Institute of Neuroanatomy, University Medical Center, Georg-August-University Goettingen, 37075, Goettingen, Germany.
Zoology Department, Faculty of Science, Alexandria University, Alexandria, Egypt.
Mol Neurobiol. 2018 Nov;55(11):8306-8327. doi: 10.1007/s12035-018-0987-y. Epub 2018 Mar 12.
The postnatal mammalian olfactory epithelium (OE) represents a major aspect of the peripheral olfactory system. It is a pseudostratified tissue that originates from the olfactory placode and is composed of diverse cells, some of which are specialized receptor neurons capable of transducing odorant stimuli to afford the perception of smell (olfaction). The OE is known to offer a tractable miniature model for studying the systematic generation of neurons and glia that typify neural tissue development. During OE development, stem/progenitor cells that will become olfactory sensory neurons and/or non-neuronal cell types display fine spatiotemporal expression of neuronal and non-neuronal genes that ensures their proper proliferation, differentiation, survival, and regeneration. Many factors, including transcription and epigenetic factors, have been identified as key regulators of the expression of such requisite genes to permit normal OE morphogenesis. Typically, specific interactive regulatory networks established between transcription and epigenetic factors/cofactors orchestrate histogenesis in the embryonic and adult OE. Hence, investigation of these regulatory networks critical for OE development promises to disclose strategies that may be employed in manipulating the stepwise transition of olfactory precursor cells to become fully differentiated and functional neuronal and non-neuronal cell types. Such strategies potentially offer formidable means of replacing injured or degenerated neural cells as therapeutics for nervous system perturbations. This review recapitulates the developmental cellular diversity of the olfactory neuroepithelium and discusses findings on how the precise and cooperative molecular control by transcriptional and epigenetic machinery is indispensable for OE ontogeny.
产后哺乳动物嗅上皮(OE)是外周嗅觉系统的主要组成部分。它是一种假复层组织,起源于嗅基板,由多种细胞组成,其中一些是专门的受体神经元,能够将气味刺激转化为嗅觉(嗅觉)。OE 被认为是研究典型神经组织发育中神经元和神经胶质系统生成的可行微型模型。在 OE 发育过程中,将成为嗅觉感觉神经元和/或非神经元细胞类型的干细胞/祖细胞表现出神经元和非神经元基因的精细时空表达,以确保其适当的增殖、分化、存活和再生。许多因素,包括转录和表观遗传因素,已被确定为调控此类必需基因表达的关键调节剂,以允许正常 OE 形态发生。通常,转录和表观遗传因子/共因子之间建立的特定交互调节网络协调胚胎和成年 OE 的组织发生。因此,对这些对 OE 发育至关重要的调节网络的研究有望揭示可用于操纵嗅觉前体细胞逐步过渡为完全分化和功能神经元和非神经元细胞类型的策略。这些策略可能为神经系统紊乱的治疗提供有价值的手段,即用替代受损或退化的神经细胞。本综述概括了嗅神经上皮的发育细胞多样性,并讨论了转录和表观遗传机制的精确和协作分子控制对 OE 个体发生的不可或缺性。