Gene Therapy Using Efficient Direct Lineage Reprogramming Technology for Neurological Diseases

被引:4
作者
Chang, Yujung [1 ,2 ]
Lee, Sungwoo [3 ]
Kim, Jieun [4 ]
Kim, Chunggoo [1 ]
Shim, Hyun Soo [1 ]
Lee, Seung Eun [5 ]
Park, Hyeok Ju [6 ]
Kim, Jeongwon [3 ]
Lee, Soohyun [3 ]
Lee, Yong Kyu [6 ]
Park, Sungho [3 ]
Yoo, Junsang [1 ]
机构
[1] Stand Up Therapeut, Lab Regenerat Med Neurodegenerat Dis, Hannamdaero 98, Seoul 04418, South Korea
[2] Nuturn Sci, Dept Mol Biol, Sinsadong 559-8, Seoul 06037, South Korea
[3] Sungkyunkwan Univ, Dept Chem, 2066 Seobu Ro, Suwon 16419, South Korea
[4] Kangwon Natl Univ, Coll Biomed Sci, Dept Biohlth Technol, 1 Kangwondeahak Gil, Chunchon 24341, South Korea
[5] Korea Inst Sci & Technol, Res Anim Resource Ctr, Hwarang Ro 14 Gil, Seoul 02792, South Korea
[6] Dongguk Univ Seoul, Dept Comp Sci & Engn, Database Lab, Pildong Ro 1 Gil 30, Seoul 04620, South Korea
基金
新加坡国家研究基金会;
关键词
cell fate conversion; direct lineage reprogramming; spinal cord injury; gene therapy; nanoporous particle-based gene delivery; LEBER CONGENITAL AMAUROSIS; BLOOD-BRAIN-BARRIER; DIRECT CONVERSION; IN-VIVO; PARKINSONS-DISEASE; DOPAMINE NEURONS; FUNCTIONAL-NEURONS; NONHUMAN-PRIMATES; HUMAN FIBROBLASTS; OPEN-LABEL;
D O I
10.3390/nano13101680
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Gene therapy is an innovative approach in the field of regenerative medicine. This therapy entails the transfer of genetic material into a patient's cells to treat diseases. In particular, gene therapy for neurological diseases has recently achieved significant progress, with numerous studies investigating the use of adeno-associated viruses for the targeted delivery of therapeutic genetic fragments. This approach has potential applications for treating incurable diseases, including paralysis and motor impairment caused by spinal cord injury and Parkinson's disease, and it is characterized by dopaminergic neuron degeneration. Recently, several studies have explored the potential of direct lineage reprogramming (DLR) for treating incurable diseases, and highlighted the advantages of DLR over conventional stem cell therapy. However, application of DLR technology in clinical practice is hindered by its low efficiency compared with cell therapy using stem cell differentiation. To overcome this limitation, researchers have explored various strategies such as the efficiency of DLR. In this study, we focused on innovative strategies, including the use of a nanoporous particle-based gene delivery system to improve the reprogramming efficiency of DLR-induced neurons. We believe that discussing these approaches can facilitate the development of more effective gene therapies for neurological disorders.
引用
收藏
页数:17
相关论文
共 50 条
  • [31] There Must Be a Way Out of Here: Identifying a Safe and Efficient Combination of Promoter, Transgene, and Vector Backbone for Gene Therapy of Neurological Disease
    Lowenstein, P. R.
    Yadav, Viveka Nand
    Chockley, Peter
    Castro, Maria
    MOLECULAR THERAPY, 2014, 22 (02) : 246 - 247
  • [32] Application and perspective of CRISPR/Cas9 genome editing technology in human diseases modeling and gene therapy
    Zhang, Man-Ling
    Li, Hong-Bin
    Jin, Yong
    FRONTIERS IN GENETICS, 2024, 15
  • [33] Aspects of Gene Therapy Products Using Current Genome-Editing Technology in Japan
    Yamaguchi, Teruhide
    Uchida, Eriko
    Okada, Takashi
    Ozawa, Keiya
    Onodera, Masafumi
    Kume, Akihiro
    Shimada, Takashi
    Takahashi, Satoru
    Tani, Kenzaburo
    Nasu, Yasutomo
    Mashimo, Tomoji
    Mizuguchi, Hiroyuki
    Mitani, Kohnosuke
    Maki, Kazushige
    HUMAN GENE THERAPY, 2020, 31 (19-20) : 1043 - 1053
  • [34] Gene therapy for human ovarian cancer cells using efficient expression of Fas gene combined with γδT cells
    Lin, Jiajing
    Zeng, Dingyuan
    He, Hongying
    Tan, Guangping
    Lan, Ying
    Jiang, Fuyan
    Sheng, Shuting
    MOLECULAR MEDICINE REPORTS, 2017, 16 (04) : 3791 - 3798
  • [35] CTGCT, Centre of Excellence for the Technologies of Gene and Cell Therapy: Collaborative translation of scientific discoveries into advanced treatments for neurological rare genetic diseases and cancer
    Presen, Darja Marolt
    Lainscek, Dusko
    Kinghorn, Jane
    Sebestyen, Zsolt
    Kuball, Jurgen
    Amini, Leila
    Reinke, Petra
    Fuchs, Anke
    Jerala, Roman
    Bencina, Mojca
    COMPUTATIONAL AND STRUCTURAL BIOTECHNOLOGY JOURNAL, 2025, 27 : 10 - 16
  • [36] Efficient Transduction of Corneal Stroma by Adeno-Associated Viral Serotype Vectors for Implications in Gene Therapy of Corneal Diseases
    Lu, Yi
    Ai, Jianzhong
    Gessler, Dominic
    Su, Qin
    Tran, Karen
    Zheng, Qiang
    Xu, Xun
    Gao, Guangping
    HUMAN GENE THERAPY, 2016, 27 (08) : 598 - 608
  • [37] Efficient CNS targeting in adult mice by intrathecal infusion of single-stranded AAV9-GFP for gene therapy of neurological disorders
    Bey, K.
    Ciron, C.
    Dubreil, L.
    Deniaud, J.
    Ledevin, M.
    Cristini, J.
    Blouin, V.
    Aubourg, P.
    Colle, M-A
    GENE THERAPY, 2017, 24 (05) : 325 - 332
  • [38] A gene therapy approach to treat demyelinating diseases using nonreplicative herpetic vectors engineered to produce cytokines
    Martino, G
    Furlan, R
    Galbiati, F
    Poliani, PL
    Bergami, A
    Grimaldi, LME
    Adorini, L
    Comi, G
    MULTIPLE SCLEROSIS, 1998, 4 (03): : 222 - 227
  • [39] Adenovirus for neurodegenerative diseases: In vivo strategies and ex vivo gene therapy using human neural progenitors
    Sabate, O
    Barkats, M
    BucCaron, MH
    CastelBarthe, MN
    Finiels, F
    Horellou, P
    Revah, F
    Mallet, J
    CLINICAL NEUROSCIENCE, 1996, 3 (05) : 317 - 321
  • [40] Efficient siRNA delivery using water soluble lipopolymer for anti-anglogenic gene therapy
    Kim, Won Jong
    Chang, Chien-Wen
    Lee, Minhyung
    Kim, Sung Wan
    JOURNAL OF CONTROLLED RELEASE, 2007, 118 (03) : 357 - 363