›› 2008, Vol. 39 ›› Issue (5): 615-619.doi:

• 论著 •    下一篇

体外培养的人源神经干-祖细胞超微结构分析

赵耀东2 ;张天一1 ;黄强2* ;王爱东2 ;董军2 ;兰青2 ;秦正红2; 顾晓松1*   

  1. 1.南通大学神经再生重点实验室,江苏 南通 226004;2.苏州大学附属第二医院神经外科暨苏州大学衰老与神经疾病实验室,江苏 苏州 215004
  • 收稿日期:2007-08-31 修回日期:2007-10-25 出版日期:2008-10-06
  • 通讯作者: 黄强;顾晓松

ULTRASTRUCTURE ANALYSIS OF HUMAN NEURAL STEM CELLS/PROGENITORS CULTIVATED EM>IN VITRO/EM>

  1. 1.Key Laboratory of Neuroregeneration,Nantong University,Jiangsu Nantong 226361, China;2.Deparment of Cerebral Surgery of the Second Affiliated Hospital of Suzhou University, the Laboratory of Aging and Neuro-disease of Suzhou University, Jiangsu Suzhou 215004,China
  • Received:2007-08-31 Revised:2007-10-25 Online:2008-10-06
  • Contact: HUANG Qiang;GU Xiao-song

关键词: 神经干-祖细胞, 神经球, 超微结构, 电子显微镜, 人胚胎

Abstract: Objective Neural stem cells have become a major concern in the current research of neuroscience, for they are involved in the neural injuries and recoveries, the origin of neural tumors, as well as other fields. The study on their ultrastructures, which is still limited at present, is indispensible. To offer more information is the aim of this paper. Methods Neural stem cells/progenitors from human fetal brain tissue were cultivated EM>in vitro/EM> and observed under a scanning electron microscope (SEM) and a transmission electron microscope (TEM). Results Neural stem cells/progenitors presented to be neurospherelike after days of culture EM>in vitro/EM>. The neruospheres were made up of neural stem cells/progenitors and nonfixiform material inside, and cells in neruospheres could be divided into lucent and dark ones according to electron densities. Between adjacent cells as well as on the cytoplasmic sides of the apposed plasma membranes, there were vesiclelike structures. Cell membrane fusions were also observed between some adjacent cells. Single neural stem cell /progenitor was spherical with rough surface under SEM. Many kinds of organellas, e.g. Golgi’s complex and endocytoplasmic reticulum, were underdeveloped in neural stem cells/progenitors, which generally had big, nuclei and scanty cytoplasm. The numbers, types and maturities of cellular organs in different cells were not always identical, which showed their heterogeneities. For instance, both neurofilaments and microtubules could only be observed in a few neural stem cells/progenitors; lysosomes were very abundant in some, but even hardly founded in others. What’s more, autophagosomes at different stages and in differernt formations could be seen in most cells. The nuclei, frenquently containing huge amounts of euchromatin and a small quantity of heterochromatin, mostly were globular, sometimes reniform or lobulated; most neural stem cells/progenitors had only one chromatospherite, seldom two or more, and sometimes no obvious chromatospherite could be seen. Conclusion Developed autophagosomes, vesiclelike structures between adjacent cells as well as on the cytoplasmic sides of the apposed plasma membranes and cellular membrane fusions could be seen in the human embryooriginated neural stem cells/progenitors and

Key words: Neuro-precursor cells, Neurosphere, Ultrastructure, Electron microscopy, Human embryo

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