Tassoni Alessia, Gutteridge Alex, Barber Amanda C, Osborne Andrew, Martin Keith R
Department of Clinical Neurosciences, John van Geest Centre for Brain Repair, University of Cambridge, Cambridge, United Kingdom.
Pfizer Neusentis, Granta Park, Cambridge, United Kingdom.
Stem Cells. 2015 Oct;33(10):3006-16. doi: 10.1002/stem.2095. Epub 2015 Jul 29.
A variety of diseases lead to degeneration of retinal ganglion cells (RGCs) and their axons within the optic nerve resulting in loss of visual function. Although current therapies may delay RGC loss, they do not restore visual function or completely halt disease progression. Regenerative medicine has recently focused on stem cell therapy for both neuroprotective and regenerative purposes. However, significant problems remain to be addressed, such as the long-term impact of reactive gliosis occurring in the host retina in response to transplanted stem cells. The aim of this work was to investigate retinal glial responses to intravitreally transplanted bone marrow mesenchymal stem cells (BM-MSCs) to help identify factors able to modulate graft-induced reactive gliosis. We found in vivo that intravitreal BM-MSC transplantation is associated with gliosis-mediated retinal folding, upregulation of intermediate filaments, and recruitment of macrophages. These responses were accompanied by significant JAK/STAT3 and MAPK (ERK1/2 and JNK) cascade activation in retinal Muller glia. Lipocalin-2 (Lcn-2) was identified as a potential new indicator of graft-induced reactive gliosis. Pharmacological inhibition of STAT3 in BM-MSC cocultured retinal explants successfully reduced glial fibrillary acidic protein expression in retinal Muller glia and increased BM-MSC retinal engraftment. Inhibition of stem cell-induced reactive gliosis is critical for successful transplantation-based strategies for neuroprotection, replacement, and regeneration of the optic nerve.
多种疾病会导致视网膜神经节细胞(RGCs)及其在视神经内的轴突发生退化,从而导致视觉功能丧失。尽管目前的治疗方法可能会延缓RGCs的丧失,但它们并不能恢复视觉功能或完全阻止疾病进展。再生医学最近将重点放在了用于神经保护和再生目的的干细胞治疗上。然而,仍有一些重大问题有待解决,比如宿主视网膜中因移植干细胞而发生的反应性胶质增生的长期影响。这项工作的目的是研究视网膜胶质细胞对玻璃体内移植的骨髓间充质干细胞(BM-MSCs)的反应,以帮助确定能够调节移植诱导的反应性胶质增生的因素。我们在体内发现,玻璃体内BM-MSC移植与胶质增生介导的视网膜折叠、中间丝上调以及巨噬细胞募集有关。这些反应伴随着视网膜Muller胶质细胞中显著的JAK/STAT3和MAPK(ERK1/2和JNK)级联激活。脂质运载蛋白-2(Lcn-2)被确定为移植诱导的反应性胶质增生的一个潜在新指标。在与BM-MSC共培养的视网膜外植体中对STAT3进行药理学抑制,成功降低了视网膜Muller胶质细胞中胶质纤维酸性蛋白的表达,并增加了BM-MSC在视网膜中的植入。抑制干细胞诱导的反应性胶质增生对于基于移植的视神经神经保护、替代和再生策略的成功至关重要。