RANTES/CL5信号从颌骨空洞到多发性硬化的认识——研究和病例研究。

Degenerative Neurological and Neuromuscular Disease Pub Date : 2021-07-05 eCollection Date: 2021-01-01 DOI:10.2147/DNND.S315321
Johann Lechner, Volker von Baehr, Fabian Schick
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引用次数: 4

摘要

背景:信号通路在与多发性硬化症(MS)进展相关的细胞间通讯中所起的作用已成为研究的一个关键领域。趋化因子RANTES(在激活时调节,正常T细胞表达和分泌),也称为趋化因子C-C基序配体5(CCL5;R/C),是一种因其与MS发展有关而在神经炎症研究中被研究的蛋白质。目的:研究颌骨骨髓缺损(BMDJ),其形态表现为颌骨脂肪变性骨坏死(FDOJ),在受累区域表现为R/C信号过度表达。在这里,我们试图阐明颚骨衍生的R/C和MS之间的潜在联系。方法:使用基于珠的Luminex®分析,对从17名MS患者中提取的17份BMDJ/FDOJ样本以及19名健康对照的样本进行R/C表达分析。检测了10例MS患者的血清R/C水平。此外,在两个临床病例研究中分析了骨密度、组织学和R/C表达。结果:在MS组获得的所有BMDJ/FDOJ样品中均发现高R/C过表达。MS组的血清R/C水平也上调。MS队列的R/C血清水平高于健康对照组。相反,BMDJ/FDOJ样品的组织学显示没有炎症细胞。讨论:科学文献中广泛讨论了R/C诱导的MS“无声炎症”,以及R/C触发中枢神经系统炎症,这可能是MS发展的关键。结论:作者怀疑BMDJ/FDOJ可能通过R/C过表达触发MS进展。因此,牙科和医学界应了解多发性硬化症患者的BMDJ/FDOJ。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

RANTES/CCL5 Signaling from Jawbone Cavitations to Epistemology of Multiple Sclerosis - Research and Case Studies.

RANTES/CCL5 Signaling from Jawbone Cavitations to Epistemology of Multiple Sclerosis - Research and Case Studies.

RANTES/CCL5 Signaling from Jawbone Cavitations to Epistemology of Multiple Sclerosis - Research and Case Studies.

RANTES/CCL5 Signaling from Jawbone Cavitations to Epistemology of Multiple Sclerosis - Research and Case Studies.

Background: The role played by signaling pathways in the cell-cell communication associated with multiple sclerosis (MS) progression has become a critical area in research. Chemokine RANTES (regulated upon activation, normal T-cell expressed and secreted), also named chemokine C-C motif ligand 5 (CCL5; R/C), is a protein that has been investigated in neuroinflammatory research due to its link to MS development.

Objective: Research on bone marrow defects in the jawbone (BMDJ), which morphologically presents as fatty-degenerative osteonecrosis of the jawbone (FDOJ), presents overexpression of R/C signaling in affected areas. Here, we try to elucidate the potential link between jawbone-derived R/C and MS.

Methods: Seventeen BMDJ/FDOJ samples extracted from 17 MS patients, as well as samples from 19 healthy controls, were analyzed for R/C expression using bead-based Luminex® analysis. The serum R/C levels from 10 MS patients were examined. Further, bone density, histology, and R/C expression were analyzed in two clinical case studies.

Results: High R/C overexpression was found in all BMDJ/FDOJ samples obtained from the MS group. Serum R/C levels were also upregulated in the MS group. R/C serum levels in the MS cohort were higher than in the healthy controls. In contrast, the histology of BMDJ/FDOJ samples showed no inflammatory cells.

Discussion: R/C-induced "silent inflammation" in MS is widely discussed in the scientific literature, along with R/C triggering of inflammation in the central nervous system, which might be key in the development of MS.

Conclusion: The authors suspect that BMDJ/FDOJ may serve as a trigger of MS progression via R/C overexpression. As such, the dental and medical communities should be made aware of BMDJ/FDOJ in cases of MS.

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