实验性肥胖中脂肪组织贮库特异性表达和纤维化相关基因和蛋白质的调控。

IF 2.7 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Mammalian Genome Pub Date : 2024-03-01 Epub Date: 2023-10-26 DOI:10.1007/s00335-023-10022-3
Kristina Eisinger, Philipp Girke, Christa Buechler, Sabrina Krautbauer
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引用次数: 0

摘要

转化生长因子β(Tgfb)是一种研究充分的促纤维化细胞因子,它上调细胞通讯网络因子2(Ccn2)、胶原和肌动蛋白α2、平滑肌(Acta2)的表达。肥胖会导致脂肪组织纤维化,从而导致代谢性疾病。本工作旨在分析Tgfb、Ccn2、胶原1A1(Col1a1)、Acta2、BMP和激活素膜结合抑制剂(Bambi)在喂食标准食物的小鼠、喂食高脂饮食(HFD)的小鼠和ob/ob小鼠的不同脂肪组织库中的表达。主要是,这些基因在棕色脂肪组织中低表达,而这种差异在ob/ob小鼠中不太明显。HFD喂养后,脂肪组织中没有诱导Ccn2和Bambi蛋白以及mRNA表达和胶原1a1 mRNA,而白色脂肪库中的Tgfb和Acta2 mRNA增加。免疫印迹分析显示,Acta2蛋白在这些小鼠的皮下和肾周脂肪中较高。在ob/ob小鼠中,Ccn2mRNA和Ccn2蛋白在脂肪库中上调。在此,Tgfb、Acta2和Col1a1 mRNA水平以及血清Tgfb蛋白增加。然而,Acta2蛋白在这些小鼠的皮下和肾周脂肪中并不高。Col6a1信使核糖核酸以前在肥胖脂肪组织中显示较高。目前的分析证明,在HFD喂养的小鼠的皮下脂肪中诱导了Col6a1蛋白。值得注意的是,与相应的对照组相比,ob/ob小鼠的肾周脂肪中的Col6a1减少。3T3-L1细胞表达Ccn2和Bambi蛋白,其水平不受脂肪酸、瘦素、脂多糖、肿瘤坏死因子和白细胞介素-6的影响。所有这些因素都导致3T3-L1脂肪细胞培养基中Tgfb升高,但没有增加其mRNA水平。游离脂肪酸诱导坏死,而细胞凋亡在任何体外孵育中都没有发生,细胞死亡是细胞培养基中Tgfb升高的主要原因。总之,Tgfb mRNA在肥胖的白色脂肪组织中持续被诱导,但其靶基因的明显增加并没有与之平行。此外,观察到Acta2的mRNA和蛋白质表达之间的差异。在肥胖中,脂肪细胞似乎对更高的Tgfb mRNA水平没有贡献。当与代谢功能障碍和纤维化相关的肥胖相关代谢产物攻击时,这些细胞会释放更多的Tgfb蛋白。
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Adipose tissue depot specific expression and regulation of fibrosis-related genes and proteins in experimental obesity.

Transforming growth factor beta (Tgfb) is a well-studied pro-fibrotic cytokine, which upregulates cellular communication network factor 2 (Ccn2), collagen, and actin alpha 2, smooth muscle (Acta2) expression. Obesity induces adipose tissue fibrosis, which contributes to metabolic diseases. This work aimed to analyze the expression of Tgfb, Ccn2, collagen1a1 (Col1a1), Acta2 and BMP and activin membrane-bound inhibitor (Bambi), which is a negative regulator of Tgfb signaling, in different adipose tissue depots of mice fed a standard chow, mice fed a high fat diet (HFD) and ob/ob mice. Principally, these genes were low expressed in brown adipose tissues and this difference was less evident for the ob/ob mice. Ccn2 and Bambi protein as well as mRNA expression, and collagen1a1 mRNA were not induced in the adipose tissues upon HFD feeding whereas Tgfb and Acta2 mRNA increased in the white fat depots. Immunoblot analysis showed that Acta2 protein was higher in subcutaneous and perirenal fat of these mice. In the ob/ob mice, Ccn2 mRNA and Ccn2 protein were upregulated in the fat depots. Here, Tgfb, Acta2 and Col1a1 mRNA levels and serum Tgfb protein were increased. Acta2 protein was, however, not higher in subcutaneous and perirenal fat of these mice. Col6a1 mRNA was shown before to be higher in obese fat tissues. Current analysis proved the Col6a1 protein was induced in subcutaneous fat of HFD fed mice. Notably, Col6a1 was reduced in perirenal fat of ob/ob mice in comparison to the respective controls. 3T3-L1 cells express Ccn2 and Bambi protein, whose levels were not changed by fatty acids, leptin, lipopolysaccharide, tumor necrosis factor and interleukin-6. All of these factors led to higher Tgfb in 3T3-L1 adipocyte media but did not increase its mRNA levels. Free fatty acids induced necrosis whereas apoptosis did not occur in any of the in vitro incubations excluding cell death as a main reason for higher Tgfb in cell media. In summary, Tgfb mRNA is consistently induced in white fat tissues in obesity but this is not paralleled by a clear increase of its target genes. Moreover, discrepancies between mRNA and protein expression of Acta2 were observed. Adipocytes seemingly do not contribute to higher Tgfb mRNA levels in obesity. These cells release more Tgfb protein when challenged with obesity-related metabolites connecting metabolic dysfunction and fibrosis.

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来源期刊
Mammalian Genome
Mammalian Genome 生物-生化与分子生物学
CiteScore
4.00
自引率
0.00%
发文量
33
审稿时长
6-12 weeks
期刊介绍: Mammalian Genome focuses on the experimental, theoretical and technical aspects of genetics, genomics, epigenetics and systems biology in mouse, human and other mammalian species, with an emphasis on the relationship between genotype and phenotype, elucidation of biological and disease pathways as well as experimental aspects of interventions, therapeutics, and precision medicine. The journal aims to publish high quality original papers that present novel findings in all areas of mammalian genetic research as well as review articles on areas of topical interest. The journal will also feature commentaries and editorials to inform readers of breakthrough discoveries as well as issues of research standards, policies and ethics.
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