دورية أكاديمية

Hyaluronic acid: targeting immune modulatory components of the extracellular matrix in atherosclerosis.

التفاصيل البيبلوغرافية
العنوان: Hyaluronic acid: targeting immune modulatory components of the extracellular matrix in atherosclerosis.
المؤلفون: Bot PT; Dept. of Cardiology, AMC Amsterdam, the Netherlands., Hoefer IE, Piek JJ, Pasterkamp G
المصدر: Current medicinal chemistry [Curr Med Chem] 2008; Vol. 15 (8), pp. 786-91.
نوع المنشور: Journal Article; Review
اللغة: English
بيانات الدورية: Publisher: Bentham Science Publishers Country of Publication: United Arab Emirates NLM ID: 9440157 Publication Model: Print Cited Medium: Print ISSN: 0929-8673 (Print) Linking ISSN: 09298673 NLM ISO Abbreviation: Curr Med Chem Subsets: MEDLINE
أسماء مطبوعة: Publication: Saif Zone, Sharjah, U.A.E. : Bentham Science Publishers
Original Publication: Schiphol, The Netherlands : Bentham Science Publishers,
مواضيع طبية MeSH: Atherosclerosis/*metabolism , Extracellular Matrix/*metabolism , Hyaluronic Acid/*physiology, Animals ; Atherosclerosis/immunology ; Cell Movement ; Humans ; Hyaluronan Receptors/metabolism
مستخلص: Purpose of Review: Atherosclerosis is a chronic inflammatory disease of the vessel wall. Although it has become common knowledge that hyaluronic acid (HA), an important component of the extracellular matrix, is strongly involved in atherosclerotic disease development it has only recently become evident that HA, instead of being a static matrix polymer, is an active modulator of proliferation and inflammation of the atherosclerotic plaque. This review discusses the regulatory capacity of HA in atherosclerotic lesions and its effects on plaque stability.
Recent Findings: The mechanisms by which HA might alter plaque stability are diverse. It regulates cellular migration and proliferation, lipid accumulation, and intraplaque angiogenesis. Smooth muscle cell migration is enhanced upon accumulation of HA, potentially stabilizing atherosclerotic plaques. On the other hand, HA is an important ligand for CD44, which stimulates inflammatory cell recruitment to lesions, leukocyte migration and cell proliferation in atherosclerotic plaques. Furthermore, HA forms complexes with low density lipoproteins, and uptake of these complexes by macrophages is increased compared to native LDL, indicating a more detrimental effect on atherosclerosis. The dynamic functional role of HA might be based on the functional difference between short and larger size fragments of this polymer, with either an inflammatory or an anti-inflammatory besides a pro-mitogenic and anti-mitogenic effect. Low molecular weight HA has been shown to be pro-angiogenic, whereas high molecular weight HA has an anti-angiogenic effect. The cause of these differential actions might be that HA synthesis is regulated by three different genes: HAS1, 2 and 3 leading to different size HA products. These genes are specifically expressed under certain conditions, e.g. HAS1 and HAS3 are selectively induced in inflammation, suggesting an important role of their products in this process.
Summary: Hyaluronic acid is an active regulatory component of atherosclerotic lesions. Further studies are warranted to gain more insight into the mechanisms which decide on the role of HA in atherosclerosis and plaque stability.
Number of References: 108
المشرفين على المادة: 0 (Hyaluronan Receptors)
9004-61-9 (Hyaluronic Acid)
تواريخ الأحداث: Date Created: 20080409 Date Completed: 20080605 Latest Revision: 20190823
رمز التحديث: 20231215
DOI: 10.2174/092986708783955554
PMID: 18393848
قاعدة البيانات: MEDLINE
الوصف
تدمد:0929-8673
DOI:10.2174/092986708783955554