浏览全部资源
扫码关注微信
1.中国中医科学院 中药研究所,北京 100700
2.中国中医科学院 青蒿素研究中心,北京 100700
邓硕秋,在读硕士,从事中药学、心血管药理学研究,E-mail:dengshuoqiu98@163.com
陈利娜,助理研究员,从事青蒿素及其衍生物、脑型疟相关研究,E-mail:lnchen@icmm.ac.cn
李玉洁,研究员,从事中药学、心血管药理学研究,Tel:010-64097152,E-mail:yjli@icmm.ac.cn
纸质出版日期:2023-01-05,
网络出版日期:2022-09-19,
收稿日期:2022-06-27,
扫 描 看 全 文
邓硕秋,瞿水清,张雨等.CRISPR/Cas9基因编辑技术在脑科学中的技术优化进展及在中医药领域应用[J].中国实验方剂学杂志,2023,29(01):169-180.
DENG Shuoqiu,QU Shuiqing,ZHANG Yu,et al.Optimized CRISPR/Cas9 System in Brain Science and Application Prospects in Field of Traditional Chinese Medicine[J].Chinese Journal of Experimental Traditional Medical Formulae,2023,29(01):169-180.
邓硕秋,瞿水清,张雨等.CRISPR/Cas9基因编辑技术在脑科学中的技术优化进展及在中医药领域应用[J].中国实验方剂学杂志,2023,29(01):169-180. DOI: 10.13422/j.cnki.syfjx.20221803.
DENG Shuoqiu,QU Shuiqing,ZHANG Yu,et al.Optimized CRISPR/Cas9 System in Brain Science and Application Prospects in Field of Traditional Chinese Medicine[J].Chinese Journal of Experimental Traditional Medical Formulae,2023,29(01):169-180. DOI: 10.13422/j.cnki.syfjx.20221803.
成簇规律间隔的短回文重复序列(CRISPR)/CRISPR相关蛋白(CRISPR/Cas9)是在细菌和古细菌中发现的一种自身防御系统,根据其原理可实现定向基因编辑,因其普适、高效、简便的特点,已为多个领域的疾病病理机制、预防或治疗等提供了良好的技术支持。脑血管疾病和神经系统疾病严重危害人类健康,卒中由遗传、不良生活习惯、慢性疾病等因素相关。脑组织结构复杂,细胞类型多样,普适的基因编辑平台较难安全、特异和高效地对靶基因进行研究。学者们不断改进和优化基因编辑技术,发掘了基因编辑技术的潜力和研究方法,推动了脑科学的研究进程。该文在简介CRISPR/Cas9技术原理的基础上,主要从递送方式、腺相关病毒组装、纳米新材料等方面综述了其在脑和神经科学领域中的系统优化进展,从血管稳态、小胶质细胞稳态、血管形成、血脑屏障、药物筛选等方面总结了其在脑血管研究和中风等相关疾病中的应用,并对其在中医药领域的发展进行了展望,以期为相关研究设计提供参考。
Clustered regularly interspaced short palindromic repeats(CRISPR)/CRISPR associated nuclease 9 (CRISPR/Cas9) is a self-defense system found in bacteria and archaea that enables targeted gene editing based on the principle. Due to its universality, efficiency, and simplicity, CRISPR/Cas9 has been applied in the pathological mechanism and prevention and treatment of diseases in many fields. Cerebrovascular diseases and central nervous system diseases seriously endanger human health. Stroke is related to genetics, unhealthy living habits, chronic diseases, and other factors. The brain tissue structure is complex and the cell types are diverse. It is difficult for a universal gene editing platform to study target genes safely, specifically, and efficiently. Scholars have continuously improved and optimized gene editing technology, explored the potential and research methods of gene editing technology, and promoted the research process of brain science. After a brief introduction to the mechanism of CRISPR/Cas9, this paper mainly summarized the optimization of the system in the fields of cerebral science including delivery methods, adeno-associated virus assembly, and new nanomaterials. Its application in cerebrovascular research including vascular homeostasis, microglial homeostasis, angiogenesis, blood-brain barrier, and drug screening was also summarized. Finally, this paper prospected the development of CRISPR/Cas9 in traditional Chinese medicine, hoping to provide references for related research design.
成簇规律间隔的短回文重复序列(CRISPR)/CRISPR相关蛋白(CRISPR/Cas9)基因编辑脑科学中药
clustered regularly interspaced short palindromic repeats(CRISPR)/CRISPR associated nuclease 9 (CRISPR/Cas9)gene editingbrain sciencetraditional Chinese medicine
GONZÁLEZ CASTRO N,BJELIC J,MALHOTRA G,et al.Comparison of the feasibility, efficiency, and safety of genome editing technologies[J].Int J Mol Sci,2021,22(19):10355.
