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circMyt1l/rno-let-7d-5p/BDNF在少突胶质细胞前体细胞中的作用研究
作者:朱丽华1  王新宇2  韩奕文1  莫思思3  疏佳萍4  蒋犁3 
单位:1. 江苏卫生健康职业学院, 江苏 南京 211800;
2. 扬州大学 附属医院, 江苏 扬州 225012;
3. 东南大学 附属中大医院, 江苏 南京 210009;
4. 东南大学 医学院, 江苏 南京 210009
关键词:少突胶质前体细胞 环状RNA 脑源性神经营养因子 氧糖剥夺 SD大鼠 
分类号:R-33; R742
出版年·卷·期(页码):2023·42·第三期(451-456)
摘要:

目的: 探讨circMyt1l/rno-let-7d-5p/脑源性神经营养因子(BDNF)在少突胶质细胞前体细胞(OPCs)中的表达变化和相互作用。方法: 运用生物信息学分析方法,分析脑室周围白质损伤幼鼠脑组织中具有差异表达的circMyt1l,和其相互作用的miRNA和mRNA;分离培养出OPCs,将其分为对照组(Mock组)和氧糖剥夺(OGD)1、2、3 h组,即OGD1、OGD2、OGD3组,采用qRT-PCR法检测circMyt1l、rno-let-7d-5p基因表达水平,使用蛋白质印迹法检测BDNF蛋白表达水平。结果: 生物信息学分析提示circMyt1l、rno-let-7d-5p、BDNF存在相互作用。OGD1、OGD2、OGD3 3组OPCs内circMyt1l的表达较Mock组均降低,差异均有统计学意义(P<0.01);而rno-let-7d-5p的表达较Mock组均升高,差异均有统计学意义(P<0.01);OGD1与Mock组间BDNF蛋白的表达差异无统计学意义(P>0.05),OGD2、OGD3两组与Mock组比较差异均有统计学意义(P<0.05)。结论: circMyt1l/rno-let-7d-5p/BDNF三者在OGD的OPCs中表达具有相互关系,circMyt1l表达的降低对rno-let-7d-5p的作用减弱,促进了其靶向BDNF的表达。

Objective: To investigate the expression and interaction of circMyt1l/rno-let-7d-5p/brain-derived neurotrophic factor(BDNF) in oligodendrocyte progenitor cells(OPCs). Methods: Bioinformatics analysis was used to analyze the differentially expressed circMyt1l and it's interacting miRNAs and mRNAs in the brain tissues of young rats with periventricular white matter injury. OPCs were isolated and cultured, and divided into control group(Mock group) and oxygen glucose deprivation(OGD) groups for 1 h, 2 h and 3 h, Namely OGD1, OGD2 and OGD3 groups. The expression levels of circMyt1l and rno-let-7d-5p genes were detected by qRT-PCR, and the expression levels of BDNF protein were detected by Western Blotting. Results: Bioinformatics analysis suggested that circMyt1l, rno-let-7d-5p and BDNF interact with each other. The expression of circMyt1l in OPCs in OGD1, OGD2 and OGD3 groups was lower than that in Mock group, and the differences were statistically significant(P<0.01).The expression of rno-let-7d-5p was higher than that of Mock group, and the differences were statistically significant(P<0.01). The expression of BDNF protein showed no significant difference between OGD1 and the Mock group(P>0.05), while there were significant differences between OGD2, OGD3 groups and the Mock group(P<0.05). Conclusion: The expression of circMyt1l/rno-let-7d-5p/BDNF is interrelated in OPCs of OGD. Decreased expression of circMyt1l weakened the effect on rno-let-7d-5p and promoted the expression of its targeted BDNF.

参考文献:

