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联合使用软骨素酶 ABC 和 NEP1-40 对器官型共培养物中皮质脊髓束轴突生长的影响。

The effects of combining chondroitinase ABC and NEP1-40 on the corticospinal axon growth in organotypic co-cultures.

机构信息

Department of Orthopaedic Surgery, Graduate School of Biomedical Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima 734-8551, Japan.

出版信息

Neurosci Lett. 2010 May 26;476(1):14-7. doi: 10.1016/j.neulet.2010.03.049. Epub 2010 Mar 25.

Abstract

The area surrounding the injured spinal cord is a non-permissive milieu for axonal growth due to the inhibitory factors, especially chondroitin sulfate proteoglycan (CSPG) and Nogo. Recent studies have reported that chondroitinase ABC (ChABC) or Nogo-66(1-40) antagonist peptide (NEP1-40) promote axonal growth after spinal cord injury. But no study has addressed the effects on spinal cord injury of combining ChABC and NEP1-40. Previously, we described an organotypic co-culture system using the brain cortex and spinal cord from neonatal rats. In this study, we examined whether the combination of ChABC and NEP1-40 creates an action that promotes corticospinal axon growth in organotypic co-cultures. Organotypic co-cultures of brain and spinal cord were prepared from rats, and ChABC or NEP1-40 was delivered to them. To examine the effects of this combination these two drugs were applied together. We counted the number of labeled axons with DiI and assessed the immunoreactivity of CSPG and Nogo. Axonal growth was enhanced by infusing ChABC or NEP1-40 compared with that in the control group, whereas synergistic effects of combined administration of ChABC and NEP1-40 on axonal growth were not observed. There is a possibility that ChABC and NEP1-40 affect the same intracellular pathways and have no synergistic influence on axonal growth.

摘要

损伤脊髓周围区域由于抑制因子(尤其是软骨素硫酸盐蛋白聚糖(CSPG)和 Nogo)的存在,不利于轴突生长。最近的研究报道,软骨素酶 ABC(ChABC)或 Nogo-66(1-40)拮抗剂肽(NEP1-40)可促进脊髓损伤后的轴突生长。但目前尚无研究探讨 ChABC 和 NEP1-40 联合应用对脊髓损伤的影响。此前,我们描述了一种使用新生大鼠大脑皮质和脊髓的器官型共培养系统。在这项研究中,我们研究了 ChABC 和 NEP1-40 的联合应用是否会产生促进器官型共培养中皮质脊髓轴突生长的作用。从大鼠中制备脑和脊髓的器官型共培养物,并将 ChABC 或 NEP1-40 递送至其中。为了研究这种联合作用的效果,将这两种药物一起应用。我们用 DiI 标记轴突并评估 CSPG 和 Nogo 的免疫反应性。与对照组相比,给予 ChABC 或 NEP1-40 可增强轴突生长,而 ChABC 和 NEP1-40 联合给药对轴突生长的协同作用则不明显。ChABC 和 NEP1-40 可能影响相同的细胞内途径,对轴突生长没有协同影响。

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