国际眼科纵览

• 综述 • 上一篇    下一篇

弱视视觉可塑性相关基因研究

曹朝霞,刘安国,严兴科,马重兵,李小娟,魏玉婷   

  1. 730000 兰州,甘肃中医药大学针灸推拿学院(曹朝霞、刘安国、严兴科、马重兵、李小娟、魏玉婷);635000 四川, 达州市中西医结合医院(曹朝霞)
  • 出版日期:2018-06-22 发布日期:2018-06-28
  • 通讯作者: 严兴科, Email:yanxingke@126.com
  • 基金资助:

    国家自然科学基金(81660816、81260560);甘肃中医药大学中青年科研基金(ZQ2015-1);甘肃中医药大学研究生创新基金(2018CX31)

The research of visual plasticity related genes in amblyopia

CAO Zhao-xia1.2, LIU An-guo1, YAN Xing-ke1, MA Chong-bing1, LI Xiao-juan1, WEI Yu-ting1   

  1. 1. School of Acupuncture and Tuina, Gansu University of Chinese Medicine, Lanzhou 730000, China; 2. Dazhou Hospital of Integrated Traditional Chinese and Western Medicine, Sichuan 635000,China
  • Online:2018-06-22 Published:2018-06-28
  • Contact: YAN Xing-ke, Email: yanxingke@126.com
  • Supported by:

    National Natural Science Foundation of China (81660816, 81260560); Science Fund Project for Middle-Young Age of Gansu University of Chinese Medicine (ZQ2015-1); Graduate Innovation Fund of Gansu University of Chinese Medicine (2018CX31)

摘要:

可能与弱视发病密切相关的部分基因有抗凋亡基因(Bcl-2、Bax)、即刻早期基因(c-jun、c-fos)、视觉可塑性神经递质相关基因(N-甲基-D-天冬氨酸受体1亚单位基因)、视觉可塑性神经营养因子相关基因(Neuritin mRNA、GDNF mRNA、BDNF mRNA、GAP-43 mRNA)、PTPσ mRNA、β-catenin mRNA等。Bcl-2、Bax可能通过调节视觉系统相关神经细胞的存活来参与弱视的发病;c-jun、c-fos进入细胞核后能够改变靶基因的转录活性从而调节视皮质神经元的功能状态;N-甲基-D-天冬氨酸受体1亚单位基因位于突触后膜,可以通过调节不同亚单位的表达水平来调节视皮层突触的可塑性;视觉可塑性神经营养因子相关基因中的Neuritin mRNA编码一种活性分子,这种活性分子可以促进树突的生长,从而调节视觉系统发育过程中神经元的活动;GDNF mRNA存在于视皮层和外侧膝状体,对各种损伤后的神经元具有保护和修复作用,能通过影响视觉系统正常发育过程中的转录来参与对视觉发育的调控,BDNF mRNA具有调节神经系统突触发育可塑性的效应,参与视觉发育关键期突触的可塑性变化;PTPσ mRNA、β-catenin mRNA参与了成年大鼠视皮层可塑性关键期的终止及可塑性再激活的过程。(国际眼科纵览, 2018,  42:   163-168)

Abstract:

Some genes such as anti-apoptotic genes (Bcl-2, Bax), immediate early genes (c-jun, c-fos), visual plasticity neurotransmitter related genes (N- methyl-D-aspartic acid receptor, NMDAR-1 subunit gene), visual plasticity neurotrophic factors related genes (Neuritin mRNA, GDNF mRNA, BDNF mRNA, GAP-43 mRNA), PTPσ mRNA, β-catenin mRNA and so on  may be closely related to the onset of amblyopia. Bcl-2 and Bax may participate in the pathogenesis of amblyopia by regulating the survival of the related neurons in the visual system. C-jun and c-fos can alter the transcriptional activity of the target gene and regulate the functional state of the cortical neurons after entering the nucleus of neurons. NMDAR-1 subunit gene of the aspartate receptor is located in the postsynaptic membrane, which regulates the plasticity of the synapses in the visual cortex by regulating the expression level of different subunits. The neuritin mRNA encodes a kind of active molecule, which can promote the growth of dendrites and regulate the visual system. GDNF mRNA exists in the visual cortex and lateral geniculate body, which protects and repairs neurons after various injuries. It can regulate visual development by influencing the transcription of the normal development process of the visual system. BDNF mRNA regulates the plasticity of synaptic development in nervous system. The PTPσ mRNA and β-catenin mRNA are involved in the termination of the critical stage of visual cortex and the process of plasticity reactivation in the visual cortex of adult rats.(Int Rev Ophthalmol, 2018, 42:  163-168)