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在体外单核细胞中鉴定转谷氨酰胺酶 2 活性抑制剂及其在多发性硬化症小鼠模型中的作用。

Characterization of Transglutaminase 2 activity inhibitors in monocytes in vitro and their effect in a mouse model for multiple sclerosis.

机构信息

Department of Anatomy and Neurosciences, Amsterdam Neuroscience, VU University Medical Center, Amsterdam, The Netherlands.

Covalab, Villeurbanne, France.

出版信息

PLoS One. 2018 Apr 24;13(4):e0196433. doi: 10.1371/journal.pone.0196433. eCollection 2018.

Abstract

The neurodegenerative disease multiple sclerosis (MS) is pathologically characterized by the massive influx of immune cells into the central nervous system. This contributes to demyelination and axonal damage which causes symptoms such as motor and cognitive dysfunctions. The migration of leukocytes from the blood vessel is orchestrated by a multitude of factors whose determination is essential in reducing cellular influx in MS patients and the experimental autoimmune encephalomyelitis (EAE) animal model. The here studied enzyme tissue Transglutaminase (TG2) is present intracellularly, on the cell surface and extracellularly. There it contributes to cellular adhesion and migration via its transamidation activity and possibly by facilitating cellular interaction with the extracellular matrix. Previous data from our group showed reduced motor symptoms and cellular infiltration after using a pharmacological TG2 transamidation activity inhibitor in a rat EAE model. However, it remained elusive if the cross-linking activity of the enzyme resulted in the observed effects. To follow-up, we now characterized two new small molecule TG2 activity inhibitors, BJJF078 and ERW1041E. Both compounds are potent inhibitor of recombinant human and mouse Transglutaminase enzyme activity, mainly TG2 and the close related enzyme TG1. In addition they did not affect the binding of TG2 to the extracellular matrix substrate fibronectin, a process via which TG2 promotes cellular adhesion and migration. We found, that ERW1041E but not BJJF078 resulted in reduced EAE disease motor-symptoms while neither caused apparent changes in pathology (cellular influx), Transglutaminase activity or expression of inflammation related markers in the spinal cord, compared to vehicle treated controls. Although we cannot exclude issues on bioavailability and in vivo efficacy of the used compounds, we hypothesize that extracellular TG1/TG2 activity is of greater importance than (intra-)cellular activity in mouse EAE pathology.

摘要

神经退行性疾病多发性硬化症(MS)的病理学特征是大量免疫细胞涌入中枢神经系统。这导致脱髓鞘和轴突损伤,从而导致运动和认知功能障碍等症状。白细胞从血管迁移是由多种因素协调的,确定这些因素对于减少 MS 患者和实验性自身免疫性脑脊髓炎(EAE)动物模型中的细胞内流至关重要。这里研究的酶组织转谷氨酰胺酶(TG2)存在于细胞内、细胞表面和细胞外。在那里,它通过其转酰胺活性促进细胞黏附和迁移,并可能通过促进细胞与细胞外基质的相互作用。我们小组的先前数据表明,在大鼠 EAE 模型中使用药理学 TG2 转酰胺活性抑制剂后,运动症状和细胞浸润减少。然而,酶的交联活性是否导致了观察到的效果仍不清楚。为了跟进,我们现在描述了两种新的小分子 TG2 活性抑制剂,BJJF078 和 ERW1041E。这两种化合物都是重组人源和鼠源转谷氨酰胺酶活性的有效抑制剂,主要是 TG2 和密切相关的酶 TG1。此外,它们不影响 TG2 与细胞外基质底物纤维连接蛋白的结合,这一过程通过 TG2 促进细胞黏附和迁移。我们发现,与 vehicle 处理对照组相比,ERW1041E 而非 BJJF078 可降低 EAE 疾病的运动症状,而两者均未导致明显的病理学变化(细胞内流)、转谷氨酰胺酶活性或脊髓中炎症相关标志物的表达。尽管我们不能排除所用化合物的生物利用度和体内疗效问题,但我们假设细胞外 TG1/TG2 活性比(细胞内)活性在小鼠 EAE 病理学中更为重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4d0/5918173/54abccc840dc/pone.0196433.g001.jpg

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