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建立用于细胞治疗研究的老龄大鼠慢性颈脊髓损伤模型。

Modeling chronic cervical spinal cord injury in aged rats for cell therapy studies.

机构信息

Unidad de Producción y Reprogramación celular (UPRC), Red Andaluza de Diseño y Traslación de Terapias Avanzadas (RAdytTA), 41092 Sevilla, Spain; Grupo de Neurociencia Aplicada, Instituto de Investigaciones Biomédicas de Sevilla (IBIS), 41013 Sevilla, Spain; Programa de Doctorado en Biología Molecular, Biomedicina e Investigación Clínica, Universidad de Sevilla, Sevilla, Spain.

Departamento de Biología Celular, Genética y Fisiología, Universidad de Málaga, 29071 Málaga, Spain; Centro de Investigación Biomédica en Red de Bioingeniería, Biomateriales y Nanomedicina, (CIBER-BBN), 29071 Málaga, Spain.

出版信息

J Clin Neurosci. 2021 Dec;94:76-85. doi: 10.1016/j.jocn.2021.09.042. Epub 2021 Oct 12.

Abstract

With an expanding elderly population, an increasing number of older adults will experience spinal cord injury (SCI) and might be candidates for cell-based therapies, yet there is a paucity of research in this age group. The objective of the present study was to analyze how aged rats tolerate behavioral testing, surgical procedures, post-operative complications, intra-spinal cell transplantation and immunosuppression, and to examine the effectiveness of human iPSC-derived Neural Progenitor Cells (IMR90-hiPSC-NPCs) in a model of SCI. We performed behavioral tests in rats before and after inducing cervical hemi-contusions at C4 level with a fourth-generation Ohio State University Injury Device. Four weeks later, we injected IMR90-hiPSC-NPCs in animals that were immunosuppressed by daily cyclosporine injection. Four weeks after injection we analyzed locomotor behavior and mortality, and histologically assessed the survival of transplanted human NPCs. As rats aged, their success at completing behavioral tests decreased. In addition, we observed high mortality rates during behavioral training (41.2%), after cervical injury (63.2%) and after cell injection (50%). Histological analysis revealed that injected cells survived and remained at and around the grafted site and did not cause tumors. No locomotor improvement was observed in animals four weeks after IMR90-hiPSC-NPC transplantation. Our results show that elderly rats are highly vulnerable to interventions, and thus large groups of animals must be initially established to study the potential efficacy of cell-based therapies in age-related chronic myelopathies.

摘要

随着老年人口的不断增加,越来越多的老年人可能会经历脊髓损伤 (SCI),并可能成为细胞治疗的候选者,但针对这一年龄组的研究很少。本研究的目的是分析老年大鼠如何耐受行为测试、手术程序、术后并发症、脊髓内细胞移植和免疫抑制,并研究人诱导多能干细胞衍生的神经祖细胞 (IMR90-hiPSC-NPCs) 在 SCI 模型中的有效性。我们在大鼠 C4 水平进行了第四代俄亥俄州立大学损伤装置诱导的半挫伤后,在术前和术后进行了行为测试。四周后,我们对接受每日环孢素注射免疫抑制的动物进行了 IMR90-hiPSC-NPC 注射。注射后四周,我们分析了运动行为和死亡率,并对移植的人 NPC 存活情况进行了组织学评估。随着大鼠年龄的增长,它们完成行为测试的成功率下降。此外,我们在行为训练期间(41.2%)、颈椎损伤后(63.2%)和细胞注射后(50%)观察到高死亡率。组织学分析显示,注射的细胞存活并留在和围绕移植部位,没有引起肿瘤。在 IMR90-hiPSC-NPC 移植后四周,动物的运动功能没有改善。我们的研究结果表明,老年大鼠对干预措施非常敏感,因此必须首先建立大量动物模型来研究细胞治疗在与年龄相关的慢性脊髓病中的潜在疗效。

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