The genetically modified human foreskin fibroblast cell line (YhFF#۸) stably expressing Cas۹ gene: A lab resource report

سال انتشار: 1402
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 109

فایل این مقاله در 8 صفحه با فرمت PDF قابل دریافت می باشد

استخراج به نرم افزارهای پژوهشی:

لینک ثابت به این مقاله:

شناسه ملی سند علمی:

JR_IJRM-22-1_007

تاریخ نمایه سازی: 7 اسفند 1402

چکیده مقاله:

Background: Stable Cas۹ (CRISPR-associated protein ۹)-expressing cell lines have emerged as valuable tools in genetic research, enhancing the efficiency of the CRISPR/Cas۹ system and streamlining gene editing procedures. These cell lines enable simultaneous editing of multiple genes and reduce the overall editing time. Objective: This study aimed to develop a stable human fibroblast cell line capable of genetic conversion into a mutant form, serving as a cellular model for a specific genetic disease. The established cell line facilitates investigation of disease mechanisms, testing of potential treatments, and gaining insights into underlying molecular processes. Materials and Methods: Human embryonic kidney ۲۹۳LTV cells were used to produce pseudo-virus particles, while Yazd human foreskin fibroblasts batch ۸ (YhFF#۸) cells were targeted for genetic modification. Transfection of human embryonic kidney ۲۹۳LTV cells with pCDH-Cas۹ plasmid DNA generated pseudo-viral particles. YhFF#۸ cells were transduced and selected using antibiotics. Green fluorescent protein (GFP) detection confirmed successful transduction and selection. Relative expression levels of the Cas۹ gene were determined by quantitative polymerase chain reaction. Results: The study validated the fidelity of the Cas۹ gene cassette sequence and its transcriptional activity. Transduced YhFF#۸ cells exhibited green fluorescence, with antibiotic selection resulting in nearly ۱۰۰% transduced cells. A reporter GFP gene enabled real-time monitoring of YhFF#۸-Cas۹-GFP-PuroR cells using fluorescence microscopy. Conclusion: YhFF#۸-Cas۹-GFP-PuroR cells, labeled and susceptible to genomic editing, provide an optimal source for generating induced pluripotent stem cell lines for future biomedical research.

نویسندگان

Farzad Soheilipour

Stem Cell Biology Research Center, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran. Department of Biology, Faculty of Basic Sciences, Gonbad Kavous University, Gonbad Kavous, Iran.

Sohrab Boozarpour

Department of Biology, Faculty of Basic Sciences, Gonbad Kavous University, Gonbad Kavous, Iran.

Shiva Aghaei

Stem Cell Biology Research Center, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.

Ehsan Farashahi Yazd

Stem Cell Biology Research Center, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.

مراجع و منابع این مقاله:

لیست زیر مراجع و منابع استفاده شده در این مقاله را نمایش می دهد. این مراجع به صورت کاملا ماشینی و بر اساس هوش مصنوعی استخراج شده اند و لذا ممکن است دارای اشکالاتی باشند که به مرور زمان دقت استخراج این محتوا افزایش می یابد. مراجعی که مقالات مربوط به آنها در سیویلیکا نمایه شده و پیدا شده اند، به خود مقاله لینک شده اند :
  • Carrillo-Ávila JA, Catalina P, Aguilar-Quesada R. Quality control of cell ...
  • Capes-Davis A, Bairoch A, Barrett T, Burnett EC, Dirks WG, ...
  • Dumont J, Euwart D, Mei B, Estes S, Kshirsagar R. ...
  • Genzel Y. Designing cell lines for viral vaccine production: Where ...
  • Peng Y, Ma A, Xiao Zh, Hao J, Feng R, ...
  • Xu Y, Li Zh. CRISPR-Cas systems: Overview, innovations and applications ...
  • Caneparo Ch, Baratange C, Chabaud S, Bolduc S. Conditioned medium ...
  • Fernandes IR, Russo FB, Pignatari GC, Evangelinellis MM, Tavolari S, ...
  • Mesdom P, Colle R, Lebigot E, Trabado S, Deflesselle E, ...
  • Han X, Liu Z, Jo MC, Zhang K, Li Y, ...
  • DeWitt MA, Corn JE, Carroll D. Genome editing via delivery ...
  • Suchý T, Kaczmarek I, Maricic T, Zieschang C, Schöneberg T, ...
  • Javaid N, Choi S. CRISPR/Cas system and factors affecting its ...
  • Aregger M, Chandrashekhar M, Tong AHY, Chan K, Moffat J. ...
  • Yu H, Wu Zh, Chen X, Ji Q, Tao Sh. ...
  • Dong W, Kantor B. Lentiviral vectors for delivery of gene-editing ...
  • Liao JQ, Zhou G, Zhou Y. Generation of monoclonal iPSC ...
  • Aubrey BJ, Kelly GL, Kueh AJ, Brennan MS, O'Connor L, ...
  • Pfaffl MW. A new mathematical model for relative quantification in ...
  • Fernandez JP, Vejnar ChE, Giraldez AJ, Rouet R, Moreno-Mateos MA. ...
  • Lino CA, Harper JC, Carney JP, Timlin JA. Delivering CRISPR: ...
  • Campa CC, Weisbach NR, Santinha AJ, Incarnato D, Platt RJ. ...
  • Lo ChA, Greben AW, Chen BE. Generating stable cell lines ...
  • Hajizadeh-Tafti F, Golzadeh J, Farashahi-Yazd E, Heidarian-Meimandi H, Aflatoonian B. ...
  • Ryø LB, Thomsen EA, Mikkelsen JG. Production and validation of ...
  • Wang X, Xu Zh, Tian Zh, Zhang X, Xu D, ...
  • Wen J, Wu J, Cao T, Zhi S, Chen Y, ...
  • Ellis J. Silencing and variegation of gammaretrovirus and lentivirus vectors. ...
  • Schlesinger Sh, Goff SP. Silencing of proviruses in embryonic cells: ...
  • Herbst F, Ball CR, Tuorto F, Nowrouzi A, Wang W, ...
  • Khacho M, Mekhail K, Pilon-Larose K, Pause A, Côté J, ...
  • نمایش کامل مراجع