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miR-204调控眼科疾病的研究进展 被引量:6

Research progress of miR-204 in the regulation of ophthalmic diseases
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摘要 微小RNA(miRNA)是一类广泛存在于真核生物体内、长度为20~25个核苷酸、具有调控功能的非编码单链RNA,参与机体的各种生命进程,包括细胞的生长、分化、增生、凋亡和自噬。miRNA-204—5p(miR-204.5p)是由位于染色体9q21.12上的TRPM3大内含子6表达。研究发现,miR-204在角膜损伤愈合过程中起着十分重要的作用,亦能够保持静止状态下血一视网膜屏障的稳定,并且在人小梁网细胞中,miR-204与细胞的凋亡、生存能力以及炎症介质的表达有着重要联系。这些研究都表明miR-204在眼部呈多维表达,提示miR-204很可能是不同眼部疾病的关键miRNA。本文从miRNA的生物合成,miR-204与糖尿病性角膜病变、视网膜色素上皮细胞、人小梁网细胞、年龄相关性白内障、糖尿病视网膜病变、视网膜母细胞瘤的关系,以及miR-204与自噬的相关研究等几个方面,就miR-204调控眼科疾病的研究进展进行综述,为探寻眼部难治性疾病的防治方法寻找新的靶点。 MicroRNAs (miRNAs) are endogenous short nucleotide non-coding RNAs which widely exist in eukaryotic organisms,involved in the body's life process, including cell growth, differentiation, proliferation, apoptosis and autophagy. MiR-204-Sp is located on chromosome TRPM3 in the 9q21.12 large intron 6 expression, and miR-204 plays an important role in corneal wound healing process; and it regulates retinal pigment epithelium (RPE) tight junction integrity and maintains the blood retina barrier in a quiescent state;in human trabecular meshwork cells, miR- 204 appears to play an important role in the regulation of responses to endoplasmic reticulum stress, apoptosis, and production of inflammatory mediators. Identification of additional target genes will be necessary to fully understand the biological functions of miR-204. These studies found that it is a multidimensional expression in the eye, suggesting that miR-204 is likely to be the key miRNA in different eye diseases. This article reviews the biosynthesis of miRNA,the relationship between miR-204 and diabetic keratopathy, RPE cells, human trabecular meshwork cells, age-related cataract,diabetic retinopathy, retinoblastoma and autophagy, and explore the prevention of ocular refractory diseases with new targets.
出处 《中华实验眼科杂志》 CAS CSCD 北大核心 2017年第8期761-763,共3页 Chinese Journal Of Experimental Ophthalmology
基金 江西省自然科学基金项目(20151BAB205096)
关键词 眼科疾病 微小RNA 自噬 Ophthalmic diseases MicroRNA Autophagy
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  • 1柳向军,张令强,刘小林,贺福初.细胞凋亡中的Bcl-2家族蛋白及其BH3结构域的功能研究[J].生物化学与生物物理进展,2006,33(3):221-225. 被引量:21
  • 2周桔,罗荣保,汤长发,瞿树林.Bcl-2蛋白家族和p53基因在细胞凋亡中的调控效应[J].中国组织工程研究与临床康复,2007,11(10):1950-1952. 被引量:85
  • 3Yang Cao Daniel J Klionsky.Physiological functions of Atg6/Beclin 1: a unique autophagy-related protein[J].Cell Research,2007,17(10):839-849. 被引量:104
  • 4Geng J, Baba M, Nair U, Klionsky DJ. Quantitative analysis of autophagy-related protein stoichiometry by fluorescence microscopy. J Cell Biol 2008; 182: 129-140.
  • 5Mizushima N, Yamamoto A, Hatano M, et al. Dissection of autophagosome formation using Apg5-deficient mouse embryonic stem cells. J Cell Biol 2001; 152:657-668.
  • 6Fujita N, Hayashi-Nishino M, Fukumoto H, et al. An Atg4B mutant hampers the lipidation of LC3 paralogues and causes defects in autophagosome closure. Mol Biol Cell 2008; 19:4651-4659.
  • 7Singh R, Cuervo AM. Autophagy in the cellular energetic balance. Cell Metab 2011; 13:495-504.
  • 8Baba M, Osumi M, Scott SV, Klionsky DJ, Ohsumi Y. Two distinct pathways for targeting proteins from the cytoplasm to the vacuole/lysosome. J Cell Biol 1997; 139:1687-1695.
  • 9Mizushima N, Ohsumi Y, Yoshimori T. Autophagosome formation in mammalian cells. Cell Struct Funct 2002; 27:421-429.
  • 10Fujita N, Yoshimori T. Ubiquitination-mediated autophagy against invading bacteria. Curr Opin Cell Biol 2011; 23:492- 497.

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