YAP and TAZ regulate remyelination in the central nervous system

IF 5.4 2区 医学 Q1 NEUROSCIENCES Glia Pub Date : 2023-09-19 DOI:10.1002/glia.24467
Jiayue Hong, Julia M. Kirkland, Jenica Acheta, Leandro N. Marziali, Brianna Beck, Haley Jeanette, Urja Bhatia, Grace Davis, Jacob Herron, Clémence Roué, Charly Abi-Ghanem, M. Laura Feltri, Kristen L. Zuloaga, Marie E. Bechler, Yannick Poitelon, Sophie Belin
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Abstract

Myelinating cells are sensitive to mechanical stimuli from their extracellular matrix. Ablation of YAP and TAZ mechanotransducers in Schwann cells abolishes the axon–Schwann cell recognition, myelination, and remyelination in the peripheral nervous system. It was unknown if YAP and TAZ are also required for myelination and remyelination in the central nervous system. Here we define the importance of oligodendrocyte (OL) YAP and TAZ in vivo, by specific deletion in oligodendroglial cells in adult OLs during myelin repair. Blocking YAP and TAZ expression in OL lineage cells did not affect animal viability or any major defects on OL maturation and myelination. However, using a mouse model of demyelination/remyelination, we demonstrate that YAP and TAZ modulate the capacity of OLs to remyelinate axons, particularly during the early stage of the repair process, when OL proliferation is most important. These results indicate that YAP and TAZ signaling is necessary for effective remyelination of the mouse brain.

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YAP和TAZ调节中枢神经系统的髓鞘再生
髓鞘细胞对来自细胞外基质的机械刺激敏感。消融雪旺细胞中的YAP和TAZ机械转导可消除周围神经系统中轴突-雪旺细胞识别、髓鞘形成和再髓鞘形成。目前尚不清楚YAP和TAZ是否也是中枢神经系统髓鞘形成和再髓鞘形成所必需的。在这里,我们定义了少突胶质细胞(OL) YAP和TAZ在体内的重要性,通过在成人OL中髓鞘修复过程中少突胶质细胞的特异性缺失。阻断OL谱系细胞中YAP和TAZ的表达不会影响动物的生存能力,也不会对OL成熟和髓鞘形成产生任何重大缺陷。然而,通过小鼠脱髓鞘/再髓鞘形成模型,我们证明了YAP和TAZ调节OL轴突再髓鞘形成的能力,特别是在修复过程的早期阶段,当OL增殖是最重要的。这些结果表明,YAP和TAZ信号是小鼠大脑有效髓鞘再生的必要条件。
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来源期刊
Glia
Glia 医学-神经科学
CiteScore
13.10
自引率
4.80%
发文量
162
审稿时长
3-8 weeks
期刊介绍: GLIA is a peer-reviewed journal, which publishes articles dealing with all aspects of glial structure and function. This includes all aspects of glial cell biology in health and disease.
期刊最新文献
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