Cardiovascular Effects Mediated by HMMR and CD44

Kinga Jaskuła1, Mariusz Sacharczuk1,2, Zbigniew Gaciong3

  • 1Department of Experimental Genomics, Institute of Genetics and Animal Biotechnology, Polish Academy of Sciences, Postępu 36A, Jastrzebiec, Poland.

Insights

Cardiovascular disease (CVD) involves chronic inflammation, with hyaluronic acid receptors CD44 and RHAMM playing key roles. This review explores their specific involvement in CVD development and potential as therapeutic targets.

Area of Science:

  • Cardiovascular research
  • Inflammation biology
  • Molecular cell biology

Background:

  • Cardiovascular disease (CVD) is a major global health concern, with myocardial infarction and stroke as critical outcomes.
  • Chronic inflammation, vascular damage, and oxidative stress are implicated in CVD pathogenesis.
  • Hyaluronic acid (HA) signaling, mediated by receptors CD44 and RHAMM, is crucial in inflammatory processes.

Purpose of the Study:

  • To elucidate the roles of hyaluronic acid receptors CD44 and RHAMM in the development of cardiovascular disease.
  • To review the current understanding of CD44 and RHAMM functions in the context of CVD.
  • To identify potential therapeutic strategies targeting these receptors for CVD treatment.

Main Methods:

  • Literature review of studies investigating hyaluronic acid, CD44, RHAMM, and cardiovascular disease.
  • Analysis of research on the molecular mechanisms linking inflammation and CVD.
  • Synthesis of data on the cellular functions of CD44 and RHAMM in disease models.

Main Results:

  • Both CD44 and RHAMM are implicated in cellular processes relevant to CVD, including inflammation and cell migration.
  • While their structures differ, CD44 and RHAMM may exhibit synergistic or overlapping functions in disease.
  • The precise contribution and interplay of these receptors in CVD pathogenesis require further investigation.

Conclusions:

  • Hyaluronic acid receptors CD44 and RHAMM are significant players in the inflammatory pathways associated with cardiovascular disease.
  • Understanding the specific roles of CD44 and RHAMM in CVD may reveal novel therapeutic targets.
  • Further research is warranted to fully delineate the mechanisms and therapeutic potential of targeting CD44 and RHAMM in CVD.