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Effect of type-2 astrocytes on the viability of dorsal root ganglion neurons and length of neuronal processes
引用本文:Chunling Fan,Hui Wang,Dan Chen,Xiaoxin Cheng,Kun Xiong,Xuegang Luo,Qilin Cao. Effect of type-2 astrocytes on the viability of dorsal root ganglion neurons and length of neuronal processes[J]. 中国神经再生研究, 2014, 9(2): 119-128. DOI: 10.4103/1673-5374.125339
作者姓名:Chunling Fan  Hui Wang  Dan Chen  Xiaoxin Cheng  Kun Xiong  Xuegang Luo  Qilin Cao
基金项目:This study was supported by the NIH Foundation of the USA, No. RO1 NS061975, and the Natural Science Foundation of Hunan Province in China, No. 11JJ6077.
摘    要:The role of type-2 astrocytes in the repair of central nervous system injury remains poorly un- derstood. In this study, using a relatively simple culture condition in vitro, type-2 astrocytes, differentiated from oligodendrocyte precursor cells by induction with bone morphogenetic pro- tein-4, were co-cultured with dorsal root ganglion neurons. We examined the effects of type-2 astrocytes differentiated from oligodendrocyte precursor cells on the survival and growth of dorsal root ganglion neurons. Results demonstrated that the number of dorsal root ganglion neurons was higher following co-culture of oligodendrocyte precursor cells and type-2 astrocytes than when cultured alone, but lower than that of neurons co-cultured with type-1 astrocytes. The length of the longest process and the length of all processes of a single neuron were shortest in neurons cultured alone, followed by neurons co-cultured with type-2 astroc~es, then neurons co-cultured with oligodendrocyte precursor cells, and longest in neurons co-cultured with type-1 astrocytes. These results indicate that co-culture with type-2 astrocytes can increase neuronal survival rate and process length. However, compared with type-1 astrocytes and oligodendrocyte precursor cells, the promotion effects of type-2 astrocytes on the growth of dorsal root ganglion neurons were weaker.

关 键 词:背根神经节神经元  星形胶质细胞  存活率  2型  长度  中枢神经系统损伤  前体细胞  培养条件

Effect of type-2 astrocytes on the viability of dorsal root ganglion neurons and length of neuronal processes
Chunling Fan,Hui Wang,Dan Chen,Xiaoxin Cheng,Kun Xiong,Xuegang Luo,Qilin Cao. Effect of type-2 astrocytes on the viability of dorsal root ganglion neurons and length of neuronal processes[J]. Neural Regeneration Research, 2014, 9(2): 119-128. DOI: 10.4103/1673-5374.125339
Authors:Chunling Fan  Hui Wang  Dan Chen  Xiaoxin Cheng  Kun Xiong  Xuegang Luo  Qilin Cao
Affiliation:[1]Department of Human Anatomy and Neurobiology, Xiangya School of Medicine, Central South University, Changsha, Hunan Province, China [2]The Vivian L Smith Department of Neurosurgery, UT Medical School at Houston, Houston, TX, USA
Abstract:The role of type-2 astrocytes in the repair of central nervous system injury remains poorly understood. In this study, using a relatively simple culture condition in vitro, type-2 astrocytes, differentiated from oligodendrocyte precursor cells by induction with bone morphogenetic protein-4, were co-cultured with dorsal root ganglion neurons. We examined the effects of type-2 astrocytes differentiated from oligodendrocyte precursor cells on the survival and growth of dorsal root ganglion neurons. Results demonstrated that the number of dorsal root ganglion neurons was higher following co-culture of oligodendrocyte precursor cells and type-2 astrocytes than when cultured alone, but lower than that of neurons co-cultured with type-1 astrocytes. The length of the longest process and the length of all processes of a single neuron were shortest in neurons cultured alone, followed by neurons co-cultured with type-2 astrocytes, then neurons co-cultured with oligodendrocyte precursor cells, and longest in neurons co-cultured with type-1 astrocytes. These results indicate that co-culture with type-2 astrocytes can increase neuronal survival rate and process length. However, compared with type-1 astrocytes and oligodendrocyte precursor cells, the promotion effects of type-2 astrocytes on the growth of dorsal root ganglion neurons were weaker.
Keywords:nerve regeneration  spinal cord injury  oligodendrocyte  oligodendrocyte precursor cells  astrocytes  bone morphogenetic protein  neurons  neurites  dorsal root ganglion  NIH grant  neuralregeneration
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