Uncovering the link between diabetes and cardiovascular diseases: insights from adipose-derived stem cells

被引:1
|
作者
Meechem, Megan B. [1 ,2 ]
Jadli, Anshul S. [1 ,2 ]
Patel, Vaibhav B. [1 ,2 ]
机构
[1] Univ Calgary, Cumming Sch Med, Dept Physiol & Pharmacol, Calgary, AB, Canada
[2] Univ Calgary, Libin Cardiovasc Inst, Calgary, AB, Canada
关键词
adipose-derived stem cells; adipose tissue; diabetes; cardiovascular disease; REGENERATIVE CELLS; SIGNALING PATHWAY; REACTIVE OXYGEN; RISK-FACTORS; TISSUE; APOPTOSIS; TRANSPLANTATION; OBESITY; MODEL; PATHOPHYSIOLOGY;
D O I
10.1139/cjpp-2023-0282
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cardiovascular diseases (CVDs) are the leading causes of morbidity and mortality worldwide. The escalating global occurrence of obesity and diabetes mellitus (DM) has led to a significant upsurge in individuals afflicted with CVDs. As the prevalence of CVDs continues to rise, it is becoming increasingly important to identify the underlying cellular and molecular mechanisms that contribute to their development and progression, which will help discover novel therapeutic avenues. Adipose tissue (AT) is a connective tissue that plays a crucial role in maintaining lipid and glucose homeostasis. However, when AT is exposed to diseased conditions, such as DM, this tissue will alter its phenotype to become dysfunctional. AT is now recognized as a critical contributor to CVDs, especially in patients with DM. AT is comprised of a heterogeneous cellular population, which includes adipose -derived stem cells (ADSCs). ADSCs resident in AT are believed to regulate physiological cardiac function and have potential cardioprotective roles. However, recent studies have also shown that ADSCs from various adipose tissue depots become pro-apoptotic, pro -inflammatory, less angiogenic, and lose their ability to differentiate into various cell lineages upon exposure to diabetic conditions. This review aims to summarize the current understanding of the physiological roles of ADSCs, the impact of DM on ADSC phenotypic changes, and how these alterations may contribute to the pathogenesis of CVDs.
引用
收藏
页码:229 / 241
页数:13
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