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FPR2特异性肽WKYMVm对成年小鼠神经干细胞迁移和增殖的刺激作用

Stimulation of the Migration and Expansion of Adult Mouse Neural Stem Cells by the FPR2-Specific Peptide WKYMVm.

作者信息

Kwon Yang Woo, Bae Sungwon, Jo Yeon Suk, Seo Youngsuk, Yoon Jong Hyuk

机构信息

Neurodegenerative Diseases Research Group, Korea Brain Research Institute, Daegu 41062, Korea.

Department of Brain-Cognitive Science, Daegu-Gyeongbuk Institute of Science and Technology (DGIST), Daegu 42988, Korea.

出版信息

Life (Basel). 2021 Nov 17;11(11):1248. doi: 10.3390/life11111248.

Abstract

Neural stem cells (NSCs) are multipotent cells capable of self-renewal and differentiation into different nervous system cells. Mouse NSCs (mNSCs) are useful tools for studying neurogenesis and the therapeutic applications of neurodegenerative diseases in mammals. Formyl peptide receptor 2 (FPR2), expressed in the central nervous system and brain, is involved in the migration and differentiation of murine embryonic-derived NSCs. In this study, we explored the effect of FPR2 activation in adult mNSCs using the synthetic peptide Trp-Lys-Tyr-Met-Val-D-Met-NH2 (WKYMVm), an agonist of FPR2. After isolation of NSCs from the subventricular zone of the adult mouse brain, they were cultured in two culture systems-neurospheres or adherent monolayers-to demonstrate the expression of NSC markers and phenotypes. Under different conditions, mNSCs differentiated into neurons and glial cells such as astrocytes, microglia, and oligodendrocytes. Treatment with WKYMVm stimulated the chemotactic migration of mNSCs. Moreover, WKYMVm-treated mNSCs were found to promote proliferation; this result was confirmed by the expansion of mNSCs in Matrigel and the increase in the number of Ki67-positive cells. Incubation of mNSCs with WKYMVm in a supplement-free medium enhanced the survival rate of the mNSCs. Together, these results suggest that WKYMVm-induced activation of FPR2 stimulates cellular responses in adult NSCs.

摘要

神经干细胞(NSCs)是具有自我更新能力且能分化为不同神经系统细胞的多能细胞。小鼠神经干细胞(mNSCs)是研究哺乳动物神经发生及神经退行性疾病治疗应用的有用工具。在中枢神经系统和大脑中表达的甲酰肽受体2(FPR2)参与了小鼠胚胎来源神经干细胞的迁移和分化。在本研究中,我们使用FPR2激动剂合成肽Trp-Lys-Tyr-Met-Val-D-Met-NH2(WKYMVm)探索了FPR2激活对成年mNSCs的影响。从成年小鼠脑室下区分离神经干细胞后,将它们培养在两种培养体系中——神经球或贴壁单层培养,以展示神经干细胞标志物和表型的表达。在不同条件下,mNSCs分化为神经元和胶质细胞,如星形胶质细胞、小胶质细胞和少突胶质细胞。WKYMVm处理刺激了mNSCs的趋化迁移。此外,发现WKYMVm处理的mNSCs能促进增殖;mNSCs在基质胶中的扩增以及Ki67阳性细胞数量的增加证实了这一结果。在无补充培养基中用WKYMVm孵育mNSCs提高了mNSCs的存活率。总之,这些结果表明WKYMVm诱导的FPR2激活刺激了成年神经干细胞中的细胞反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2ec/8622362/9a6aad8f1231/life-11-01248-g001.jpg

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