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Tst-1/Oct-6/SCIP调节外周髓鞘形成中的一个独特步骤,是正常呼吸所必需的。

Tst-1/Oct-6/SCIP regulates a unique step in peripheral myelination and is required for normal respiration.

作者信息

Bermingham J R, Scherer S S, O'Connell S, Arroyo E, Kalla K A, Powell F L, Rosenfeld M G

机构信息

Department of Medicine, University of California, San Diego, La Jolla, 92093-0648, USA.

出版信息

Genes Dev. 1996 Jul 15;10(14):1751-62. doi: 10.1101/gad.10.14.1751.

Abstract

The terminal differentiation of myelinating glia involves complex interactions that culminate in the formation of myelin. The POU domain transcription factor Tst-1/Oct-6/SCIP is expressed transiently during myelination, and we report here that it has a critical role in this developmental process. Deletion of the Tst-1/Oct-6/SCIP gene produces a severe defect in peripheral myelination by arresting Schwann cell maturation before axonal wrapping. Unexpectedly, the activation of major myelin-specific genes appears to be unaffected by the Tst-1/Oct-6/SCIP mutation, demonstrating that multiple, independently regulated events are required for terminal differentiation of Schwann cells. In addition, aberrant differentiation and migration of specific neurons in Tst-1/Oct-6/SCIP mutant homozygotes is associated with a fatal breathing defect, providing a model for investigating the regulation of pulmonary homeostasis.

摘要

形成髓鞘的神经胶质细胞的终末分化涉及复杂的相互作用,最终导致髓鞘的形成。POU结构域转录因子Tst-1/Oct-6/SCIP在髓鞘形成过程中短暂表达,我们在此报告它在这一发育过程中起关键作用。Tst-1/Oct-6/SCIP基因的缺失通过在轴突包裹前阻止施万细胞成熟而导致外周髓鞘形成严重缺陷。出乎意料的是,主要髓鞘特异性基因的激活似乎不受Tst-1/Oct-6/SCIP突变的影响,这表明施万细胞的终末分化需要多个独立调节的事件。此外,Tst-1/Oct-6/SCIP突变纯合子中特定神经元的异常分化和迁移与致命的呼吸缺陷有关,为研究肺内稳态的调节提供了一个模型。

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