An update on the lithogenic mechanisms of cholecystokinin a receptor (Cckar), an important gallstone gene for lith13

Helen H. Wang, Piero Portincasa, Min Liu, Patrick Tso, David Q.H. Wang

Research output: Contribution to journalReview articlepeer-review

1 Scopus citations

Abstract

The cholecystokinin A receptor (CCKAR) is expressed predominantly in the gallbladder and small intestine in the digestive system, where it is responsible for CCK’s regulation of gallbladder and small intestinal motility. The effect of CCKAR on small intestinal transit is a physiological response for regulating intestinal cholesterol absorption. The Cckar gene has been identified to be an important gallstone gene, Lith13, in inbred mice by a powerful quantitative trait locus analysis. Knockout of the Cckar gene in mice enhances cholesterol cholelithogenesis by impairing gallbladder contraction and emptying, promoting cholesterol crystallization and crystal growth, and increasing intestinal cholesterol absorption. Clinical and epidemiological studies have demonstrated that several variants in the CCKAR gene are associated with increased prevalence of cholesterol cholelithiasis in humans. Dysfunctional gallbladder emptying in response to exogenously administered CCK-8 is often found in patients with cholesterol gallstones, and patients with pigment gallstones display an intermediate degree of gallbladder motility defect. Gallbladder hypomotility is also revealed in some subjects without gallstones under several conditions: pregnancy, total parenteral nutrition, celiac disease, oral contraceptives and conjugated estrogens, obesity, diabetes, the metabolic syndrome, and administration of CCKAR antagonists. The physical–chemical, genetic, and molecular studies of Lith13 show that dysfunctional CCKAR enhances susceptibility to cholesterol gallstones through two primary mechanisms: impaired gallbladder emptying is a key risk factor for the development of gallbladder hypomotility, biliary sludge (the precursor of gallstones), and microlithiasis, as well as delayed small intestinal transit augments cholesterol absorption as a major source for the hepatic hypersecretion of biliary cholesterol and for the accumulation of excess cholesterol in the gallbladder wall that further worsens impaired gallbladder motor function. If these two defects in the gallbladder and small intestine could be prevented by the potent CCKAR agonists, the risk of developing cholesterol gallstones could be dramatically reduced.

Original languageEnglish (US)
Article number1438
Pages (from-to)1-21
Number of pages21
JournalGenes
Volume11
Issue number12
DOIs
StatePublished - Dec 2020

Keywords

  • Bile salts
  • Biliary sludge
  • Cholesterol nucleation and crystallization
  • Gallbladder motility
  • Intestinal cholesterol absorption
  • Lith genes
  • Lithogenic bile
  • Microlithiasis
  • Mucin gel

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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