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多巴胺D2受体在应激诱导的髓鞘丢失中的作用。

Role of Dopamine D2 Receptor in Stress-Induced Myelin Loss.

作者信息

Choi Mi-Hyun, Na Ji Eun, Yoon Ye Ran, Lee Hyo Jin, Yoon Sehyoun, Rhyu Im Joo, Baik Ja-Hyun

机构信息

Molecular Neurobiology Laboratory, Department of Life Sciences, Korea University, Seoul, 02841, Korea.

Department of Anatomy, College of Medicine, Korea University, Seoul, 02841, Korea.

出版信息

Sci Rep. 2017 Sep 14;7(1):11654. doi: 10.1038/s41598-017-10173-9.

DOI:10.1038/s41598-017-10173-9
PMID:28912499
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5599541/
Abstract

Dopaminergic systems play a major role in reward-related behavior and dysregulation of dopamine (DA) systems can cause several mental disorders, including depression. We previously reported that dopamine D2 receptor knockout (D2R) mice display increased anxiety and depression-like behaviors upon chronic stress. Here, we observed that chronic stress caused myelin loss in wild-type (WT) mice, while the myelin level in D2R mice, which was already lower than that in WT mice, was not affected upon stress. Fewer mature oligodendrocytes (OLs) were observed in the corpus callosum of stressed WT mice, while in D2R mice, both the control and stressed group displayed a decrease in the number of mature OLs. We observed a decrease in the number of active β-catenin (ABC)-expressing and TCF4-expressing cells among OL lineage cells in the corpus callosum of stressed WT mice, while such regulation was not found in D2R mice. Administration of lithium normalized the behavioral impairments and myelin damage induced by chronic stress in WT mice, and restored the number of ABC-positive and TCF4-positive OLs, while such effect was not found in D2R mice. Together, our findings indicate that chronic stress induces myelin loss through the Wnt/β-catenin signaling pathway in association with DA signaling through D2R.

摘要

多巴胺能系统在与奖赏相关的行为中起主要作用,多巴胺(DA)系统的失调会导致多种精神障碍,包括抑郁症。我们之前报道过,多巴胺D2受体基因敲除(D2R)小鼠在慢性应激后会表现出焦虑和抑郁样行为增加。在此,我们观察到慢性应激导致野生型(WT)小鼠出现髓鞘丢失,而D2R小鼠的髓鞘水平本就低于WT小鼠,在应激后并未受到影响。在应激的WT小鼠胼胝体中观察到成熟少突胶质细胞(OLs)数量减少,而在D2R小鼠中,对照组和应激组的成熟OLs数量均减少。我们观察到应激的WT小鼠胼胝体中OL谱系细胞中表达活性β-连环蛋白(ABC)和TCF4的细胞数量减少,而在D2R小鼠中未发现这种调节情况。给予锂可使WT小鼠因慢性应激诱导的行为障碍和髓鞘损伤恢复正常,并使ABC阳性和TCF4阳性OLs的数量恢复,而在D2R小鼠中未发现这种效果。总之,我们的研究结果表明,慢性应激通过Wnt/β-连环蛋白信号通路与通过D2R的DA信号传导相关联,从而诱导髓鞘丢失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/262f/5599541/5ff4b2aa0ef4/41598_2017_10173_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/262f/5599541/f38212ab344f/41598_2017_10173_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/262f/5599541/0866729678f6/41598_2017_10173_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/262f/5599541/9823d0e0ec56/41598_2017_10173_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/262f/5599541/c6178724f30d/41598_2017_10173_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/262f/5599541/4fe99a0bd812/41598_2017_10173_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/262f/5599541/5ff4b2aa0ef4/41598_2017_10173_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/262f/5599541/f38212ab344f/41598_2017_10173_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/262f/5599541/0866729678f6/41598_2017_10173_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/262f/5599541/9823d0e0ec56/41598_2017_10173_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/262f/5599541/c6178724f30d/41598_2017_10173_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/262f/5599541/4fe99a0bd812/41598_2017_10173_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/262f/5599541/5ff4b2aa0ef4/41598_2017_10173_Fig6_HTML.jpg

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