[1] ZHAO X,DU F,LIU X,et al.Brain-derived neurotrophic factor(BDNF)is expressed in buffalo(Bubalus bubalis)ovarian follicles and promotes oocyte maturation and early embryonic development[J].Theriogenology,2019,130:79-88.
[2] LEE-HOTTA S,UCHIYAMA Y,KAMETAKA S.Role of the BDNF-TrkB pathway in KCC2 regulation and rehabilitation following neuronal injury:a mini review[J].Neurochem Int,2019,128:32-38.
[3] WONG I,LOAO H,BAI X,et al.ProBDNF inhibits infiltration of ED1+macrophages after spinal cord injury[J].Brain Behav Immun,2010,24(4): 585-597.
[4] VONDRAN M W,SINGH H,HONEYWELL J Z,et al.Levels of BDNF impact oligodendrocyte lineage cells following a cuprizone lesion[J].J Neurosci,2011,31(40):14182-14190.
[5] QU Y,ZHU J,LIU J,et al.Circular RNA circ_0079593 indicates a poor prognosis and facilitates cell growth and invasion by sponging miR-182 and miR-433 in glioma[J].J Cell Biochem,2019,120(10):18005-18013.
[6] WANG X,LIU H,LIAO X,et al.Dissecting the roles of LncRNAs in the development of periventricular white matter damage[J].Front Genet,2021,12:641526.
[7] ZHU L,ZHAO R,HUANG L,et al.Circular RNA expression in the brain of a neonatal rat model of periventricular white matter damage[J].Cell Physiol Biochem, 2018,49(6):2264-2276.
[8] 莫思思,朱丽华,李棒棒,等.SD 大鼠少突胶质前体细胞的纯化及氧糖剥夺对其活性的影响[J].东南大学学报(医学版),2019,38(4):572-578.
[9] RONAZNO R,THETIOT M,LUBETZKI C,et al.Myelin plasticity and repair: neuro-glial choir sets the tuning[J].Front Cell Neurosci,2020,14:00042.
[10] HUANG Y,SONG Y J,ISAAC M,et al.Tropomyosin receptor kinase B expressed in oligodendrocyte lineage cells functions to promote myelin following a demyelinating lesion[J].ASN Neuro,2020,12:1-13.
[11] ZHAO D,ZHANG M L,YANG L L,et al.GPR68 Improves nerve damage and myelination in an immature rat model induced by sevoflurane anesthesia by activating cAMP/CREB to mediate BDNF[J].ACS Chem Neurosci,2022,13(3):423-431.
[12] XIAO J,WONG A W,WILLINGHAM M M,et al.Brain-derived neurotrophic factor promotes central nervous system myelination via a direct effect upon oligodendrocytes[J].Neurosignals,2010,18(3):186-202.
[13] HUNG P L,HSU M H,YU H R,et al.Thyroxin protects white matter from hypoxic-ischemic insult in the immature sprague-dawley rat brain by regulating periventricular white matter and cortex BDNF and CREB pathways[J].Int J Mol Sci, 2018,19(9):2573.
[14] LI M,XIA M,CHEN W,et al.Lithium treatment mitigates white matter injury after intracerebral hemorrhage through brain-derived neurotrophic factor signaling in mice[J].Transl Res,2020,217: 61-74.
[15] LIU S,GUO W,ZHOU H X,et al.ProBDNF inhibits the proliferation and migration of OLN-93 oligodendrocytes[J]. Mol Med Rep,2018,18(4):3809-3817.
[16] 高笑妮,杨丽君,张囡,等.新生未成熟大鼠缺氧缺血性脑损伤时微小RNA-200b对缺氧诱导因子1α的调控作用[J].中华新生儿科杂志(中英文),2019, 34(1):58-62.
[17] CHO K H T,XU B,BLENKIRON C,et al.Emerging roles of miRNAs in brain development and perinatal brain injury[J].Front Physiol,2019,10:00227.
[18] YANG Q,WU M F,ZHU L H,et al.Long non-coding RNA Snhg3 protects against hypoxia/ischemia-induced neonatal brain injury[J].Exp Mol Pathol,2020,112:104343.
[19] ZHU L H,HUANG L,MO S S,et al.RNA-sequencing analysis of long non-coding RNAs in a neonatal rat brain model of periventricular white matter damage[J].Nanosci Nanotechnol Lett,2019,11(4):524-532.
[20] 魏思萌,肖谧,郑曦,等.环状RNA在炎症所致早产小鼠脑损伤中的作用及机制初步研究[J].中国当代儿科杂志,2021,23(7):730-734.
[21] QIAO L,MO S,ZHOU Y,et al.Circular RNA expression alteration in whole blood of premature infants with periventricular white matter damage[J].Genomics,2020, 112(4):2875-2885.
[22] 胡志刚,赵鹏新,马维远,等.微小RNA-489调控脑源性神经营养因子在甲状腺乳头状癌中的作用机制研究[J].中国耳鼻咽喉头颈外科,2020,27(5):243-247.
[23] 宋晋,梁婷,王强,等.miR-134/CREB/BDNF通路在低频重复经颅磁刺激影响癫痫大鼠抑郁、焦虑样行为中的作用[J].中国老年学杂志,2022,42(14):3562-3565.
[24] LIU C X,LI X,NAN F,et al.Structure and degradation of circular RNAs regulate PKR activation in innate immunity[J].Cell,2019,177(4):865-880.
[25] WANG Q,QU L,CHEN X,et al.Progress in understanding the relationship between circular RNAs and neurological disorders[J].J Mol Neurosci,2018,65(4): 546-556.
[26] HANSEN T B,JENSEN T I,CLAUSEN B H,et al.Natural RNA circles function as efficient microRNA sponges[J].Nature,2013,495(7441):384-388.

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