Sodium taurocholate cotransporting polypeptide (SLC10A1) deficiency: Conjugated hypercholanemia without a clear clinical phenotype

F M. Vaz, C.C. Paulusma, H. Huidekoper, M. de Ru, C. Lim, J. Koster, K. Ho-Mok, A.H. Bootsma, A.K. Groen, F.G. Schaap, R.P. Oude Elferink, H.R. Waterham, R.J. Wanders

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Abstract

The enterohepatic circulation of bile salts is an important physiological route to recycle bile salts and ensure intestinal absorption of dietary lipids. The Na+ -taurocholate cotransporting polypeptide SLC10A1 (NTCP) plays a key role in this process as the major transporter of conjugated bile salts from the plasma compartment into the hepatocyte. Here we present the first patient with NTCP deficiency, who was clinically characterized by mild hypotonia, growth retardation and delayed motor milestones. Total bile salts in plasma were extremely elevated (up to 1500 microM, ref. <16.3) but there were no clinical signs of cholestatic jaundice, pruritis or liver dysfunction. Bile salt synthesis and intestinal bile salt signaling were not affected as evidenced by normal plasma 7alpha-hydroxy-4-cholesten-3-one (C4) and FGF19 levels. Importantly, the presence of secondary bile salts in the circulation suggested residual enterohepatic cycling of bile salts. Sequencing of the SLC10A1 gene revealed a single homozygous non-synonymous point mutation in the coding sequence of the gene resulting in an arginine to histidine substitution at position 252. Functional studies showed that this mutation resulted in a markedly reduced uptake activity of taurocholic acid. Immunofluorescence studies and surface biotinylation experiments demonstrated that the mutant protein is virtually absent from the plasma membrane. Conclusion: we describe the identification of NTCP deficiency as a new inborn error of metabolism with a relatively mild clinical phenotype. The identification of NTCP deficiency confirms that this transporter is the main import system for conjugated bile salts into the liver but also indicates that auxiliary transporters are able to sustain the enterohepatic cycle in its absence. (Hepatology 2014;).
Original languageEnglish
Pages (from-to)260-267
Number of pages8
JournalHepatology
Volume61
Issue number1
DOIs
Publication statusPublished - 1 Jan 2015

Keywords

  • BILE-ACID TRANSPORTERS
  • FAMILIAL INTRAHEPATIC CHOLESTASIS
  • LIVER
  • HEPATOCYTES
  • EXPRESSION
  • MUTATIONS
  • DRUG

Cite this

Vaz, F. M., Paulusma, C. C., Huidekoper, H., de Ru, M., Lim, C., Koster, J., Ho-Mok, K., Bootsma, A. H., Groen, A. K., Schaap, F. G., Oude Elferink, R. P., Waterham, H. R., & Wanders, R. J. (2015). Sodium taurocholate cotransporting polypeptide (SLC10A1) deficiency: Conjugated hypercholanemia without a clear clinical phenotype. Hepatology, 61(1), 260-267. https://doi.org/10.1002/hep.27240