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直链醛类可引发B16黑色素瘤细胞中的钙反应。

Linear chain aldehydes evoke calcium responses in B16 melanoma cells.

作者信息

Ishikawa Yuki, Ohara Kazuyuki, Ohshima Toshiaki, Ushio Hideki

机构信息

Department of Food Science and Technology, Tokyo University of Marine Science and Technology, 5-7 Konan 4, Minato, Tokyo 108-8477, Japan.

Laboratory of Marine Biochemistry, Graduate School of Agriculture and Life Sciences, The University of Tokyo, 1-1 Yayoi 1, Bunkyo, Tokyo 113-8657, Japan.

出版信息

EXCLI J. 2011 Dec 9;10:303-311. eCollection 2011.

Abstract

Oxidative stress is involved in various physiological impairing stages, such as aging, diabetes, atherosclerosis, cirrhosis, and neurological disorders. Recent research indicates that aldehyde compounds derived from oxidized lipids increase in cancer patients compared to healthy individuals. Among of them, hexanal, a six-carbon liner chain aldehyde, is commonly found in cancer patients. Lipid oxidation products including aldehydes are in general chemically unstable and react with biological molecules such as proteins. The purpose of this study is to investigate effects of lipid-derived aldehydes and the related compounds on intracellular Ca responses in B16 melanoma cells. Hexanal-induced [Ca] elevation is observed in B16 cells in a dose dependent manner, but [Ca] changes were observed neither in 3T3-L1 cells nor Caco-2 cells. Propanal, a chain length analogue of hexanal, elicited no change in [Ca], but nonanal initiated [Ca] increases. Analogue compounds of hexanal failed to induce [Ca] elevation. Furthermore, unsaturated aldehydes known as TRPA1 channel agonists also failed to alter [Ca] levels in B16 melanoma cells. Pharmacological spectra using inhibitors against intracellular Ca signaling suggest that hexanal-induced [Ca] responses in B16 cells might be involved in TRP channels other than TRPA1. Our results suggest that saturated aliphatic chain aldehydes would be novel compounds for initiating [Ca] increases through very strict recognitions of chain saturation, aldehydic base structures, and chain lengths in B16 melanoma cells. B16 cells would have sensing mechanisms for oxidative status and/or metabolic activities in their growth environment.

摘要

氧化应激参与了各种生理损伤阶段,如衰老、糖尿病、动脉粥样硬化、肝硬化和神经紊乱。最近的研究表明,与健康个体相比,癌症患者体内源自氧化脂质的醛类化合物有所增加。其中,己醛,一种六碳直链醛,在癌症患者中普遍存在。包括醛类在内的脂质氧化产物一般化学性质不稳定,会与蛋白质等生物分子发生反应。本研究的目的是探究脂质衍生醛类及其相关化合物对B16黑色素瘤细胞内钙反应的影响。在B16细胞中观察到己醛诱导的[Ca]升高呈剂量依赖性,但在3T3-L1细胞和Caco-2细胞中均未观察到[Ca]的变化。丙醛,己醛的链长类似物,未引起[Ca]的变化,但壬醛引发了[Ca]的增加。己醛的类似化合物未能诱导[Ca]升高。此外,作为TRPA1通道激动剂的不饱和醛类也未能改变B16黑色素瘤细胞中的[Ca]水平。使用针对细胞内钙信号传导抑制剂的药理学光谱表明,B16细胞中己醛诱导的[Ca]反应可能涉及TRPA1以外的TRP通道。我们的结果表明,饱和脂肪链醛类可能是通过对链饱和度、醛基结构和链长的非常严格的识别在B16黑色素瘤细胞中引发[Ca]增加的新型化合物。B16细胞可能在其生长环境中具有感知氧化状态和/或代谢活性的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed3b/5611634/b1c364276fa8/EXCLI-10-303-g-001.jpg

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