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调节小鼠嗅觉上皮中神经发生和程序性细胞死亡的因素。

Factors regulating neurogenesis and programmed cell death in mouse olfactory epithelium.

作者信息

Calof A L, Rim P C, Askins K J, Mumm J S, Gordon M K, Iannuzzelli P, Shou J

机构信息

Department of Anatomy & Neurobiology, University of California, Irvine, College of Medicine 92697-1275, USA.

出版信息

Ann N Y Acad Sci. 1998 Nov 30;855:226-9. doi: 10.1111/j.1749-6632.1998.tb10571.x.

Abstract

To identify factors regulating neurogenesis and programmed cell death in mouse olfactory epithelium (OE), and to determine the mechanisms by which these factors act, we have studied mouse OE using two major experimental paradigms: tissue culture of embryonic OE and cell types isolated from it; and ablation of the olfactory bulb ('bulbectomy') of adult mice, a procedure that induces programmed cell death of olfactory receptor neurons (ORNS) and a subsequent surge of neurogenesis in the OE in vivo. Such experiments have been used to characterize the cellular stages in the ORN lineage, leading to the realization that there are at least two distinct stages of proliferating neuronal progenitor cells interposed between the ORN and the stem cell that ultimately gives rise to it. The identification of a number of different factors that act to regulate proliferation and survival of ORNs and progenitor cells suggests that these multiple cell stages may each serve as a control point at which neuron number in the OE is regulated. Our recent studies of neuronal colony-forming progenitors (putative stem cells) of the OE suggest that even these cells, at the earliest stage in the ORN lineage so far identified, are subject to such regulation: if colony-forming progenitors are cultured in the presence of a large excess of differentiated ORNs, then the production of new neurons by progenitors is dramatically inhibited. This result suggests that differentiated ORNs produce a signal that feeds back to inhibit neurogenesis by their own progenitors, and provides a possible explanation for the observation that ORN death, consequent to bulbectomy, results in increased neurogenesis in the OE in vivo: death of ORNs may release neuronal progenitor cells from this inhibitory signal, produced by the differentiated ORNs that lie near them in the OE. Our current experiments are directed toward identifying the molecular basis of this inhibitory signal, and the cellular mechanism(s) by which it acts.

摘要

为了确定调节小鼠嗅上皮(OE)中神经发生和程序性细胞死亡的因素,并确定这些因素发挥作用的机制,我们使用了两种主要的实验范式来研究小鼠OE:胚胎OE的组织培养及其分离出的细胞类型;以及成年小鼠嗅球切除(“嗅球切除术”),该手术会诱导嗅觉受体神经元(ORN)程序性细胞死亡,并随后在体内OE中引发神经发生激增。此类实验已用于表征ORN谱系中的细胞阶段,从而认识到在ORN和最终产生它的干细胞之间至少存在两个不同的增殖神经元祖细胞阶段。已鉴定出许多调节ORN和祖细胞增殖与存活的不同因素,这表明这些多个细胞阶段可能各自作为调控OE中神经元数量的控制点。我们最近对OE的神经元集落形成祖细胞(假定的干细胞)的研究表明,即使是这些在迄今已鉴定的ORN谱系最早阶段的细胞,也受到这种调控:如果在大量分化的ORN存在下培养集落形成祖细胞,那么祖细胞产生新神经元的能力会受到显著抑制。这一结果表明,分化的ORN产生一种信号,反馈抑制其自身祖细胞的神经发生,并为以下观察结果提供了一种可能的解释:嗅球切除术后ORN死亡会导致体内OE中神经发生增加,ORN死亡可能使神经元祖细胞从OE中与其相邻的分化ORN产生的这种抑制信号中释放出来。我们目前的实验旨在确定这种抑制信号的分子基础及其作用的细胞机制。

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