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Sphingolipids in Atherosclerosis: Chimeras in Structure and Function

期刊

出版社

MDPI
DOI: 10.3390/ijms231911948

关键词

cardiovascular disease; atherosclerosis; sphingolipids; ceramide; sphingosine-1-phosphate; dihydrocerammide; lactosylceramide; glucosylceramide; sphingomyelin

资金

  1. German Research Foundation [SFB-TR84 A, SFB 1449 B1, SFB 1470 A4, KU1218/9-1, KU1218/11-1, KU1218/12-1]
  2. German Centre for Cardiovascular Research (DZHK)
  3. German Ministry of Education and Research (BMBF) [01ZX1906A, 01KI20160A]
  4. DZHK
  5. German Foundation for Heart Research

向作者/读者索取更多资源

Atherosclerosis is a global health issue, and understanding the underlying cellular and molecular mechanisms like sphingolipids is crucial for disease treatment.
Atherosclerosis-a systemic inflammatory disease-is the number one cause of mortality and morbidity worldwide. As such, the prevention of disease progression is of global interest in order to reduce annual deaths at a significant scale. Atherosclerosis is characterized by plaque formation in the arteries, resulting in vascular events such as ischemic stroke or myocardial infarction. A better understanding of the underlying pathophysiological processes at the cellular and molecular level is indispensable to identify novel therapeutic targets that may alleviate disease initiation or progression. Sphingolipids-a lipid class named after the chimeric creature sphinx-are considered to play a critical and, metaphorically, equally chimeric regulatory role in atherogenesis. Previous studies identified six common sphingolipids, namely dihydroceramide (DhCer), ceramide (Cer), sphingosine-1-phosphate (S1P), sphingomyelin (SM), lactosylceramide (LacCer), and glucosylceramide (GluCer) in carotid plaques, and demonstrated their potential as inducers of plaque inflammation. In this review, we point out their specific roles in atherosclerosis by focusing on different cell types, carrier molecules, enzymes, and receptors involved in atherogenesis. Whereas we assume mainly atheroprotective effects for GluCer and LacCer, the sphingolipids DhCer, Cer, SM and S1P mediate chimeric functions. Initial studies demonstrate the successful use of interventions in the sphingolipid pathway to prevent atherosclerosis. However, as atherosclerosis is a multifactorial disease with a variety of underlying cellular processes, it is imperative for future research to emphasize the circumstances in which sphingolipids exert protective or progressive functions and to evaluate their therapeutic benefits in a spatiotemporal manner.

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