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通过在发育中的脊髓器官培养物中用 rAAV 介导 jGCaMP8s 的表达来探索髓鞘形成少突胶质细胞中的 Ca 动力学。

Exploring Ca Dynamics in Myelinating Oligodendrocytes through rAAV-Mediated jGCaMP8s Expression in Developing Spinal Cord Organ Cultures.

机构信息

Scuola Internazionale Superiore di Studi Avanzati, Trieste 34146, Italy

Scuola Internazionale Superiore di Studi Avanzati, Trieste 34146, Italy.

出版信息

eNeuro. 2024 Jun 4;11(6). doi: 10.1523/ENEURO.0540-23.2024. Print 2024 Jun.

DOI:10.1523/ENEURO.0540-23.2024
PMID:38744490
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11151195/
Abstract

Oligodendrocytes, the myelin-producing glial cells of the central nervous system (CNS), crucially contribute to myelination and circuit function. An increasing amount of evidence suggests that intracellular calcium (Ca) dynamics in oligodendrocytes mediates activity-dependent and activity-independent myelination. Unraveling how myelinating oligodendrocytes orchestrate and integrate Ca signals, particularly in relation to axonal firing, is crucial for gaining insights into their role in the CNS development and function, both in health and disease. In this framework, we used the recombinant adeno-associated virus/Olig001 capsid variant to express the genetically encoded Ca indicator jGCaMP8s, under the control of the myelin basic protein promoter. In our study, this tool exhibits excellent tropism and selectivity for myelinating and mature oligodendrocytes, and it allows monitoring Ca activity in myelin-forming cells, both in isolated primary cultures and organotypic spinal cord explants. By live imaging of myelin Ca events in oligodendrocytes within organ cultures, we observed a rapid decline in the amplitude and duration of Ca events across different in vitro developmental stages. Active myelin sheath remodeling and growth are modulated at the level of myelin-axon interface through Ca signaling, and, during early myelination in organ cultures, this phase is finely tuned by the firing of axon action potentials. In the later stages of myelination, Ca events in mature oligodendrocytes no longer display such a modulation, underscoring the involvement of complex Ca signaling in CNS myelination.

摘要

少突胶质细胞是中枢神经系统(CNS)中产生髓鞘的神经胶质细胞,对髓鞘形成和回路功能至关重要。越来越多的证据表明,少突胶质细胞内钙离子(Ca)动力学介导了活动依赖性和非活动依赖性的髓鞘形成。阐明髓鞘形成的少突胶质细胞如何协调和整合 Ca 信号,特别是与轴突放电的关系,对于深入了解它们在 CNS 发育和功能中的作用至关重要,无论是在健康还是疾病状态下。在这个框架中,我们使用重组腺相关病毒/Olig001 衣壳变体表达受髓鞘碱性蛋白启动子控制的基因编码 Ca 指示剂 jGCaMP8s。在我们的研究中,这种工具对髓鞘形成和成熟的少突胶质细胞具有优异的靶向性和选择性,它允许在体外培养的原代培养物和器官型脊髓外植体中监测形成髓鞘的细胞中的 Ca 活性。通过对器官培养物中少突胶质细胞髓鞘 Ca 事件的活体成像,我们观察到不同体外发育阶段的 Ca 事件的幅度和持续时间迅速下降。通过 Ca 信号调节髓鞘-轴突界面处的活跃髓鞘鞘重塑和生长,并且在器官培养物中的早期髓鞘形成过程中,该阶段通过轴突动作电位的放电进行精细调节。在髓鞘形成的后期阶段,成熟少突胶质细胞中的 Ca 事件不再显示这种调节,这突出了复杂的 Ca 信号在中枢神经系统髓鞘形成中的参与。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0909/11151195/cb362910b1f0/eneuro-11-ENEURO.0540-23.2024-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0909/11151195/6a9ee5965468/eneuro-11-ENEURO.0540-23.2024-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0909/11151195/d2dfc62f623e/eneuro-11-ENEURO.0540-23.2024-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0909/11151195/b3552eab6a3a/eneuro-11-ENEURO.0540-23.2024-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0909/11151195/cb362910b1f0/eneuro-11-ENEURO.0540-23.2024-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0909/11151195/6a9ee5965468/eneuro-11-ENEURO.0540-23.2024-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0909/11151195/d2dfc62f623e/eneuro-11-ENEURO.0540-23.2024-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0909/11151195/b3552eab6a3a/eneuro-11-ENEURO.0540-23.2024-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0909/11151195/cb362910b1f0/eneuro-11-ENEURO.0540-23.2024-g004.jpg

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