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短链脂肪酸通过免疫机制改善脑卒中后恢复。

Short-Chain Fatty Acids Improve Poststroke Recovery via Immunological Mechanisms.

机构信息

Institute for Stroke and Dementia Research, University Hospital, Ludwig-Maximilians-University LMU, 81377, Munich, Germany.

Munich Cluster for Systems Neurology (SyNergy), 81377, Munich, Germany.

出版信息

J Neurosci. 2020 Jan 29;40(5):1162-1173. doi: 10.1523/JNEUROSCI.1359-19.2019. Epub 2019 Dec 30.

Abstract

Recovery after stroke is a multicellular process encompassing neurons, resident immune cells, and brain-invading cells. Stroke alters the gut microbiome, which in turn has considerable impact on stroke outcome. However, the mechanisms underlying gut-brain interaction and implications for long-term recovery are largely elusive. Here, we tested the hypothesis that short-chain fatty acids (SCFAs), key bioactive microbial metabolites, are the missing link along the gut-brain axis and might be able to modulate recovery after experimental stroke. SCFA supplementation in the drinking water of male mice significantly improved recovery of affected limb motor function. Using wide-field calcium imaging, we observed that SCFAs induced altered contralesional cortex connectivity. This was associated with SCFA-dependent changes in spine and synapse densities. RNA sequencing of the forebrain cortex indicated a potential involvement of microglial cells in contributing to the structural and functional remodeling. Further analyses confirmed a substantial impact of SCFAs on microglial activation, which depended on the recruitment of T cells to the infarcted brain. Our findings identified that microbiota-derived SCFAs modulate poststroke recovery via effects on systemic and brain resident immune cells. Previous studies have shown a bidirectional communication along the gut-brain axis after stroke. Stroke alters the gut microbiota composition, and in turn, microbiota dysbiosis has a substantial impact on stroke outcome by modulating the immune response. However, until now, the mediators derived from the gut microbiome affecting the gut-immune-brain axis and the molecular mechanisms involved in this process were unknown. Here, we demonstrate that short-chain fatty acids, fermentation products of the gut microbiome, are potent and proregenerative modulators of poststroke neuronal plasticity at various structural levels. We identified that this effect was mediated via circulating lymphocytes on microglial activation. These results identify short-chain fatty acids as a missing link along the gut-brain axis and as a potential therapeutic to improve recovery after stroke.

摘要

中风后的恢复是一个涉及神经元、固有免疫细胞和侵入大脑的细胞的多细胞过程。中风改变了肠道微生物组,而肠道微生物组反过来又对中风的结果有很大的影响。然而,肠道-大脑相互作用的机制以及对长期恢复的影响在很大程度上还不清楚。在这里,我们测试了这样一个假设,即短链脂肪酸(SCFAs)是关键的生物活性微生物代谢产物,是沿肠道-大脑轴缺失的一环,并且可能能够调节实验性中风后的恢复。在雄性小鼠的饮用水中补充 SCFA 显著改善了受影响肢体运动功能的恢复。通过宽场钙成像,我们观察到 SCFA 诱导了对侧皮质连接的改变。这与 SCFA 依赖性的棘突和突触密度变化有关。对前脑皮层的 RNA 测序表明,小胶质细胞的潜在参与可能有助于结构和功能重塑。进一步的分析证实,SCFAs 对小胶质细胞的激活有很大的影响,这取决于 T 细胞向梗死大脑的募集。我们的研究结果表明,微生物群衍生的 SCFAs 通过对系统性和大脑驻留免疫细胞的影响来调节中风后的恢复。以前的研究表明,中风后沿肠道-大脑轴存在双向通讯。中风改变了肠道微生物组的组成,而肠道微生物组的失调通过调节免疫反应对中风的结果有很大的影响。然而,直到现在,影响肠道-免疫-大脑轴的源自肠道微生物组的介质以及涉及这一过程的分子机制尚不清楚。在这里,我们证明了短链脂肪酸,即肠道微生物群的发酵产物,是各种结构水平中风后神经元可塑性的有效且再生性的调节剂。我们发现,这种作用是通过循环淋巴细胞对小胶质细胞的激活来介导的。这些结果将短链脂肪酸确定为肠道-大脑轴上缺失的一环,并作为改善中风后恢复的潜在治疗方法。

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本文引用的文献

1
Microglia monitor and protect neuronal function through specialized somatic purinergic junctions.
Science. 2020 Jan 31;367(6477):528-537. doi: 10.1126/science.aax6752. Epub 2019 Dec 12.
2
In vivo widefield calcium imaging of the mouse cortex for analysis of network connectivity in health and brain disease.
Neuroimage. 2019 Oct 1;199:570-584. doi: 10.1016/j.neuroimage.2019.06.014. Epub 2019 Jun 7.
3
Stroke Dysbiosis Index (SDI) in Gut Microbiome Are Associated With Brain Injury and Prognosis of Stroke.
Front Neurol. 2019 Apr 24;10:397. doi: 10.3389/fneur.2019.00397. eCollection 2019.
4
Ischaemic stroke in mice induces lung inflammation but not acute lung injury.
Sci Rep. 2019 Mar 6;9(1):3622. doi: 10.1038/s41598-019-40392-1.
5
Double-negative T cells remarkably promote neuroinflammation after ischemic stroke.
Proc Natl Acad Sci U S A. 2019 Mar 19;116(12):5558-5563. doi: 10.1073/pnas.1814394116. Epub 2019 Feb 28.
6
Developmental Heterogeneity of Microglia and Brain Myeloid Cells Revealed by Deep Single-Cell RNA Sequencing.
Neuron. 2019 Jan 16;101(2):207-223.e10. doi: 10.1016/j.neuron.2018.12.006. Epub 2018 Dec 31.
7
Short-chain fatty acids and gut microbiota in multiple sclerosis.
Acta Neurol Scand. 2019 Mar;139(3):208-219. doi: 10.1111/ane.13045. Epub 2018 Dec 3.
8
Short-chain fatty acids: microbial metabolites that alleviate stress-induced brain-gut axis alterations.
J Physiol. 2018 Oct;596(20):4923-4944. doi: 10.1113/JP276431. Epub 2018 Aug 28.
9
Sex-Specific Features of Microglia from Adult Mice.
Cell Rep. 2018 Jun 19;23(12):3501-3511. doi: 10.1016/j.celrep.2018.05.048.
10
The gut microbiome primes a cerebroprotective immune response after stroke.
J Cereb Blood Flow Metab. 2018 Aug;38(8):1293-1298. doi: 10.1177/0271678X18780130. Epub 2018 May 30.

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