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TRPV2:中枢神经系统髓鞘形成障碍的关键因素。

TRPV2: A Key Player in Myelination Disorders of the Central Nervous System.

机构信息

Biophysics Unit, Department of Biochemistry and Molecular Biology, School of Medicine, Universitat Autònoma de Barcelona, 08193 Cerdanyola del Vallès, Catalonia, Spain.

Institut de Neurociències, Universitat Autònoma de Barcelona, 08193 Cerdanyola del Vallès, Catalonia, Spain.

出版信息

Int J Mol Sci. 2022 Mar 25;23(7):3617. doi: 10.3390/ijms23073617.

Abstract

Transient potential receptor vanilloid 2 (TRPV2) is widely expressed through the nervous system and specifically found in neuronal subpopulations and some glial cells. TRPV2 is known to be sensitized by methionine oxidation, which results from inflammation. Here we aim to characterize the expression and regulation of TRPV2 in myelination pathologies, such as hypomyelination and demyelination. We validated the interaction between TRPV2 and its putative interactor Opalin, an oligodendrocyte marker, in mixed glial cultures under pro- and anti-inflammatory conditions. Then, we characterized TRPV2 time-course expression in experimental animal models of hypomyelination (jimpy mice) and de-/remyelination (cuprizone intoxication and experimental autoimmune encephalomyelitis (EAE)). TRPV2 showed upregulation associated with remyelination, inflammation in cuprizone and EAE models, and downregulation in hypomyelinated jimpy mice. TRPV2 expression was altered in human samples of multiple sclerosis (MS) patients. Additionally, we analyzed the expression of methionine sulfoxide reductase A (MSRA), an enzyme that reduces oxidated methionines in TRPV2, which we found increased in inflammatory conditions. These results suggest that TRPV2 may be a key player in myelination in accordance with the recapitulation hypothesis, and that it may become an interesting clinical target in the treatment of demyelination disorders.

摘要

瞬时受体电位香草酸 2 型(TRPV2)广泛表达于神经系统,特异性存在于神经元亚群和一些神经胶质细胞中。TRPV2 已知可被炎症导致的蛋氨酸氧化所敏化。在此,我们旨在研究 TRPV2 在髓鞘形成病理中的表达和调控,如少突胶质细胞髓鞘形成不足和脱髓鞘。我们验证了 TRPV2 与其假定相互作用蛋白 Opalin(少突胶质细胞标志物)在促炎和抗炎条件下混合神经胶质细胞培养物中的相互作用。然后,我们在少突胶质细胞髓鞘形成不足(jimpy 小鼠)和脱髓鞘/再髓鞘(铜中毒和实验性自身免疫性脑脊髓炎(EAE))的动物模型中对 TRPV2 的时间表达进行了特征描述。TRPV2 的表达与再髓鞘化、杯状朊病毒和 EAE 模型中的炎症上调,以及少突胶质细胞髓鞘形成不足的 jimpy 小鼠中的下调有关。TRPV2 的表达在多发性硬化症(MS)患者的人类样本中发生改变。此外,我们分析了还原 TRPV2 中氧化蛋氨酸的酶——蛋氨酸亚砜还原酶 A(MSRA)的表达,我们发现其在炎症条件下增加。这些结果表明,TRPV2 可能是髓鞘形成中的关键参与者,符合重演假说,并且它可能成为脱髓鞘疾病治疗中的一个有趣的临床靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b42e/8999035/4013729c53b2/ijms-23-03617-g001.jpg

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