DETERMINATION OF THE CIRCADIAN OSCILLATION PATTERN OF UNFOLDED PROTEIN RESPONSE SIGNALING COMPONENTS IN HUMAN EMBRYONIC KIDNEY HEK293 CELLS

Q4 Pharmacology, Toxicology and Pharmaceutics
Y. Erzurumlu, Hatice Kübra Doğan, Deniz Çataklı
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Abstract

Objective: The circadian rhythm is one of the primary regulatory systems with near 24-hour oscillations. It has a crucial role in regulating physiological conditions in the human body, including body temperature and the secretion of hormones. Numerous disorders, such as cancer and diabetes, have been linked to disruptions of the cellular circadian rhythm. Herein, we aimed to investigate the relationship between the circadian rhythm and unfolded protein response (UPR) signaling, which is one of the important physiological mechanisms in mammalian cells and has recently been associated with drug resistance, invasion and metastasis in cancer. Material and Method: Human embryonic kidney cell line HEK293 was provided from the American Type Culture Collection and propagated in DMEM containing 10% FBS and growth ingredients. For in vitro circadian synchronization, cells were exposed to 50% and then the oscillation pattern of gene and protein expression of UPR-related target genes was analyzed by agarose gel electrophoresis and immunoblotting, respectively. The oscillation pattern was commented on through curve-fitting analysis. Result and Discussion: Our findings demonstrated that UPR components, including IRE1α, XBP-1s, eIF2α, phospho(Ser51)-eIF2α, PERK, ATF4, GADD34 and ATF6, tightly exhibit oscillation patterns under a circadian rhythm on a 48-hour time scale like the PER1 gene that is a core component of the circadian rhythm. Moreover, endoplasmic reticulum (ER) stress genes, BiP/GRP78 and CHOP, were similar to UPR components under the circadian rhythm. Additionally, we found the activation of UPR signaling harmoniously modulated with the circadian rhythm. Present data indicated that the expression level of UPR components exhibited strict oscillation under the circadian rhythm. Our findings may guide experimental studies of new-generation UPR-targeted drugs to be developed to treat various pathologies in accordance with the circadian rhythm.
确定人类胚胎肾脏 hek293 细胞中折叠蛋白反应信号成分的昼夜振荡模式
目的:昼夜节律是近 24 小时振荡的主要调节系统之一。它在调节人体生理状况(包括体温和激素分泌)方面起着至关重要的作用。癌症和糖尿病等许多疾病都与细胞昼夜节律紊乱有关。昼夜节律是哺乳动物细胞的重要生理机制之一,最近发现它与癌症的耐药性、侵袭和转移有关。材料与方法:人胚胎肾细胞系 HEK293 由美国类型培养物保藏中心提供,在含有 10% FBS 和生长成分的 DMEM 中繁殖。为实现体外昼夜同步,将细胞暴露于 50%的温度,然后分别通过琼脂糖凝胶电泳和免疫印迹法分析 UPR 相关靶基因的基因和蛋白质表达的振荡模式。结果与讨论:我们的研究结果表明,UPR成分,包括IRE1α、XBP-1s、eIF2α、phospho(Ser51)-eIF2α、PERK、ATF4、GADD34和ATF6,与作为昼夜节律核心成分的PER1基因一样,在昼夜节律下紧密表现出48小时时间尺度的振荡模式。此外,内质网(ER)应激基因 BiP/GRP78 和 CHOP 与昼夜节律下的 UPR 成分相似。此外,我们还发现 UPR 信号的激活与昼夜节律协调调节。目前的数据表明,UPR成分的表达水平在昼夜节律下呈现严格的振荡。我们的发现可能会指导新一代 UPR 靶向药物的实验研究,从而开发出符合昼夜节律的药物来治疗各种病症。
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来源期刊
Ankara Universitesi Eczacilik Fakultesi Dergisi
Ankara Universitesi Eczacilik Fakultesi Dergisi Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
0.80
自引率
0.00%
发文量
70
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