弹性蛋白衍生肽VGVAPG可减少小鼠胚胎成纤维细胞(3T3-L1)向脂肪细胞的分化。

IF 3.5 4区 生物学 Q2 ENDOCRINOLOGY & METABOLISM
Konrad A Szychowski, Bartosz Skóra, Jakub Tobiasz, Jan Gmiński
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引用次数: 8

摘要

弹性蛋白是存在于结缔组织中的一种高弹性蛋白。由于蛋白酶的活性,弹性蛋白水解发生,在这个过程中,弹性蛋白衍生肽(EDPs)被释放。组成重复的弹性蛋白和EDP构建序列之一是六肽VGVAPG。因此,我们的研究目的是确定VGVAPG肽对小鼠3T3-L1细胞系脂肪生成的影响。3T3-L1细胞按照先前描述的方案分化,并暴露于浓度增加的VGVAPG或VVGPGA肽中。结果表明,VGVAPG肽不刺激活性氧(ROS)的产生、caspase-1的激活和3T3-L1细胞的增殖。在第二部分实验中,通过油红O染色证实了VGVAPG肽降低了脂质积累,并通过未分化前脂肪细胞表达标记物的增加谱证实了这一点。在我们的实验中,添加10 nM VGVAPG分化为脂肪细胞,与罗格列酮(PPARγ激动剂)处理组相比,Pref-1、serpin E1和脂联素的表达增加,同时与罗格列酮处理组相比,VEGF和抵抗素的表达降低。结果表明,VGVAPG肽维持3T3细胞处于未分化状态。缩写:DMSO:二甲基亚砜;弹性结合蛋白;EDPs:弹性蛋白衍生肽;胎牛血清;Glb1: β -半乳糖苷酶基因;低密度脂蛋白:低密度脂蛋白;PAI-1 (Serpin E1):纤溶酶原激活物抑制剂-1;PBS:磷酸盐缓冲盐水;PPARγ:过氧化物酶体增殖物激活受体;Pref-1:前脂肪细胞因子1;ROS:活性氧;VEGF-A:血管内皮生长因子a;VGVAPG: Val-Gly-Val-Ala-Pro-Gly;β加:苷;ORO:油红O;IBMX: 3-isobutyl-1-methylxanthine;H2DCFDA: 2',7'-二氯二氢荧光素二乙酸酯;DMEM: Dulbecco's Modified Eagle's Medium;VVGPGA: Val-Val-Gly-Pro-Gly-Ala。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Elastin-derived peptide VGVAPG decreases differentiation of mouse embryo fibroblast (3T3-L1) cells into adipocytes.

Elastin-derived peptide VGVAPG decreases differentiation of mouse embryo fibroblast (3T3-L1) cells into adipocytes.

Elastin-derived peptide VGVAPG decreases differentiation of mouse embryo fibroblast (3T3-L1) cells into adipocytes.

Elastin-derived peptide VGVAPG decreases differentiation of mouse embryo fibroblast (3T3-L1) cells into adipocytes.

Elastin is a highly elastic protein present in connective tissue. As a result of protease activity, elastin hydrolysis occurs, and during this process, elastin-derived peptides (EDPs) are released. One of the constitutively repeating elastin and EDP building sequences is the hexapeptide VGVAPG. Therefore, the aim of our research was to define the effect of VGVAPG peptide on adipogenesis in a mouse 3T3-L1 cell line. 3T3-L1 cells were differentiated according to a previously described protocol and exposed to increasing concentrations of VGVAPG or VVGPGA peptide. The obtained results showed that VGVAPG peptide does not stimulate reactive oxygen species (ROS) production, caspase-1 activation, and 3T3-L1 cell proliferation. In the second part of the experiments, it was proved that VGVAPG peptide decreased lipid accumulation as measured by oil red O staining, which was confirmed by the profile of increased expression markers of undifferentiated preadipocytes. In our experiments, 10 nM VGVAPG added for differentiating to adipocytes increased the expression of Pref-1, serpin E1, and adiponectin as compared to rosiglitazone (PPARγ agonist)-treated group and simultaneously decreased the expression of VEGF and resistin as compared to the rosiglitazone-treated group. The obtained results show that VGVAPG peptide sustains 3T3 cells in undifferentiated state.

Abbreviations: DMSO: dimethyl sulphoxide; EBP: elastin-binding protein; EDPs: elastin-derived peptides; FBS: foetal bovine serum; Glb1: gene for beta-galactosidase; LDL: low-density-lipoprotein; PAI-1 (Serpin E1): plasminogen activator inhibitor-1; PBS: phosphate-buffered saline; PPARγ: peroxisome proliferator-activated receptor gamma; Pref-1: preadipocyte factor 1; ROS: reactive oxygen species; VEGF-A: vascular endothelial growth factor-A; VGVAPG: Val-Gly-Val-Ala-Pro-Gly; β-Gal: beta-galactosidase; ORO: oil red O; IBMX: 3-isobutyl-1-methylxanthine; H2DCFDA: 2',7'-dichlorodihydrofluorescein diacetate; DMEM: Dulbecco's Modified Eagle's Medium; VVGPGA: Val-Val-Gly-Pro-Gly-Ala.

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来源期刊
Adipocyte
Adipocyte Medicine-Histology
CiteScore
6.50
自引率
3.00%
发文量
46
审稿时长
32 weeks
期刊介绍: Adipocyte recognizes that the adipose tissue is the largest endocrine organ in the body, and explores the link between dysfunctional adipose tissue and the growing number of chronic diseases including diabetes, hypertension, cardiovascular disease and cancer. Historically, the primary function of the adipose tissue was limited to energy storage and thermoregulation. However, a plethora of research over the past 3 decades has recognized the dynamic role of the adipose tissue and its contribution to a variety of physiological processes including reproduction, angiogenesis, apoptosis, inflammation, blood pressure, coagulation, fibrinolysis, immunity and general metabolic homeostasis. The field of Adipose Tissue research has grown tremendously, and Adipocyte is the first international peer-reviewed journal of its kind providing a multi-disciplinary forum for research focusing exclusively on all aspects of adipose tissue physiology and pathophysiology. Adipocyte accepts high-profile submissions in basic, translational and clinical research.
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