期刊文献+

细胞自噬在斑马鱼中的研究进展 被引量:1

Research Progress of Cell Autophagy in Zebrafish
原文传递
导出
摘要 细胞自噬是一种维持细胞内稳态的重要方式,并被发现与许多人类疾病相关。由于其具有重大的理论研究价值和潜在应用前景,是近年来生命科学领域的热点之一。细胞自噬的功能与机制在物种间是高度保守的,对它的研究已在多种模式生物中展开。斑马鱼是一种常用的脊椎模式动物,具有影像学、遗传学和发育生物学等学科研究的优势,也可用于高通量药物筛选,是研究细胞自噬的理想材料。目前在斑马鱼中展开的细胞自噬相关研究取得了很多进展。本研究首先简要地描述了自噬的发生过程,重点综述应用于斑马鱼中的自噬检测方法,以及利用斑马鱼模型进行的与自噬相关人类疾病的研究。 Autophagy is an important mechanism to maintain cellular homeostasis within cells, and has been linked to many human diseases. Due to its both great value in basic research and high potential in medical application,autophagy has become a hot field in life science in recent years. Cell autophagy is highly conserved both in functions and molecular mechanisms among species, and it has been reported in many model organisms. Zebrafish is a widely used vertebrate animal model, with advantages in imaging, genetics, developmental biology and high throughput drug screening, making this animal an ideal material for cell autophagy investigation. Much progress has been made in this field using zebrafish. Here we first introduce the occurrence process of autophagy, putting emphasis on the autophagy detection methods used in zebrafish and the studies of autophagy related human diseases using zebrafish.
作者 刘欢 靳天志 杨金畅 董国萍 阮华 Liu Huan;Jin Tianzhi;Yang Jinchang;Dong Guoping;Ruan Hua(Key Laboratory of Freshwater Fish Reproduction and Development Ministry of Education,School of Life Sciences,Southwest University,Chongqing,400715)
出处 《基因组学与应用生物学》 CAS CSCD 北大核心 2019年第8期3527-3532,共6页 Genomics and Applied Biology
基金 西南大学中央高校基本科研业务费(XDJK2017D107,XDJK2017A102)资助
关键词 细胞自噬 斑马鱼 检测方法 疾病模型 Autophagy Zebrafish Method Disease model
  • 相关文献

参考文献1

二级参考文献160

  • 1Mizushima N, Klionsky DJ. Protein turnover via autophagy: implications for metabolism. Annu Rev Nutr 2007; 27: 19-40.
  • 2Mari M, Tooze SA, Reggiori F. The puzzling origin of the autophagosomal membrane. F1000 Biol Rep 2011; 3: 25.
  • 3Mizushima N, Yoshimori T, Ohsumi Y. The role of Atg proteins in autophagosome formation. Annu Rev Cell Dev Biol 2011; 27:107-132.
  • 4Hara T, Takamura A, Kishi C, et al. FIP200, a ULK-interacting protein, is required for autophagosome formation in mammalian cells. J Cell Biol 2008; 181:497-510.
  • 5Chan EY, Longatti A, McKnight NC, Tooze SA. Kinase-inactivated ULK proteins inhibit autophagy via their conserved C-terminal domains using an Atg13-independent mechanism. Mol Cell Biol 2009; 29: 157 -171.
  • 6Ganley IG, Lam du H, Wang J, Ding X, Chen S, Jiang X. ULK1.ATG 13.FIP200 complex mediates mTOR signaling and is essential for autophagy. J Biol Chem 2009; 284:12297- 12305.
  • 7Hosokawa N, Hara T, Kaizuka T, et al. Nutrient-dependent mTORCI association with the ULKI-Atg13-FIP200 complex required for autophagy. Mol Biol Cell 2009; 20:1981-1991.
  • 8Jung CH, Jun CB, Ro SH, et al. ULK-Atg13-FIP200 complexes mediate mTOR signaling to the autophagy machinery. Mol Biol Cell 2009; 20: 1992-2003.
  • 9Hosokawa N, Sasaki T, Iemura S, Natsume T, Hara T, Mizushima N. AtglO1, a novel mammalian autophagy protein interacting with Atg13. Autophagy 2009; 5:973-979.
  • 10Herman PK, Emr SD. Characterization ofVPS34, a gene required for vacuolar protein sorting and vacuole segregation in Saccharomyces cerevisiae. Mol Cell Biol 1990; 10:6742-6754.

共引文献70

同被引文献24

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部