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胰腺发生:从芽到丛到腺。

Pancreas organogenesis: from bud to plexus to gland.

出版信息

Dev Dyn. 2011 Mar;240(3):530-65. doi: 10.1002/dvdy.22584.

Abstract

Pancreas oganogenesis comprises a coordinated and highly complex interplay of signaling events and transcriptional networks that guide a step-wise process of organ development from early bud specification all the way to the final mature organ state. Extensive research on pancreas development over the last few years, largely driven by a translational potential for pancreatic diseases (diabetes, pancreatic cancer, and so on), is markedly advancing our knowledge of these processes. It is a tenable goal that we will one day have a clear, complete picture of the transcriptional and signaling codes that control the entire organogenetic process, allowing us to apply this knowledge in a therapeutic context, by generating replacement cells in vitro, or perhaps one day to the whole organ in vivo. This review summarizes findings in the past 5 years that we feel are amongst the most significant in contributing to the deeper understanding of pancreas development. Rather than try to cover all aspects comprehensively, we have chosen to highlight interesting new concepts, and to discuss provocatively some of the more controversial findings or proposals. At the end of the review, we include a perspective section on how the whole pancreas differentiation process might be able to be unwound in a regulated fashion, or redirected, and suggest linkages to the possible reprogramming of other pancreatic cell-types in vivo, and to the optimization of the forward-directed-differentiation of human embryonic stem cells (hESC), or induced pluripotential cells (iPSC), towards mature β-cells.

摘要

胰腺器官发生包括信号事件和转录网络的协调和高度复杂的相互作用,这些信号事件和转录网络指导器官从早期芽的特化到最终成熟器官状态的逐步发育过程。近年来,由于对胰腺疾病(糖尿病、胰腺癌等)的转化潜力的研究,对胰腺发育的研究有了显著进展,这显著地促进了我们对这些过程的认识。我们的目标是,有一天我们能够清楚地、完整地了解控制整个器官发生过程的转录和信号编码,以便我们能够在治疗学上应用这些知识,通过体外产生替代细胞,或者有一天在体内产生整个器官。这篇综述总结了过去 5 年中我们认为对深入了解胰腺发育最重要的发现。我们没有试图全面涵盖所有方面,而是选择突出一些有趣的新概念,并富有启发性地讨论一些更有争议的发现或建议。在综述的最后,我们包括了一个关于整个胰腺分化过程如何能够以受调控的方式展开或重新定向的观点部分,并提出了与体内其他胰腺细胞类型的可能重编程以及人类胚胎干细胞(hESC)或诱导多能细胞(iPSC)向成熟β细胞的正向分化的优化的联系。

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