神经管有机体:研究发育时间的新系统

IF 4.5 3区 医学 Q2 CELL & TISSUE ENGINEERING
Stem Cell Reviews and Reports Pub Date : 2024-11-01 Epub Date: 2024-09-04 DOI:10.1007/s12015-024-10785-5
Alexa Rabeling, Amy van der Hoven, Nathalie Andersen, Mubeen Goolam
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引用次数: 0

摘要

神经管(NT)是胚胎发育过程中形成的瞬时结构,可发育成大脑和脊髓。虽然小鼠模型常用来代替人类胚胎研究神经管的发育,但物种间的差异限制了其适用性。其中一个主要的差异是发育时间,人的神经管从神经板形成需要16天,而小鼠只需4天,而且形成神经元亚型和完成神经发生所需的时间也不同。神经管器官组织(NTOs)是研究NT体外发育的一种新方法。虽然小鼠和人类的 NTOs 已被证明能再现神经管形成的主要发育过程,但其是否能再现物种特异性的发育时间(也称为异时性)还不得而知。本综述总结了目前使用小鼠和人类 NTO 进行的研究,并比较了发育时间事件,以评估器官组织中是否保持了异时性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Neural Tube Organoids: A Novel System to Study Developmental Timing.

Neural Tube Organoids: A Novel System to Study Developmental Timing.

The neural tube (NT) is a transient structure formed during embryogenesis which develops into the brain and spinal cord. While mouse models have been commonly used in place of human embryos to study NT development, species-specific differences limit their applicability. One major difference is developmental timing, with NT formation from the neural plate in 16 days in humans compared to 4 days in mice, as well as differences in the time taken to form neuronal subtypes and complete neurogenesis. Neural tube organoids (NTOs) represent a new way to study NT development in vitro. While mouse and human NTOs have been shown to recapitulate the major developmental events of NT formation; it is unknown whether species-specific developmental timing, also termed allochrony, is also recapitulated. This review summarises current research using both mouse and human NTOs and compares developmental timing events in order to assess if allochrony is maintained in organoids.

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来源期刊
Stem Cell Reviews and Reports
Stem Cell Reviews and Reports 医学-细胞生物学
CiteScore
9.30
自引率
4.20%
发文量
0
审稿时长
3 months
期刊介绍: The purpose of Stem Cell Reviews and Reports is to cover contemporary and emerging areas in stem cell research and regenerative medicine. The journal will consider for publication: i) solicited or unsolicited reviews of topical areas of stem cell biology that highlight, critique and synthesize recent important findings in the field. ii) full length and short reports presenting original experimental work. iii) translational stem cell studies describing results of clinical trials using stem cells as therapeutics. iv) papers focused on diseases of stem cells. v) hypothesis and commentary articles as opinion-based pieces in which authors can propose a new theory, interpretation of a controversial area in stem cell biology, or a stem cell biology question or paradigm. These articles contain more speculation than reviews, but they should be based on solid rationale. vi) protocols as peer-reviewed procedures that provide step-by-step descriptions, outlined in sufficient detail, so that both experts and novices can apply them to their own research. vii) letters to the editor and correspondence. In order to facilitate this exchange of scientific information and exciting novel ideas, the journal has created five thematic sections, focusing on: i) the role of adult stem cells in tissue regeneration; ii) progress in research on induced pluripotent stem cells, embryonic stem cells and mechanism governing embryogenesis and tissue development; iii) the role of microenvironment and extracellular microvesicles in directing the fate of stem cells; iv) mechanisms of stem cell trafficking, stem cell mobilization and homing with special emphasis on hematopoiesis; v) the role of stem cells in aging processes and cancerogenesis.
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