Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Instituto de Engenharia Nuclear, Comissão Nacional de Energia Nuclear, Rio de Janeiro, Brazil.
Stem Cells Dev. 2020 May 1;29(9):586-598. doi: 10.1089/scd.2019.0176. Epub 2020 Apr 9.
Intracerebral hemorrhage (ICH) is as a life-threatening condition that can occur in young adults, often causing long-term disability. Recent preclinical data suggest mesenchymal stromal cell (MSC)-based therapies as promising options to minimize brain damage after ICH. However, therapeutic evidence and mechanistic insights are still limited, particularly when compared with other disorders such as ischemic stroke. Herein, we employed a model of collagenase-induced ICH in young adult rats to investigate the potential therapeutic effects of an intravenous injection of human umbilical cord Wharton's jelly-derived MSCs (hUC-MSCs). Two doses of collagenase were used to cause moderate or severe hemorrhages. Magnetic resonance imaging showed that animals treated with hUC-MSCs after moderate ICH had smaller residual hematoma volumes than vehicle-treated rats, whereas the cell therapy failed to decrease the hematoma volume in animals with a severe ICH. Functional assessments (rotarod and elevated body swing tests) were performed for up to 21 days after ICH. Enduring neurological impairments were seen only in animals subjected to severe ICH, but the cell therapy did not induce statistically significant improvements in the functional recovery. The biodistribution of Technetium-99m-labeled hUC-MSCs was also evaluated, showing that most cells were found in organs such as the spleen and lungs 24 h after transplantation. Nevertheless, it was possible to detect a weak signal in the brain, which was higher in the ipsilateral hemisphere of rats subjected to a severe ICH. These data indicate that hUC-MSCs have moderately beneficial effects in cases of less severe brain hemorrhages in rats by decreasing the residual hematoma volume, and that optimization of the therapy is still necessary.
脑出血(ICH)是一种危及生命的疾病,可发生于年轻人,常导致长期残疾。最近的临床前数据表明,间充质基质细胞(MSC)为基础的治疗方法作为一种有前途的选择,以最大限度地减少 ICH 后的脑损伤。然而,治疗证据和机制见解仍然有限,特别是与其他疾病如缺血性中风相比。在此,我们采用胶原酶诱导的年轻成年大鼠 ICH 模型,研究静脉注射人脐带华通氏胶来源的 MSC(hUC-MSC)的潜在治疗效果。使用两种剂量的胶原酶引起中度或重度出血。磁共振成像显示,中度 ICH 后接受 hUC-MSC 治疗的动物比接受载体治疗的大鼠的残余血肿体积更小,而细胞治疗未能减少重度 ICH 动物的血肿体积。ICH 后进行长达 21 天的功能评估(旋转棒和高架体摆动试验)。只有在接受重度 ICH 的动物中才会出现持久的神经损伤,但细胞治疗并未在功能恢复方面引起统计学上的显著改善。还评估了锝-99m 标记的 hUC-MSC 的生物分布,结果表明,移植后 24 小时,大多数细胞存在于脾脏和肺部等器官中。然而,在接受重度 ICH 的大鼠的同侧半球中,可以检测到较弱的信号。这些数据表明,hUC-MSC 通过减少残余血肿体积对大鼠较轻的脑出血具有适度的有益作用,并且仍需要对治疗进行优化。