摘要
背景:烟雾病(MMD)是一种慢性进行性狭窄或闭塞脑血管疾病。典型的烟雾血管是源于起始颈内动脉的狭窄,强调增生或者异常的血管生成,血管和动脉性过程均被涉及到疾病的病理生理性过程当中了。目的:在此,我们总结了目前参与多血管形成的最重要的信号通路的知识,特别专注于生长因子的表达以及内皮祖细胞(EPCs)的作用。方法和结果:更高血浆浓度的血管内皮生长因子,基质金属蛋白酶、肝细胞生长因子和白介素-1β,在烟雾病中均有报道。特别高水平的基本纤维细胞生长因子在病人的脑脊液中也有发现,最后,内皮祖细胞的数量和功能也有所增加。尽管数据可用,迄今为止报道的方法和结果并没有说明在生长因子的表达水平和烟雾病严重性之间存在明显的相关性。此外,研究内皮祖细胞提供的有争议的结果使得这些细胞的烟雾病的病理生理学真实过程难以理解。结论:进一步的研究应该因此被执行来扩展我们在调节动脉狭窄和侧枝血管的过度形成过程中的知识。此外,我们建议将集成方法和功能分析提前以响应生物和临床数据,为开发烟雾病新的治疗申请方案。
关键词: 血管生成,动脉生成, 侧枝化
Current Medicinal Chemistry
Title:Vasculogenic and Angiogenic Pathways in Moyamoya Disease
Volume: 23 Issue: 4
Author(s): Gloria Bedini, Kinga G. Blecharz, Sara Nava, Peter Vajkoczy, Giulio Alessandri, Michela Ranieri, Francesco Acerbi, Paolo Ferroli, Daria Riva, Silvia Esposito, Chiara Pantaleoni, Nardo Nardocci and Federica Zibordi, Elisa Ciceri, Eugenio A. Parati and Anna Bersano
Affiliation:
关键词: 血管生成,动脉生成, 侧枝化
摘要: Background. Moyamoya disease (MMD) is a slowly progressing steno-occlusive cerebrovascular disease. The typical moyamoya vessels, which originate from an initial stenosis of the internal carotid, highlight that increased and/or abnormal angiogenic, vasculogenic and arteriogenic processes are involved in the disease pathophysiology. Objective. Herein, we summarize the current knowledge on the most important signaling pathways involved in MMD vessel formation, particularly focusing on the expression of growth factors and function of endothelial progenitor cells (EPCs). Methods and Results. Higher plasma concentrations of vascular endothelial growth factor, matrix metalloproteinase, hepatocyte growth factor, and interleukin-1β were reported in MMD. A specific higher level of basic fibroblast growth factor was also found in the cerebrospinal fluid of these patients. Finally, the number and the functionality of EPCs were found to be increased. In spite of the available data, the approaches and findings reported so far do not give an evident correlation between the expression levels of the aforementioned growth factors and MMD severity. Furthermore, the controversial results provided by studies on EPCs, do not permit to understand the true involvement of these cells in MMD pathophysiology. Conclusion. Further studies should thus be implemented to extend our knowledge on processes regulating both the arterial stenosis and the excessive formation of collateral vessels. Moreover, we suggest advances of integrated approaches and functional assays to correlate biological and clinical data, arguing for the development of new therapeutic applications for MMD.
Export Options
About this article
Cite this article as:
Gloria Bedini, Kinga G. Blecharz, Sara Nava, Peter Vajkoczy, Giulio Alessandri, Michela Ranieri , Francesco Acerbi, Paolo Ferroli, Daria Riva, Silvia Esposito, Chiara Pantaleoni, Nardo Nardocci and Federica Zibordi, Elisa Ciceri, Eugenio A. Parati and Anna Bersano , Vasculogenic and Angiogenic Pathways in Moyamoya Disease, Current Medicinal Chemistry 2016; 23 (4) . https://dx.doi.org/10.2174/092986732304160204181543
DOI https://dx.doi.org/10.2174/092986732304160204181543 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
- Author Guidelines
- Graphical Abstracts
- Fabricating and Stating False Information
- Research Misconduct
- Post Publication Discussions and Corrections
- Publishing Ethics and Rectitude
- Increase Visibility of Your Article
- Archiving Policies
- Peer Review Workflow
- Order Your Article Before Print
- Promote Your Article
- Manuscript Transfer Facility
- Editorial Policies
- Allegations from Whistleblowers
- Announcements
Related Articles
-
Remodelling of the Ca2+ Toolkit in Tumor Endothelium as a Crucial Responsible for the Resistance to Anticancer Therapies
Current Signal Transduction Therapy The Role of Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) in Cardiovascular Homeostasis: A Non-Systematic Literature Review
Current Cardiology Reviews Chronic Inflammation and Colorectal Cancer: The Role of Vascular Endothelial Growth Factor
Current Pharmaceutical Design Endothelial Dysfunction, Obesity and Insulin Resistance
Current Vascular Pharmacology Cerebral Amyloid Angiopathy-related Intracerebral Hemorrhage Score For Predicting Outcome
Current Neurovascular Research A More Accurate Approach to Molecular Genetics Analysis in Vascular Disease
Cardiovascular & Hematological Disorders-Drug Targets EDITORIAL (Thematic Issue: Serpins as Therapeutics – A Potential Biologic Source for Unique Protein-based Therapeutics)
Cardiovascular & Hematological Disorders-Drug Targets Transcription Factors in Autoimmune Diseases
Current Pharmaceutical Design Cyclophosphamide: Time to Say Goodnight and Goodbye?
Current Rheumatology Reviews Harnessing CD36 to Rein in Inflammation
Endocrine, Metabolic & Immune Disorders - Drug Targets An Update on the Management of Severe Cutaneous Drug Hypersensitivity Reactions
Current Pharmaceutical Design New Insights into Inflammatory Bowel Disease Pathophysiology: Paving the Way for Novel Therapeutic Targets
Current Drug Targets Selective Elevation of Circulating CCL2/MCP1 Levels in Patients with Longstanding Post-vaccinal Macrophagic Myofasciitis and ASIA
Current Medicinal Chemistry Hepatic Manifestations in Juvenile Systemic Lupus Erythematosus
Recent Patents on Inflammation & Allergy Drug Discovery Treatment of Central Nervous System Tuberculosis Infections and Neurological Complications of Tuberculosis Treatment
Current Pharmaceutical Design Oncogenic Fusion Tyrosine Kinases as Molecular Targets for Anti-Cancer Therapy
Anti-Cancer Agents in Medicinal Chemistry Current and Emerging Therapeutic Approaches in HCV-Related Mixed Cryoglobulinemia
Current Medicinal Chemistry Skeletal Muscle in Cancer Cachexia: The Ideal Target of Drug Therapy
Current Cancer Drug Targets The Role of Alpha-lipoic Acid Supplementation in the Prevention of Diabetes Complications: A Comprehensive Review of Clinical Trials
Current Diabetes Reviews Targeted Gene Deletion of Prolyl Hydroxylase Domain Protein 3 Triggers Angiogenesis and Preserves Cardiac Function by Stabilizing Hypoxia Inducible Factor 1 Alpha Following Myocardial Infarction
Current Pharmaceutical Design