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基质金属蛋白酶-9而非基质金属蛋白酶-2的表达升高促进颅外动静脉畸形的进展。

Elevated Expression of Matrix Metalloproteinase-9 not Matrix Metalloproteinase-2 Contributes to Progression of Extracranial Arteriovenous Malformation.

作者信息

Wei Ting, Zhang Haihong, Cetin Neslihan, Miller Emily, Moak Teri, Suen James Y, Richter Gresham T

机构信息

Center for Investigation of Congenital Anomalies of Vascular Development, Arkansas Vascular Biology Program, Arkansas Children's Hospital, University of Arkansas for Medical Sciences, Little Rock, AR, USA.

Department of Pathology, Arkansas Children's Hospital, University of Arkansas for Medical Sciences, Little Rock, AR, USA.

出版信息

Sci Rep. 2016 Apr 14;6:24378. doi: 10.1038/srep24378.

Abstract

Extracranial arteriovenous malformations (AVMs) are rare but dangerous congenital lesions arising from direct arterial-venous shunts without intervening capillaries. Progressive infiltration, expansion, and soft tissue destruction lead to bleeding, pain, debilitation and disfigurement. The pathophysiology of AVMs is not well understood. Matrix Metalloproteinases (MMPs) are thought to play an important role in pathologic processes underlying many diseases. This study investigates the expression of MMP-9 and MMP-2 in aggressive extracranial AVMs. The differential expression of MMP-9 and its regulatory factors is also examined. Herein we demonstrate that mRNA and protein expressions of MMP-9, but not MMP-2, are significantly higher in AVM tissues compared to normal tissues. The serum level of MMP-9, but not MMP-2, is also elevated in AVM patients compared to healthy controls. MMP-9/neutrophil gelatinase-associated lipocalin (NGAL) complex is also significantly increased in AVM tissues. The MMP-9/ tissue inhibitor of metalloproteases-1 (TIMP-1) complex presents as a major form detected in normal tissues. The increased and aberrant expression of MMP-9 and specific MMP-9 forms may help explain the constitutive vascular remodeling and infiltrative nature of these lesions. Specific MMP-9 inhibitors would be a promising treatment for AVMs.

摘要

颅外动静脉畸形(AVM)虽罕见但危险,是一种由无毛细血管介入的直接动静脉分流引起的先天性病变。进行性浸润、扩张和软组织破坏会导致出血、疼痛、身体虚弱和容貌损毁。AVM的病理生理学尚未完全明确。基质金属蛋白酶(MMP)被认为在许多疾病的病理过程中起重要作用。本研究调查MMP-9和MMP-2在侵袭性颅外AVM中的表达情况。同时也检测MMP-9及其调节因子的差异表达。在此我们证明,与正常组织相比,AVM组织中MMP-9的mRNA和蛋白表达显著升高,而MMP-2则不然。与健康对照组相比,AVM患者血清中MMP-9水平升高,而MMP-2则不然。AVM组织中MMP-9/中性粒细胞明胶酶相关脂质运载蛋白(NGAL)复合物也显著增加。MMP-9/金属蛋白酶组织抑制剂-1(TIMP-1)复合物是正常组织中检测到的主要形式。MMP-9及其特定形式的表达增加和异常可能有助于解释这些病变的持续性血管重塑和浸润性本质。特异性MMP-9抑制剂可能是治疗AVM的一种有前景的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8715/4830979/cbc639aee183/srep24378-f1.jpg

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