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非肥胖非糖尿病与肥胖非糖尿病皮马印第安人前脂肪细胞/基质血管细胞中基质金属蛋白酶3(MMP3)的差异表达

Differential expression of matrix metalloproteinase 3 (MMP3) in preadipocytes/stromal vascular cells from nonobese nondiabetic versus obese nondiabetic Pima Indians.

作者信息

Traurig Michael T, Permana Paska A, Nair Saraswathy, Kobes Sayuko, Bogardus Clifton, Baier Leslie J

机构信息

NIDDK, NIH, 445 North 5th St., Phoenix, AZ 85004, USA.

出版信息

Diabetes. 2006 Nov;55(11):3160-5. doi: 10.2337/db06-0373.

Abstract

Prior microarray studies comparing global gene expression patterns in preadipocytes/stromal vascular cells isolated from nonobese nondiabetic versus obese nondiabetic Pima Indians showed that matrix metalloproteinase 9 (MMP9) is upregulated in obese subjects. The current study targeted analysis of nine additional MMP genes that cluster to a region on chromosome 11q22 that is linked to BMI and percent body fat. Differential-display PCR showed that MMP3 is downregulated in preadipocytes/stromal vascular cells from obese subjects, and real-time PCR showed that MMP3 expression levels are negatively correlated with percent body fat. To determine whether variants within MMP3 are responsible for its altered expression, MMP3 was sequenced, and seven representative variants were genotyped in 1,037 Pima subjects for association analyses. Two variants were associated with both BMI and type 2 diabetes, and two additional variants were associated with type 2 diabetes alone; however, none of these variants were associated with MMP3 expression levels. We propose that the MMP3 pathway is altered in human obesity, but this alteration may be the result of a combination of genetic variation within the MMP3 locus itself, as well as variation in additional factors, either primary or secondary to obesity, that regulate expression of the MMP3 gene.

摘要

先前的微阵列研究比较了从非肥胖非糖尿病与肥胖非糖尿病皮马印第安人分离出的前脂肪细胞/基质血管细胞中的整体基因表达模式,结果显示基质金属蛋白酶9(MMP9)在肥胖受试者中上调。当前研究针对另外9个MMP基因进行分析,这些基因聚集在11号染色体q22区域,该区域与体重指数(BMI)和体脂百分比相关。差异显示PCR表明,肥胖受试者的前脂肪细胞/基质血管细胞中MMP3表达下调,实时PCR显示MMP3表达水平与体脂百分比呈负相关。为了确定MMP3内的变异是否导致其表达改变,对MMP3进行了测序,并在1037名皮马受试者中对7个代表性变异进行基因分型以进行关联分析。两个变异与BMI和2型糖尿病均相关,另外两个变异仅与糖尿病相关;然而,这些变异均与MMP3表达水平无关。我们提出,人类肥胖中MMP3途径发生改变,但这种改变可能是MMP3基因座本身的遗传变异以及肥胖原发性或继发性的其他调节MMP3基因表达的因素变异共同作用的结果。

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