Morita Tomonori, Sasaki Masanori, Kataoka-Sasaki Yuko, Nakazaki Masahito, Nagahama Hiroshi, Oka Shinichi, Oshigiri Tsutomu, Takebayashi Tsuneo, Yamashita Toshihiko, Kocsis Jeffery D, Honmou Osamu
Department of Neural Regenerative Medicine, Research Institute for Frontier Medicine, Sapporo Medical University School of Medicine, Sapporo 060-8556, Japan; Department of Orthopaedic Surgery, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.
Department of Neural Regenerative Medicine, Research Institute for Frontier Medicine, Sapporo Medical University School of Medicine, Sapporo 060-8556, Japan; Department of Neurology, Yale University School of Medicine, New Haven, CT 06510, USA; Center for Neuroscience and Regeneration Research, VA Connecticut Healthcare System, West Haven, CT 06516, USA.
Neuroscience. 2016 Oct 29;335:221-31. doi: 10.1016/j.neuroscience.2016.08.037. Epub 2016 Aug 30.
Intravenous infusion of mesenchymal stem cells (MSCs) derived from adult bone marrow improves behavioral function in rat models of spinal cord injury (SCI). However, most studies have focused on the acute or subacute phase of SCI. In the present study, MSCs derived from bone marrow of rats were intravenously infused 10weeks after the induction of a severe contusive SCI. Open field locomotor function was assessed weekly until 20weeks post-SCI. Motor recovery was greater in the MSC-treated group with rapid improvement beginning in earlier post-infusion times than in the vehicle-treated group. Blood spinal cord barrier (BSCB) integrity was assessed by the intravenous infusion of Evans Blue (EvB) with spectrophotometric quantitation of its leakage into the parenchyma. In MSC-treated rats, BSCB leakage was reduced. Immunohistochemical staining for RECA-1 and PDGFR-β showed increased microvasculature/repair-neovascularization in MSC-treated rats. There was extensive remyelination around the lesion center and increased sprouting of the corticospinal tract and serotonergic fibers after MSC infusion. These results indicate that the systemic infusion of MSCs results in functional improvement that is associated with structural changes in the chronically injured spinal cord including stabilization of the BSCB, axonal sprouting/regeneration and remyelination.
静脉输注源自成年骨髓的间充质干细胞(MSCs)可改善脊髓损伤(SCI)大鼠模型的行为功能。然而,大多数研究集中在SCI的急性期或亚急性期。在本研究中,在严重挫伤性SCI诱导10周后静脉输注源自大鼠骨髓的MSCs。每周评估旷场运动功能,直至SCI后20周。与载体治疗组相比,MSCs治疗组的运动恢复更好,在输注后较早时间开始快速改善。通过静脉输注伊文思蓝(EvB)并分光光度法定量其渗入实质来评估血脊髓屏障(BSCB)的完整性。在MSCs治疗的大鼠中,BSCB渗漏减少。对RECA-1和PDGFR-β进行免疫组织化学染色显示,MSCs治疗的大鼠中微血管/修复性新生血管形成增加。MSCs输注后,损伤中心周围有广泛的髓鞘再生,皮质脊髓束和5-羟色胺能纤维的芽生增加。这些结果表明,全身输注MSCs可导致功能改善,这与慢性损伤脊髓的结构变化有关,包括BSCB的稳定、轴突发芽/再生和髓鞘再生。