The Origin and Regulation of Neuromesodermal Progenitors (NMPs) in Embryos.

Cells

Laboratory for Embryology, Institute for Advanced Medical Sciences, Tokushima University, Tokushima 770-8503, Japan.

Published: March 2024

AI Article Synopsis

  • Neuromesodermal progenitors (NMPs) are key players in both neural and paraxial mesoderm development during embryogenesis, sparking interest for their role in organ formation and in vitro modeling.
  • The study emphasizes several aspects of NMPs, including their tissue organization, the influence of N1 enhancer activity from the epiblast, and the importance of Tbx6 in the development of paraxial mesoderm.
  • Additionally, it highlights the identification of nephric mesenchyme as an NMP derivative, the changeover from tissue-specific progenitors to NMPs at the forelimb bud level, and the role of Wnt3a signaling in supporting the growth of N

Article Abstract

Neuromesodermal progenitors (NMPs), serving as the common origin of neural and paraxial mesodermal development in a large part of the trunk, have recently gained significant attention because of their critical importance in the understanding of embryonic organogenesis and the design of in vitro models of organogenesis. However, the nature of NMPs at many essential points remains only vaguely understood or even incorrectly assumed. Here, we discuss the nature of NMPs, focusing on their dynamic migratory behavior during embryogenesis and the mechanisms underlying their neural vs. mesodermal fate choice. The discussion points include the following: (1) How the sinus rhomboidals is organized; the tissue where the neural or mesodermal fate choice of NMPs occurs. (2) NMPs originating from the broad posterior epiblast are associated with N1 enhancer activity. (3) Tbx6-dependent repression occurs during NMP-derived paraxial mesoderm development. (4) The nephric mesenchyme, a component of the intermediate mesoderm, was newly identified as an NMP derivative. (5) The transition of embryonic tissue development from tissue-specific progenitors in the anterior part to that from NMPs occurs at the forelimb bud axial level. (6) The coexpression of Sox2 and Bra in NMPs is conditional and is not a hallmark of NMPs. (7) The ability of the NMP pool to sustain axial embryo growth depends on Wnt3a signaling in the NMP population. Current in vitro models of NMPs are also critically reviewed.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10968745PMC
http://dx.doi.org/10.3390/cells13060549DOI Listing

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