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通过二维电泳进行蛋白质组学分析,以鉴定由肿瘤坏死因子α和白细胞介素-1β刺激的正常人软骨细胞蛋白质组。

Proteomic analysis by two-dimensional electrophoresis to identify the normal human chondrocyte proteome stimulated by tumor necrosis factor alpha and interleukin-1beta.

作者信息

Cillero-Pastor Berta, Ruiz-Romero Cristina, Caramés Beatriz, López-Armada María J, Blanco Francisco J

机构信息

INIBIC, Complejo Hospitalario Universitario A Coruña, A Coruña, Spain.

出版信息

Arthritis Rheum. 2010 Mar;62(3):802-14. doi: 10.1002/art.27265.

Abstract

OBJECTIVE

To determine the intracellular proteome of normal human chondrocytes stimulated with interleukin-1beta (IL-1beta) and tumor necrosis factor alpha (TNFalpha) and to ascertain differences in the protein expression patterns of these 2 cytokines.

METHODS

Normal human knee cartilage chondrocytes were incubated for 48 hours without stimulation or stimulated with IL-1beta (5 ng/ml) or with TNFalpha (10 ng/ml). For each culture condition, protein extracts from 4 normal subjects were pooled and resolved using 2-dimensional electrophoresis. Protein spots were visualized with Sypro stain, and qualitative and quantitative analyses were performed using PDQuest software. Protein spots were then identified by mass spectrometry, using matrix-assisted laser desorption ionization-time-of-flight/time-of-flight technology.

RESULTS

We identified 37 spots by mass spectrometry (MS) or by MS/MS, corresponding to 35 different proteins. In IL-1beta-stimulated chondrocytes, IL-1beta was found to modulate 22 proteins, as compared with unstimulated chondrocytes. All of these proteins except connective tissue growth factor (CCND2) were up-regulated. Proteins involved in cellular metabolism and energy (23%) that were up-regulated or induced by IL-1beta included nicotinamide phosphoribosyltransferase, long-chain fatty acid-coenzyme A ligase 4, delta-aminolevulinic acid dehydratase, triosephosphate isomerase, and an isoform of glyceraldehyde-3-phosphate dehydrogenase. In TNFalpha-stimulated chondrocytes, TNFalpha was found to modulate 20 proteins, as compared with unstimulated chondrocytes. All of these except chitinase 3-like 1 (cartilage glycoprotein 39), proteasome activator complex subunit 2, and G3PDH, were up-regulated. Eighteen proteins were differently modulated by IL-1beta and TNFalpha. Of these, 45% were related to metabolism.

CONCLUSION

IL-1beta and TNFalpha induce different profiles of intracellular protein expression in healthy human chondrocytes. Most of the proteins that are differently regulated are proteins that are implicated in the generation of cellular energy and in glycolysis.

摘要

目的

确定白细胞介素-1β(IL-1β)和肿瘤坏死因子α(TNFα)刺激下正常人软骨细胞的细胞内蛋白质组,并确定这两种细胞因子在蛋白质表达模式上的差异。

方法

将正常人膝关节软骨细胞在无刺激条件下培养48小时,或用IL-1β(5 ng/ml)或TNFα(10 ng/ml)刺激。对于每种培养条件,将来自4名正常受试者的蛋白质提取物合并,并使用二维电泳进行分离。用Sypro染色剂使蛋白质斑点可视化,并使用PDQuest软件进行定性和定量分析。然后使用基质辅助激光解吸电离飞行时间/飞行时间技术通过质谱法鉴定蛋白质斑点。

结果

我们通过质谱(MS)或串联质谱(MS/MS)鉴定了37个斑点,对应于35种不同的蛋白质。与未刺激的软骨细胞相比,在IL-1β刺激的软骨细胞中,发现IL-1β调节了22种蛋白质。除结缔组织生长因子(CCND2)外,所有这些蛋白质均上调。IL-1β上调或诱导的参与细胞代谢和能量代谢(23%)的蛋白质包括烟酰胺磷酸核糖基转移酶、长链脂肪酸辅酶A连接酶4、δ-氨基乙酰丙酸脱水酶、磷酸丙糖异构酶和甘油醛-3-磷酸脱氢酶的一种同工型。与未刺激的软骨细胞相比,在TNFα刺激的软骨细胞中,发现TNFα调节了20种蛋白质。除几丁质酶3样1(软骨糖蛋白39)、蛋白酶体激活复合物亚基2和甘油醛-3-磷酸脱氢酶外,所有这些蛋白质均上调。18种蛋白质受到IL-1β和TNFα的不同调节。其中,45%与代谢有关。

结论

IL-1β和TNFα在健康人软骨细胞中诱导不同的细胞内蛋白质表达谱。大多数受到不同调节的蛋白质是与细胞能量产生和糖酵解有关的蛋白质。

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