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γ射线照射诱导大鼠肝细胞线粒体自噬与再生的研究 被引量:3

Study on γ-ray induced mitochondrial autophagy and regeneration of liver cells in rats
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摘要 目的探讨线粒体自噬在细胞损伤后再生中的作用。方法在体外利用γ射线照射诱导大鼠肝细胞损伤,在亚细胞水平上观察肝细胞的损伤修复情况与线粒体自噬的关系,并利用分子生物学技术进行DNA凋亡片段的分析和线粒体RNA的RT-PCR分析。结果受损线粒体清除过程存在线粒体自噬,随着修复过程的进行细胞DNA凋亡程度下降,细胞自噬现象减少,细胞凋亡和线粒体自噬同时存在于损伤细胞中,通过RT-PCR分析发现肝组织的损伤修复与线粒体自噬后的线粒体再生有关。结论线粒体自噬可能为组织的损伤修复提供某种分子信号,促使新的线粒体再生。 Objective To explore the role of mitochondrial autophagy in wound healing. Methods Damages of liver cells in rats after γ-ray irradiation with a total dose of 8 Gy were investigated. The relationship between mitoehondrial autophagy and repair of liver cells, was observed uhrastrueturally. Apoptosis-related DNA fragment and mitoehondrial RNA levels were analyzed. Results Most of the damaged mitochondria were removed through mitoehondrial autophagy. Apoptosis-related DNA fragment analysis implied that, accompanied with reduction of mitoehondrial autophagy, the amount of cellular apoptosis was decreased during wound healing. Wound healing was related to mitoehondrial regeneration after mitoehondrial autophagy. Conclusion Mitochondrial autophagy may release some molecular signals for wound healing so as to accelerate sufficiently the regeneration of newly formed mitoehondria.
出处 《中华放射医学与防护杂志》 CAS CSCD 北大核心 2006年第1期50-52,共3页 Chinese Journal of Radiological Medicine and Protection
基金 广东省专项课题基金资助项目(A302020401) 广东省科技攻关基金资助项目(2KM05503S) 广州市科技攻关基金资助项目(2002Z1-E0037)
关键词 Γ射线照射 线粒体自噬 凋亡 线粒体再生 γ-ray irradiation Mitochondrial autophagy Apoptosis Mitochondrial regeneration
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参考文献9

  • 1Piao YJ,Ogawa K,Ono K,et al.The relationship between heterophagy and autophagy in the splenic macrophage of rats after gamma-ray irradiation.ACTA Histochem Cytochem,1983,16:353-367.
  • 2Gutierrez MG,Master SS,Singh SB,et al.Autophagy is a defense mechanism inhibiting BCG and Mycobacterium tuberculosis survival in infected macrophages.Cell,2004,119:753-766.
  • 3Nisoli E,Clementi E,Paolucci C,et al.Mitochondrial biogenesis in mammals:the role of endogenous nitric oxide.Science,2003,299:896-899.
  • 4Raben N,Fukuda T,Gilbert AL,et al.Replacing acid alphaglucosidase in Pompe disease:recombinant and transgenic enzymes are equipotent,but neither completely clears glycogen from type Ⅱ muscle fibers.Mol Ther,2005,11:48-56.
  • 5Kotoulas OB,Kalamidas SA,Kondomerkos DJ.Glycogen autophagy.Microsc Res Tech,2004,64:10-20.
  • 6Klionsky DJ,Emr SD.Autophagy as a regulated pathway of cellular degradation.Science,2000,290:1717-1721.
  • 7Vinarsky V,Atkinson DL,Stevenson TJ,et al.Normal newt limb regeneration requires matrix metalloproteinase function.Dev Biol,2005,279:86-98.
  • 8Yamada T,Dumont JN,Moret R,et al.Autophagy in dedifferentiating newt iris epithelial cells in vitro.Differentiation,1978,11:133-147.
  • 9Shintani T,Klionsky DJ.Autophagy in health and disease:a doubleedged sword.Science,2004,306:990-995.

同被引文献27

  • 1赵学谦,范京安,谢成伦,秦蓁,李刚,朱军,曾大兵,孔繁春.^(60)Co-γ射线对柑桔大实蝇幼虫的影响研究[J].西南农业大学学报(自然科学版),1995,17(2):126-129. 被引量:5
  • 2Alison MR, Poulsom R, Forbes S,et al.An introduction to stem cells[J]. J Pathol, 2002, 197(1): 419-423.
  • 3Blau HM, Brazelton TR,Weimann JM .The evolving concept of a stem cell: entity or function[J].Cell, 2001, 105(2): 829-841.
  • 4Chen S, Zhang Q, Wu X, et al. Dedifferentiation of lineage-committed cells by a small molecule[J].J Am Chem Soc, 2004,126(1) :410-411.
  • 5Anastasia L, Sampaolesi M, Papini N, et al. Reversine-treated fibroblasts acquire myogenic competence in vitro and in Regenerating skeletal muscle[J].Cell Death Differ,2006,13(2):2042-2051.
  • 6Mariko K, Chad S, Qikai X,et al. An orderly retreat: Dedifferentiation is a regulated process [J]. PNAS, 2004, 101 (1):7005 - 7010.
  • 7Cai S, Fu X, Sheng Z. Dedifferentiation: A new approach in stem cell research[J]. Bio Science, 2007,57(2):655-662.
  • 8Tsonis PA. Stem cells from differentiated cells[J]. Mol Interv, 2004, 4(1): 81-83.
  • 9Lee EK, Bae GU, You Js, et al. Reversine increases the plasticity of lineage-committed cells toward neuroectodermal lineage [J]. J Biol Chem, 2009, 284(5):2891-2901.
  • 10Shan SW, Tang MK , Chow PH, et al. Induction of growth arrest and polycomb gene expression by reversine allows C2C12 cells to be reprogrammed to various differentiated cell types[J]. Proteomics, 2007, 7 (2):4303 - 4316.

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