Human Intestinal PEPT1 Transporter Expression and Localization in Preterm and Term Infants

Drug Metab Dispos. 2016 Jul;44(7):1014-9. doi: 10.1124/dmd.115.068809. Epub 2016 Apr 14.

Abstract

The intestinal influx oligopeptide transporter peptide transporter 1 (PEPT1) (SLC15A1) is best known for nutrient-derived di- and tripeptide transport. Its role in drug absorption is increasingly recognized. To better understand the disposition of PEPT1 substrate drugs in young infants, we studied intestinal PEPT1 mRNA expression and tissue localization across the pediatric age range. PEPT1 mRNA expression was determined using real-time reverse-transcription polymerase chain reaction in small intestinal tissues collected from surgical procedures (neonates and infants) or biopsies (older children and adolescents). PEPT1 mRNA relative to villin mRNA expression was compared between neonates/infants and older children/adolescents. PEPT1 was visualized in infant tissue using immunohistochemical staining. Other transporters [multidrug resistance protein 1 (MDR1), multidrug resistance-like protein 2 (MRP2), and organic anion transporter polypeptide 2B1 (OATP2B1)] were also stained to describe the localization in relation to PEPT1. Twenty-six intestinal samples (n = 20 neonates/infants, n = 2 pediatric, n = 4 adolescents) were analyzed. The young infant samples were collected at a median (range) gestational age at birth of 29.2 weeks (24.7-40) and postnatal age of 2.4 weeks (0-16.6). The PEPT1 mRNA expression of the neonates/infants was only marginally lower (0.8-fold) than the older children (P < 0.05). Similar and clear apical PEPT1 and MRP2 staining, apical and lateral MDR1 staining, and intraepithelial OATP2B1 staining at the basolateral membrane of the enterocyte were detected in 12 infant and 2 adolescent samples. Although small intestinal PEPT1 expression tended to be lower in neonates than in older children, this difference is small and tissue distribution is similar. This finding suggests similar oral absorption of PEPT1 substrates across the pediatric age range.

Publication types

  • Comparative Study

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B / metabolism
  • Adolescent
  • Age Factors
  • Child
  • Child, Preschool
  • Enterocytes / metabolism
  • Female
  • Gene Expression Regulation, Developmental
  • Gestational Age
  • Humans
  • Infant
  • Infant, Newborn
  • Infant, Premature*
  • Intestine, Small / metabolism*
  • Male
  • Multidrug Resistance-Associated Proteins / metabolism
  • Organic Anion Transporters / metabolism
  • Peptide Transporter 1 / genetics
  • Peptide Transporter 1 / metabolism*
  • Premature Birth*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Term Birth*

Substances

  • ABCB1 protein, human
  • ATP Binding Cassette Transporter, Subfamily B
  • Multidrug Resistance-Associated Proteins
  • Organic Anion Transporters
  • Peptide Transporter 1
  • RNA, Messenger
  • SLC15A1 protein, human
  • SLCO2B1 protein, human
  • multidrug resistance-associated protein 2