Department of Medical Laser, Medical Laser Research Center, Yara Institute, ACECR, Tehran, Iran; Sina Trauma and Surgery Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Laboratory of Neuro-Organic Chemistry, Institute of Biochemistry and Biophysics (IBB), University of Tehran, Tehran, Iran.
Injury. 2020 Nov;51(11):2390-2401. doi: 10.1016/j.injury.2020.07.007. Epub 2020 Jul 7.
To acquire evidence-based knowledge in temporal and spatial patterns of microglia/macrophages changes to facilitate finding proper intervention time for functional restoration after traumatic spinal cord injury (TSCI).
Sina Trauma and Surgery Research Center, Tehran University of Medical Sciences, Tehran, Iran.
We searched PubMed and EMBASE via Ovid SP with no temporal and linguistic restrictions. Besides, hand-search was performed in the bibliographies of relevant studies. The experimental non-interventional and non-transgenic animal studies confined to the rat species which assess the pathological change of microglia /macrophages at the specified time were included.
We found 15,315 non-duplicate studies. Screening through title and abstract narrowed down to 607 relevant articles, 31 of them were selected based on the inclusion criteria. The reactivity of the microglia/macrophages initiates in early hours PI in contusion, compression and transection models. Cells activity reached a maximum within 48 h to 28 days in compression, 7 days in contusion and between 4 and 60 days in transection models. Inflammatory response occurred at the epicenter, in or near the lesion site in both gray and white matter in all three injury models with a maximum extension of one centimeter caudal and rostral to the epicenter in the gray matter in contusion and transection models.
This study was designed to study spatial-temporal changes in the activation of microglia/macrophages overtime after TSCI. We were able to demonstrate time-dependent cell morphological changes after TSCI. The peak times of cell reactivity and the areas where the cells responded to the injury were determined.
获取关于小胶质细胞/巨噬细胞时空变化的循证知识,以便为创伤性脊髓损伤(TSCI)后功能恢复找到合适的干预时间。
伊朗德黑兰大学医学科学新浪创伤与外科研究中心。
我们通过 Ovid SP 在 PubMed 和 EMBASE 进行了无时间和语言限制的检索。此外,还对相关研究的参考文献进行了手工检索。纳入了仅评估特定时间小胶质细胞/巨噬细胞病理变化的实验性非干预性和非转基因动物研究,仅限于大鼠物种。
我们发现了 15315 篇非重复研究。通过标题和摘要筛选,缩小到 607 篇相关文章,其中 31 篇基于纳入标准进行了选择。挫伤、压迫和横断模型中,小胶质细胞/巨噬细胞的反应性在损伤后早期开始。细胞活性在压迫模型中 48 小时至 28 天内、在挫伤模型中 7 天内、在横断模型中 4 至 60 天内达到最大值。在三种损伤模型中,炎症反应发生在损伤中心,灰质和白质中的损伤部位或其附近,在挫伤和横断模型中,灰质中炎症反应向损伤中心的尾侧和头侧延伸可达 1 厘米。
本研究旨在研究 TSCI 后小胶质细胞/巨噬细胞激活的时空变化。我们能够证明 TSCI 后细胞形态学的时间依赖性变化。确定了细胞反应的峰值时间和细胞对损伤反应的区域。