RUI Y,WILSON D R,GREEN J J.Non-viral delivery to enable genome editing[J].Trends Biotechnol,2019,37(3):281-293.
SHIVRAM H,CRESS B F,KNOTT G J,et al.Controlling and enhancing CRISPR systems[J].Nat Chem Biol,2021,17(1):10-19.
SAYED N,ALLAWADHI P,KHURANA A,et al.Gene therapy: Comprehensive overview and therapeutic applications[J].Life Sci,2022,294:120375.
ADLI M.The CRISPR tool kit for genome editing and beyond[J].Nat Commun,2018,9(1):1911.
PAWLUK A,DAVIDSON A R,MAXWELL K L.Anti-CRISPR: Discovery, mechanism and function[J].Nat Rev Microbiol,2018,16(1):12-17.
FANG H,BYGRAVE A M,ROTH R H,et al.An optimized CRISPR/Cas9 approach for precise genome editing in neurons[J].Elife,2021,10:e65202.
SHINMYO Y,KAWASAKI H.CRISPR/Cas9-mediated gene knockout in the mouse brain using in utero electroporation[J].Curr Protoc Neurosci,2017,doi:10.1002/cpns.26http://dx.doi.org/10.1002/cpns.26.
STAAHL B T,BENEKAREDDY M,COULON-BAINIER C,et al.Efficient genome editing in the mouse brain by local delivery of engineered Cas9 ribonucleoprotein complexes[J].Nat Biotechnol,2017,35(5):431-434.
ZHENG Y,SHEN W,ZHANG J,et al.CRISPR interference-based specific and efficient gene inactivation in the brain[J].Nat Neurosci,2018,21(3):447-454.
HENDRIKS D,CLEVERS H,ARTEGIANI B.CRISPR-cas tools and their application in genetic engineering of human stem cells and organoids[J].Cell Stem Cell,2020,27(5):705-731.
WILBIE D,WALTHER J,MASTROBATTISTA E.Delivery aspects of CRISPR/Cas for in vivo genome editing[J].Acc Chem Res,2019,52(6):1555-1564.
ABE T,INOUE K I,FURUTA Y,et al.Pronuclear microinjection during S-phase increases the efficiency of CRISPR-Cas9-assisted knockin of large DNA donors in mouse zygotes[J].Cell Rep,2020,31(7):107653.
LIN J C,VAN EENENNAAM A L.Electroporation-mediated genome editing of livestock zygotes[J].Front Genet,2021,12:648482.
CHEN S,SUN S,MOONEN D,et al.CRISPR-READI: Efficient generation of knockin mice by CRISPR RNP electroporation and AAV donor infection[J].Cell Rep,2019,27(13):3780-3789.
WAKE Y,KANEKO T.Production of genome-edited mice by visualization of nucleases introduced into the embryos using electroporation[J].J Reprod Dev,2020,66(5):469-473.
SWIECH L,HEIDENREICH M,BANERJEE A,et al.In vivo interrogation of gene function in the mammalian brain using CRISPR-Cas9[J].Nat Biotechnol,2015,33(1):102-106.
CHAN K Y,JANG M J,YOO B B,et al.Engineered AAVs for efficient noninvasive gene delivery to the central and peripheral nervous systems[J].Nat Neurosci,2017,20(8):1172-1179.
HEIDE M,HAFFNER C,MURAYAMA A,et al.Human-specific ARHGAP11B increases size and folding of primate neocortex in the fetal marmoset[J].Science,2020,369(6503):546-550.
HARRIS J C.Animal models of neurodevelopmental disorders with behavioral phenotypes[J].Curr Opin Psychiatry,2021,34(2):87-93.
GRAFALS-RUIZ N,RIOS-VICIL C I,LOZADA-DELGADO E L,et al.Brain targeted gold liposomes improve RNAi delivery for glioblastoma[J].Int J Nanomedicine,2020,15:2809-2828.
SATO M,NAKAMURA S,INADA E,et al.Recent advances in the production of genome-edited rats[J].Int J Mol Sci,2022,23(5)
BÄCK S,NECARSULMER J,WHITAKER L R,et al.Neuron-specific genome modification in the adult rat brain using CRISPR-Cas9 transgenic rats[J].Neuron,2019,102(1):105-119.
