Faruqu Farid N, Zhou Shuai, Sami Noor, Gheidari Fatemeh, Lu Han, Al-Jamal Khuloud T
Institute of Pharmaceutical Science King's College London London UK.
Genomics Centre King's College London London UK.
FASEB Bioadv. 2020 Jun 28;2(7):419-433. doi: 10.1096/fba.2020-00025. eCollection 2020 Jul.
Stem cell-derived exosomes have been identified as novel cell-free therapeutics for regenerative medicine. Three-dimensional (3D) culture of stem cells were reported to improve their "stemness" and therapeutic efficacy. This work focused on establishing serum-free 3D culture of dental pulp pluripotent-like stem cells (DPPSCs)-a newly characterized pluripotent-like stem cell for exosome production. DPPSCs were expanded in regular 2D culture in human serum-supplemented (HS)-medium and transferred to a micropatterned culture plate for 3D culture in HS-medium (default) and medium supplemented with KnockOut™ serum replacement (KO-medium). Bright-field microscopy observation throughout the culture period (24 days) revealed that DPPSCs in KO-medium formed spheroids of similar morphology and size to that in HS-medium. qRT-PCR analysis showed similar gene expression in DPPSC spheroids in both HS-medium and KO-medium, but expression significantly increased in the latter. Vesicles isolated from DPPSC spheroids in KO-medium in the first 12 days of culture showed sizes that fall within the exosomal size range by nanoparticle tracking analysis (NTA) and express the canonical exosomal markers. It is concluded that 3D culture of DPPSCs in KO-medium provided an optimal serum-free condition for successful isolation of DPPSC-derived exosomes for subsequent applications in regenerative medicine.
干细胞衍生的外泌体已被确定为再生医学中新型的无细胞疗法。据报道,干细胞的三维(3D)培养可改善其“干性”和治疗效果。这项工作的重点是建立牙髓多能样干细胞(DPPSCs)的无血清3D培养体系,DPPSCs是一种新鉴定的用于生产外泌体的多能样干细胞。DPPSCs在添加人血清(HS)的培养基中进行常规二维培养扩增,然后转移到微图案培养板中,在HS培养基(默认)和添加KnockOut™血清替代物的培养基(KO培养基)中进行3D培养。在整个培养期(24天)的明场显微镜观察显示,KO培养基中的DPPSCs形成的球体在形态和大小上与HS培养基中的相似。qRT-PCR分析表明,HS培养基和KO培养基中DPPSC球体的基因表达相似,但在后者中表达显著增加。通过纳米颗粒跟踪分析(NTA),从培养前12天KO培养基中的DPPSC球体中分离出的囊泡大小在外泌体大小范围内,并表达典型的外泌体标志物。得出的结论是,在KO培养基中对DPPSCs进行3D培养为成功分离DPPSC衍生的外泌体提供了最佳的无血清条件,以便随后应用于再生医学。