Schwob J E, Youngentob S L, Mezza R C
Department of Anatomy and Cell Biology, State University of New York Health Science Center, Syracuse 13210, USA.
J Comp Neurol. 1995 Aug 14;359(1):15-37. doi: 10.1002/cne.903590103.
The olfactory epithelium and its neuronal population are known to have a substantial capacity to recover after either direct injury or damage to the olfactory nerve. However, the mechanisms underlying that capacity for recovery, and indeed the limits on the recovery process, are not well understood. The aim of this study is to describe in detail the way in which the olfactory epithelium reconstitutes after direct injury. Adult male rats were exposed to 330 ppm methyl bromide (MeBr) gas for a single 6-hour period. The exposure destroys all of the neurons and sustentacular cells in over 95% of the olfactory epithelium of food-restricted rats and in over 90% of the epithelium in ad-libitum-fed rats of the same weight, yet substantial recovery of the olfactory epithelium occurs. In response to the lesion, cellular proliferation increases markedly beginning between 24 and 48 hours, peaks at 1 week, and persists at levels higher than the control level for more than 4 weeks after MeBr exposure. Even though proliferation accelerates promptly, the beginning of neuronal reconstitution is delayed; only a few immature neurons are observed 3 days after the lesion, yet they reappear in large numbers by the end of the first week. The first mature neurons emerge between 7 and 14 days after lesion and increase to near normal numbers by 4-6 weeks. In association with the restoration of the neuronal population, basal cell proliferation returns to control levels between 4 and 6 weeks after damage. Likewise, sustentacular cells, identifiable by anticytokeratin 18 labeling, reappear rapidly and reform a distinct lamina in the superficial aspect of the epithelium. They closely resemble their counterparts in control epithelium with regard to disposition and shape by 3 weeks after lesion and with regard to expression of olfactory-specific cytochrome P450s by 8 weeks. Thus, most areas of the epithelium are restored to a near normal appearance and cellular composition by the end of 8 weeks, suggesting that the MeBr paradigm for lesioning the epithelium offers significant advantages over techniques such as Triton X-100 or ZnSO4 irrigation. However, not all measures of epithelial status are normal even at 8 weeks. Immature neurons remain slightly more numerous than normal at this time. Furthermore, some areas of the olfactory epithelium do not recover after MeBr lesion and are replaced by respiratory epithelium.(ABSTRACT TRUNCATED AT 400 WORDS)
已知嗅觉上皮及其神经元群体在受到直接损伤或嗅神经受损后具有显著的恢复能力。然而,这种恢复能力背后的机制以及恢复过程的限度尚未得到充分理解。本研究的目的是详细描述嗅觉上皮在直接损伤后重新构建的方式。成年雄性大鼠在单一的6小时内暴露于330 ppm的溴甲烷(MeBr)气体中。这种暴露会破坏限食大鼠超过95%的嗅觉上皮以及相同体重的自由采食大鼠超过90%的上皮中的所有神经元和支持细胞,但嗅觉上皮仍会出现显著恢复。针对损伤,细胞增殖在24至48小时之间开始显著增加,在1周时达到峰值,并在MeBr暴露后持续高于对照水平4周以上。尽管增殖迅速加速,但神经元重构的开始却延迟了;损伤后3天仅观察到少数未成熟神经元,但到第一周结束时它们大量重新出现。第一批成熟神经元在损伤后7至14天出现,并在4至6周时增加到接近正常数量。随着神经元群体的恢复,基底细胞增殖在损伤后4至6周恢复到对照水平。同样,通过抗细胞角蛋白18标记可识别的支持细胞迅速重新出现,并在上皮的浅表形成一个明显的层。在损伤后3周,它们在分布和形状上与对照上皮中的对应细胞非常相似,在8周时在嗅觉特异性细胞色素P450s的表达方面也相似。因此,到8周结束时,上皮的大部分区域恢复到接近正常的外观和细胞组成,这表明用于损伤上皮的MeBr模型比诸如Triton X - 100或硫酸锌冲洗等技术具有显著优势。然而,即使在8周时,上皮状态的所有指标也并非都正常。此时未成熟神经元的数量仍略多于正常水平。此外,嗅觉上皮的一些区域在MeBr损伤后无法恢复,并被呼吸道上皮取代。(摘要截断于400字)