation  

Use of this site constitutes acceptance of our Terms of Service and Privacy Policy. All content on this Web site, including medical opinion and any other health-related information, is for informational purposes only and should not be used for a specific diagnosis or individual treatment plan for any situation. Use of this site and the information contained herein does not create a doctor-patient relationship. Always seek the direct advice of your doctor in connection with any questions or issues you may have regarding your own health or the health of others.