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Leukocyte Adhesion Molecules in Diabetic Retinopathy
Diabetes is a systemic disease that causes a number of metabolic and physiologic abnormalities. One of the major microvascular complications of diabetes is diabetic retinopathy (DR), a leading cause of blindness in people over age 50. The mechanisms underlying the development of DR are not fully und...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3216271/ https://www.ncbi.nlm.nih.gov/pubmed/22132315 http://dx.doi.org/10.1155/2012/279037 |
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author | Noda, Kousuke Nakao, Shintaro Ishida, Susumu Ishibashi, Tatsuro |
author_facet | Noda, Kousuke Nakao, Shintaro Ishida, Susumu Ishibashi, Tatsuro |
author_sort | Noda, Kousuke |
collection | PubMed |
description | Diabetes is a systemic disease that causes a number of metabolic and physiologic abnormalities. One of the major microvascular complications of diabetes is diabetic retinopathy (DR), a leading cause of blindness in people over age 50. The mechanisms underlying the development of DR are not fully understood; however, extensive studies have recently implicated chronic, low-grade inflammation in the pathophysiology of DR. During inflammation leukocytes undergo sequential adhesive interactions with endothelial cells to migrate into the inflamed tissues, a process known as the “leukocyte recruitment cascade” which is orchestrated by precise adhesion molecule expression on the cell surface of leukocytes and the endothelium. This paper summarizes the recent clinical and preclinical works on the roles of leukocyte adhesion molecules in DR. |
format | Online Article Text |
id | pubmed-3216271 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-32162712011-11-30 Leukocyte Adhesion Molecules in Diabetic Retinopathy Noda, Kousuke Nakao, Shintaro Ishida, Susumu Ishibashi, Tatsuro J Ophthalmol Review Article Diabetes is a systemic disease that causes a number of metabolic and physiologic abnormalities. One of the major microvascular complications of diabetes is diabetic retinopathy (DR), a leading cause of blindness in people over age 50. The mechanisms underlying the development of DR are not fully understood; however, extensive studies have recently implicated chronic, low-grade inflammation in the pathophysiology of DR. During inflammation leukocytes undergo sequential adhesive interactions with endothelial cells to migrate into the inflamed tissues, a process known as the “leukocyte recruitment cascade” which is orchestrated by precise adhesion molecule expression on the cell surface of leukocytes and the endothelium. This paper summarizes the recent clinical and preclinical works on the roles of leukocyte adhesion molecules in DR. Hindawi Publishing Corporation 2012 2011-11-02 /pmc/articles/PMC3216271/ /pubmed/22132315 http://dx.doi.org/10.1155/2012/279037 Text en Copyright © 2012 Kousuke Noda et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Noda, Kousuke Nakao, Shintaro Ishida, Susumu Ishibashi, Tatsuro Leukocyte Adhesion Molecules in Diabetic Retinopathy |
title | Leukocyte Adhesion Molecules in Diabetic Retinopathy |
title_full | Leukocyte Adhesion Molecules in Diabetic Retinopathy |
title_fullStr | Leukocyte Adhesion Molecules in Diabetic Retinopathy |
title_full_unstemmed | Leukocyte Adhesion Molecules in Diabetic Retinopathy |
title_short | Leukocyte Adhesion Molecules in Diabetic Retinopathy |
title_sort | leukocyte adhesion molecules in diabetic retinopathy |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3216271/ https://www.ncbi.nlm.nih.gov/pubmed/22132315 http://dx.doi.org/10.1155/2012/279037 |
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