Bacallao Ketty, Monje Paula V
The Miami Project to Cure Paralysis, University of Miami Miller School of Medicine, Miami, Florida, United States of America.
The Miami Project to Cure Paralysis, University of Miami Miller School of Medicine, Miami, Florida, United States of America; Department of Neurological Surgery, University of Miami Miller School of Medicine, Miami, Florida, United States of America.
PLoS One. 2015 Feb 23;10(2):e0116948. doi: 10.1371/journal.pone.0116948. eCollection 2015.
Isolated Schwann cells (SCs) respond to cAMP elevation by adopting a differentiated post-mitotic state that exhibits high levels of Krox-20, a transcriptional enhancer of myelination, and mature SC markers such as the myelin lipid galactocerebroside (O1). To address how cAMP controls myelination, we performed a series of cell culture experiments which compared the differentiating responses of isolated and axon-related SCs to cAMP analogs and ascorbate, a known inducer of axon ensheathment, basal lamina formation and myelination. In axon-related SCs, cAMP induced the expression of Krox-20 and O1 without a concomitant increase in the expression of myelin basic protein (MBP) and without promoting axon ensheathment, collagen synthesis or basal lamina assembly. When cAMP was provided together with ascorbate, a dramatic enhancement of MBP expression occurred, indicating that cAMP primes SCs to form myelin only under conditions supportive of basal lamina formation. Experiments using a combination of cell permeable cAMP analogs and type-selective adenylyl cyclase (AC) agonists and antagonists revealed that selective transmembrane AC (tmAC) activation with forskolin was not sufficient for full SC differentiation and that the attainment of an O1 positive state also relied on the activity of the soluble AC (sAC), a bicarbonate sensor that is insensitive to forskolin and GPCR activation. Pharmacological and immunological evidence indicated that SCs expressed sAC and that sAC activity was required for morphological differentiation and the expression of myelin markers such as O1 and protein zero. To conclude, our data indicates that cAMP did not directly drive myelination but rather the transition into an O1 positive state, which is perhaps the most critical cAMP-dependent rate limiting step for the onset of myelination. The temporally restricted role of cAMP in inducing differentiation independently of basal lamina formation provides a clear example of the uncoupling of signals controlling differentiation and myelination in SCs.
分离的施万细胞(SCs)通过进入分化后的有丝分裂后状态来响应cAMP升高,该状态表现出高水平的Krox-20(一种髓鞘形成的转录增强因子)以及成熟的SCs标志物,如髓鞘脂质半乳糖脑苷脂(O1)。为了研究cAMP如何控制髓鞘形成,我们进行了一系列细胞培养实验,比较了分离的和与轴突相关的SCs对cAMP类似物和抗坏血酸(一种已知的轴突包裹、基膜形成和髓鞘形成诱导剂)的分化反应。在与轴突相关的SCs中,cAMP诱导Krox-20和O1的表达,但髓鞘碱性蛋白(MBP)的表达没有随之增加,也没有促进轴突包裹、胶原蛋白合成或基膜组装。当cAMP与抗坏血酸一起提供时,MBP表达显著增强,表明cAMP仅在支持基膜形成的条件下促使SCs形成髓鞘。使用细胞可渗透的cAMP类似物与类型选择性腺苷酸环化酶(AC)激动剂和拮抗剂组合的实验表明,用福司可林选择性激活跨膜AC(tmAC)不足以实现SCs的完全分化,并且达到O1阳性状态还依赖于可溶性AC(sAC)的活性,sAC是一种对福司可林和GPCR激活不敏感的碳酸氢盐传感器。药理学和免疫学证据表明SCs表达sAC,并且sAC活性是形态分化以及髓鞘标志物如O1和蛋白零表达所必需的。总之,我们的数据表明cAMP并不直接驱动髓鞘形成而是驱动向O1阳性状态的转变,这可能是髓鞘形成开始时最关键的cAMP依赖性限速步骤。cAMP在独立于基膜形成诱导分化方面的时间受限作用提供了一个明确的例子,说明控制SCs分化和髓鞘形成的信号是解偶联的。