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鼠脐带血细胞可减轻新生大鼠缺氧缺血性脑损伤。

Rat umbilical cord blood cells attenuate hypoxic-ischemic brain injury in neonatal rats.

机构信息

Department of Perinatology, Institute for Developmental Research, Aichi Human Service Center, 713-8 Kagiya-cho, Kasugai, Aichi, 480-0392, Japan.

Division of Neonatology, Center for Maternal-Neonatal Care, Nagoya University Hospital, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8560, Japan.

出版信息

Sci Rep. 2017 Mar 10;7:44111. doi: 10.1038/srep44111.

Abstract

Increasing evidence has suggested that human umbilical cord blood cells (hUCBC) have a favorable effect on hypoxic-ischemic (HI) brain injury. However, the efficacy of using hUCBCs to treat this injury has been variable and the underlying mechanism remains elusive. Here, we investigated its effectiveness using stereological analysis in an allogeneic system to examine whether intraperitoneal injection of cells derived from UCBCs of green fluorescent protein (GFP)-transgenic rats could ameliorate brain injury in neonatal rats. Three weeks after the HI event, the estimated residual brain volume was larger and motor function improved more in the cell-injected rats than in the control (PBS-treated) rats. The GFP-positive cells were hardly detectable in the brain (0.0057% of injected cells) 9 days after injection. Although 60% of GFP-positive cells in the brain were Iba1-positive, none of these were positive for NeuroD or DCX. While the number of proliferating cells increased in the hippocampus, that of activated microglia/macrophages decreased and a proportion of M2 microglia/macrophages increased in the ipsilateral hemisphere of cell-injected rats. These results suggest that intraperitoneal injection of cells derived from UCBCs could ameliorate HI injury, possibly through an endogenous response and not by supplying differentiated neurons derived from the injected stem cells.

摘要

越来越多的证据表明,人脐带血细胞(hUCBC)对缺氧缺血(HI)脑损伤有有利影响。然而,使用 hUCBC 治疗这种损伤的疗效各不相同,其潜在机制仍难以捉摸。在这里,我们在同种异体系统中使用体视学分析来研究其效果,以检查来自 GFP 转基因大鼠 UCBC 的细胞腹腔内注射是否可以改善新生大鼠的脑损伤。HI 事件发生后 3 周,与对照组(PBS 处理组)相比,细胞注射组的估计残留脑体积更大,运动功能改善更多。注射后 9 天,大脑中几乎检测不到 GFP 阳性细胞(注射细胞的 0.0057%)。尽管大脑中 60%的 GFP 阳性细胞为 Iba1 阳性,但没有一个为 NeuroD 或 DCX 阳性。虽然海马中的增殖细胞数量增加,但活化的小胶质细胞/巨噬细胞数量减少,并且细胞注射大鼠对侧半球的 M2 小胶质细胞/巨噬细胞比例增加。这些结果表明,来自 UCBC 的细胞腹腔内注射可以改善 HI 损伤,可能通过内源性反应而不是通过注射干细胞分化的神经元来实现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87a2/5345001/45d7efd7833d/srep44111-f1.jpg

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