SUN H,ZHENG J,YI M,et al.Conditional genome editing in the mammalian brain using CRISPR-Cas9[J].Neurosci Bull,2021,37(3):423-426.
SUN H,FU S,CUI S,et al.Development of a CRISPR-SaCas9 system for projection- and function-specific gene editing in the rat brain[J].Sci Adv,2020,6(12):eaay6687.
TIAN R,GACHECHILADZE M A,LUDWIG C H,et al.CRISPR interference-based platform for multimodal genetic screens in human iPSC-derived neurons[J].Neuron,2019,104(2):239-255.
MURLIDHARAN G,SAKAMOTO K,RAO L,et al.CNS-restricted transduction and CRISPR/Cas9-mediated gene deletion with an engineered AAV vector[J].Mol Ther Nucleic Acids,2016,5(7):e338.
SAVELL K E,BACH S V,ZIPPERLY M E,et al.A neuron-optimized CRISPR/dCas9 activation system for robust and specific gene regulation[J].eNeuro,2019,6(1):143.
ZHOU H,SU J,HU X,et al.Glia-to-neuron conversion by CRISPR-CasRx alleviates symptoms of neurological disease in mice[J].Cell,2020,181(3):590-603.
DENES C E,COLE A J,AKSOY Y A,et al.Approaches to enhance precise CRISPR/Cas9-mediated genome editing[J].Int J Mol Sci,2021,22(16):8571.
ZHANG J,CHEN L,ZHANG J,et al.Drug Inducible CRISPR/Cas Systems[J].Comput Struct Biotechnol J,2019,17:1171-1177.
WANG X,DONG K,KONG D,et al.A far-red light-inducible CRISPR-Cas12a platform for remote-controlled genome editing and gene activation[J].Sci Adv,2021,7(50):eabh2358.
HOFFMANN M D,BUBECK F,NIOPEK D.Light-inducible CRISPR labeling[J].Methods Mol Biol,2020,2173:137-150.
DE SOLIS C A,HO A,HOLEHONNUR R,et al.The development of a viral mediated CRISPR/Cas9 system with doxycycline dependent gRNA expression for inducible in vitro and in vivo genome editing[J].Front Mol Neurosci,2016,9:70.
KUMAR N,STANFORD W,DE SOLIS C,et al.The development of an AAV-based CRISPR SaCas9 genome editing system that can be delivered to neurons in vivo and regulated via doxycycline and cre-recombinase[J].Front Mol Neurosci,2018,11:413.
DAI Z,LI R,HOU Y,et al.Inducible CRISPRa screen identifies putative enhancers[J].J Genet Genomics,2021,48(10):917-927.
THAMODARAN V,RANI S,VELAYUDHAN S R.Gene editing in human induced pluripotent stem cells using doxycycline-inducible CRISPR-Cas9 system[J].Methods Mol Biol,2022,2454:755-773.
LIU X S,JAENISCH R.Editing the epigenome to tackle brain disorders[J].Trends Neurosci,2019,42(12):861-870.
LIU X S,WU H,JI X,et al.Editing DNA methylation in the mammalian genome[J].Cell,2016,167(1):233-247.
LIU X S,WU H,KRZISCH M,et al.Rescue of fragile X syndrome neurons by DNA methylation editing of the FMR1 gene[J].Cell,2018,172(5):979-992.
KOENNING M,WANG X,KARKI M,et al.Neuronal SETD2 activity links microtubule methylation to an anxiety-like phenotype in mice[J].Brain,2021,144(8):2527-2540.
TANG H,ZHAO X,JIANG X.Synthetic multi-layer nanoparticles for CRISPR-Cas9 genome editing[J].Adv Drug Deliv Rev,2021,168:55-78.
LEE K,CONBOY M,PARK H M,et al.Nanoparticle delivery of Cas9 ribonucleoprotein and donor DNA in vivo induces homology-directed DNA repair[J].Nat Biomed Eng,2017,1:889-901.
LEE B,LEE K,PANDA S,et al.Nanoparticle delivery of CRISPR into the brain rescues a mouse model of fragile X syndrome from exaggerated repetitive behaviours[J].Nat Biomed Eng,2018,2(7):497-507.
PARK H,OH J,SHIM G,et al.In vivo neuronal gene editing via CRISPR-Cas9 amphiphilic nanocomplexes alleviates deficits in mouse models of Alzheimer's disease[J].Nat Neurosci,2019,22(4):524-528.
