C1q/TNF-related Protein 1, a Multifunctional Adipokine: An Overview of Current Data

Am J Med Sci. 2020 Sep;360(3):222-228. doi: 10.1016/j.amjms.2020.05.036. Epub 2020 May 28.

Abstract

The present review aimed to present the research highlights on C1q/TNF-related protein 1 (CTRP1), a member of the recently discovered family of highly conserved adiponectin paralog proteins, C1q tumor necrosis factor-related proteins. CTRP1 plays an important role in regulating body energy homeostasis and sensitivity to insulin. Studies on animal models have shown that it lowers the concentration of glucose. Elevated concentrations of CTRP1 reduce weight gain and diet-induced insulin resistance. CTRP1 limits the extent of ischemia-reperfusion injury in acute myocardial infarction. It inhibits platelet aggregation by blocking von Willebrand factor binding to collagen. In patients with chronic kidney disease, an increase in CTRP1 levels is associated with a lesser degree of disease progression. CTRP1 stimulates aldosterone synthesis in the adrenal cortex by affecting aldosterone synthase expression. In dehydration, an increase in CTRP1 concentration helps to maintain normotension. It participates in processes related to the proliferation and maturation of chondrocytes. It also promotes atherosclerosis, and a surge in its concentration is correlated with a higher cardiovascular risk in patients with coronary atherosclerosis. In vascular smooth muscle cells, it induces the expression of proinflammatory cytokines. An increase in CTRP1 levels is correlated with the progression of the neoplastic process in patients with glioblastoma.

Keywords: C1qTNF-related protein 1; Chronic kidney disease; Coronary artery disease; Glucose and lipid metabolism; Inflammation.

Publication types

  • Review

MeSH terms

  • Adipokines / physiology*
  • Animals
  • Cardiovascular Diseases
  • Chondrogenesis / physiology
  • Energy Metabolism
  • Glucose / metabolism
  • Homeostasis / physiology
  • Humans
  • Inflammation
  • Insulin Resistance / physiology
  • Kidney Diseases
  • Lipid Metabolism / physiology
  • MEDLINE
  • Neoplasms
  • Proteins / physiology*
  • PubMed

Substances

  • Adipokines
  • C1QTNF1 protein, human
  • Proteins
  • Glucose