Adipose tissue-derived stem cells rescue Purkinje neurons and alleviate inflammatory responses in Niemann-Pick disease type C mice

被引:0
作者
Jae-sung Bae
Janet E. Carter
Hee Kyung Jin
机构
[1] Kyungpook National University,Department of Physiology, Cell and Matrix Research Institute, BSEI, World Class University Program, School of Medicine
[2] University College London,Department of Mental Health Sciences, Royal Free and University College Medical School
[3] Kyungpook National University,Department of Laboratory Animal Medicine, College of Veterinary Medicine, Cell and Matrix Research Institute
[4] Kyungpook National University,School of Medicine
[5] Kyungpook National University,College of Veterinary Medicine
来源
Cell and Tissue Research | 2010年 / 340卷
关键词
Niemann-Pick type C disease model; Adipose tissue-derived stem cell; Cerebellum; Transplantation; Therapeutic potential; Mouse (BALB/c npc; );
D O I
暂无
中图分类号
学科分类号
摘要
Adult stem cells offer special therapeutic prospects because they can be isolated for autologous transplantation, expanded ex vivo, and differentiated into various cell types. We previously reported that bone marrow-derived mesenchymal stem cells improve neurological deficits in neurodegenerative disease animal models. However, the efficacy of adipose tissue-derived stem cells (ADSCs) transplantation in similar models remains unknown. Herein, we demonstrate that ADSCs, when transplanted into Niemann-Pick disease type C (NP-C) mouse cerebellum, elicit rescue of Purkinje neurons and restoration of motor coordination together with alleviation of inflammatory responses as verified by immunohistochemistry and real-time PCR using glial fibrillary acidic protein (GFAP), F4/80, IL-1β, IL-6, and TNF-α. Most importantly, ADSCs enhance electrically active Purkinje neurons with functional synaptic formation after transplantation in NP-C disease model mice. This report demonstrates for the first time that ADSCs can rescue imperiled Purkinje neurons and alleviate the inflammatory response in NP-C disease model mice, thereby signifying the therapeutic potential of ADSCs for neurodegenerative diseases.
引用
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页码:357 / 369
页数:12
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