BJÖRKEGREN J,LUSIS A J.Atherosclerosis: Recent developments[J].Cell,2022,185(10):1630-1645.
LYDEN P D.Cerebroprotection for acute ischemic stroke: Looking ahead[J].Stroke,2021,52(9):3033-3044.
KLEINDORFER D O,TOWFIGHI A,CHATURVEDI S,et al.2021 guideline for the prevention of stroke in patients with stroke and transient ischemic attack: A guideline from the american heart association/American stroke association[J].Stroke,2021,52(7):e364-e467.
AKOVA M,UNAL S.A randomized, double-blind, placebo-controlled phase Ⅲ clinical trial to evaluate the efficacy and safety of SARS-CoV-2 vaccine (inactivated, Vero cell): A structured summary of a study protocol for a randomised controlled trial[J].Trials,2021,22(1):276.
KRAUSE M D,HUANG R T,WU D,et al.Genetic variant at coronary artery disease and ischemic stroke locus 1p32.2 regulates endothelial responses to hemodynamics[J].Proc Natl Acad Sci USA,2018,115(48):E11349-E11358.
VAR S R,SHETTY A V,GRANDE A W,et al.Microglia and macrophages in neuroprotection, neurogenesis, and emerging therapies for stroke[J].Cells,2021,10(12):156.
COSTA J,MARTINS S,FERREIRA P A,et al.The old guard: Age-related changes in microglia and their consequences[J].Mech Ageing Dev,2021,197:111512.
PLUVINAGE J V,HANEY M S,SMITH B,et al.CD22 blockade restores homeostatic microglial phagocytosis in ageing brains[J].Nature,2019,568(7751):187-192.
MARSCHALLINGER J,IRAM T,ZARDENETA M,et al.Lipid-droplet-accumulating microglia represent a dysfunctional and proinflammatory state in the aging brain[J].Nat Neurosci,2020,23(2):194-208.
HU J,WANG W,HAO Q,et al.Suppressors of cytokine signalling (SOCS)-1 inhibits neuroinflammation by regulating ROS and TLR4 in BV2 cells[J].Inflamm Res,2020,69(1):27-39.
SI W,LI Y,YE S,et al.Methyltransferase 3 mediated miRNA m6A methylation promotes stress granule formation in the early stage of acute ischemic stroke[J].Front Mol Neurosci,2020,13:103.
LI W,YANG F,GAO J,et al.Over-expression of TRPC6 via CRISPR based synergistic activation mediator in BMSCs ameliorates brain injury in a rat model of cerebral ischemia/reperfusion[J].Neuroscience,2019,415:147-160.
SI W,LI Z,HUANG Z,et al.RNA binding protein Motif 3 inhibits oxygen-glucose deprivation/reoxygenation-induced apoptosis through promoting stress granules formation in PC12 cells and rat primary cortical neurons[J].Front Cell Neurosci,2020,14:559384.
PETERSEN M A,RYU J K,CHANG K J,et al.Fibrinogen activates BMP signaling in oligodendrocyte progenitor cells and inhibits remyelination after vascular damage[J].Neuron,2017,96(5):1003-1012.
ZHOU Y F,LI Y N,JIN H J,et al.Sema4D/PlexinB1 inhibition ameliorates blood-brain barrier damage and improves outcome after stroke in rats[J].FASEB J,2018,32(4):2181-2196.
MATEI N,CAMARA J,MCBRIDE D,et al.Intranasal wnt3a attenuates neuronal apoptosis through Frz1/PIWIL1a/FOXM1 pathway in MCAO rats[J].J Neurosci,2018,38(30):6787-6801.
HANKEY G J.Secondary stroke prevention[J].Lancet Neurol,2014,13(2):178-194.
左玲,陈建新,王伟,等.中医信息学与表型组学:症状的遗传突变与证候的生物学基础初探[J].北京中医药大学学报,2022,45(2):140-147.
XU H,SONG J,LUO H,et al.Analysis of the genome sequence of the medicinal plant Salvia miltiorrhiza[J].Mol Plant,2016,9(6):949-952.
ZHENG S G,HU Y D,ZHAO R X,et al.Genome-wide researches and applications on Dendrobium[J].Planta,2018,248(4):769-784.
LIANG Q,LI H,LI S,et al.The genome assembly and annotation of yellowhorn (Xanthoceras sorbifolium Bunge)[J].Gigascience,2019,8(6):gi2071.
张亚男,邹忆怀,罗树云,等.邹忆怀教授论治缺血性中风经验[J].陕西中医,2019,40(12):1765-1767.
