Höving Anna L, Windmöller Beatrice A, Knabbe Cornelius, Kaltschmidt Barbara, Kaltschmidt Christian, Greiner Johannes F W
Department of Cell Biology, University of Bielefeld, Bielefeld, Germany.
Institute for Laboratory- and Transfusion Medicine, Heart and Diabetes Centre North Rhine-Westphalia (NRW), Ruhr University Bochum, Bad Oeynhausen, Germany.
Front Cell Dev Biol. 2021 Apr 8;9:662754. doi: 10.3389/fcell.2021.662754. eCollection 2021.
Stem cells of the neural crest (NC) vitally participate to embryonic development, but also remain in distinct niches as quiescent neural crest-derived stem cell (NCSC) pools into adulthood. Although NCSC-populations share a high capacity for self-renewal and differentiation resulting in promising preclinical applications within the last two decades, inter- and intrapopulational differences exist in terms of their expression signatures and regenerative capability. Differentiation and self-renewal of stem cells in developmental and regenerative contexts are partially regulated by the niche or culture condition and further influenced by single cell decision processes, making cell-to-cell variation and heterogeneity critical for understanding adult stem cell populations. The present review summarizes current knowledge of the cellular heterogeneity within NCSC-populations located in distinct craniofacial and trunk niches including the nasal cavity, olfactory bulb, oral tissues or skin. We shed light on the impact of intrapopulational heterogeneity on fate specifications and plasticity of NCSCs in their niches as well as during culture. We further discuss underlying molecular regulators determining fate specifications of NCSCs, suggesting a regulatory network including NF-κB and NC-related transcription factors like SLUG and SOX9 accompanied by Wnt- and MAPK-signaling to orchestrate NCSC stemness and differentiation. In summary, adult NCSCs show a broad heterogeneity on the level of the donor and the donors' sex, the cell population and the single stem cell directly impacting their differentiation capability and fate choices and . The findings discussed here emphasize heterogeneity of NCSCs as a crucial parameter for understanding their role in tissue homeostasis and regeneration and for improving their applicability in regenerative medicine.
神经嵴(NC)干细胞在胚胎发育中起着至关重要的作用,而且在成年后,它们还作为静止的神经嵴衍生干细胞(NCSC)库存在于不同的微环境中。尽管在过去二十年中,NCSC群体具有高度的自我更新和分化能力,在临床前应用方面前景广阔,但在表达特征和再生能力方面,群体间和群体内存在差异。在发育和再生环境中,干细胞的分化和自我更新部分受微环境或培养条件的调节,并进一步受到单细胞决策过程的影响,这使得细胞间的变异和异质性对于理解成体干细胞群体至关重要。本综述总结了目前关于位于不同颅面和躯干微环境(包括鼻腔、嗅球、口腔组织或皮肤)中的NCSC群体细胞异质性的知识。我们阐明了群体内异质性对NCSC在其微环境以及培养过程中的命运决定和可塑性的影响。我们进一步讨论了决定NCSC命运决定的潜在分子调节因子,提出了一个包括NF-κB和NC相关转录因子(如SLUG和SOX9)以及Wnt和MAPK信号的调节网络,以协调NCSC的干性和分化。总之,成年NCSC在供体及其性别、细胞群体和单个干细胞水平上表现出广泛的异质性,这直接影响它们的分化能力和命运选择。这里讨论的研究结果强调了NCSC的异质性是理解它们在组织稳态和再生中的作用以及提高它们在再生医学中适用性的关键参数。