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人类动脉树的异质性和分化:聚焦血管疾病中的 microRNA 表达。

Heterogeneity and Differentiation of the Human Arterial Tree: Focus on microRNA Expression in Vascular Disease.

机构信息

Department of Medical and Surgical Sciences (DIMEC), University of Bologna, 40138 Bologna, Italy.

Alma Mater Institute on Healthy Planet, University of Bologna, 40138 Bologna, Italy.

出版信息

Biomolecules. 2024 Mar 12;14(3):343. doi: 10.3390/biom14030343.

Abstract

Human arteries show structural and functional peculiarities according to the nutrient and oxygen needs of a specific vascular district. This architectural heterogeneity is reflected in the pathological setting of cardiovascular diseases (CVDs). Indeed, the responsiveness to cardiovascular risk factors, and the morphological and molecular patterns are discriminating factors among CVDs affecting different vascular beds. MicroRNAs (miRNAs) are endogenous regulators of gene expression and fine-tuners of vascular cell differentiation; thus, these non-coding RNAs can modulate arterial heterogeneity. The identification of an artery-specific miRNA signature would be promising in the therapy of CVDs, especially in patients who are frail and elderly. In the present review, we will provide a concise description of the arterial tree heterogeneity on a structural and cellular basis, mainly in the pathological context. Secondly, we will address the miRNA potential as crucial mediators of arterial heterogeneity, focusing on the abdominal aorta and femoral artery, with the final goal of strengthening the search for more targeted therapies in CVDs and stratification approaches in patients who are frail and elderly.

摘要

人类动脉根据特定血管区域的营养和氧气需求表现出结构和功能上的特点。这种结构异质性反映在心血管疾病(CVDs)的病理环境中。事实上,对心血管危险因素的反应以及形态和分子模式是区分不同血管床影响的 CVDs 的区分因素。微小 RNA(miRNAs)是基因表达的内源性调节剂,也是血管细胞分化的微调因子;因此,这些非编码 RNA 可以调节动脉的异质性。动脉特异性 miRNA 特征的鉴定在 CVDs 的治疗中很有前途,特别是在体弱和老年患者中。在本综述中,我们将主要在病理环境中,简要描述结构和细胞基础上的动脉树异质性。其次,我们将探讨 miRNA 作为动脉异质性关键介质的潜力,重点关注腹主动脉和股动脉,最终目标是加强针对 CVDs 的更具针对性的治疗方法和体弱和老年患者的分层方法的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a97/10967886/1ba003594cee/biomolecules-14-00343-g001.jpg

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