Kobayashi Hideyuki, Nakajima Koichi, Oka Yusuke, Tai Toshihiro, Nagao Koichi, Ishii Nobuhisa
Department of Urology Toho University School of Medicine 6-11-1 Omori-Nishi 143-8541 Ota-ku Tokyo Japan.
Reprod Med Biol. 2011 Feb 16;10(2):105-112. doi: 10.1007/s12522-011-0077-6. eCollection 2011 Jun.
Induced pluripotent stem (iPS) cells have been generated from mouse and human fibroblasts by several groups; however, transplanted mouse iPS cells can cause teratomas, depending on their tissue of origin. Therefore, human iPS cells are preferable, and various tissues are being evaluated for their potential to generate human iPS cells.
We examined whether adult human testicular tissue had undergone reprogramming by introducing four transcription factors, OCT4, SOX2, KLF4, and C-MYC, using lentiviral vectors.
We obtained embryonic stem (ES)-like cells derived from human testicular tissue by introducing four cDNAs, encoding the transcription factors OCT4, SOX2, KLF4, and C-MYC, using lentiviral vectors. We showed that DAZL and VASA were expressed in testicular cells but down-regulated in ES-like cells, indicating that the cells had undergone reprogramming. ES-like cells could develop tumors, which is a hallmark of pluripotency, when SCID mice were injected with these cells.
We induced iPS cells from adult human testicular tissue by introducing four transcription factors, OCT4, SOX2, KLF4, and C-MYC, using lentiviral vectors. Future studies on these cells may elucidate the causes of male infertility, and eventually lead to treatments with autologous testicular tissue-derived iPS cells.
多个研究小组已从小鼠和人类成纤维细胞中诱导生成了诱导多能干细胞(iPS细胞);然而,移植的小鼠iPS细胞可能会形成畸胎瘤,这取决于其来源组织。因此,人类iPS细胞更具优势,目前正在评估各种组织生成人类iPS细胞的潜力。
我们使用慢病毒载体导入四种转录因子OCT4、SOX2、KLF4和C-MYC,检测成人睾丸组织是否发生重编程。
我们通过使用慢病毒载体导入编码转录因子OCT4、SOX2、KLF4和C-MYC的四个cDNA,从人类睾丸组织中获得了胚胎干细胞(ES)样细胞。我们发现DAZL和VASA在睾丸细胞中表达,但在ES样细胞中表达下调,这表明细胞已经历重编程。当将这些ES样细胞注射到SCID小鼠体内时,它们能够形成肿瘤,这是多能性的一个标志。
我们通过使用慢病毒载体导入四种转录因子OCT4、SOX2、KLF4和C-MYC,从成人睾丸组织中诱导生成了iPS细胞。对这些细胞的进一步研究可能会阐明男性不育的原因,并最终实现用自体睾丸组织来源的iPS细胞进行治疗。