Generation of functional organs and tissues using organism interspecific blastocyst complementation

利用生物体种间囊胚互补生成功能器官和组织

• 批准号: 10182224
• 负责人: Juan Carlos Izpisua Belmonte
• 金额: $ 48.1万
• 依托单位: SALK INSTITUTE FOR BIOLOGICAL STUDIES
• 依托单位国家: 美国
• 财政年份: 2016
• 资助国家: 美国
• 起止时间: 2016-09-30 至 2022-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10182224
• 关键词: Address; Animals; Architecture; CRISPR/Cas technology; Cell Lineage; Cells; Complement; Development; Disease; Embryonic Development; Evolution; Family suidae; Future; Generations; Genes; Genetic; Genetic Complementation Test; Genetic Processes; Genome engineering; Guide RNA; Human; In Vitro; Injections; Knock-out; Life; Mediating; Messenger RNA; Molecular Genetics; Nature; Organ; Organ Donor; Organ Transplantation; Organism; Pluripotent Stem Cells; Primates; Production; Regenerative Medicine; Replacement Therapy; Safety; System; Tissues; Work; base; blastocyst; blastomere structure; cell type; clinical application; complement system; genome editing; in vivo; knockout animal; knockout gene; nonhuman primate; novel; organ growth; programs; spatiotemporal; tool; zygote

PROJECT SUMMARY: In vitro differentiation of cultured pluripotent stem cells (PSCs) provides a promising tool for the generation of specific cell types useful for cell replacement therapies. Despite rapid progress over the last decade, numerous challenges encompassing cell-production quantity, quality and safety remain to be addressed before full-fledged clinical application becomes a reality. Moreover, generation of functional organs from cultured PSCs, a much needed breakthrough to meet the rising demands for organ donors, remains improbable. This is largely due to our limited understanding of molecular and genetic processes underlying in vivo tissue/organ generation, which has been perfected through millions of years’ evolution. Nature has evolved a sophisticated and robust system to generate functional tissues and organs during normal course of embryo development. The intrinsic genetic program works seamlessly with extrinsic developmental niches in a perfect spatiotemporal manner to enable embryonic cells to commit to specific cell lineages and be organized into higher-order tissue architectures. Blastocyst complementation is based on emptying these developmental niches created by knocking out gene(s) critical for the specific tissue/organ development and use donor chimeric-competent PSCs to colonize the vacant niche and generate desired tissues/organs of donor origin. With the booming of CRISPR/CAS9-mediated genome engineering gene knockout animals can be generated with high efficiency by co-injection of Cas9 mRNA and gRNAs directly into zygotes. Also, chimeric-competent primate PSCs have seen several promising developments very recently. By combining the strength of zygote genome editing and chimeric-competent primate PSCs, we propose to establish a novel interspecific blastocyst complementation system for the generation of functional organs in a large animal host, the pig. For this first study, we will focus on using PSCs derived from non-human primate species, to evaluate the efficacy and safety of our proposed strategy. Our study will provide critical information for future application into humans. If successful, this approach will lead to a paradigm shift in regenerative medicine and will help to overcome the shortage of organ donors.

项目总结： 培养的多能干细胞(PSCs)的体外分化为产生用于细胞替代治疗的特定细胞类型提供了一种有前途的工具。尽管在过去十年中取得了快速进展，但在全面临床应用成为现实之前，围绕细胞生产数量、质量和安全性的众多挑战仍有待解决。此外，从培养的PSCs中产生功能器官仍然是不可能的，这是满足日益增长的器官捐赠者需求所亟需的突破。这在很大程度上是因为我们对体内组织/器官生成背后的分子和遗传过程的了解有限，这一过程已经经过数百万年的进化而完善。自然界已经进化出一种复杂而强大的系统，在胚胎发育的正常过程中产生功能组织和器官。内在遗传程序以完美的时空方式与外部发育的利基环境无缝合作，使胚胎细胞能够致力于特定的细胞谱系，并被组织成更高级别的组织结构。胚泡互补是基于清空这些通过敲除对特定组织/器官发育至关重要的基因(S)而产生的发育生态位，并使用供体嵌合能力强的PSCs来定植空白的生态位并产生所需的供体来源的组织/器官。随着CRISPR/Cas9介导的基因组工程的蓬勃发展，通过将Cas9mRNA和gRNAs共同注射到受精卵中，可以高效地产生基因敲除动物。此外，具有嵌合能力的灵长类PSCs最近也有了一些很有前途的发展。通过结合受精卵基因组编辑和嵌合能力强的灵长类PSCs的优势，我们建议建立一种新的种间囊胚互补系统，用于大型动物宿主猪的功能器官的生成。在第一项研究中，我们将重点使用来自非人类灵长类物种的PSCs，以评估我们建议的策略的有效性和安全性。我们的研究将为将来应用于人类提供关键信息。如果成功，这种方法将导致再生医学范式的转变，并将有助于克服器官捐赠者短缺的问题。

项目成果

CRISPR-Cas9 mediated one-step disabling of pancreatogenesis in pigs.

• DOI: 10.1038/s41598-017-08596-5
• 发表时间: 2017-09-05
• 期刊: Scientific reports
• 影响因子: 4.6
• 作者: Wu J;Vilarino M;Suzuki K;Okamura D;Bogliotti YS;Park I;Rowe J;McNabb B;Ross PJ;Belmonte JCI
• 通讯作者: Belmonte JCI