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脊髓损伤的严重程度决定了免疫神经源性肽后的炎症基因表达模式。

The Severity of Spinal Cord Injury Determines the Inflammatory Gene Expression Pattern after Immunization with Neural-Derived Peptides.

机构信息

Centro de Investigación en Ciencias de la Salud, Facultad de Ciencias de la Salud, Universidad Anáhuac México Campus Norte, Av. Universidad Anáhuac No. 46, Col. Lomas Anáhuac, C.P. 52786, Huixquilucan Edo. de México, México.

Centro de Investigación del Proyecto CAMINA A.C., 14050, Mexico City, Mexico.

出版信息

J Mol Neurosci. 2018 Jun;65(2):190-195. doi: 10.1007/s12031-018-1077-3. Epub 2018 May 23.

Abstract

Previous studies revealed that the intensity of spinal cord injury (SCI) plays a key role in the therapeutic effects induced by immunizing with neural-derived peptides (INDP), as severe injuries abolish the beneficial effects induced by INDP. In the present study, we analyzed the expression of some inflammation-related genes (IL6, IL12, IL-1β, IFNɣ, TNFα, IL-10, IL-4, and IGF-1) by quantitative PCR in rats subjected to SCI and INDP. We investigated the expression of these genes after a moderate or severe contusion. In addition, we evaluated the effect of INDP by utilizing two different peptides: A91 and Cop-1. After moderate injury, both A91 and Cop-1 elicited a pattern of genes characterized by a significant reduction of IL6, IL1β, and TNFα but an increase in IL10, IL4, and IGF-1 expression. There was no effect on IL-12 and INFɣ. In contrast, the opposite pattern was observed when rats were subjected to a severe spinal cord contusion. Immunization with either peptide caused a significant increase in the expression of IL-12, IL-1β, IFNɣ (pro-inflammatory genes), and IGF-1. There was no effect on IL-4 and IL-10 compared to controls. After a moderate SCI, INDP reduced pro-inflammatory gene expression and generated a microenvironment prone to neuroprotection. Nevertheless, severe injury elicits the expression of pro-inflammatory genes that could be aggravated by INDP. These findings correlate with our previous results demonstrating that severe injury inhibits the beneficial effects of protective autoimmunity.

摘要

先前的研究表明,脊髓损伤(SCI)的严重程度在通过免疫神经源性肽(INDP)诱导的治疗效果中起着关键作用,因为严重的损伤会消除 INDP 诱导的有益效果。在本研究中,我们通过定量 PCR 分析了 SCI 和 INDP 大鼠中一些与炎症相关的基因(IL6、IL12、IL-1β、IFNɣ、TNFα、IL-10、IL-4 和 IGF-1)的表达。我们研究了这些基因在中度或重度挫伤后的表达。此外,我们还通过利用两种不同的肽:A91 和 Cop-1 来评估 INDP 的作用。在中度损伤后,A91 和 Cop-1 均引起了一种基因表达模式,其特征是 IL6、IL1β 和 TNFα 的显著减少,但 IL10、IL4 和 IGF-1 的表达增加。对 IL-12 和 INFɣ 没有影响。相比之下,当大鼠受到严重脊髓挫伤时,观察到相反的模式。用任一肽免疫接种都会导致 IL-12、IL-1β、IFNɣ(促炎基因)和 IGF-1 的表达显著增加。与对照组相比,对 IL-4 和 IL-10 没有影响。在中度 SCI 后,INDP 减少了促炎基因的表达,并产生了有利于神经保护的微环境。然而,严重的损伤会引发促炎基因的表达,而 INDP 可能会加重这些基因的表达。这些发现与我们之前的结果相关,表明严重的损伤抑制了保护性自身免疫的有益效果。

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