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胎肝来源Sca-1^+细胞在体内分化为神经细胞研究 被引量:1

Fetal liver - derived Sca- 1^+ cells can differentiate into both neurons and astrocytes in vivo
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摘要 目的:为了了解胎肝干细胞是否具有向神经组织细胞分化的潜能。方法:PCR检测sry基因分析孕14.5d胚胎鼠性别;采用免疫磁珠法分离雄性胎鼠肝的Sca-1^+细胞,尾静脉注射Sca-1^+细胞(2.0×10~3个/小鼠)到致死剂量放射线照射的雌性小鼠。移植60、120、180 d后采用免疫组化和FISH双染色检测受体小鼠脑组织中供体来源细胞特性。结果:受体雌鼠脑组织内存在大最Y染色体阳性细胞。免疫组化分析显示,部分Y染色体阳性细胞表达神经组织特异标志,如神经元核特异蛋白(NeuN,Neuron-specific nuclei protein)、部分Y染色体阳性细胞表达星形胶质细胞特异标志,如胶质纤维酸性蛋白(GFAP,Glial fibrillary acidic protein)等。结论:移植的胎肝Sca-1^+细胞,含造血干细胞,能分化成神经细胞和星形胶质细胞。 AIM: To determine whether Sca-1^+ cells from fetal liver can differentiate into neural cells. METHODS: The sex of 14.5-day-old murine fetuses was determined by PCR analysis of sry gene, and Sca-1^+ cells from male fetal liver were isolated with a magnetic cell sorting kit, 2×10~3 of which were then transplanted into lethally irradiated female mice. The donor cells and their characteristics in recipient brains were identified and detected by FISH and immunohistochemistry double-staining analysis at 60, 120, 180 days after transplantation. RESULTS: There existed many male cells in brains of female recipients, some of them express neuron-specific nuclear protein (NeuN), and some of them express the astrocyte-specific marker, i.e. glial fibrillary acidic protein (GFAP). CONCLUSION: Sca-1^+ cells from fetal liver, which contain hematopoietic stem cells, can differentiate into neuronal cells and astrocytes in the brains of adult mice.
作者 刘革修 张洹
出处 《中国病理生理杂志》 CAS CSCD 北大核心 2004年第3期354-358,共5页 Chinese Journal of Pathophysiology
基金 Supported by Foundation of Science and Technology of Guangdong Province(No.99M01204G) Science and Technology of Guangzhou City(No.2001-2-037-01) Key Science Foundation of Guangdong Province(No.021195).
关键词 分化 胎肝 神经元 SCA-1^+细胞 Differentiation Fetal liver Neurons Sca-1^+ cells
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  • 1Koopman P, Gubbay J, Vivian N, et al. Male development of chromosomally female mice transgenic for Sry [J]. Nature,1991,351(6322): 117 - 121.
  • 2Kim CJ, Khoo JC, Gillotte- Taylor K, et al. Polymerase chain reaction - based method for quantifying recruitment of monocytes to mouse atherosclerotic lesions in vivo- enhancement by tumor necrosis factor-alpha and interleukin- 1 beta[J]. Arterioscler Thromb Vasc Biol, 2000,20(8): 1976-1982.
  • 3Greenlee AR, Krisher RL, Plotka ED. Rapid sexing of murine preimplantation embryos using a nested, multiplex polymerase chain reaction(PCR) [J]. Mol Reprod Dev,1998,49(3):261 - 267.
  • 4Lambert JF, Benoit BO, Colvin GA, et al. Quick sex determination of mouse fetuses [J]. J Neurosci Methods, 2000, 95(2) : 127 - 132.
  • 5Miyatake S, Yokota T, Lee F, et al. Structure of the chromosomal gene for murine interleukin- 3 [J]. Proc Natl Acad Sci USA, 1985,82(2) :316- 320.
  • 6van de Corput MP, Grosveld FG. Fluorescence in situ hybridization analysis of transcript dynamics in cells [J]. Methods, 2001,25(1):111 - 118.

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