Bdnf and Ntrk2 functions promote but are not essential for spinal cord myelination in larval zebrafish

IF 2.2 3区 生物学 Q4 CELL BIOLOGY
Kristen Russell , Christina A. Kearns , Macie B. Walker , Christopher S. Knoeckel , Angeles B. Ribera , Caleb A. Doll , Bruce Appel
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Abstract

Myelin, a specialized membrane produced by oligodendroglial cells in the central nervous system, wraps axons to enhance conduction velocity and maintain axon health. Not all axons are myelinated, and not all myelinated axons are uniformly wrapped along their lengths. Several lines of evidence indicate that neuronal activity can influence myelination, however, the cellular and molecular mechanisms that mediate communication between axons and oligodendrocytes remain poorly understood. Prior research showed that the neurotrophic growth factor Bdnf and its receptor Ntrk2 promote myelination in rodents, raising the possibility that Bdnf and Ntrk2 convey myelin-promoting signals from neurons to oligodendrocytes. We explored this possibility using a combination of gene expression analyses, gene function tests, and myelin sheath formation assays in zebrafish larvae. Altogether, our data indicate that, although not essential for myelination, Bdnf-Ntrk2 signaling contributes to the timely formation of myelin in the developing zebrafish spinal cord.
Bdnf和Ntrk2的功能促进了斑马鱼幼体脊髓髓鞘形成,但不是必需的
髓磷脂是由中枢神经系统少突胶质细胞产生的一种特殊膜,包裹轴突以提高传导速度,维持轴突健康。并不是所有的轴突都有髓鞘,也不是所有有髓鞘的轴突沿其长度均匀包裹。一些证据表明,神经元活动可以影响髓鞘形成,然而,介导轴突和少突胶质细胞之间通讯的细胞和分子机制仍然知之甚少。先前的研究表明,神经营养生长因子Bdnf及其受体Ntrk2促进啮齿动物的髓鞘形成,这提出了Bdnf和Ntrk2将髓鞘促进信号从神经元传递到少突胶质细胞的可能性。我们通过对斑马鱼幼虫的基因表达分析、基因功能测试和髓鞘形成分析来探索这种可能性。总之,我们的数据表明,尽管Bdnf-Ntrk2信号不是髓鞘形成所必需的,但它有助于发育中的斑马鱼脊髓髓鞘的及时形成。
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来源期刊
Differentiation
Differentiation 生物-发育生物学
CiteScore
4.10
自引率
3.40%
发文量
38
审稿时长
51 days
期刊介绍: Differentiation is a multidisciplinary journal dealing with topics relating to cell differentiation, development, cellular structure and function, and cancer. Differentiation of eukaryotes at the molecular level and the use of transgenic and targeted mutagenesis approaches to problems of differentiation are of particular interest to the journal. The journal will publish full-length articles containing original work in any of these areas. We will also publish reviews and commentaries on topics of current interest. The principal subject areas the journal covers are: • embryonic patterning and organogenesis • human development and congenital malformation • mechanisms of cell lineage commitment • tissue homeostasis and oncogenic transformation • establishment of cellular polarity • stem cell differentiation • cell reprogramming mechanisms • stability of the differentiated state • cell and tissue interactions in vivo and in vitro • signal transduction pathways in development and differentiation • carcinogenesis and cancer • mechanisms involved in cell growth and division especially relating to cancer • differentiation in regeneration and ageing • therapeutic applications of differentiation processes.
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