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大鼠嗅觉上皮的逆转录病毒谱系研究。

Retroviral lineage studies of the rat olfactory epithelium.

作者信息

Schwob J E, Huard J M, Luskin M B, Youngentob S L

机构信息

Department of Anatomy and Cell Biology, SUNY Health Science Center, Syracuse 13210, USA.

出版信息

Chem Senses. 1994 Dec;19(6):671-82. doi: 10.1093/chemse/19.6.671.

Abstract

Replication-incompetent retroviral vectors that encode the heritable marker enzyme, beta-galactosidase, were used to study the lineage relationships of cells in the olfactory epithelium of unmanipulated animals and in the olfactory epithelium as it reconstitutes after lesion. Virally-marked cells are categorized as to type based on their position in the epithelium and on expression of NCAM (limited to neurons) and the carbohydrate moiety recognized by Griffonia lectin (limited to the dark/horizontal basal cells and the microvillar class of supporting cells). Direct injections of the vectors into the olfactory epithelium of otherwise intact animals produce clusters of beta-galactosidase-labeled cells when assessed 6-10 days after infection; these clusters are composed of neurons and NCAM-negative/lectin-negative light/globose basal cells exclusively. In contrast, clusters of virally-marked cells after MeBr-induced lesion of the epithelium frequently contain both neurons and supporting cells, as well as both types of basal cells. Other clusters contain supporting cells and/or Bowman's gland/duct cells. It is likely that the clusters of marked cells are derived from a single founder cell, i.e. the cells are clonal and lineally related, since the clusters are widely dispersed. Furthermore, infusion of mixtures of viruses that can be distinguished on the basis of the type and subcellular localization of the marker enzyme that is expressed produce clusters that are homogenous with respect to enzyme type, providing strong evidence in favor of the notion that the clusters are clonal in nature. Thus, the founders of the clones that contain neurons, supporting cells and basal cells are pluripotent in their capacity for differentiation. It is unlikely that the pluripotent cells are found in Bowman's gland/duct, since we have yet to observe a clone that contains neurons and cells in Bowman's gland/duct. Hence, the pluripotent stem cells are to be found in the basal cell compartment of the epithelium. However, the exact nature of these stem cells remains unknown and a subject for future investigation.

摘要

编码可遗传标记酶β-半乳糖苷酶的无复制能力逆转录病毒载体,被用于研究未受操作动物嗅上皮细胞以及损伤后重构的嗅上皮细胞之间的谱系关系。根据病毒标记细胞在上皮中的位置、神经细胞黏附分子(NCAM,仅限于神经元表达)以及被非洲豆蔻凝集素识别的碳水化合物部分(仅限于暗/水平基底细胞和微绒毛类支持细胞)的表达情况,对病毒标记细胞进行类型分类。在感染后6 - 10天进行评估时,将载体直接注射到原本完好动物的嗅上皮中会产生β-半乳糖苷酶标记细胞簇;这些细胞簇仅由神经元和NCAM阴性/凝集素阴性的亮/球状基底细胞组成。相比之下,甲基溴诱导上皮损伤后,病毒标记细胞簇通常既包含神经元和支持细胞,也包含两种类型的基底细胞。其他细胞簇则包含支持细胞和/或鲍曼腺/导管细胞。由于这些细胞簇广泛分散,标记细胞簇很可能源自单个起始细胞,即细胞是克隆性且有谱系关联的。此外,注入基于所表达标记酶的类型和亚细胞定位可区分的病毒混合物,会产生在酶类型上同质的细胞簇,这有力地证明了这些细胞簇本质上是克隆性的这一观点。因此,包含神经元、支持细胞和基底细胞的克隆的起始细胞具有多能分化能力。多能细胞不太可能存在于鲍曼腺/导管中,因为我们尚未观察到包含神经元和鲍曼腺/导管细胞的克隆。所以,多能干细胞存在于上皮的基底细胞区室中。然而,这些干细胞的确切性质仍然未知,是未来研究的一个课题。

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