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Intestinal IMINO transporter SIT1 is not expressed in human newborns


Meier, Chantal Florence; Camargo, Simone M R; Hunziker, Schirin; Moehrlen, Ueli; Gros, Stephanie J; Bode, Peter Karl; Leu, Svenja; Meuli, Martin; Holland-Cunz, Stefan; Verrey, François; Vuille-Dit-Bille, Raphael Nicolas (2018). Intestinal IMINO transporter SIT1 is not expressed in human newborns. American Journal Of Physiology. Gastrointestinal And Liver Physiology, 315(5):G887-G895.

Abstract

The expression of amino acid transporters in small intestine epithelium of human newborns has not been studied yet. It is further not known whether the maturation of imino acid (proline) transport is delayed as in kidney proximal tubule. The possibility to obtain small intestinal tissue from patients undergoing surgery for jejunal or ileal atresia during their first days after birth was used to address these questions. As control, adult terminal ileum tissue was sampled during routine endoscopies. Gene expression of luminal imino- and amino acid transporter SIT1 (SLC6A20) was approximately 3-fold lower in newborns versus adults. mRNA levels of all other luminal and basolateral amino acid transporters and accessory proteins tested were similar in newborn mucosa compared to adults. At the protein level, the major luminal neutral amino acid transporter BAT1 (SLC6A19) and its accessory protein angiotensin-converting enzyme 2 (ACE2) were shown by immunofluorescence to be expressed similarly in newborns and in adults. SIT1 protein was not detectable in the small intestine of human newborns, in contrast to adults. The morphology of newborn intestinal mucosa proximal and distal to the obstruction was generally normal but a decreased proliferation rate was visualized distally of the atresia by lower levels of the mitosis marker Ki-67. The mRNA level of the 13 tested amino acid transporters and accessory proteins was nontheless similar, suggesting that the intestinal obstruction and interruption of amniotic fluid passage through the small intestinal lumen did not affect amino acid transporter expression.

Abstract

The expression of amino acid transporters in small intestine epithelium of human newborns has not been studied yet. It is further not known whether the maturation of imino acid (proline) transport is delayed as in kidney proximal tubule. The possibility to obtain small intestinal tissue from patients undergoing surgery for jejunal or ileal atresia during their first days after birth was used to address these questions. As control, adult terminal ileum tissue was sampled during routine endoscopies. Gene expression of luminal imino- and amino acid transporter SIT1 (SLC6A20) was approximately 3-fold lower in newborns versus adults. mRNA levels of all other luminal and basolateral amino acid transporters and accessory proteins tested were similar in newborn mucosa compared to adults. At the protein level, the major luminal neutral amino acid transporter BAT1 (SLC6A19) and its accessory protein angiotensin-converting enzyme 2 (ACE2) were shown by immunofluorescence to be expressed similarly in newborns and in adults. SIT1 protein was not detectable in the small intestine of human newborns, in contrast to adults. The morphology of newborn intestinal mucosa proximal and distal to the obstruction was generally normal but a decreased proliferation rate was visualized distally of the atresia by lower levels of the mitosis marker Ki-67. The mRNA level of the 13 tested amino acid transporters and accessory proteins was nontheless similar, suggesting that the intestinal obstruction and interruption of amniotic fluid passage through the small intestinal lumen did not affect amino acid transporter expression.

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Additional indexing

Item Type:Journal Article, refereed, original work
Communities & Collections:04 Faculty of Medicine > University Hospital Zurich > Institute of Pathology and Molecular Pathology
04 Faculty of Medicine > Institute of Physiology
07 Faculty of Science > Institute of Physiology

04 Faculty of Medicine > Center for Integrative Human Physiology
04 Faculty of Medicine > University Children's Hospital Zurich > Clinic for Surgery
Dewey Decimal Classification:610 Medicine & health
Language:English
Date:30 August 2018
Deposited On:11 Dec 2018 14:37
Last Modified:12 Dec 2018 11:39
Publisher:American Physiological Society
ISSN:0193-1857
OA Status:Closed
Free access at:Publisher DOI. An embargo period may apply.
Publisher DOI:https://doi.org/10.1152/ajpgi.00318.2017
PubMed ID:30160974

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