LIBBY P,BURING J E,BADIMON L,et al.Atherosclerosis[J].Nat Rev Dis Primers,2019,5(1):56.
DICHGANS M,PULIT S L,ROSAND J.Stroke genetics: discovery, biology, and clinical applications[J].Lancet Neurol,2019,18(6):587-599.
陈浪欣,张桂莹,李其富,等.染色体6p21.1区遗传变异与缺血性脑卒中易感性的研究进展[J].中华神经医学杂志,2021,20(9):952-955.
刘靖.6、7和9号染色体基因多态性与汉族和哈萨克族脑梗塞的相关性研究[D].武汉:华中科技大学,2017.
BEHR M,ZHOU J,XU B,et al.In vivo delivery of CRISPR-Cas9 therapeutics: Progress and challenges[J].Acta Pharm Sin B,2021,11(8):2150-2171.
REES H A,MINELLA A C,BURNETT C A,et al.CRISPR-derived genome editing therapies: Progress from bench to bedside[J].Mol Ther,2021,29(11):3125-3139.
LI B,NIU Y,JI W,et al.Strategies for the CRISPR-based therapeutics[J].Trends Pharmacol Sci,2020,41(1):55-65.
SHARMA G,SHARMA A R,BHATTACHARYA M,et al.CRISPR-Cas9: A preclinical and clinical perspective for the treatment of human diseases[J].Mol Ther,2021,29(2):571-586.
KAMINSKI M M,ABUDAYYEH O O,GOOTENBERG J S,et al.CRISPR-based diagnostics[J].Nat Biomed Eng,2021,5(7):643-656.
LI J,HONG S,CHEN W,et al.Advances in detecting and reducing off-target effects generated by CRISPR-mediated genome editing[J].J Genet Genomics,2019,46(11):513-521.
LEVY Y,LEVY D.A friend and a Foe: 50 years of the apolipoprotein e research trail[J].Isr Med Assoc J,2021,23(10):665-669.
CARROLL K J,MAKAREWICH C A,MCANALLY J,et al.A mouse model for adult cardiac-specific gene deletion with CRISPR/Cas9[J].Proc Natl Acad Sci USA,2016,113(2):338-343.
VERMERSCH E,JOUVE C,HULOT J S.CRISPR/Cas9 gene-editing strategies in cardiovascular cells[J].Cardiovasc Res,2020,116(5):894-907.
KAMPMANN M.CRISPR-based functional genomics for neurological disease[J].Nat Rev Neurol,2020,16(9):465-480.
ESPINO-SALDAÑA A E,RODRÍGUEZ-ORTIZ R,PEREIDA-JARAMILLO E,et al.Modeling neuronal diseases in zebrafish in the era of CRISPR[J].Curr Neuropharmacol,2020,18(2):136-152.
YAN S,TU Z,LI S,et al.Use of CRISPR/Cas9 to model brain diseases[J].Prog Neuropsychopharmacol Biol Psychiatry,2018,81:488-492.
NISHIYAMA J.Genome editing in the mammalian brain using the CRISPR-Cas system[J].Neurosci Res,2019,141:4-12.
NISHIZONO H,YASUDA R,LAVIV T.Methodologies and challenges for CRISPR/Cas9 mediated genome editing of the mammalian brain[J].Front Genome Ed,2020,2:602970.
LUTHER D C,LEE Y W,NAGARAJ H,et al.Delivery approaches for CRISPR/Cas9 therapeutics in vivo: Advances and challenges[J].Expert Opin Drug Deliv,2018,15(9):905-913.
VERDERA H C,KURANDA K,MINGOZZI F.AAV vector immunogenicity in humans: A long journey to successful gene transfer[J].Mol Ther,2020,28(3):723-746.
WANG D,ZHANG F,GAO G.CRISPR-based therapeutic genome editing: Strategies and in vivo delivery by AAV vectors[J].Cell,2020,181(1):136-150.
TORRES-RUIZ R,RODRIGUEZ-PERALES S.CRISPR-Cas9 technology: Applications and human disease modelling[J].Brief Funct Genomics,2017,16(1):4-12.
CHO S,SHIN J,CHO B K.Applications of CRISPR/Cas system to bacterial metabolic engineering[J].Int J Mol Sci,2018,19(4):1089.
BROKOWSKI C,ADLI M.CRISPR ethics: Moral considerations for applications of a powerful tool[J].J Mol Biol,2019,431(1):88-101.
0
浏览量
13
下载量
0
CSCD
关联资源
相关文章
相关作者
相关机构