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嗅觉上皮中的神经发生与细胞死亡

Neurogenesis and cell death in olfactory epithelium.

作者信息

Calof A L, Hagiwara N, Holcomb J D, Mumm J S, Shou J

机构信息

Department of Anatomy and Neurobiology, University of California, Irvine, College of Medicine 92717-1275, USA.

出版信息

J Neurobiol. 1996 May;30(1):67-81. doi: 10.1002/(SICI)1097-4695(199605)30:1<67::AID-NEU7>3.0.CO;2-E.

Abstract

The olfactory epithelium (OE) of the mammal is uniquely suited as a model system for studying how neurogenesis and cell death interact to regulate neuron number during development and regeneration. To identify factors regulating neurogenesis and neuronal death in the OE, and to determine the mechanisms by which these factors act, investigators studied OE using two major experimental paradigms: tissue culture of OE; and ablation of the olfactory bulb or severing the olfactory nerve in adult animals, procedures that induce cell death and a subsequent surge of neurogenesis in the OE in vivo. These studies characterized the cellular stages in the olfactory receptor neuron (ORN) lineage, leading to the realization that at least three distinct stages of proliferating neuronal precursor cells are employed in generating ORNs. The identification of a number of factors that act to regulate proliferation and survival of ORNs and their precursors suggests that these multiple developmental stages may serve as control points at which cell number is regulated by extrinsic factors. In vivo surgical studies, which have shown that all cell types in the neuronal lineage of the OE undergo apoptotic cell death, support this idea. These studies, and the possible coregulation of neuronal birth and apoptosis in the OE, are discussed.

摘要

哺乳动物的嗅觉上皮(OE)是研究神经发生和细胞死亡如何相互作用以在发育和再生过程中调节神经元数量的独特模型系统。为了确定调节OE中神经发生和神经元死亡的因素,并确定这些因素的作用机制,研究人员使用了两种主要的实验范式来研究OE:OE的组织培养;以及在成年动物中切除嗅球或切断嗅神经,这些操作会在体内诱导OE中的细胞死亡以及随后的神经发生激增。这些研究对嗅觉受体神经元(ORN)谱系中的细胞阶段进行了表征,从而认识到在生成ORN的过程中至少使用了三个不同阶段的增殖神经元前体细胞。对一些调节ORN及其前体细胞增殖和存活的因素的鉴定表明,这些多个发育阶段可能作为控制点,在这些点上细胞数量由外在因素调节。体内手术研究表明,OE神经元谱系中的所有细胞类型都会经历凋亡性细胞死亡,这支持了这一观点。本文讨论了这些研究以及OE中神经元生成和凋亡可能的共同调节。

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