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基因芯片分析显示 IBSP 在人颈动脉斑块中过表达。

Microarray analysis reveals overexpression of IBSP in human carotid plaques.

机构信息

University Claude Bernard Lyon, Faculty of Pharmacy, Laboratory of Pharmacology, INSERM team on vascular attacks and tissue responses, Lyon, France.

出版信息

Adv Med Sci. 2012;57(2):334-40. doi: 10.2478/v10039-012-0056-0.

Abstract

PURPOSE

Vascular calcification was considered to be a passive, degenerative, and end-stage process of vascular disease. However, bone associated proteins such as bone morphogenetic proteins, osteopontin, osteonectin, osteocalcin, and matrix Gla protein (MGP) have been found in the calcified atherosclerotic lesions. We studied by microarray analysis whether intact tissue and carotid plaque from the same patient differ in transcriptional profiling in response to arterial calcification.

MATERIAL AND METHODS

mRNA gene expression was measured by an Affymetrix GeneChip Human Gene 1.0 ST arrays (Affymetrix, Santa Clara, CA, USA) using RNA prepared from 68 specimens of endarterectomy from 34 patients.

RESULTS

Integrin-binding sialoprotein (IBSP) was found to be differentially expressed. IBSP mRNA is over expressed in atheroma plaque (3.74 fold, p = 1.41E-09) in an intraindividual comparison. Besides, Carbonic anhydrase II (CA2) which known to be a putative calcification inhibitory molecule is over expressed more than 1.7 fold in carotid plaque (p = 1.26E-06).

CONCLUSION

Although further evidence is needed, our results support previously available data. To our knowledge, this is the first report comparing gene expression between intact arterial tissue and carotid plaque using microarray analysis in order to identify calcification related genes. We suggest that plaques show a more pronounced induction of IBSP that may cause arterial calcification.

摘要

目的

血管钙化被认为是血管疾病的一种被动、退行性和终末期过程。然而,骨形态发生蛋白、骨桥蛋白、骨连接素、骨钙素和基质 Gla 蛋白(MGP)等骨相关蛋白已在钙化的动脉粥样硬化病变中被发现。我们通过微阵列分析研究了同一患者的完整组织和颈动脉斑块在对动脉钙化的转录谱反应方面是否存在差异。

材料和方法

使用来自 34 名患者的 68 个内膜切除术标本制备的 RNA,通过 Affymetrix GeneChip Human Gene 1.0 ST 阵列(Affymetrix,Santa Clara,CA,USA)测量 mRNA 基因表达。

结果

发现整合素结合唾液蛋白(IBSP)表达差异。IBSP mRNA 在个体内比较中在动脉粥样硬化斑块中过度表达(3.74 倍,p = 1.41E-09)。此外,已知是潜在钙化抑制分子的碳酸酐酶 II(CA2)在颈动脉斑块中的表达超过 1.7 倍(p = 1.26E-06)。

结论

尽管需要进一步的证据,但我们的结果支持先前可用的数据。据我们所知,这是首次使用微阵列分析比较完整动脉组织和颈动脉斑块之间的基因表达以鉴定与钙化相关的基因。我们认为斑块中 IBSP 的诱导更为明显,这可能导致动脉钙化。

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