Block Copolymer Nanomicelle-Encapsulated Curcumin Attenuates Cerebral Ischemia Injury and Affects Stem Cell Marker Expression by Inhibiting lncRNA GAS5.

IF 3.8 3区 医学 Q2 CELL & TISSUE ENGINEERING
Stem Cells International Pub Date : 2023-02-17 eCollection Date: 2023-01-01 DOI:10.1155/2023/9821500
Fengguang Li, Yan Xu, Xinghua Wang, Xuan Cai, Wanli Li, Wei Cheng, Xing Li, Gangli Yan
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引用次数: 0

Abstract

Stroke has become the most common cause of death among residents in China, among which ischemic stroke accounts for the vast majority reaching 70% to 80%. It is of great importance to actively investigate the protective mechanism of cerebral ischemia injury after IS (ischemic stroke). We constructed cerebral ischemia injury models in vivo MACO rat and in vitro (oxygen-glucose deprivation cell model) and set up different interference groups. RT-PCR (reverse transcription PCR) was conducted to detect the expression of lncRNA in neuronal cells, brain tissue, and plasma of different groups, and ELISA (enzyme-linked immunosorbent assay) and western blot were used to detect the expression of the protein in neuronal cells, brain tissue, and plasma of different groups. Cell activity was detected by the CCK-8 assay, while cell apoptosis was examined by TUNEL (terminal deoxynucleotidyl transferase dUTP nick end labeling) assay. In the rats' neuronal cells and brain tissue, curcumin can inhibit the expression of lncRNA GAS5 (long noncoding RNA growth arrest-specific 5). In oxygen-glucose-deprived neuronal cells in vitro, curcumin and low-expressed lncRNA GAS5 can enhance cell activity and decline cell apoptosis, but the addition of curcumin and overexpressed lncRNA GAS5 can make this phenomenon disappear. In neuronal cells, plasma, and brain tissue, curcumin and the low-expressed lncRNA GAS5 can inhibit the expression of IL-1β (interleukin 1 beta), TNF-α (tumor necrosis factor alpha), IL-6 (interleukin 6), Sox2 (SRY-box transcription factor 2), Nanog, and Oct4 (octamer-binding transcription factor 4). However, overexpressed lncRNA GAS5 and curcumin made the inhibitory effect disappear. In conclusion, this study demonstrated that curcumin could inhibit the expression of lncRNA GAS5, thereby inhibiting the expression of inflammation-related factors IL-1β, TNF-α, and IL-6, and ultimately achieve the purpose of attenuating cerebral ischemic cell damage. However, curcumin and lncRNA GAS5 may not alleviate cerebral ischemic cell damage by affecting stem cell differentiation.

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嵌段共聚物纳米胶囊包裹的姜黄素通过抑制lncRNA GAS5减轻脑缺血损伤并影响干细胞标记表达
脑卒中已成为我国居民最常见的死亡原因,其中缺血性脑卒中占绝大多数,达到70%-80%。积极研究IS(缺血性脑卒中)后脑缺血损伤的保护机制具有重要意义。我们构建了体内 MACO 大鼠脑缺血损伤模型和体外(氧-葡萄糖剥夺细胞模型)脑缺血损伤模型,并设立了不同的干扰组。通过RT-PCR(逆转录PCR)检测不同组神经细胞、脑组织和血浆中lncRNA的表达,通过ELISA(酶联免疫吸附试验)和Western blot检测不同组神经细胞、脑组织和血浆中蛋白的表达。细胞活性检测采用 CCK-8 法,细胞凋亡检测采用 TUNEL(末端脱氧核苷酸转移酶 dUTP 缺口标记)法。在大鼠的神经细胞和脑组织中,姜黄素能抑制 lncRNA GAS5(长非编码 RNA 生长停滞特异性 5)的表达。在缺氧-缺糖的体外神经元细胞中,姜黄素和低表达的lncRNA GAS5能增强细胞活性,减少细胞凋亡,但添加姜黄素和高表达的lncRNA GAS5能使这一现象消失。在神经元细胞、血浆和脑组织中,姜黄素和低表达的lncRNA GAS5能抑制IL-1β(白细胞介素1β)、TNF-α(肿瘤坏死因子α)、IL-6(白细胞介素6)、Sox2(SRY盒转录因子2)、Nanog和Oct4(八聚体结合转录因子4)的表达。然而,过表达的lncRNA GAS5和姜黄素会使抑制作用消失。总之,本研究表明姜黄素能抑制lncRNA GAS5的表达,从而抑制炎症相关因子IL-1β、TNF-α和IL-6的表达,最终达到减轻脑缺血细胞损伤的目的。然而,姜黄素和lncRNA GAS5可能不会通过影响干细胞分化来减轻脑缺血细胞损伤。
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来源期刊
Stem Cells International
Stem Cells International CELL & TISSUE ENGINEERING-
CiteScore
8.10
自引率
2.30%
发文量
188
审稿时长
18 weeks
期刊介绍: Stem Cells International is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies in all areas of stem cell biology and applications. The journal will consider basic, translational, and clinical research, including animal models and clinical trials. Topics covered include, but are not limited to: embryonic stem cells; induced pluripotent stem cells; tissue-specific stem cells; stem cell differentiation; genetics and epigenetics; cancer stem cells; stem cell technologies; ethical, legal, and social issues.
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