Combined treatment of vascular endothelial growth factor and human neural stem cells in experimental focal cerebral ischemia

• Published in: Neuroscience research Vol. 53; no. 4; pp. 384 - 390
• Main Authors: Chu, Kon, Park, Kyung-Il, Lee, Soon-Tae, Jung, Keun-Hwa, Ko, Song-Yi, Kang, Lami, Sinn, Dong-In, Lee, Yong-Seok, Kim, Seung U., Kim, Manho, Roh, Jae-Kyu
• Format: Journal Article
• Language: English
• Published: Ireland Elsevier Ireland Ltd 01.12.2005
• Subjects: Animals; Brain - blood supply; Brain - pathology; Brain Ischemia - pathology; Brain Ischemia - therapy; Cell Line; Cell Transplantation; Focal ischemia; Humans; Male; Neural stem cell; Neurons - transplantation; Rats; Rats, Sprague-Dawley; Recovery; Recovery of Function; Stem Cell Transplantation; Transplantation; Vascular Endothelial Growth Factor A - therapeutic use; VEGF; Focal ischemia; Transplantation; Recovery; VEGF; Neural stem cell
• ISSN: 0168-0102; 1872-8111
• DOI: 10.1016/j.neures.2005.08.010

Recent studies have indicated the beneficial effects of vascular endothelial growth factor (VEGF), and transplanted neural stem cells (NSCs) in cerebral ischemia. We investigated the effects of the combined administration of NSCs and VEGF on focal cerebral ischemia in adult rats. Four groups ( n = 12, respectively) – group 1 (ischemia-only), group 2 (ischemia + VEGF), group 3 (ischemia + NSCs) and group 4 (ischemia + NSCs + VEGF) – were compared. Human NSCs (HB1.F3), labeled with Lac Z + or PKH26, were given intravenously 24 h after surgery (5 × 10 6 cells). At 48 h after surgery, recombinant human VEGF (50 μg/kg) was infused intravenously (1 μg/(kg min)). Behavioral tests using the modified limb placing and rotarod tests were performed every week following ischemia. Immunohistochemistry for endothelial barrier antigen (EBA), VEGF and Nissl staining were performed at day 35 after ischemia. Group 4 showed better behavioral recovery at 7, 14 and 28 days than group 3 ( p = 0.020, 0.005 and 0.043, respectively). These functional recoveries were correlated with enhanced EBA immunoreactivities at day 35 after ischemia, especially in the ipsilesional striatum. Group 4 showed lesser degree of brain atrophy in cortex and striatum, when compared with other groups. The distribution of VEGF was not co-localized with NSCs. Our results suggest that VEGF may act synergistically on NSC-transplanted, ischemic brain via a pro-angiogenic effect.