Endothelial cell phenotype is linked to endothelial dysfunction in individuals with a family history of type 2 diabetes.

IF 1.1 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Hormone Molecular Biology and Clinical Investigation Pub Date : 2024-11-25 DOI:10.1515/hmbci-2024-0070
Noé Alvarado-Vásquez, Bettina Sommer, María Eva González-Trujano
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Abstract

Objectives: The patient's family history of type 2 diabetes (FH-DM2) has been negatively associated with the functionality of endothelial cells (ECs). Our objectives in this work were to use human umbilical vein endothelial cells (HUVECs) as a model, to substantiate whether FH-DM2 influences endothelial phenotype and impairs NO and ROS synthesis, cell metabolism, and mitochondrial activity of ECs from individuals with FH-DM2.

Methods: In this study were evaluated the synthesis of reactive oxygen species (ROS) and nitric oxide (NO), mitochondrial membrane potential (MMP), mRNA of eNOS, glucose consumption, and lactate synthesis in HUVECs from newborns with FH-DM2. Furthermore, we also evaluated EC complexity and cell size through flow cytometry.

Results: Our results showed significant differences in HUVECs with FH-DM2, regarding their complexity and cell size, in the synthesis of ROS (p<0.01), and NO (p<0.05); they also reflected diminished glucose consumption and slight changes in the lactate levels.

Conclusion: In conclusion, our results showed that HUVECs from children with FH-DM2 have a reduced capability of synthesizing ROS and NO, which might be linked to the metabolism of endothelial cells. These results are relevant since early endothelial dysfunction has been reported in individuals with FH-DM2, and could be used to establish preventive measures to reduce the risk of developing atherosclerosis or cardiovascular diseases in healthy individuals, but with this family background.

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内皮细胞表型与 2 型糖尿病家族史患者的内皮功能障碍有关。
研究目的患者的 2 型糖尿病家族史(FH-DM2)与内皮细胞(ECs)的功能呈负相关。我们这项工作的目的是以人脐静脉内皮细胞(HUVECs)为模型,证实 FH-DM2 是否会影响内皮表型并损害 FH-DM2 患者内皮细胞的 NO 和 ROS 合成、细胞代谢和线粒体活性:本研究评估了 FH-DM2 新生儿 HUVECs 中活性氧(ROS)和一氧化氮(NO)的合成、线粒体膜电位(MMP)、eNOS 的 mRNA、葡萄糖消耗和乳酸合成。此外,我们还通过流式细胞术评估了EC的复杂性和细胞大小:结果:我们的结果表明,患有 FH-DM2 的 HUVECs 在 ROS 合成(pC)、复杂性和细胞大小方面存在明显差异:总之,我们的研究结果表明,FH-DM2 患儿的 HUVECs 合成 ROS 和 NO 的能力下降,这可能与内皮细胞的新陈代谢有关。这些结果很有意义,因为有报道称,FH-DM2 患儿会出现早期内皮功能障碍,这些结果可用于制定预防措施,以降低健康人患动脉粥样硬化或心血管疾病的风险。
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来源期刊
Hormone Molecular Biology and Clinical Investigation
Hormone Molecular Biology and Clinical Investigation BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
2.60
自引率
0.00%
发文量
55
期刊介绍: Hormone Molecular Biology and Clinical Investigation (HMBCI) is dedicated to the provision of basic data on molecular aspects of hormones in physiology and pathophysiology. The journal covers the treatment of major diseases, such as endocrine cancers (breast, prostate, endometrium, ovary), renal and lymphoid carcinoma, hypertension, cardiovascular systems, osteoporosis, hormone deficiency in menopause and andropause, obesity, diabetes, brain and related diseases, metabolic syndrome, sexual dysfunction, fetal and pregnancy diseases, as well as the treatment of dysfunctions and deficiencies. HMBCI covers new data on the different steps and factors involved in the mechanism of hormone action. It will equally examine the relation of hormones with the immune system and its environment, as well as new developments in hormone measurements. HMBCI is a blind peer reviewed journal and publishes in English: Original articles, Reviews, Mini Reviews, Short Communications, Case Reports, Letters to the Editor and Opinion papers. Ahead-of-print publishing ensures faster processing of fully proof-read, DOI-citable articles.
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