Ramaswamy Krishna, Yik Wing Yan, Wang Xiao-Ming, Oliphant Erin N, Lu Wange, Shibata Darryl, Ryder Oliver A, Hacia Joseph G
Department of Biochemistry and Molecular Biology, University of Southern California, Los Angeles, CA, USA.
Department of Preventive Medicine, University of Southern California, Los Angeles, CA, USA.
BMC Res Notes. 2015 Oct 16;8:577. doi: 10.1186/s13104-015-1567-0.
Orangutans are an endangered species whose natural habitats are restricted to the Southeast Asian islands of Borneo and Sumatra. Along with the African great apes, orangutans are among the closest living relatives to humans. For potential species conservation and functional genomics studies, we derived induced pluripotent stem cells (iPSCs) from cryopreserved somatic cells obtained from captive orangutans.
Primary skin fibroblasts from two Sumatran orangutans were transduced with retroviral vectors expressing the human OCT4, SOX2, KLF4, and c-MYC factors. Candidate orangutan iPSCs were characterized by global gene expression and DNA copy number analysis. All were consistent with pluripotency and provided no evidence of large genomic insertions or deletions. In addition, orangutan iPSCs were capable of producing cells derived from all three germ layers in vitro through embryoid body differentiation assays and in vivo through teratoma formation in immune-compromised mice.
We demonstrate that orangutan skin fibroblasts are capable of being reprogrammed into iPSCs with hallmark molecular signatures and differentiation potential. We suggest that reprogramming orangutan somatic cells in genome resource banks could provide new opportunities for advancing assisted reproductive technologies relevant for species conservation efforts. Furthermore, orangutan iPSCs could have applications for investigating the phenotypic relevance of genomic changes that occurred in the human, African great ape, and/or orangutan lineages. This provides opportunities for orangutan cell culture models that would otherwise be impossible to develop from living donors due to the invasive nature of the procedures required for obtaining primary cells.
猩猩是一种濒危物种,其天然栖息地仅限于东南亚的婆罗洲和苏门答腊岛。与非洲大猩猩一样,猩猩是现存与人类亲缘关系最近的物种之一。为了进行潜在的物种保护和功能基因组学研究,我们从圈养猩猩的冷冻保存体细胞中获得了诱导多能干细胞(iPSC)。
用表达人类OCT4、SOX2、KLF4和c-MYC因子的逆转录病毒载体转导两只苏门答腊猩猩的原代皮肤成纤维细胞。通过全基因组表达和DNA拷贝数分析对候选猩猩iPSC进行表征。所有结果均与多能性一致,且未提供大的基因组插入或缺失的证据。此外,猩猩iPSC能够通过胚状体分化试验在体外产生来自所有三个胚层的细胞,并通过在免疫缺陷小鼠体内形成畸胎瘤在体内产生这些细胞。
我们证明猩猩皮肤成纤维细胞能够被重编程为具有标志性分子特征和分化潜能的iPSC。我们认为,在基因组资源库中对猩猩体细胞进行重编程可为推进与物种保护相关的辅助生殖技术提供新机会。此外,猩猩iPSC可用于研究人类、非洲大猩猩和/或猩猩谱系中发生的基因组变化的表型相关性。这为猩猩细胞培养模型提供了机会,否则由于获取原代细胞所需程序的侵入性,从活体供体中无法开发出这样的模型。