Gut microbiota regulates optic nerve fiber myelination.

IF 4.6 2区 生物学 Q2 CELL BIOLOGY
Frontiers in Cell and Developmental Biology Pub Date : 2025-02-20 eCollection Date: 2025-01-01 DOI:10.3389/fcell.2025.1526855
Giulia Ronchi, Davide Pellegrino, Marwa El Soury, Olga Amato, Francesco Gaia, Sajjad Farzin, Raffaele Nuzzi, Marijana Basic, Silvia Bolsega, Stefano Geuna, Matilde Cescon, Kirsten Haastert-Talini, Giovanna Gambarotta
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Abstract

Introduction: Recent evidence supports the hypothesis of an association between gut microbiota and the pathogenesis of retinal and eye diseases, suggesting the existence of a gut-eye axis. However, no data are available on the possible effect of the gut microbiota on the optic nerve fiber maturation and myelin development.

Methods: We investigated the impact of gut microbiota on the optic nerves collected from neonatal and young adult germ-free (GF), gnotobiotic (stably colonized with 12 bacteria strains, OMM12) and control (colonized with a complex gut microbiota, CGM) mice, by performing stereological and morphoquantitative analyses with transmission electron microscopy and gene expression analysis by quantitative real-time PCR.

Results: Young adult GF and OMM12 optic nerve axons are smaller and hypermyelinated compared to CGM ones, while no such differences were detected in neonatal optic nerves. The transcription factors Olig1, Olig2, and Sox10 (oligodendrocyte myelination positive regulators) are downregulated in CGM and OMM12 young adult mice compared to the respective neonates. Such developmental downregulation was not observed in GF optic nerves, suggesting that the absence of the gut microbiota prolongs the stimulation of optic nerve fiber myelination, possibly through mechanisms that are yet to be identified.

Discussion: Altogether, these data underscore the gut microbiota pivotal role in driving optic nerve myelination, contributing to our knowledge about both the gut-eye axis and the gut-brain axis, and opening new horizons for further investigations that will explore the role of the microbiota also in pathologies, injuries and regeneration associated with the optic nerve.

肠道微生物群调节视神经纤维髓鞘化
最近的证据支持肠道微生物群与视网膜和眼部疾病发病机制之间存在关联的假设,表明存在肠-眼轴。然而,肠道微生物群对视神经纤维成熟和髓鞘发育的可能影响尚无数据。方法:采用透射电子显微镜和实时荧光定量PCR技术对视神经进行体视学和形态定量分析,研究肠道菌群对新生小鼠、无细菌小鼠(GF)、无细菌小鼠(稳定定植12株细菌OMM12)和对照小鼠(复杂肠道菌群CGM)视神经的影响。结果:与CGM相比,青年GF和OMM12视神经轴突更小,髓鞘增生,而新生儿视神经未见此差异。转录因子Olig1, Olig2和Sox10(少突胶质细胞髓鞘形成阳性调节因子)在CGM和OMM12年轻成年小鼠中与各自的新生儿相比下调。在GF视神经中没有观察到这种发育下调,这表明肠道微生物群的缺失延长了视神经纤维髓鞘形成的刺激,可能是通过尚未确定的机制。讨论:总之,这些数据强调了肠道微生物群在驱动视神经髓鞘形成中的关键作用,有助于我们了解肠-眼轴和肠-脑轴,并为进一步研究探索微生物群在视神经病理、损伤和再生中的作用开辟了新的视野。
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来源期刊
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
9.70
自引率
3.60%
发文量
2531
审稿时长
12 weeks
期刊介绍: Frontiers in Cell and Developmental Biology is a broad-scope, interdisciplinary open-access journal, focusing on the fundamental processes of life, led by Prof Amanda Fisher and supported by a geographically diverse, high-quality editorial board. The journal welcomes submissions on a wide spectrum of cell and developmental biology, covering intracellular and extracellular dynamics, with sections focusing on signaling, adhesion, migration, cell death and survival and membrane trafficking. Additionally, the journal offers sections dedicated to the cutting edge of fundamental and translational research in molecular medicine and stem cell biology. With a collaborative, rigorous and transparent peer-review, the journal produces the highest scientific quality in both fundamental and applied research, and advanced article level metrics measure the real-time impact and influence of each publication.
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