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多发性硬化症中的黏附分子与基质金属蛋白酶:β-干扰素诱导的效应

Adhesion molecules and matrix metalloproteinases in Multiple Sclerosis: effects induced by Interferon-beta.

作者信息

Avolio C, Giuliani F, Liuzzi G M, Ruggieri M, Paolicelli D, Riccio P, Livrea P, Trojano M

机构信息

Neurology Unit, University of Foggia, Foggia, Italy.

出版信息

Brain Res Bull. 2003 Aug 15;61(3):357-64. doi: 10.1016/s0361-9230(03)00098-4.

Abstract

In Multiple Sclerosis (MS) pathology, early inflammation involves leukocyte migration across the blood-brain barrier (BBB) within the central nervous system. In this process, adhesion molecules (AMs), both membrane-bound and soluble-circulating forms, and matrix metalloproteinases (MMPs) certainly play a regulatory role. In MS, recombinant Interferon-beta (rIFNbeta) is effective in reducing gadolinium contrast-enhancing lesions on magnetic resonance imaging and this suggests that it may reduce BBB damage or even restore its integrity by different mechanisms that include interference with both AM and MMP pathways. This review will highlight the effects induced by rIFNbeta, both in vitro and in vivo, on cell-bound and soluble forms of AMs and on MMPs.

摘要

在多发性硬化症(MS)病理学中,早期炎症涉及白细胞穿越血脑屏障(BBB)进入中枢神经系统。在此过程中,粘附分子(AMs),包括膜结合形式和可溶性循环形式,以及基质金属蛋白酶(MMPs)肯定发挥着调节作用。在MS中,重组干扰素-β(rIFNβ)在磁共振成像中可有效减少钆对比增强病变,这表明它可能通过包括干扰AM和MMP途径在内的不同机制减少血脑屏障损伤甚至恢复其完整性。本综述将重点介绍rIFNβ在体外和体内对细胞结合形式和可溶性形式的AMs以及对MMPs所诱导的影响。

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